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TargetUbiquitin carboxyl-terminal hydrolase isozyme L1
LigandBDBM50411562
Substrate/Competitorn/a
Meas. Tech.ChEMBL_455564 (CHEMBL903551)
Ki>30000±n/a nM
Citation Mermerian, AHCase, AStein, RLCuny, GD Structure-activity relationship, kinetic mechanism, and selectivity for a new class of ubiquitin C-terminal hydrolase-L1 (UCH-L1) inhibitors. Bioorg Med Chem Lett17:3729-32 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Ubiquitin carboxyl-terminal hydrolase isozyme L1
Name:Ubiquitin carboxyl-terminal hydrolase isozyme L1
Synonyms:Neuron cytoplasmic protein 9.5 | PGP 9.5 | PGP9.5 | UCH-L1 | UCHL1 | UCHL1_HUMAN | Ubiquitin thioesterase L1
Type:PROTEIN
Mol. Mass.:24819.03
Organism:Homo sapiens (Human)
Description:ChEMBL_974327
Residue:223
Sequence:
MQLKPMEINPEMLNKVLSRLGVAGQWRFVDVLGLEEESLGSVPAPACALLLLFPLTAQHE
NFRKKQIEELKGQEVSPKVYFMKQTIGNSCGTIGLIHAVANNQDKLGFEDGSVLKQFLSE
TEKMSPEDRAKCFEKNEAIQAAHDAVAQEGQCRVDDKVNFHFILFNNVDGHLYELDGRMP
FPVNHGASSEDTLLKDAAKVCREFTEREQGEVRFSAVALCKAA
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BDBM50411562
n/a
NameBDBM50411562
Synonyms:CHEMBL540118
TypeSmall organic molecule
Emp. Form.C10H8N2O4S
Mol. Mass.252.247
SMILESCC(=O)c1sc2[nH]c(=O)c(cc2c1N)C(O)=O
Structure
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