Structure of PDB 5f2v Chain S Binding Site BS01
Receptor Information
>5f2v Chain S (length=182) Species:
1415167
(Bacillus subtilis PY79) [
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DKQWERFLVPYRQAVEELKVKLKGIRTLYEYEDDHSPIEFVTGRVKPVAS
ILEKARRKSIPLHEIETMQDIAGLRIMCQFVDDIQIVKEMLFARKDFTVV
DRSYHLVVLYPLQTVSGEKHVLVEIQIRTLAMNFWATIEHSLNYKYSGNI
PEKVKLRLQRASEAASRLDEEMSEIRGEVQEA
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
5f2v Chain S Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
5f2v
Catalytic mechanism and allosteric regulation of an oligomeric (p)ppGpp synthetase by an alarmone.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
D72 E139
Binding residue
(residue number reindexed from 1)
D70 E124
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.6.5
: GTP diphosphokinase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0005525
GTP binding
GO:0008728
GTP diphosphokinase activity
GO:0016301
kinase activity
GO:0046872
metal ion binding
Biological Process
GO:0015969
guanosine tetraphosphate metabolic process
GO:0015970
guanosine tetraphosphate biosynthetic process
GO:0016310
phosphorylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:5f2v
,
PDBe:5f2v
,
PDBj:5f2v
PDBsum
5f2v
PubMed
26460002
UniProt
O31611
|YJBM_BACSU GTP pyrophosphokinase YjbM (Gene Name=yjbM)
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