Structure of PDB 8czh Chain A Binding Site BS01
Receptor Information
>8czh Chain A (length=157) Species:
9606
(Homo sapiens) [
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GSMSEEQVAQDTEEVFRSYVFYRHQQEQPADPEMVTLPLQPSSTMGQVGR
QLAIIGDDINRRYDSEFQTMLQHLQPTAENAYEYFTKIATSLFESGINWG
RVVALLGFGYRLALHVYQHGLTGFLGQVTRFVVDFMLHHSIARWIAQRGG
WVAALNL
Ligand information
>8czh Chain B (length=23) Species:
32630
(synthetic construct) [
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APYLEQVARTLRKIGEEINEALR
Receptor-Ligand Complex Structure
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PDB
8czh
Peptides from human BNIP5 and PXT1 and non-native binders of pro-apoptotic BAK can directly activate or inhibit BAK-mediated membrane permeabilization.
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
R88 Y89 E92 F93 M96 H99 L100 Y110 I114 S117 L118 N124 G126 F134
Binding residue
(residue number reindexed from 1)
R62 Y63 E66 F67 M70 H73 L74 Y84 I88 S91 L92 N98 G100 F108
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:8czh
,
PDBe:8czh
,
PDBj:8czh
PDBsum
8czh
PubMed
36706751
UniProt
Q16611
|BAK_HUMAN Bcl-2 homologous antagonist/killer (Gene Name=BAK1)
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