Structure of PDB 2jgq Chain B Binding Site BS01

Receptor Information
>2jgq Chain B (length=231) Species: 85962 (Helicobacter pylori 26695) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TKIAMANFKSAMPIFKSHAYLKELEKTLKPQHFDRVFVFPDFFGLLPNSF
LHFTLGVQNAYPRDCGAFTGEITSKHLEELKIHTLLIGHSERRTLLKESP
SFLKEKFDFFKSKNFKIVYCIGEELTTREKGFKAVKEFLSEQLENIDLNY
PNLVVAYEPIWAIGTSASLEDIYLTHGFLKQILNQKTPLLYGGSVNTQNA
KEILGIDSVDGLLIGSASWELENFKTIISFL
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 chain2jgq Chain B Residue 1235 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB2jgq Kinetics and Structural Properties of Triosephosphate Isomerase from Helicobacter Pylori
Resolution2.3 Å
Binding residue
(original residue number in PDB)
K10 I164 G165 S197 G218 S219
Binding residue
(residue number reindexed from 1)
K9 I163 G164 S194 G215 S216
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) N8 K10 H90 E92 E159 G165 S197
Catalytic site (residue number reindexed from 1) N7 K9 H89 E91 E158 G164 S194
Enzyme Commision number 5.3.1.1: triose-phosphate isomerase.
Gene Ontology
Molecular Function
GO:0004807 triose-phosphate isomerase activity
GO:0016853 isomerase activity
Biological Process
GO:0006094 gluconeogenesis
GO:0006096 glycolytic process
GO:0019563 glycerol catabolic process
GO:0046166 glyceraldehyde-3-phosphate biosynthetic process
Cellular Component
GO:0005737 cytoplasm
GO:0005829 cytosol

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Cellular Component
External links
PDB RCSB:2jgq, PDBe:2jgq, PDBj:2jgq
PDBsum2jgq
PubMed17957775
UniProtP56076|TPIS_HELPY Triosephosphate isomerase (Gene Name=tpiA)

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