Structure of PDB 4b5w Chain D Binding Site BS02
Receptor Information
>4b5w Chain D (length=253) Species:
481805
(Escherichia coli ATCC 8739) [
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MENSFKAALKAGRPQIGLWLGLSSSYSAELLAGAGFDWLLIDGEHAPNNV
QTVLTQLQAIAPYPSQPVVAPSWNDPVQIKQLLDVGTQTLLVPMVQNADE
AREAVRATRYPPAGIRGVGSALARASRWNRIPDYLQKANDQMCVLVQIET
REAMKNLPQILDVEGVDGVFIGPADLSADMGYAGNPQHPEVQAAIEQAIV
QIRESGKAPGILIANEQLAKRYLELGALFVAVGVDTTLLARAAEALAARF
GAQ
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
4b5w Chain D Residue 1256 [
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Receptor-Ligand Complex Structure
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PDB
4b5w
Crystal Structure of Reaction Intermediates in Pyruvate Class II Aldolase: Substrate Cleavage, Enolate Stabilization and Substrate Specificity
Resolution
1.792 Å
Binding residue
(original residue number in PDB)
Q147 E149 G172 P173 A174 D175
Binding residue
(residue number reindexed from 1)
Q147 E149 G172 P173 A174 D175
Annotation score
5
Binding affinity
MOAD
: Kd=26.9mM
Enzymatic activity
Catalytic site (original residue number in PDB)
H45 A70 D84 E149 D175
Catalytic site (residue number reindexed from 1)
H45 A70 D84 E149 D175
Enzyme Commision number
4.1.2.52
: 4-hydroxy-2-oxoheptanedioate aldolase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0043863
4-hydroxy-2-ketopimelate aldolase activity
GO:0046872
metal ion binding
GO:0061677
2-dehydro-3-deoxy-D-gluconate aldolase activity
Biological Process
GO:0009056
catabolic process
GO:0010124
phenylacetate catabolic process
Cellular Component
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:4b5w
,
PDBe:4b5w
,
PDBj:4b5w
PDBsum
4b5w
PubMed
22908224
UniProt
B1IS70
|HPCH_ECOLC 4-hydroxy-2-oxo-heptane-1,7-dioate aldolase (Gene Name=hpcH)
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