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Literature summary for 1.1.1.34 extracted from

  • Campos, N.; Arro, M.; Ferrer, A.; Boronat, A.
    Determination of 3-hydroxy-3-methylglutaryl CoA reductase activity in plants (2014), Methods Mol. Biol., 1153, 21-40.
    View publication on PubMed

Activating Compound

Activating Compound Comment Organism Structure
DTT
-
Vigna radiata var. radiata
DTT
-
Hordeum vulgare
DTT
-
Spinacia oleracea
DTT
-
Pisum sativum
DTT
-
Zea mays
DTT
-
Solanum tuberosum
DTT
-
Nicotiana tabacum
DTT
-
Glycine max
DTT
-
Lithospermum erythrorhizon
DTT
-
Arabidopsis thaliana
DTT
-
Picea abies
DTT
-
Brassica napus
DTT
-
Arachis hypogaea
DTT
-
Medicago sativa
DTT
-
Daucus carota
DTT
-
Solanum lycopersicum
DTT
-
Helianthus tuberosus
DTT
-
Raphanus sativus
DTT
-
Gossypium hirsutum
DTT
-
Ochromonas malhamensis
DTT
-
Hevea brasiliensis
DTT
-
Persea americana
DTT
-
Cucumis melo
DTT
-
Cannabis sativa
DTT
-
Sinapis alba
DTT
-
Ipomoea batatas
DTT
-
Malus domestica
DTT
-
Dunaliella salina
DTT
-
Euphorbia lathyris
DTT
-
Nepeta cataria
DTT
-
Pimpinella anisum
DTT
-
Parthenium argentatum
DTT
-
Gossypium barbadense
DTT
-
Artemisia annua
DTT
-
Nicotiana benthamiana
DTT
-
Stevia rebaudiana
DTT
-
Salvia miltiorrhiza
DTT
-
Taraxacum brevicorniculatum
DTT
-
Solanum virginianum
DTT
-
Bixa orellana
EDTA increases the apparent HMGR activity in sweet potato extracts Ipomoea batatas

Inhibitors

Inhibitors Comment Organism Structure
EDTA inhibits the subsequent reactions of the mevalonate pathway in Hevea latex Hevea brasiliensis

Localization

Localization Comment Organism GeneOntology No. Textmining
endoplasmic reticulum membrane
-
Vigna radiata var. radiata 5789
-
endoplasmic reticulum membrane
-
Hordeum vulgare 5789
-
endoplasmic reticulum membrane
-
Spinacia oleracea 5789
-
endoplasmic reticulum membrane
-
Pisum sativum 5789
-
endoplasmic reticulum membrane
-
Zea mays 5789
-
endoplasmic reticulum membrane
-
Solanum tuberosum 5789
-
endoplasmic reticulum membrane
-
Nicotiana tabacum 5789
-
endoplasmic reticulum membrane
-
Glycine max 5789
-
endoplasmic reticulum membrane
-
Lithospermum erythrorhizon 5789
-
endoplasmic reticulum membrane
-
Picea abies 5789
-
endoplasmic reticulum membrane
-
Brassica napus 5789
-
endoplasmic reticulum membrane
-
Arachis hypogaea 5789
-
endoplasmic reticulum membrane
-
Medicago sativa 5789
-
endoplasmic reticulum membrane
-
Daucus carota 5789
-
endoplasmic reticulum membrane
-
Solanum lycopersicum 5789
-
endoplasmic reticulum membrane
-
Helianthus tuberosus 5789
-
endoplasmic reticulum membrane
-
Raphanus sativus 5789
-
endoplasmic reticulum membrane
-
Gossypium hirsutum 5789
-
endoplasmic reticulum membrane
-
Ochromonas malhamensis 5789
-
endoplasmic reticulum membrane
-
Hevea brasiliensis 5789
-
endoplasmic reticulum membrane
-
Persea americana 5789
-
endoplasmic reticulum membrane
-
Cucumis melo 5789
-
endoplasmic reticulum membrane
-
Cannabis sativa 5789
-
endoplasmic reticulum membrane
-
Sinapis alba 5789
-
endoplasmic reticulum membrane
-
Ipomoea batatas 5789
-
endoplasmic reticulum membrane
-
Malus domestica 5789
-
endoplasmic reticulum membrane
-
Dunaliella salina 5789
-
endoplasmic reticulum membrane
-
Euphorbia lathyris 5789
-
endoplasmic reticulum membrane
-
Nepeta cataria 5789
-
endoplasmic reticulum membrane
-
Pimpinella anisum 5789
-
endoplasmic reticulum membrane
-
Parthenium argentatum 5789
-
endoplasmic reticulum membrane
-
Gossypium barbadense 5789
-
endoplasmic reticulum membrane
-
Artemisia annua 5789
-
endoplasmic reticulum membrane
-
Nicotiana benthamiana 5789
-
endoplasmic reticulum membrane
-
Stevia rebaudiana 5789
-
endoplasmic reticulum membrane
-
Salvia miltiorrhiza 5789
-
endoplasmic reticulum membrane
-
Taraxacum brevicorniculatum 5789
-
endoplasmic reticulum membrane
-
Solanum virginianum 5789
-
endoplasmic reticulum membrane
-
Bixa orellana 5789
-
endoplasmic reticulum membrane the enzyme spans the endoplasmic reticulum membrane twice. Both the N-terminal region and the highly conserved catalytic domain are in the cytosol, whereas only a short stretch of the protein is in the endoplasmic reticulum lumen. Insertion in the endoplasmic reticulum membrane is mediated by the signal recognition particle (SRP) that recognizes the two hydrophobic sequences which will become membrane spanning segments Arabidopsis thaliana 5789
-
microsome the HMGR activity is detected in the final microsomal pellet after ultracentrifugation Arabidopsis thaliana
-
-

