Structure of PDB 1fgs Chain A Binding Site BS01
Receptor Information
>1fgs Chain A (length=393) Species:
1582
(Lacticaseibacillus casei) [
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MNYTETVAYIHSFPRLAGDHRRILTLLHALGNPQQQGRYIHVTGTNGKGS
AANAIAHVLEASGLTVGLYTSPFIMRFNERIMIDHEPIPDAALVNAVAFV
RAALERLQQQQADFNVTEFEFITALAYWYFRQRQVDVAVIEVGDSTNVIT
PVVSVLTEVALDTITAIAKHKAGIIKRGIPVVTGNLVPDAAAVVAAKVAT
TGSQWLRFDRDFSVPKAKLHGWGQRFTYEDQDGRISDLEVPLVGDYQQRN
MAIAIQTAKVYAKQTEWPLTPQNIRQGLAASHWPARLEKISDTPLIVIDG
AHNPDGINGLITALKQLFSQPITVIAGYAAMADRLTAAFSTVYLVPVPGT
PRGRLKDSWQEALAASLNDVPDQPIVITGSLYLASAVRQTLLG
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
1fgs Chain A Residue 998 [
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Receptor-Ligand Complex Structure
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PDB
1fgs
Structural homologies with ATP- and folate-binding enzymes in the crystal structure of folylpolyglutamate synthetase.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
S73 E143
Binding residue
(residue number reindexed from 1)
S71 E141
Annotation score
1
Enzymatic activity
Enzyme Commision number
6.3.2.17
: tetrahydrofolate synthase.
Gene Ontology
Molecular Function
GO:0004326
tetrahydrofolylpolyglutamate synthase activity
GO:0005524
ATP binding
GO:0008841
dihydrofolate synthase activity
GO:0016874
ligase activity
GO:0016881
acid-amino acid ligase activity
GO:0046872
metal ion binding
Biological Process
GO:0006730
one-carbon metabolic process
GO:0006761
dihydrofolate biosynthetic process
GO:0009058
biosynthetic process
GO:0009396
folic acid-containing compound biosynthetic process
GO:0046901
tetrahydrofolylpolyglutamate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1fgs
,
PDBe:1fgs
,
PDBj:1fgs
PDBsum
1fgs
PubMed
9618466
UniProt
P15925
|FPGS_LACCA Folylpolyglutamate synthase (Gene Name=fpgS)
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