Structure of PDB 8czg Chain A Binding Site BS01
Receptor Information
>8czg Chain A (length=157) Species:
9606
(Homo sapiens) [
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SMSEEQVAQDTEEVFRSYVFYRHQQEQPADPEMVTLPLQPSSTMGQVGRQ
LAIIGDDINRRYDSEFQTMLQHLQPTAENAYEYFTKIATSLFESGINWGR
VVALLGFGYRLALHVYQHGLTGFLGQVTRFVVDFMLHHSIARWIAQRGGW
VAALNLG
Ligand information
>8czg Chain E (length=22) Species:
32630
(synthetic construct) [
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SLLEKLAEELRQLADELNKKFE
Receptor-Ligand Complex Structure
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PDB
8czg
Peptides from human BNIP5 and PXT1 and non-native binders of pro-apoptotic BAK can directly activate or inhibit BAK-mediated membrane permeabilization.
Resolution
1.99 Å
Binding residue
(original residue number in PDB)
I81 R88 Y89 F93 M96 H99 L100 Y110 I114 S117 L118 N124 W125 G126 R127
Binding residue
(residue number reindexed from 1)
I54 R61 Y62 F66 M69 H72 L73 Y83 I87 S90 L91 N97 W98 G99 R100
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:8czg
,
PDBe:8czg
,
PDBj:8czg
PDBsum
8czg
PubMed
36706751
UniProt
Q16611
|BAK_HUMAN Bcl-2 homologous antagonist/killer (Gene Name=BAK1)
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