Structure of PDB 4b5w Chain C Binding Site BS01
Receptor Information
>4b5w Chain C (length=252) Species:
481805
(Escherichia coli ATCC 8739) [
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MENSFKAALKAGRPQIGLWLGLSSSYSAELLAGAGFDWLLIDGEHAPNNV
QTVLTQLQAIAPYPSQPVVAPSWNDPVQIKQLLDVGTQTLLVPMVQNADE
AREAVRATRYPPAGIRGVGSALARASRWNRIPDYLQKANDQMCVLVQIET
REAMKNLPQILDVEGVDGVFIGPADLSADMGYAGNPQHPEVQAAIEQAIV
QIRESGKAPGILIANEQLAKRYLELGALFVAVGVDTTLLARAAEALAARF
GA
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
4b5w Chain C Residue 1253 [
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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)
E149 D175
Binding residue
(residue number reindexed from 1)
E149 D175
Annotation score
1
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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