Structure of PDB 3pe7 Chain A Binding Site BS01

Receptor Information
>3pe7 Chain A (length=376) Species: 393305 (Yersinia enterocolitica subsp. enterocolitica 8081) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MAKGKQIPLTFDTYQDASTGAQVTRLTPPDVTCHRNYFYQKCFTRDGSKL
LFGGAFDGPWNYYLLDLNTQVATQLTEGRGDNTFGGFLSPDDDALFYVKD
GRNLMRVDLATLEENVVYQVPAEWVGYGTWVANSDCTKLVGIEIRREDWV
PLTDWKKFHEFYFTKPCCRLMRVDLKTGESTVILQENQWLGHPIYRPYDD
STVAFCHEGPHDLVDARMWLINEDGTNMRKVKTHAEGESCTHEFWVPDGS
ALVYVSYLKGSPDRFIYSADPETLENRQLTSMPACSHLMSNYDGSLMVGD
GSDAENDPFLYVFNMKNGTQHRVARHDTSWKVFEGDRQVTHPHPSFTPDD
KQILFTSDVHGKPALYLATLPESVWK
Ligand information
Ligand IDMN
InChIInChI=1S/Mn/q+2
InChIKeyWAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341[Mn++]
FormulaMn
NameMANGANESE (II) ION
ChEMBL
DrugBankDB06757
ZINC
PDB chain3pe7 Chain A Residue 389 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB3pe7 The active site of oligogalacturonate lyase provides unique insights into cytoplasmic oligogalacturonate beta-elimination.
Resolution1.65 Å
Binding residue
(original residue number in PDB)
H287 Q350 H353 H355
Binding residue
(residue number reindexed from 1)
H287 Q338 H341 H343
Annotation score1
Enzymatic activity
Enzyme Commision number ?
Gene Ontology
Molecular Function
GO:0016829 lyase activity
GO:0046872 metal ion binding
GO:0047487 oligogalacturonide lyase activity
Biological Process
GO:0045490 pectin catabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:3pe7, PDBe:3pe7, PDBj:3pe7
PDBsum3pe7
PubMed20851883
UniProtA1JMA5

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