Structure of PDB 5vwz Chain A Binding Site BS01
Receptor Information
>5vwz Chain A (length=166) Species:
9606
(Homo sapiens) [
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SMSEEQVAQDTEEVFRSYVFYRHQQEQEAEGVAAPADPEMVTLPLQPSST
MGQVGRQLAIIGDDINRRYDSEFQTMLQHLQPTAENAYEYFTKIATSLFE
SGINWGRVVALLGFGYRLALHVYQHGLTGFLGQVTRFVVDFMLHHSIARW
IAQRGGWVAALNLGNG
Ligand information
>5vwz Chain B (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)
R42 I81 G82 I85 N86 R88 Y89 E92 F93 M96 I114 S117 L118 S121 N124 G126 R127 V129 A130 F134 R137 G184
Binding residue
(residue number reindexed from 1)
R22 I61 G62 I65 N66 R68 Y69 E72 F73 M76 I94 S97 L98 S101 N104 G106 R107 V109 A110 F114 R117 G164
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0042981
regulation of apoptotic process
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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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