Structure of PDB 1dxf Chain A Binding Site BS01
Receptor Information
>1dxf Chain A (length=253) Species:
562
(Escherichia coli) [
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DVFPNKFKAALAAKQVQIGCWSALSNPISTEVLGLAGFDWLVLDGEHAPN
DISTFIPQLMALKGSASAPVVRVPTNEPVIIKRLLDIGFYNFLIPFVETK
EEAELAVASTRYPPEGIRGVSVSHRANMFGTVADYFAQSNKNITILVQIE
SQQGVDNVDAIAATEGVDGIFVGPSDLAAALGHLGNASHPDVQKAIQHIF
NRASAHGKPSGILAPVEADARRYLEWGATFVAVGSDLGVFRSATQKLADT
FKK
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
1dxf Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1dxf
Crystal Structures of the Metal-Dependent 2-Dehydro-3-Deoxy-Galactarate Aldolase Suggest a Novel Reaction Mechanism.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
E153 G176 P177 S178 D179
Binding residue
(residue number reindexed from 1)
E150 G173 P174 S175 D176
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H50 R75 D89 E153 D179
Catalytic site (residue number reindexed from 1)
H47 R72 D86 E150 D176
Enzyme Commision number
4.1.2.20
: 2-dehydro-3-deoxyglucarate aldolase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0008672
2-dehydro-3-deoxyglucarate aldolase activity
GO:0016829
lyase activity
GO:0016830
carbon-carbon lyase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
GO:0061677
2-dehydro-3-deoxy-D-gluconate aldolase activity
Biological Process
GO:0019394
glucarate catabolic process
GO:0042838
D-glucarate catabolic process
GO:0046392
galactarate catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1dxf
,
PDBe:1dxf
,
PDBj:1dxf
PDBsum
1dxf
PubMed
10921867
UniProt
P23522
|GARL_ECOLI 5-keto-4-deoxy-D-glucarate aldolase (Gene Name=garL)
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