Structure of PDB 5ett Chain A Binding Site BS04
Receptor Information
>5ett Chain A (length=157) Species:
1280
(Staphylococcus aureus) [
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MIQAYLGLGSNIGDRESQLNDAIKILNEYDGISVSNISPIYETAPVGYTE
QPNFLNLCVEIQTTLTVLQLLECCLKTEECLHRIRKERWGPRTLDVDILL
YGEEMIDLPKLSVPHPRMNERAFVLIPLNDIAANVVEPRSKLKVKDLVFV
DDSVKRY
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
5ett Chain A Residue 205 [
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Receptor-Ligand Complex Structure
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PDB
5ett
Structural Basis for the Selective Binding of Inhibitors to 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinase from Staphylococcus aureus and Escherichia coli.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
D95 D97
Binding residue
(residue number reindexed from 1)
D95 D97
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R83 R92 D95 D97
Catalytic site (residue number reindexed from 1)
R83 R92 D95 D97
Enzyme Commision number
2.7.6.3
: 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase.
Gene Ontology
Molecular Function
GO:0003848
2-amino-4-hydroxy-6-hydroxymethyldihydropteridine diphosphokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0046872
metal ion binding
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:5ett
,
PDBe:5ett
,
PDBj:5ett
PDBsum
5ett
PubMed
27094768
UniProt
Q2G0Q5
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