Structure of PDB 3mbi Chain A Binding Site BS02
Receptor Information
>3mbi Chain A (length=287) Species:
50339
(Thermoplasma volcanium) [
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SGMKIIALRSSLKLAARIAEELKTEPVMPDERRFPDGELYLRYDEDLTGH
NIFIIGNTHSDAEVMEMILTLSAIQDYRTKSVNIIAPYYGYARQHQRYKN
GEPISSQILTEIYSSYSNSIATVDIHDEKTLSYSKVKFSDLHANDAIVRY
YKNVDVDYVVSPDDGGLARVADISAKLGKKHFFIEKKRIDDRTVEMKVPN
VDVNGKKLLIVDDIISTGGTIAKSSGLLREKGASKIYVSAVHGLFVNGSE
NKILQNADEIHVTDTVESKFSDISVYQEVCNYIRDID
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
3mbi Chain A Residue 287 [
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Receptor-Ligand Complex Structure
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PDB
3mbi
The structures of Thermoplasma volcanium phosphoribosyl pyrophosphate synthetase bound to ribose-5-phosphate and ATP analogs.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H93 H124
Binding residue
(residue number reindexed from 1)
H95 H126
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.6.1
: ribose-phosphate diphosphokinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004749
ribose phosphate diphosphokinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0046872
metal ion binding
Biological Process
GO:0006015
5-phosphoribose 1-diphosphate biosynthetic process
GO:0006164
purine nucleotide biosynthetic process
GO:0009165
nucleotide biosynthetic process
GO:0016310
phosphorylation
Cellular Component
GO:0002189
ribose phosphate diphosphokinase complex
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:3mbi
,
PDBe:3mbi
,
PDBj:3mbi
PDBsum
3mbi
PubMed
21963988
UniProt
Q97CA5
|KPRS_THEVO Ribose-phosphate pyrophosphokinase (Gene Name=prs)
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