Metals/Ions

Metals/Ions Comment Organism Structure
Ca2+ activates Vigna radiata var. radiata
Ca2+ activates Hordeum vulgare
Ca2+ activates Spinacia oleracea
Ca2+ activates Pisum sativum
Ca2+ activates Zea mays
Ca2+ activates Solanum tuberosum
Ca2+ activates Nicotiana tabacum
Ca2+ activates Glycine max
Ca2+ activates Lithospermum erythrorhizon
Ca2+ activates Arabidopsis thaliana
Ca2+ activates Picea abies
Ca2+ activates Brassica napus
Ca2+ activates Arachis hypogaea
Ca2+ activates Medicago sativa
Ca2+ activates Daucus carota
Ca2+ activates Solanum lycopersicum
Ca2+ activates Helianthus tuberosus
Ca2+ activates Raphanus sativus
Ca2+ activates Gossypium hirsutum
Ca2+ activates Ochromonas malhamensis
Ca2+ activates Hevea brasiliensis
Ca2+ activates Persea americana
Ca2+ activates Cucumis melo
Ca2+ activates Cannabis sativa
Ca2+ activates Sinapis alba
Ca2+ activates Ipomoea batatas
Ca2+ activates Malus domestica
Ca2+ activates Dunaliella salina
Ca2+ activates Euphorbia lathyris
Ca2+ activates Nepeta cataria
Ca2+ activates Pimpinella anisum
Ca2+ activates Parthenium argentatum
Ca2+ activates Gossypium barbadense
Ca2+ activates Artemisia annua
Ca2+ activates Nicotiana benthamiana
Ca2+ activates Stevia rebaudiana
Ca2+ activates Salvia miltiorrhiza
Ca2+ activates Taraxacum brevicorniculatum
Ca2+ activates Solanum virginianum
Ca2+ activates Bixa orellana

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
(R)-mevalonate + CoA + 2 NADP+ Vigna radiata var. radiata
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Hordeum vulgare
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Spinacia oleracea
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Pisum sativum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Zea mays
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Solanum tuberosum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Nicotiana tabacum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Glycine max
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Lithospermum erythrorhizon
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Arabidopsis thaliana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Picea abies
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Brassica napus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Arachis hypogaea
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Medicago sativa
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Daucus carota
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Solanum lycopersicum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Helianthus tuberosus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Raphanus sativus
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Gossypium hirsutum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Ochromonas malhamensis
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Hevea brasiliensis
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Persea americana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Cucumis melo
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Cannabis sativa
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Sinapis alba
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Ipomoea batatas
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Malus domestica
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Dunaliella salina
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Euphorbia lathyris
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Nepeta cataria
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Pimpinella anisum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Parthenium argentatum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Gossypium barbadense
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Artemisia annua
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Nicotiana benthamiana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Stevia rebaudiana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Salvia miltiorrhiza
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Taraxacum brevicorniculatum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Solanum virginianum
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+ Bixa orellana
-
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Vigna radiata var. radiata
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Hordeum vulgare
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Spinacia oleracea
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Pisum sativum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Zea mays
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum tuberosum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nicotiana tabacum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Glycine max
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Lithospermum erythrorhizon
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Arabidopsis thaliana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Picea abies
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Brassica napus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Arachis hypogaea
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Medicago sativa
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Daucus carota
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum lycopersicum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Helianthus tuberosus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Raphanus sativus
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Gossypium hirsutum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Ochromonas malhamensis
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Hevea brasiliensis
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Persea americana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Cucumis melo
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Cannabis sativa
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Sinapis alba
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Ipomoea batatas
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Malus domestica
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Dunaliella salina
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Euphorbia lathyris
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nepeta cataria
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Pimpinella anisum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Parthenium argentatum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Gossypium barbadense
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Artemisia annua
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Nicotiana benthamiana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Stevia rebaudiana
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Salvia miltiorrhiza
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Taraxacum brevicorniculatum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Solanum virginianum
-
(R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+ Bixa orellana
-
(R)-mevalonate + CoA + 2 NADP+
-
r

