Structure of PDB 3hgx Chain A Binding Site BS01
Receptor Information
>3hgx Chain A (length=99) Species:
287
(Pseudomonas aeruginosa) [
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MKTPEDCTGLADIREAIDRIDLDIVQALGRRMDYVKAASRFAASEAAIPA
PERVAAMLPERARWAEENGLDAPFVEGLFAQIIHWYIAEQIKYWRQTRG
Ligand information
Ligand ID
PYR
InChI
InChI=1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)
InChIKey
LCTONWCANYUPML-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(=O)C(O)=O
OpenEye OEToolkits 1.7.6
CC(=O)C(=O)O
ACDLabs 12.01
O=C(C(=O)O)C
Formula
C3 H4 O3
Name
PYRUVIC ACID
ChEMBL
CHEMBL1162144
DrugBank
DB00119
ZINC
ZINC000001532517
PDB chain
3hgx Chain B Residue 102 [
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Receptor-Ligand Complex Structure
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PDB
3hgx
Structure-function analyses of isochorismate-pyruvate lyase from Pseudomonas aeruginosa suggest differing catalytic mechanisms for the two pericyclic reactions of this bifunctional enzyme.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
A38 Q90
Binding residue
(residue number reindexed from 1)
A38 Q90
Annotation score
5
Enzymatic activity
Enzyme Commision number
4.2.99.21
: isochorismate lyase.
5.4.99.5
: chorismate mutase.
Gene Ontology
Molecular Function
GO:0004106
chorismate mutase activity
GO:0016829
lyase activity
GO:0016835
carbon-oxygen lyase activity
GO:0016853
isomerase activity
GO:0043904
isochorismate pyruvate lyase activity
Biological Process
GO:0009697
salicylic acid biosynthetic process
GO:0019752
carboxylic acid metabolic process
GO:0042864
pyochelin biosynthetic process
GO:0046417
chorismate metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3hgx
,
PDBe:3hgx
,
PDBj:3hgx
PDBsum
3hgx
PubMed
19432488
UniProt
Q51507
|PCHB_PSEAE Isochorismate pyruvate lyase (Gene Name=pchB)
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