Structure of PDB 1i7o Chain D Binding Site BS01
Receptor Information
>1i7o Chain D (length=421) Species:
562
(Escherichia coli) [
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MKGTIFAVALNHRSQLDAWQEAFQQSPYKAPPKTAVWFIKPRNTVIGCGE
PIPFPQGEKVLSGATVALIVGKTATKVREEDAAEYIAGYALANDVSLPEE
SFYRPAIKAKCRDGFCPIGETVALSNVDNLTIYTEINGRPADHWNTADLQ
RNAAQLLSALSEFATLNPGDAILLGTPQARVEIQPGDRVRVLAEGFPPLE
NPVVDEREVTTRKSFPTLPHPHGTLFALGLNYADHPEEPLVFLKAPNTLT
GDNQTSVRPNNIEYMHYEAELVVVIGKQARNVSEADAMDYVAGYTVCNDY
AIRDYLENYYRPNLRVKSRDGLTPMLSTIVPKEAIPDPHNLTLRTFVNGE
LRQQGTTADLIFSVPFLIAYLSEFMTLNPGDMIATGTPKGLSDVVPGDEV
VVEVEGVGRLVNRIVSEETAK
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1i7o Chain D Residue 1004 [
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Receptor-Ligand Complex Structure
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PDB
1i7o
The crystal structure of HpcE, a multi-functional enzyme fold
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
E276 E278 D307
Binding residue
(residue number reindexed from 1)
E268 E270 D299
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.1.1.68
: 5-oxopent-3-ene-1,2,5-tricarboxylate decarboxylase.
5.3.3.10
: 5-carboxymethyl-2-hydroxymuconate Delta-isomerase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008704
5-carboxymethyl-2-hydroxymuconate delta-isomerase activity
GO:0016829
lyase activity
GO:0016853
isomerase activity
GO:0018773
acetylpyruvate hydrolase activity
GO:0018800
5-oxopent-3-ene-1,2,5-tricarboxylate decarboxylase activity
GO:0046872
metal ion binding
Biological Process
GO:0009056
catabolic process
GO:1901023
4-hydroxyphenylacetate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1i7o
,
PDBe:1i7o
,
PDBj:1i7o
PDBsum
1i7o
PubMed
UniProt
P37352
|HPCE_ECOLX Homoprotocatechuate catabolism bifunctional isomerase/decarboxylase (Gene Name=hpcE)
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