Structure of PDB 3f7g Chain D Binding Site BS01
Receptor Information
>3f7g Chain D (length=100) Species:
9606
(Homo sapiens) [
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AGATLSRGPAFPGMGSEELRLASFYDWPLTAEVPPELLAAAGFFHTGHQD
KVRCFFCYGGLQSWKRGDDPWTEHAKWFPSCQFLLRSKGRDFVHSVQETH
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
3f7g Chain D Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
3f7g
Orally bioavailable antagonists of inhibitor of apoptosis proteins based on an azabicyclooctane scaffold
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
C124 C127 H144 C151
Binding residue
(residue number reindexed from 1)
C54 C57 H74 C81
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
F81
Catalytic site (residue number reindexed from 1)
F11
Enzyme Commision number
2.3.2.27
: RING-type E3 ubiquitin transferase.
External links
PDB
RCSB:3f7g
,
PDBe:3f7g
,
PDBj:3f7g
PDBsum
3f7g
PubMed
19228017
UniProt
Q96CA5
|BIRC7_HUMAN Baculoviral IAP repeat-containing protein 7 (Gene Name=BIRC7)
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