Structure of PDB 7l97 Chain A Binding Site BS02
Receptor Information
>7l97 Chain A (length=175) Species:
9606
(Homo sapiens) [
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GVEGLRCVVLPEDLCHKFLQLAESNTVRGIETCGILCGKLTHNEFTITHV
IVPKQSAGPDYCDMENVEELFNVQDQHDLLTLGWIHTHPTQTAFLSSVDL
HTHCSYQLMLPEAIAIVCSPKHKDTGIFRLTNAGMLEVSACKKKGFHPHT
KEPRLFSICKHVLVKDIKIIVLDLR
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
7l97 Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
7l97
Structural and functional characterization of ubiquitin variant inhibitors for the JAMM-family deubiquitinases STAMBP and STAMBPL1.
Resolution
2.01 Å
Binding residue
(original residue number in PDB)
H347 H349 D360
Binding residue
(residue number reindexed from 1)
H86 H88 D99
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.4.19.-
Gene Ontology
Molecular Function
GO:0008233
peptidase activity
GO:0008237
metallopeptidase activity
GO:0061578
K63-linked deubiquitinase activity
GO:0140492
metal-dependent deubiquitinase activity
Biological Process
GO:0016579
protein deubiquitination
GO:0070536
protein K63-linked deubiquitination
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Molecular Function
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Biological Process
External links
PDB
RCSB:7l97
,
PDBe:7l97
,
PDBj:7l97
PDBsum
7l97
PubMed
34425109
UniProt
Q96FJ0
|STALP_HUMAN AMSH-like protease (Gene Name=STAMBPL1)
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