Structure of PDB 3uw5 Chain A Binding Site BS03
Receptor Information
>3uw5 Chain A (length=90) Species:
9606
(Homo sapiens) [
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GPAFPGMGSEELRLASFYDWPLTAEVPPELLAAAGFFHTGHQDKVRCFFC
YGGLQSWKRGDDPWTEHAKWFPGCQFLLRSKGQEYINNIH
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
3uw5 Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
3uw5
Discovery of a Potent Small-Molecule Antagonist of Inhibitor of Apoptosis (IAP) Proteins and Clinical Candidate for the Treatment of Cancer (GDC-0152).
Resolution
1.71 Å
Binding residue
(original residue number in PDB)
C124 C127 H144 C151
Binding residue
(residue number reindexed from 1)
C47 C50 H67 C74
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.2.27
: RING-type E3 ubiquitin transferase.
External links
PDB
RCSB:3uw5
,
PDBe:3uw5
,
PDBj:3uw5
PDBsum
3uw5
PubMed
22413863
UniProt
P98170
|XIAP_HUMAN E3 ubiquitin-protein ligase XIAP (Gene Name=XIAP);
Q96CA5
|BIRC7_HUMAN Baculoviral IAP repeat-containing protein 7 (Gene Name=BIRC7)
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