Structure of PDB 7m5c Chain A Binding Site BS02
Receptor Information
>7m5c Chain A (length=151) Species:
9606
(Homo sapiens) [
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SEEQVAQDTEEVFRSYVFYRHQQEQEAADPEMVTLPSSTMGQVGRQLAII
GDDINRRYDSEFQTMLQHLQPTAENAYEYFTKIATSLFESGINWGRVVAL
LGFGYRLALHVYQHGLTGFLGQVTRFVVDFMLHHSIARWIAQRGGWVAAL
N
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
7m5c Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
7m5c
Structural basis of BAK activation in mitochondrial apoptosis initiation.
Resolution
3.06 Å
Binding residue
(original residue number in PDB)
H141 H145
Binding residue
(residue number reindexed from 1)
H110 H114
Annotation score
3
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0042981
regulation of apoptotic process
View graph for
Biological Process
External links
PDB
RCSB:7m5c
,
PDBe:7m5c
,
PDBj:7m5c
PDBsum
7m5c
PubMed
35017502
UniProt
Q16611
|BAK_HUMAN Bcl-2 homologous antagonist/killer (Gene Name=BAK1)
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