Structure of PDB 2wja Chain B Binding Site BS01

Receptor Information
>2wja Chain B (length=138) Species: 562 (Escherichia coli) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MFDSILVICTGNICRSPIGERLLRRLLPSKKINSAGVGALVDHAADESAI
RVLCLKGHRGTKFTSALARQYDLLLVMEYSHLEQISRIAPEARGKTMLFG
HWLDSKEIPDPYRMSDEAFDSVYQLLEQASKRWAEKLG
Ligand information
Ligand IDPO4
InChIInChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKeyNBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
SoftwareSMILES
CACTVS 3.341[O-][P]([O-])([O-])=O
ACDLabs 10.04[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0[O-]P(=O)([O-])[O-]
FormulaO4 P
NamePHOSPHATE ION
ChEMBL
DrugBankDB14523
ZINC
PDB chain2wja Chain B Residue 1148 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2wja Crystal Structures of Wzb of Escherichia Coli and Cpsb of Streptococcus Pneumoniae, Representatives of Two Families of Tyrosine Phosphatases that Regulate Capsule Assembly.
Resolution2.5 Å
Binding residue
(original residue number in PDB)
C13 T14 G15 N16 C18 R19 D119
Binding residue
(residue number reindexed from 1)
C9 T10 G11 N12 C14 R15 D110
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) C13 N16 C18 R19 S20 D119
Catalytic site (residue number reindexed from 1) C9 N12 C14 R15 S16 D110
Enzyme Commision number 3.1.3.48: protein-tyrosine-phosphatase.
Gene Ontology
Molecular Function
GO:0004721 phosphoprotein phosphatase activity
GO:0004725 protein tyrosine phosphatase activity
Biological Process
GO:0006470 protein dephosphorylation

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Molecular Function

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Biological Process
External links
PDB RCSB:2wja, PDBe:2wja, PDBj:2wja
PDBsum2wja
PubMed19616007
UniProtQ9X4B8

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