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S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol = S-adenosyl-L-homocysteine + plastoquinol
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol = S-adenosyl-L-homocysteine + plastoquinol
(2)
-
S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol = S-adenosyl-L-homocysteine + plastoquinol
-
-
-
-
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
(1)
-
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
-
-
-
-
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
(3)
-
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol = S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
-
-
-
-
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S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol
S-adenosyl-L-homocysteine + plastoquinol
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol
S-adenosyl-L-homocysteine + plastoquinol
-
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol
S-adenosyl-L-homocysteine + plastoquinol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
Arachis hypogaea ssp. fastigiata
-
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
-
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
-
-
-
-
?
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
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S-adenosyl-L-methionine + 2-methyl-6-all-trans-nonaprenylbenzene-1,4-diol
S-adenosyl-L-homocysteine + plastoquinol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
S-adenosyl-L-methionine + 2-methyl-6-phytylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytylbenzene-1,4-diol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
S-adenosyl-L-methionine + 6-geranylgeranyl-2-methylbenzene-1,4-diol
S-adenosyl-L-homocysteine + 6-geranylgeranyl-2,3-dimethylbenzene-1,4-diol
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
Arachis hypogaea ssp. fastigiata
-
-
-
-
?
S-adenosyl-L-methionine + 2-methyl-6-phytyl-1,4-benzoquinol
S-adenosyl-L-homocysteine + 2,3-dimethyl-6-phytyl-1,4-benzoquinone
-
-
-
?
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malfunction
-
an SLL0418 partial knockout mutant accumulates beta-tocopherol with no effect in the overall tocopherol content of the cell
evolution
Arachis hypogaea ssp. fastigiata
-
the cultivated peanut Arachis hypogaea might originate via hybridization of Arachis duranensis (A-genome) and Arachis ipaensis (B-genome), followed by a rare spontaneous duplication of chromosomes, phylogenetic analysis
evolution
the cultivated peanut Arachis hypogaea might originate via hybridization of Arachis duranensis (A-genome) and Arachis ipaensis (B-genome), followed by a rare spontaneous duplication of chromosomes, phylogenetic analysis
evolution
the cultivated peanut Arachis hypogaea might originate via hybridization of Arachis duranensis (A-genome) and Arachis ipaensis (B-genome), followed by a rare spontaneous duplication of chromosomes, phylogenetic analysis
evolution
the cultivated peanut Arachis hypogaea might originate via hybridization of Arachis duranensis (A-genome) and Arachis ipaensis (B-genome), followed by a rare spontaneous duplication of chromosomes, phylogenetic analysis
evolution
the enzyme has the typical functional domains of an SAM enzyme
metabolism
Arachis hypogaea ssp. fastigiata
-
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase is one of the critical enzymes involved in vitamin E biosynthesis in plants. The enzyme can catalyze 2-methyl-6-phytyl-1,4-benzoquinol to generate 2,3-dimethyl-6-phytyl-1,4-benzoquinone. Both compounds are cyclized by tocopherol cyclase to yield delta- and gamma-tocopherol, respectively, which are subsequently further converted to beta- and alpha-tocopherol by gamma-tocopherol methyltransferase