Organism

Organism UniProt Comment Textmining
Arabidopsis thaliana
-
-
-
Arachis hypogaea
-
-
-
Artemisia annua
-
-
-
Bixa orellana
-
-
-
Brassica napus
-
-
-
Cannabis sativa
-
-
-
Cucumis melo
-
-
-
Daucus carota
-
-
-
Dunaliella salina
-
-
-
Euphorbia lathyris
-
-
-
Glycine max
-
-
-
Gossypium barbadense
-
-
-
Gossypium hirsutum
-
-
-
Helianthus tuberosus
-
-
-
Hevea brasiliensis
-
-
-
Hordeum vulgare
-
-
-
Ipomoea batatas
-
-
-
Lithospermum erythrorhizon
-
-
-
Malus domestica
-
-
-
Medicago sativa
-
-
-
Nepeta cataria
-
-
-
Nicotiana benthamiana
-
-
-
Nicotiana tabacum
-
-
-
Ochromonas malhamensis
-
-
-
Parthenium argentatum
-
-
-
Persea americana
-
-
-
Picea abies
-
-
-
Pimpinella anisum
-
-
-
Pisum sativum
-
-
-
Raphanus sativus
-
-
-
Salvia miltiorrhiza
-
-
-
Sinapis alba
-
-
-
Solanum lycopersicum
-
-
-
Solanum tuberosum
-
-
-
Solanum virginianum
-
-
-
Spinacia oleracea
-
-
-
Stevia rebaudiana
-
-
-
Taraxacum brevicorniculatum
-
-
-
Vigna radiata var. radiata
-
-
-
Zea mays
-
-
-

Oxidation Stability

Oxidation Stability Organism
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Vigna radiata var. radiata
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Hordeum vulgare
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Spinacia oleracea
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Pisum sativum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Zea mays
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum tuberosum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nicotiana tabacum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Glycine max
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Lithospermum erythrorhizon
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Arabidopsis thaliana
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Picea abies
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Brassica napus
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Arachis hypogaea
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Medicago sativa
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Daucus carota
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum lycopersicum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Helianthus tuberosus
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Raphanus sativus
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Gossypium hirsutum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Ochromonas malhamensis
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Hevea brasiliensis
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Persea americana
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Cucumis melo
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Cannabis sativa
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Sinapis alba
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Ipomoea batatas
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Malus domestica
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Dunaliella salina
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Euphorbia lathyris
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nepeta cataria
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Pimpinella anisum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Parthenium argentatum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Gossypium barbadense
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Artemisia annua
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Nicotiana benthamiana
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Stevia rebaudiana
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Salvia miltiorrhiza
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Taraxacum brevicorniculatum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Solanum virginianum
the catalytic activity of plant HMGR depends on free thiol groups and a reducing agent is used to protect their reduced state. DTT is better than 2-mercaptoethanol or glutathione for this purpose Bixa orellana

Posttranslational Modification

Posttranslational Modification Comment Organism
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Vigna radiata var. radiata
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Hordeum vulgare
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Spinacia oleracea
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Pisum sativum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Zea mays
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum tuberosum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nicotiana tabacum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Glycine max
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Lithospermum erythrorhizon
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Arabidopsis thaliana
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Picea abies
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Brassica napus
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Arachis hypogaea
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Medicago sativa
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Daucus carota
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum lycopersicum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Helianthus tuberosus
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Raphanus sativus
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Gossypium hirsutum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Ochromonas malhamensis
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Hevea brasiliensis
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Persea americana
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Cucumis melo
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Cannabis sativa
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Sinapis alba
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Ipomoea batatas
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Malus domestica
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Dunaliella salina
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Euphorbia lathyris
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nepeta cataria
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Pimpinella anisum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Parthenium argentatum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Gossypium barbadense
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Artemisia annua
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Nicotiana benthamiana
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Stevia rebaudiana
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Salvia miltiorrhiza
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Taraxacum brevicorniculatum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Solanum virginianum
additional information protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant enzyme HMGR is posttranslationally modulated Bixa orellana
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Vigna radiata var. radiata
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Hordeum vulgare
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Spinacia oleracea
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Pisum sativum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Zea mays
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum tuberosum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nicotiana tabacum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Glycine max
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Lithospermum erythrorhizon
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Arabidopsis thaliana
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Picea abies
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Brassica napus
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Arachis hypogaea
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Medicago sativa
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Daucus carota
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum lycopersicum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Helianthus tuberosus
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Raphanus sativus
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Gossypium hirsutum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Ochromonas malhamensis
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Hevea brasiliensis
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Persea americana
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Cucumis melo
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Cannabis sativa
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Sinapis alba
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Ipomoea batatas
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Malus domestica
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Dunaliella salina
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Euphorbia lathyris
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nepeta cataria
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Pimpinella anisum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Parthenium argentatum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Gossypium barbadense
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Artemisia annua
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Nicotiana benthamiana
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Stevia rebaudiana
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Salvia miltiorrhiza
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Taraxacum brevicorniculatum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Solanum virginianum
phosphoprotein phosphorylation at a conserved site of the catalytic domain of enzyme HMGR Bixa orellana

Purification (Commentary)

Purification (Comment) Organism
native enzyme by ultracentrifugation Arabidopsis thaliana

