Structure of PDB 5vww Chain B Binding Site BS02
Receptor Information
>5vww Chain B (length=142) Species:
9606
(Homo sapiens) [
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SEEQVAQDTEEVFRSYVFYRHQQPSSTMGQVGRQLAIIGDDINRRYDSEF
QTMLQHLQPTAENAYEYFTKIATSLFESGINWGRVVALLGFGYRLALHVY
QHGLTGFLGQVTRFVVDFMLHHSIARWIAQRGGWVAALNLGN
Ligand information
>5vww Chain D (length=19) Species:
9606
(Homo sapiens) [
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RPEIRIAQELRRIGDEFNA
Receptor-Ligand Complex Structure
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PDB
5vww
Conversion of Bim-BH3 from Activator to Inhibitor of Bak through Structure-Based Design.
Resolution
2.802 Å
Binding residue
(original residue number in PDB)
I81 I85 Y89 E92 F93 M96 L100 I114 S117 L118 N124 R127 F134
Binding residue
(residue number reindexed from 1)
I38 I42 Y46 E49 F50 M53 L57 I71 S74 L75 N81 R84 F91
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0042981
regulation of apoptotic process
View graph for
Biological Process
External links
PDB
RCSB:5vww
,
PDBe:5vww
,
PDBj:5vww
PDBsum
5vww
PubMed
29149594
UniProt
Q16611
|BAK_HUMAN Bcl-2 homologous antagonist/killer (Gene Name=BAK1)
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