Structure of PDB 5vwz Chain A Binding Site BS02
Receptor Information
>5vwz Chain A (length=166) Species:
9606
(Homo sapiens) [
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SMSEEQVAQDTEEVFRSYVFYRHQQEQEAEGVAAPADPEMVTLPLQPSST
MGQVGRQLAIIGDDINRRYDSEFQTMLQHLQPTAENAYEYFTKIATSLFE
SGINWGRVVALLGFGYRLALHVYQHGLTGFLGQVTRFVVDFMLHHSIARW
IAQRGGWVAALNLGNG
Ligand information
>5vwz Chain D (length=26) Species:
9606
(Homo sapiens) [
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DMRPEIWIAQELRRIGDEFNAYYARR
Receptor-Ligand Complex Structure
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PDB
5vwz
Conversion of Bim-BH3 from Activator to Inhibitor of Bak through Structure-Based Design.
Resolution
1.622 Å
Binding residue
(original residue number in PDB)
G51 Q94
Binding residue
(residue number reindexed from 1)
G31 Q74
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0042981
regulation of apoptotic process
View graph for
Biological Process
External links
PDB
RCSB:5vwz
,
PDBe:5vwz
,
PDBj:5vwz
PDBsum
5vwz
PubMed
29149594
UniProt
Q16611
|BAK_HUMAN Bcl-2 homologous antagonist/killer (Gene Name=BAK1)
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