Source Tissue

Source Tissue Comment Organism Textmining
bark
-
Parthenium argentatum
-
BY-2 cell
-
Nicotiana tabacum
-
callus
-
Nicotiana tabacum
-
callus
-
Picea abies
-
callus
-
Nepeta cataria
-
callus
-
Bixa orellana
-
cell culture
-
Nicotiana tabacum
-
cell culture
-
Glycine max
-
cell culture
-
Lithospermum erythrorhizon
-
cell culture
-
Picea abies
-
cell culture
-
Daucus carota
-
cell culture
-
Ochromonas malhamensis
-
cell culture
-
Dunaliella salina
-
cell culture
-
Pimpinella anisum
-
cell suspension culture
-
Solanum virginianum
-
cotyledon
-
Glycine max
-
exocarp
-
Malus domestica
-
fruit
-
Solanum lycopersicum
-
fruit
-
Cucumis melo
-
hairy root
-
Lithospermum erythrorhizon
-
hairy root
-
Medicago sativa
-
hairy root
-
Salvia miltiorrhiza
-
hypocotyl
-
Glycine max
-
KY-14 cell
-
Nicotiana tabacum
-
latex
-
Hevea brasiliensis
-
latex
-
Euphorbia lathyris
-
latex
-
Taraxacum brevicorniculatum
-
leaf
-
Vigna radiata var. radiata
-
leaf
-
Spinacia oleracea
-
leaf
-
Picea abies
-
leaf
-
Solanum lycopersicum
-
leaf
-
Cannabis sativa
-
leaf
-
Euphorbia lathyris
-
leaf
-
Nepeta cataria
-
leaf
-
Artemisia annua
-
leaf
-
Nicotiana benthamiana
-
leaf
-
Stevia rebaudiana
-
leaf
-
Bixa orellana
-
leaf expanded Nicotiana tabacum
-
leaf fully expanded Parthenium argentatum
-
leaf rosette leaves and fully expanded leaves Arabidopsis thaliana
-
mesocarp
-
Persea americana
-
pericarp
-
Cucumis melo
-
root
-
Glycine max
-
root
-
Ipomoea batatas
-
seed
-
Arabidopsis thaliana
-
seed
-
Persea americana
-
seed developing Nicotiana tabacum
-
seed developing Brassica napus
-
seedling
-
Hordeum vulgare
-
seedling
-
Picea abies
-
seedling
-
Raphanus sativus
-
seedling etiolated Zea mays
-
seedling green Arachis hypogaea
-
seedling green Sinapis alba
-
seedling aerial part and full seedling Nicotiana tabacum
-
seedling apical part Glycine max
-
seedling etiolated and green seedlings Pisum sativum
-
seedling green seedling, aerial part and root Arabidopsis thaliana
-
stele
-
Gossypium hirsutum
-
stele
-
Gossypium barbadense
-
stem
-
Euphorbia lathyris
-
stem lower Parthenium argentatum
-
tuber
-
Solanum tuberosum
-
tuber explants Helianthus tuberosus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(R)-mevalonate + CoA + 2 NADP+
-
Vigna radiata var. radiata (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Hordeum vulgare (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Spinacia oleracea (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Pisum sativum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Zea mays (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Solanum tuberosum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Nicotiana tabacum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Glycine max (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Lithospermum erythrorhizon (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Arabidopsis thaliana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Picea abies (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Brassica napus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Arachis hypogaea (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Medicago sativa (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Daucus carota (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Solanum lycopersicum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Helianthus tuberosus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Raphanus sativus (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Gossypium hirsutum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Ochromonas malhamensis (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Hevea brasiliensis (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Persea americana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Cucumis melo (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Cannabis sativa (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Sinapis alba (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Ipomoea batatas (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Malus domestica (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Dunaliella salina (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Euphorbia lathyris (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Nepeta cataria (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Pimpinella anisum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Parthenium argentatum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Gossypium barbadense (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Artemisia annua (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Nicotiana benthamiana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Stevia rebaudiana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Salvia miltiorrhiza (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Taraxacum brevicorniculatum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Solanum virginianum (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(R)-mevalonate + CoA + 2 NADP+
-
Bixa orellana (S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Vigna radiata var. radiata (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Hordeum vulgare (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Spinacia oleracea (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Pisum sativum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Zea mays (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum tuberosum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nicotiana tabacum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Glycine max (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Lithospermum erythrorhizon (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Arabidopsis thaliana (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Picea abies (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Brassica napus (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Arachis hypogaea (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Medicago sativa (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Daucus carota (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum lycopersicum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Helianthus tuberosus (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Raphanus sativus (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Gossypium hirsutum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Ochromonas malhamensis (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Hevea brasiliensis (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Persea americana (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Cucumis melo (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Cannabis sativa (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Sinapis alba (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Ipomoea batatas (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Malus domestica (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Dunaliella salina (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Euphorbia lathyris (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nepeta cataria (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Pimpinella anisum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Parthenium argentatum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Gossypium barbadense (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Artemisia annua (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Nicotiana benthamiana (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Stevia rebaudiana (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Salvia miltiorrhiza (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Taraxacum brevicorniculatum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Solanum virginianum (R)-mevalonate + CoA + 2 NADP+
-
r
(S)-3-hydroxy-3-methylglutaryl-CoA + 2 NADPH + 2 H+
-
Bixa orellana (R)-mevalonate + CoA + 2 NADP+
-
r
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Vigna radiata var. radiata ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Hordeum vulgare ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Spinacia oleracea ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Pisum sativum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Zea mays ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum tuberosum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nicotiana tabacum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Glycine max ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Lithospermum erythrorhizon ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Arabidopsis thaliana ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Picea abies ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Brassica napus ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Arachis hypogaea ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Medicago sativa ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Daucus carota ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum lycopersicum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Helianthus tuberosus ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Raphanus sativus ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Gossypium hirsutum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Ochromonas malhamensis ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Hevea brasiliensis ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Persea americana ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Cucumis melo ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Cannabis sativa ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Sinapis alba ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Ipomoea batatas ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Malus domestica ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Dunaliella salina ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Euphorbia lathyris ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nepeta cataria ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Pimpinella anisum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Parthenium argentatum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Gossypium barbadense ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Artemisia annua ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Nicotiana benthamiana ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Stevia rebaudiana ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Salvia miltiorrhiza ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Taraxacum brevicorniculatum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Solanum virginianum ?
-
?
additional information assay method development: the eukaryotic enzyme HMGR catalyzes the stereospecific NADPH-dependent reductive deacylation of (3S)-HMG-CoA to (3R)-mevalonic acid. The HMGR assay reaction product is subsequently converted to mevalonolactone by heating in acid medium. The heat treatment also hydrolyses (S)-3-hydroxy-3-methylglutaryl-CoA to free hydroxy-3-methylglutaric acid and CoASH, analysis by TLC Bixa orellana ?
-
?