metabolism
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase is one of the critical enzymes involved in vitamin E biosynthesis in plants. The enzyme can catalyze 2-methyl-6-phytyl-1,4-benzoquinol to generate 2,3-dimethyl-6-phytyl-1,4-benzoquinone. Both compounds are cyclized by tocopherol cyclase to yield delta- and gamma-tocopherol, respectively, which are subsequently further converted to beta- and alpha-tocopherol by gamma-tocopherol methyltransferase
metabolism
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase is one of the critical enzymes involved in vitamin E biosynthesis in plants. The enzyme can catalyze 2-methyl-6-phytyl-1,4-benzoquinol to generate 2,3-dimethyl-6-phytyl-1,4-benzoquinone. Both compounds are cyclized by tocopherol cyclase to yield delta- and gamma-tocopherol, respectively, which are subsequently further converted to beta- and alpha-tocopherol by gamma-tocopherol methyltransferase
metabolism
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase is one of the critical enzymes involved in vitamin E biosynthesis in plants. The enzyme can catalyze 2-methyl-6-phytyl-1,4-benzoquinol to generate 2,3-dimethyl-6-phytyl-1,4-benzoquinone. Both compounds are cyclized by tocopherol cyclase to yield delta- and gamma-tocopherol, respectively, which are subsequently further converted to beta- and alpha-tocopherol by gamma-tocopherol methyltransferase
metabolism
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase (MPBQ-MT) is a vital enzyme catalyzing a key methylation step in both alpha/gamma-tocopherol and plastoquinone biosynthetic pathway
metabolism
the enzyme is involved in regulation and biosynthesis of vitamin E in safflower
physiological function
-
the enzyme is involved in the biosynthesis of plastoquinol, as well as vitamin E (tocopherols and tocotrienols)
physiological function
an isoform MT-1 homozygous mutant is non-lethal and produces 24-45% alpha-tocopherol and 55-74% beta-tocopherol as compared to 96% alpha- and 4% beta-tocopherol for wild-type
physiological function
isoform MT-2 compensates for the loss of isoform MT-1 function, and the MT-2 mutation profoundly affects the synthesis of tocopherols without adversely affecting the synthesis of plastoquinone crucial for normal plant growth and development
physiological function
loss of enzymic activity results in accumulation of delta-tocopherol and decreased gamma-tocopherol content in the seed
physiological function
loss-of-function mutant seedlings are pale green and do not survive beyond 7 days in soil. Mutation does not affect embryo growth and development
physiological function
2-methyl-6-phytyl-1,4-benzoquinol methyltransferase (MPBQ-MT) is a vital enzyme catalyzing a key methylation step in both alpha/gamma-tocopherol and plastoquinone biosynthetic pathway. Overexpression of LsMT significantly increases plastoquinone (PQ) level in lettuce. The increase of tocopherol and plastoquinone levels by LsMT overexpression conduce to the improvement of plants' tolerance and photosynthesis under high light stress, by directing excessive light energy toward photosynthetic production rather than toward generation of more photooxidative damage. No significant difference in the expression levels of HPPD, HPT, TC and gamma-TMT is observed between wild-type and transgenic plants, indicating that overexpression of LsMT does not impact on the expression of other genes up- and downstream in the tocopherol biosynthetic pathway. Mechanism by which overexpression of MPBQ-MT leads to enhanced photosynthesis and tolerance to photodamage under high light in lettuce, overview
