Structure of PDB 2vqa Chain B Binding Site BS02

Receptor Information
>2vqa Chain B (length=356) Species: 1148 (Synechocystis sp. PCC 6803) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
WRSLSNVVWGKDLPAFTYAFSKTPLVLYDGGTTKQVGTYNFPVSKGMAGV
YMSLEPGAIRELHWHANAAEWAYVMEGRTRITLTSPEGKVEIADVDKGGL
WYFPRGWGHSIEGIGPDTAKFLLVFNDGTFSEGATFSVTDWLSHTPIAWV
EENLGWTAAQVAQLPKKQVYISSYGPASGPLASATPQGQTAKIEVPHTHN
LLGQQPLVSLGGNELRLASAKEFPGSFNMTGALIHLEPGAMRQLHWHPNA
DEWQYVLDGEMDLTVFASEGKASVSRLQQGDVGYVPKGYGHAIRNSSQKP
LDIVVVFNDGDYQSIDLSTWLASNPSSVLGNTFQISPELTKKLPVQDTIF
SLPTQP
Ligand information
Ligand IDMN
InChIInChI=1S/Mn/q+2
InChIKeyWAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341[Mn++]
FormulaMn
NameMANGANESE (II) ION
ChEMBL
DrugBankDB06757
ZINC
PDB chain2vqa Chain B Residue 1002 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2vqa Protein-Folding Location Can Regulate Manganese-Binding Versus Copper- or Zinc-Binding.
Resolution2.95 Å
Binding residue
(original residue number in PDB)
H283 H285 E290 H329
Binding residue
(residue number reindexed from 1)
H245 H247 E252 H291
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) R98 H101 H103 E108 H147 E170
Catalytic site (residue number reindexed from 1) R60 H63 H65 E70 H109 E132
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0046872 metal ion binding
Biological Process
GO:0033609 oxalate metabolic process
Cellular Component
GO:0030288 outer membrane-bounded periplasmic space

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:2vqa, PDBe:2vqa, PDBj:2vqa
PDBsum2vqa
PubMed18948958
UniProtP73510

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