Subunits

Subunits Comment Organism
? x * 63000-70000 Vigna radiata var. radiata
? x * 63000-70000 Hordeum vulgare
? x * 63000-70000 Spinacia oleracea
? x * 63000-70000 Pisum sativum
? x * 63000-70000 Zea mays
? x * 63000-70000 Solanum tuberosum
? x * 63000-70000 Nicotiana tabacum
? x * 63000-70000 Glycine max
? x * 63000-70000 Lithospermum erythrorhizon
? x * 63000-70000 Arabidopsis thaliana
? x * 63000-70000 Picea abies
? x * 63000-70000 Brassica napus
? x * 63000-70000 Arachis hypogaea
? x * 63000-70000 Medicago sativa
? x * 63000-70000 Daucus carota
? x * 63000-70000 Solanum lycopersicum
? x * 63000-70000 Helianthus tuberosus
? x * 63000-70000 Raphanus sativus
? x * 63000-70000 Gossypium hirsutum
? x * 63000-70000 Ochromonas malhamensis
? x * 63000-70000 Hevea brasiliensis
? x * 63000-70000 Persea americana
? x * 63000-70000 Cucumis melo
? x * 63000-70000 Cannabis sativa
? x * 63000-70000 Sinapis alba
? x * 63000-70000 Ipomoea batatas
? x * 63000-70000 Malus domestica
? x * 63000-70000 Dunaliella salina
? x * 63000-70000 Euphorbia lathyris
? x * 63000-70000 Nepeta cataria
? x * 63000-70000 Pimpinella anisum
? x * 63000-70000 Parthenium argentatum
? x * 63000-70000 Gossypium barbadense
? x * 63000-70000 Artemisia annua
? x * 63000-70000 Nicotiana benthamiana
? x * 63000-70000 Stevia rebaudiana
? x * 63000-70000 Salvia miltiorrhiza
? x * 63000-70000 Taraxacum brevicorniculatum
? x * 63000-70000 Solanum virginianum
? x * 63000-70000 Bixa orellana