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IN37_SPIOL
344
1
38976
Swiss-Prot
Chloroplast (Reliability: 3)
BQMT1_ORYSJ
330
2
37439
Swiss-Prot
Chloroplast (Reliability: 5)
BQMT2_ORYSJ
348
1
38940
Swiss-Prot
Chloroplast (Reliability: 1)
BQMT_ARATH
338
1
37927
Swiss-Prot
Chloroplast (Reliability: 1)
BQMT_SYNY3
Synechocystis sp. (strain PCC 6803 / Kazusa)
318
1
34947
Swiss-Prot
-
A0A7C9D0K3_OPUST
332
2
37841
TrEMBL
Chloroplast (Reliability: 2)
A0A2Z6UNG5_MICAE
280
0
31245
TrEMBL
-
A0A2S0Q6R3_NODSP
272
0
31025
TrEMBL
-
A0A5A5RH78_MICAE
280
0
31206
TrEMBL
-
A0A161VDL9_CARTI
345
1
38942
TrEMBL
Chloroplast (Reliability: 4)
A0A2Z6V2V7_MICAE
336
1
37350
TrEMBL
-
A0A7U9SYA6_9FIRM
201
0
23056
TrEMBL
-
A0A2S6SRP3_9PROT
261
0
28973
TrEMBL
-
A0A2S6S9F6_9PROT
261
0
28973
TrEMBL
-
A0A2H5X8J5_9BACT
339
0
38495
TrEMBL
-
A0A7C8ZII4_OPUST
338
1
38011
TrEMBL
Chloroplast (Reliability: 5)
A0A2P6QPS5_ROSCH
318
0
35580
TrEMBL
Chloroplast (Reliability: 5)
A0A2W1JEQ3_9CYAN
Acaryochloris thomasi RCC1774
335
1
36871
TrEMBL
-
A0A2W1JJX6_9CYAN
Acaryochloris thomasi RCC1774
279
0
31388
TrEMBL
-
A0A387H628_9ACTN
282
0
30331
TrEMBL
-
A0A563W4K9_9CYAN
328
1
36615
TrEMBL
-
A0A6M1YQA2_9BACT
287
0
32924
TrEMBL
-
A0A7C9CMF6_OPUST
134
0
14766
TrEMBL
Chloroplast (Reliability: 2)
A0A498QV89_9MYCO
208
0
23214
TrEMBL
-
A0A2S8BNX2_9MYCO
190
0
20841
TrEMBL
-
A0A2P6QPX3_ROSCH
339
1
38127
TrEMBL
Chloroplast (Reliability: 5)
A0A7S8FDW5_9BACT
332
1
37209
TrEMBL
-
A0A445LNY4_GLYSO
342
1
38410
TrEMBL
Chloroplast (Reliability: 5)
A0A2G9G633_9LAMI
330
1
37536
TrEMBL
Chloroplast (Reliability: 5)
A0A5A5R3M1_MICAE
327
1
36175
TrEMBL
-
A0A445F8A7_GLYSO
295
0
33243
TrEMBL
other Location (Reliability: 5)
A0A7C8ZIC0_OPUST
338
1
37888
TrEMBL
Chloroplast (Reliability: 4)
G7ICQ0_MEDTR
347
1
39080
TrEMBL
Chloroplast (Reliability: 4)
A0A498Q8C3_9MYCO
210
0
23426
TrEMBL
-
A0A2S8BBB7_9MYCO
222
0
24113
TrEMBL
-
A0A7U9S729_9FIRM
211
0
24593
TrEMBL
-
A0A2H5WRT6_9BACT
337
0
37617
TrEMBL
-
A0A2P6PVN2_ROSCH
342
1
38360
TrEMBL
other Location (Reliability: 5)
A0A445F8A5_GLYSO
358
0
40038
TrEMBL
other Location (Reliability: 5)
A0A402DC54_MICAE
176
0
20345
TrEMBL
-
A0A0B2Q5X5_GLYSO
343
1
38765
TrEMBL
Chloroplast (Reliability: 2)
A0A5A5RMP4_MICAE
336
1
37293
TrEMBL
-
A0A445F8A3_GLYSO
322
0
36391
TrEMBL
other Location (Reliability: 5)
A0A2W1JUW9_9CYAN
Acaryochloris thomasi RCC1774
259
0
29156
TrEMBL
-
A0A5J4F860_MICAE
280
0
31321
TrEMBL
-
A0A7X5Q5N2_9BACT
283
0
32745
TrEMBL
-
A0A7C9CLN7_OPUST
108
0
12085
TrEMBL
Chloroplast (Reliability: 4)
A0A6M9BJU5_9ROSI
336
1
37866
TrEMBL
Chloroplast (Reliability: 4)
A0A402DG42_MICAE
336
1
37294
TrEMBL
-
A0A7W9BHF7_9RHOB
286
0
31407
TrEMBL
-
A0A2K8WKQ3_9CHRO
328
1
36286
TrEMBL
-
A0A679ILS9_VARPD
195
0
21851
TrEMBL
-
A0A072VMH0_MEDTR
340
1
38593
TrEMBL
Chloroplast (Reliability: 3)
A0A2G9FVX2_9LAMI
346
1
38833
TrEMBL
Chloroplast (Reliability: 5)
A0A498Q0F4_9MYCO
210
0
22709
TrEMBL
-
A0A7C8YKY3_OPUST
114
0
12647
TrEMBL
Chloroplast (Reliability: 3)
A0A5A5R7H5_MICAE
280
0
31303
TrEMBL
-
A0A5A5RNQ5_MICAE
266
0
30714
TrEMBL
-
A0A445F8G3_GLYSO
287
0
32220
TrEMBL
other Location (Reliability: 5)
A0A2J7W580_9BURK
195
0
22084
TrEMBL
-
A0A7C9CTH2_OPUST
105
0
11717
TrEMBL
Chloroplast (Reliability: 5)
A0A386A1K6_9ACTN
189
0
20703
TrEMBL
-
A0A7C8YL46_OPUST
114
0
12651
TrEMBL
Chloroplast (Reliability: 3)
A0A418PI92_VEIPA
249
0
28645
TrEMBL
-
A0A387H5B6_9ACTN
218
0
23890
TrEMBL
-
A0A2H6A6D0_9BACT
205
0
23822
TrEMBL
-
A0A6V8LQV1_9DELT
235
0
25644
TrEMBL
-
A0A7C9CR26_OPUST
114
0
12659
TrEMBL
Chloroplast (Reliability: 2)
A0A2H5YFJ6_9BACT
244
0
27558
TrEMBL
-
A0A2R8CE93_9RHOB
278
0
29906
TrEMBL
-
