Structure of PDB 1g4c Chain B Binding Site BS01
Receptor Information
>1g4c Chain B (length=158) Species:
562
(Escherichia coli) [
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TVAYIAIGSNLASPLEQVNAALKALGDIPESHILTVSSFYRTPPLGPQDQ
PDYLNAAVALETSLAPEELLNHTQRIELQQGRVRKAERWGPATLDLDIML
FGNEVINTERLTVPHYDMKNRGFMLWPLFEIAPELVFPDGEMLRQILHTR
AFDKLNKW
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
1g4c Chain B Residue 362 [
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Receptor-Ligand Complex Structure
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PDB
1g4c
Dynamic Roles of Arginine Residues 82 and 92 of Escherichia coli 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinase: Crystallographic Studies
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
D295 D297
Binding residue
(residue number reindexed from 1)
D95 D97
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R282 A292 D295 D297
Catalytic site (residue number reindexed from 1)
R82 A92 D95 D97
Enzyme Commision number
2.7.6.3
: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003848
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
Biological Process
GO:0009396
folic acid-containing compound biosynthetic process
GO:0016310
phosphorylation
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046656
folic acid biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1g4c
,
PDBe:1g4c
,
PDBj:1g4c
PDBsum
1g4c
PubMed
12578370
UniProt
P26281
|HPPK_ECOLI 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase (Gene Name=folK)
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