Synonyms

Synonyms Comment Organism
3-hydroxy-3-methylglutaryl CoA reductase
-
Vigna radiata var. radiata
3-hydroxy-3-methylglutaryl CoA reductase
-
Hordeum vulgare
3-hydroxy-3-methylglutaryl CoA reductase
-
Spinacia oleracea
3-hydroxy-3-methylglutaryl CoA reductase
-
Pisum sativum
3-hydroxy-3-methylglutaryl CoA reductase
-
Zea mays
3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum tuberosum
3-hydroxy-3-methylglutaryl CoA reductase
-
Nicotiana tabacum
3-hydroxy-3-methylglutaryl CoA reductase
-
Glycine max
3-hydroxy-3-methylglutaryl CoA reductase
-
Lithospermum erythrorhizon
3-hydroxy-3-methylglutaryl CoA reductase
-
Arabidopsis thaliana
3-hydroxy-3-methylglutaryl CoA reductase
-
Picea abies
3-hydroxy-3-methylglutaryl CoA reductase
-
Brassica napus
3-hydroxy-3-methylglutaryl CoA reductase
-
Arachis hypogaea
3-hydroxy-3-methylglutaryl CoA reductase
-
Medicago sativa
3-hydroxy-3-methylglutaryl CoA reductase
-
Daucus carota
3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum lycopersicum
3-hydroxy-3-methylglutaryl CoA reductase
-
Helianthus tuberosus
3-hydroxy-3-methylglutaryl CoA reductase
-
Raphanus sativus
3-hydroxy-3-methylglutaryl CoA reductase
-
Gossypium hirsutum
3-hydroxy-3-methylglutaryl CoA reductase
-
Ochromonas malhamensis
3-hydroxy-3-methylglutaryl CoA reductase
-
Hevea brasiliensis
3-hydroxy-3-methylglutaryl CoA reductase
-
Persea americana
3-hydroxy-3-methylglutaryl CoA reductase
-
Cucumis melo
3-hydroxy-3-methylglutaryl CoA reductase
-
Cannabis sativa
3-hydroxy-3-methylglutaryl CoA reductase
-
Sinapis alba
3-hydroxy-3-methylglutaryl CoA reductase
-
Ipomoea batatas
3-hydroxy-3-methylglutaryl CoA reductase
-
Malus domestica
3-hydroxy-3-methylglutaryl CoA reductase
-
Dunaliella salina
3-hydroxy-3-methylglutaryl CoA reductase
-
Euphorbia lathyris
3-hydroxy-3-methylglutaryl CoA reductase
-
Nepeta cataria
3-hydroxy-3-methylglutaryl CoA reductase
-
Pimpinella anisum
3-hydroxy-3-methylglutaryl CoA reductase
-
Parthenium argentatum
3-hydroxy-3-methylglutaryl CoA reductase
-
Gossypium barbadense
3-hydroxy-3-methylglutaryl CoA reductase
-
Artemisia annua
3-hydroxy-3-methylglutaryl CoA reductase
-
Nicotiana benthamiana
3-hydroxy-3-methylglutaryl CoA reductase
-
Stevia rebaudiana
3-hydroxy-3-methylglutaryl CoA reductase
-
Salvia miltiorrhiza
3-hydroxy-3-methylglutaryl CoA reductase
-
Taraxacum brevicorniculatum
3-hydroxy-3-methylglutaryl CoA reductase
-
Solanum virginianum
3-hydroxy-3-methylglutaryl CoA reductase
-
Bixa orellana
HMGR
-
Vigna radiata var. radiata
HMGR
-
Hordeum vulgare
HMGR
-
Spinacia oleracea
HMGR
-
Pisum sativum
HMGR
-
Zea mays
HMGR
-
Solanum tuberosum
HMGR
-
Nicotiana tabacum
HMGR
-
Glycine max
HMGR
-
Lithospermum erythrorhizon
HMGR
-
Arabidopsis thaliana
HMGR
-
Picea abies
HMGR
-
Brassica napus
HMGR
-
Arachis hypogaea
HMGR
-
Medicago sativa
HMGR
-
Daucus carota
HMGR
-
Solanum lycopersicum
HMGR
-
Helianthus tuberosus
HMGR
-
Raphanus sativus
HMGR
-
Gossypium hirsutum
HMGR
-
Ochromonas malhamensis
HMGR
-
Hevea brasiliensis
HMGR
-
Persea americana
HMGR
-
Cucumis melo
HMGR
-
Cannabis sativa
HMGR
-
Sinapis alba
HMGR
-
Ipomoea batatas
HMGR
-
Malus domestica
HMGR
-
Dunaliella salina
HMGR
-
Euphorbia lathyris
HMGR
-
Nepeta cataria
HMGR
-
Pimpinella anisum
HMGR
-
Parthenium argentatum
HMGR
-
Gossypium barbadense
HMGR
-
Artemisia annua
HMGR
-
Nicotiana benthamiana
HMGR
-
Stevia rebaudiana
HMGR
-
Salvia miltiorrhiza
HMGR
-
Taraxacum brevicorniculatum
HMGR
-
Solanum virginianum
HMGR
-
Bixa orellana

Temperature Optimum [°C]

Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
37
-
assay at Vigna radiata var. radiata
37
-
assay at Hordeum vulgare
37
-
assay at Spinacia oleracea
37
-
assay at Pisum sativum
37
-
assay at Zea mays
37
-
assay at Solanum tuberosum
37
-
assay at Nicotiana tabacum
37
-
assay at Glycine max
37
-
assay at Lithospermum erythrorhizon
37
-
assay at Arabidopsis thaliana
37
-
assay at Picea abies
37
-
assay at Brassica napus
37
-
assay at Arachis hypogaea
37
-
assay at Medicago sativa
37
-
assay at Daucus carota
37
-
assay at Solanum lycopersicum
37
-
assay at Helianthus tuberosus
37
-
assay at Raphanus sativus
37
-
assay at Gossypium hirsutum
37
-
assay at Ochromonas malhamensis
37
-
assay at Hevea brasiliensis
37
-
assay at Persea americana
37
-
assay at Cucumis melo
37
-
assay at Cannabis sativa
37
-
assay at Sinapis alba
37
-
assay at Ipomoea batatas
37
-
assay at Malus domestica
37
-
assay at Dunaliella salina
37
-
assay at Euphorbia lathyris
37
-
assay at Nepeta cataria
37
-
assay at Pimpinella anisum
37
-
assay at Parthenium argentatum
37
-
assay at Gossypium barbadense
37
-
assay at Artemisia annua
37
-
assay at Nicotiana benthamiana
37
-
assay at Stevia rebaudiana
37
-
assay at Salvia miltiorrhiza
37
-
assay at Taraxacum brevicorniculatum
37
-
assay at Solanum virginianum
37
-
assay at Bixa orellana

