6.3.3.2: 5-formyltetrahydrofolate cyclo-ligase
This is an abbreviated version!
For detailed information about 5-formyltetrahydrofolate cyclo-ligase, go to the full flat file.
Word Map on EC 6.3.3.2
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6.3.3.2
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mthfr
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methylenetetrahydrofolate
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one-carbon
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homocysteine
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folate-dependent
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slc19a1
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10-formyltetrahydrofolate
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trifunctional
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cyclohydrolase
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5,10-methylenetetrahydrofolate
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remethylation
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folate-mediated
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folate-related
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1-carbon
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megaloblastic
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periconceptional
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folate-metabolizing
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analysis
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pharmacology
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medicine
- 6.3.3.2
- mthfr
- methylenetetrahydrofolate
-
one-carbon
- homocysteine
-
folate-dependent
-
slc19a1
- 10-formyltetrahydrofolate
-
trifunctional
-
cyclohydrolase
- 5,10-methylenetetrahydrofolate
-
remethylation
-
folate-mediated
-
folate-related
-
1-carbon
-
megaloblastic
-
periconceptional
-
folate-metabolizing
- analysis
- pharmacology
- medicine
Reaction
Synonyms
5,10-methenyl-tetrahydrofolate synthetase, 5,10-Methenyltetrahydrofolate synthetase, 5,10-Methenyltetrahydropteroylglutamate synthetase, 5-CHO-THF cycloligase, 5-FCL, 5-Formyltetrahydrofolate cyclodehydrase, CH+-THF synthetase, Fau1p, Formyltetrahydrofolic cyclodehydrase, Methenyl THFS, Methenyl-THF synthetase, Methenyltetrahydrofolate synthetase, More, MTHFD1, MTHFS, N5-Formyltetrahydrofolic acid cyclodehydrase, Synthetase, methenyltetrahydrofolate, ygfA
ECTree
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Engineering
Engineering on EC 6.3.3.2 - 5-formyltetrahydrofolate cyclo-ligase
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D154A
site-directed mutagenesis, the mutant shows 0.9% of the wild-type catalytic activity
E61A
site-directed mutagenesis, the mutant shows 8.6% of the wild-type catalytic activity
F55A
site-directed mutagenesis, the mutant shows 53.6% of the wild-type catalytic activity
F85A
site-directed mutagenesis, the mutant shows 72.3% of the wild-type catalytic activity
K10A
site-directed mutagenesis, the mutant shows 7.5% of the wild-type catalytic activity
K150A
site-directed mutagenesis, the mutant shows wild-type catalytic activity
M58A
site-directed mutagenesis, the mutant shows 121.6% of the wild-type catalytic activity
M90A
site-directed mutagenesis, the mutant shows 49.2% of the wild-type catalytic activity
R145A
site-directed mutagenesis, the mutant shows 2.3% of the wild-type catalytic activity
R148A
site-directed mutagenesis, the mutant shows 30.7% of the wild-type catalytic activity
R14A
site-directed mutagenesis, the mutant shows 12.9% of the wild-type catalytic activity
W109A
site-directed mutagenesis, the mutant shows 39.7% of the wild-type catalytic activity
Y152A
site-directed mutagenesis, the mutant shows 24.9% of the wild-type catalytic activity
Y153A
site-directed mutagenesis, the mutant shows 3.2% of the wild-type catalytic activity
Y83A
site-directed mutagenesis, the mutant shows wild-type catalytic activity
D151A
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the mutant shows increased turnover number compared to the wild type enzyme
D81A
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the mutant shows reduced turnover number compared to the wild type enzyme
K120A
K3A
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the mutant shows strongly reduced turnover number compared to the wild type enzyme
K3D/D151K
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the mutant shows strongly reduced turnover number compared to the wild type enzyme
R125A
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the mutant shows reduced turnover number compared to the wild type enzyme
R7A
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the mutant shows severely reduced turnover number compared to the wild type enzyme
W153A
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the mutant shows reduced turnover number compared to the wild type enzyme
additional information
the mutant shows increased Km and turnover number values for ATP and 5-formyltetrahydrofolate compared to the wild type enzyme
K120A
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the mutant shows increased turnover number compared to the wild type enzyme
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insertional mutation of the gene encoding the enzyme, At5g13050 or 28D07, reduces the growth rate of the mutant plants by 20% and delayes flowering by 1 week, and leads to accumulation of 5-formyltetrahydrofolate and glycine in leaves under photorespiratory conditions, effect of 5-formyltetrahydrofolate feeding, overview
additional information
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truncation mutant comprising residues 6-202 of the enzyme is fully active and soluble
additional information
splice site mutation (c.1674G>A) identified in a patient suffering MTHFD1 deficiency leads to exon skipping
additional information
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splice site mutation (c.1674G>A) identified in a patient suffering MTHFD1 deficiency leads to exon skipping
additional information
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disruption mutants do not evoke an altered phenotype