A0A498PXN2_9MYCO
210
0
22718
TrEMBL
-
A0A2H6AXX6_9BACT
274
0
29555
TrEMBL
-
A0A445LHP4_GLYSO
305
0
34252
TrEMBL
Chloroplast (Reliability: 2)
A0A445IHE2_GLYSO
342
1
38481
TrEMBL
Chloroplast (Reliability: 5)
A0A840DX29_9BACT
309
2
34840
TrEMBL
-
A0A5A5RZZ2_MICAE
280
0
31276
TrEMBL
-
A0A2R8CGF6_9RHOB
252
0
28560
TrEMBL
-
A0A445IP28_GLYSO
396
1
45100
TrEMBL
other Location (Reliability: 3)
A0A1Z4SFP2_9NOSO
303
0
34686
TrEMBL
-
A0A5A5S019_MICAE
336
1
37319
TrEMBL
-
A0A2H6A890_9BACT
237
0
28184
TrEMBL
-
A0A402DK14_MICAE
280
0
31112
TrEMBL
-
A0A7C8ZJB1_OPUST
154
1
17477
TrEMBL
other Location (Reliability: 2)
A0A5A5RPH0_MICAE
280
0
31209
TrEMBL
-
A0A5J4F7S0_MICAE
336
1
37385
TrEMBL
-
A0A5E6MAZ4_9BACT
244
0
27561
TrEMBL
-
D2D1G3_LACSA
337
0
38006
TrEMBL
-
G3F837_ARAHY
351
0
39861
TrEMBL
-
Q2XV86_HELAN
343
0
38399
TrEMBL
-
Q2XV89_HELAN
339
0
38234
TrEMBL
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
DNA and amino acid sequence determination and analysis, the coding region is 1014bp long, divided into 3 exons by 2 introns, sequence comparisons, recombinant overexpression of the enzyme in Lactuca sativa leaves by Agrobacterium-mediated transformation using the pCAMBIA 2300 vector, quantitative PCR expression analysis showing that the transcription level of LsMT in transgenic plants increases by 1.5-5folds compared to that in wild-type plants. The transformants contain a 60%-93% higher level of gamma-tocopherol and 41%-93% higher level of alpha-tocopherol compred to wild-type. Overexpression of LsMT causes an elevation of plastoquinone level in lettuce
expressed in Escherichia coli
-
gene CtMPBQ MT, DNA and amino acid sequence determination and analysis, sequence comparisons and phylogenetic tree, quantitative real-time PCR and RACE expression analysis
gene VTE3, cloning of full-length VTE3 cDNA (designated rVTE3-1 and -2) encoding the enzyme MPBQ MT, and of the full-length DNA of VTE3 (designated gVTE3-1 and -2), DNA and amino acid sequence determination and analysis, sequence comparisons, and polymorphism analysis, phylogenetic analysis
gene VTE3, cloning, DNA and amino acid sequence determination and analysis, sequence comparisons, and polymorphism analysis, phylogenetic analysis
gene VTE3, cloning, DNA and amino acid sequence determination and analysis, sequence comparisons, and polymorphism analysis, phylogenetic analysis
Arachis hypogaea ssp. fastigiata
-
gene VTE3, cloning, DNA and amino acid sequence determination and analysis, sequence comparisons, and polymorphism analysis, phylogenetic analysis
gene VTE3, cloning, DNA and amino acid sequence determination and analysis, sequence comparisons, and polymorphism analysis, phylogenetic analysis
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
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Shintani, D.K.; Cheng, Z.; DellaPenna, D.
The role of 2-methyl-6-phytylbenzoquinone methyltransferase in determining tocopherol composition in Synechocystis sp. PCC6803
FEBS Lett.
511
1-5
2002
Synechocystis sp.
brenda
Cheng, Z.; Sattler, S.; Maeda, H.; Sakuragi, Y.; Bryant, D.A.; DellaPenna, D.
Highly divergent methyltransferases catalyze a conserved reaction in tocopherol and plastoquinone synthesis in cyanobacteria and photosynthetic eukaryotes
Plant Cell
15
2343-2356
2003
Arabidopsis thaliana (Q9LY74)
brenda
Van Eenennaam, A.L.; Lincoln, K.; Durrett, T.P.; Valentin, H.E.; Shewmaker, C.K.; Thorne, G.M.; Jiang, J.; Baszis, S.R.; Levering, C.K.; Aasen, E.D.; Hao, M.; Stein, J.C.; Norris, S.R.; Last, R.L.
Engineering vitamin E content: from Arabidopsis mutant to soy oil
Plant Cell
15
3007-3019
2003
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