pH Optimum

pH Optimum Minimum pH Optimum Maximum Comment Organism
additional information
-
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.0 and pH 75, respectively Parthenium argentatum
additional information
-
two pH optima are found, corresponding to HMGR from the heavy or the light fractions: pH 7.9 and pH 6.9, respectively Pisum sativum
6.8
-
-
Hevea brasiliensis
6.9
-
-
Pisum sativum
7
-
-
Parthenium argentatum
7.2
-
assay at Vigna radiata var. radiata
7.2
-
assay at Hordeum vulgare
7.2
-
assay at Spinacia oleracea
7.2
-
assay at Zea mays
7.2
-
assay at Solanum tuberosum
7.2
-
assay at Nicotiana tabacum
7.2
-
assay at Glycine max
7.2
-
assay at Lithospermum erythrorhizon
7.2
-
assay at Arabidopsis thaliana
7.2
-
assay at Picea abies
7.2
-
assay at Brassica napus
7.2
-
assay at Arachis hypogaea
7.2
-
assay at Medicago sativa
7.2
-
assay at Daucus carota
7.2
-
assay at Solanum lycopersicum
7.2
-
assay at Helianthus tuberosus
7.2
-
assay at Gossypium hirsutum
7.2
-
assay at Ochromonas malhamensis
7.2
-
assay at Persea americana
7.2
-
assay at Cucumis melo
7.2
-
assay at Cannabis sativa
7.2
-
assay at Sinapis alba
7.2
-
assay at Ipomoea batatas
7.2
-
assay at Malus domestica
7.2
-
assay at Dunaliella salina
7.2
-
assay at Euphorbia lathyris
7.2
-
assay at Nepeta cataria
7.2
-
assay at Pimpinella anisum
7.2
-
assay at Gossypium barbadense
7.2
-
assay at Artemisia annua
7.2
-
assay at Nicotiana benthamiana
7.2
-
assay at Stevia rebaudiana
7.2
-
assay at Salvia miltiorrhiza
7.2
-
assay at Taraxacum brevicorniculatum
7.2
-
assay at Solanum virginianum
7.2
-
assay at Bixa orellana
7.3 7.5
-
Raphanus sativus
7.5
-
-
Parthenium argentatum
7.9
-
-
Pisum sativum

Cofactor

Cofactor Comment Organism Structure
NADP+
-
Vigna radiata var. radiata
NADP+
-
Hordeum vulgare
NADP+
-
Spinacia oleracea
NADP+
-
Pisum sativum
NADP+
-
Zea mays
NADP+
-
Solanum tuberosum
NADP+
-
Nicotiana tabacum
NADP+
-
Glycine max
NADP+
-
Lithospermum erythrorhizon
NADP+
-
Arabidopsis thaliana
NADP+
-
Picea abies
NADP+
-
Brassica napus
NADP+
-
Arachis hypogaea
NADP+
-
Medicago sativa
NADP+
-
Daucus carota
NADP+
-
Solanum lycopersicum
NADP+
-
Helianthus tuberosus
NADP+
-
Raphanus sativus
NADP+
-
Gossypium hirsutum
NADP+
-
Ochromonas malhamensis
NADP+
-
Hevea brasiliensis
NADP+
-
Persea americana
NADP+
-
Cucumis melo
NADP+
-
Cannabis sativa
NADP+
-
Sinapis alba
NADP+
-
Ipomoea batatas
NADP+
-
Malus domestica
NADP+
-
Dunaliella salina
NADP+
-
Euphorbia lathyris
NADP+
-
Nepeta cataria
NADP+
-
Pimpinella anisum
NADP+
-
Parthenium argentatum
NADP+
-
Gossypium barbadense
NADP+
-
Artemisia annua
NADP+
-
Nicotiana benthamiana
NADP+
-
Stevia rebaudiana
NADP+
-
Salvia miltiorrhiza
NADP+
-
Taraxacum brevicorniculatum
NADP+
-
Solanum virginianum
NADP+
-
Bixa orellana
NADPH
-
Vigna radiata var. radiata
NADPH
-
Hordeum vulgare
NADPH
-
Spinacia oleracea
NADPH
-
Pisum sativum
NADPH
-
Zea mays
NADPH
-
Solanum tuberosum
NADPH
-
Nicotiana tabacum
NADPH
-
Glycine max
NADPH
-
Lithospermum erythrorhizon
NADPH
-
Arabidopsis thaliana
NADPH
-
Picea abies
NADPH
-
Brassica napus
NADPH
-
Arachis hypogaea
NADPH
-
Medicago sativa
NADPH
-
Daucus carota
NADPH
-
Solanum lycopersicum
NADPH
-
Helianthus tuberosus
NADPH
-
Raphanus sativus
NADPH
-
Gossypium hirsutum
NADPH
-
Ochromonas malhamensis
NADPH
-
Hevea brasiliensis
NADPH
-
Persea americana
NADPH
-
Cucumis melo
NADPH
-
Cannabis sativa
NADPH
-
Sinapis alba
NADPH
-
Ipomoea batatas
NADPH
-
Malus domestica
NADPH
-
Dunaliella salina
NADPH
-
Euphorbia lathyris
NADPH
-
Nepeta cataria
NADPH
-
Pimpinella anisum
NADPH
-
Parthenium argentatum
NADPH
-
Gossypium barbadense
NADPH
-
Artemisia annua
NADPH
-
Nicotiana benthamiana
NADPH
-
Stevia rebaudiana
NADPH
-
Salvia miltiorrhiza
NADPH
-
Taraxacum brevicorniculatum
NADPH
-
Solanum virginianum
NADPH
-
Bixa orellana

General Information

General Information Comment Organism
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Vigna radiata var. radiata
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Hordeum vulgare
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Spinacia oleracea
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Pisum sativum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Zea mays
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum tuberosum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nicotiana tabacum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Glycine max
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Lithospermum erythrorhizon
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Arabidopsis thaliana
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Picea abies
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Brassica napus
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Arachis hypogaea
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Medicago sativa
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Daucus carota
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum lycopersicum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Helianthus tuberosus
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Raphanus sativus
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Gossypium hirsutum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Ochromonas malhamensis
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Hevea brasiliensis
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Persea americana
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Cucumis melo
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Cannabis sativa
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Sinapis alba
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Ipomoea batatas
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Malus domestica
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Dunaliella salina
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Euphorbia lathyris
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nepeta cataria
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Pimpinella anisum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Parthenium argentatum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Gossypium barbadense
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Artemisia annua
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Nicotiana benthamiana
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Stevia rebaudiana
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Salvia miltiorrhiza
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Taraxacum brevicorniculatum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Solanum virginianum
evolution not only the sequence of the catalytic domain of enzyme HMGR but also its quaternary structure is conserved in high eukaryotes. HMGR is encoded by a multigene family Bixa orellana
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Vigna radiata var. radiata
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Hordeum vulgare
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Spinacia oleracea
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Pisum sativum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Zea mays
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum tuberosum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nicotiana tabacum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Glycine max
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Lithospermum erythrorhizon
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Arabidopsis thaliana
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Picea abies
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Brassica napus
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Arachis hypogaea
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Medicago sativa
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Daucus carota
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum lycopersicum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Helianthus tuberosus
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Raphanus sativus
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Gossypium hirsutum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Ochromonas malhamensis
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Hevea brasiliensis
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Persea americana
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Cucumis melo
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Cannabis sativa
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Sinapis alba
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Ipomoea batatas
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Malus domestica
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Dunaliella salina
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Euphorbia lathyris
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nepeta cataria
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Pimpinella anisum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Parthenium argentatum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Gossypium barbadense
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Artemisia annua
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Nicotiana benthamiana
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Stevia rebaudiana
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Salvia miltiorrhiza
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Taraxacum brevicorniculatum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Solanum virginianum
metabolism HMG-CoA reductase (HMGR) catalyzes the first committed step of the mevalonate pathway for isoprenoid biosynthesis, consisting in the NADPH-mediated reductive deacylation of HMG-CoA to mevalonic acid. The enzyme exerts a key regulatory role on the flux of the mevalonate pathway in all eukaryotes Bixa orellana
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Vigna radiata var. radiata
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Hordeum vulgare
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Spinacia oleracea
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Pisum sativum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Zea mays
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum tuberosum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nicotiana tabacum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Glycine max
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Lithospermum erythrorhizon
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Picea abies
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Brassica napus
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Arachis hypogaea
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Medicago sativa
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Daucus carota
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum lycopersicum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Helianthus tuberosus
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Raphanus sativus
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Gossypium hirsutum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Ochromonas malhamensis
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Hevea brasiliensis
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Persea americana
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Cucumis melo
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Cannabis sativa
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Sinapis alba
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Ipomoea batatas
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Malus domestica
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Dunaliella salina
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Euphorbia lathyris
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nepeta cataria
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Pimpinella anisum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Parthenium argentatum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Gossypium barbadense
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Artemisia annua
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Nicotiana benthamiana
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Stevia rebaudiana
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Salvia miltiorrhiza
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Taraxacum brevicorniculatum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Solanum virginianum
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated Bixa orellana
physiological function in plants, the enzyme is critical not only for normal growth and development but also for the adaptation to diverse challenging conditions. Plant HMGR is controlled at transcriptional and posttranslational levels in response to many developmental and environmental signals such as phytohormones, calcium, calmodulin, light, wounding, elicitor treatment, and pathogen attack. Protein degradation, inhibition, or activation by calcium, and phosphorylation at a conserved site of the catalytic domain are mechanisms by which plant HMGR is posttranslationally modulated. Protein phosphatase 2A (PP2A) is both a transcriptional and a posttranslational regulator of HMGR in Arabidopsis thaliana Arabidopsis thaliana