Target
Ubiquitin carboxyl-terminal hydrolase 2 [258-605]
Ligand
BDBM223978
Substrate
n/a
Meas. Tech.
Di-UB K63-2 Hydrolysis Assay
IC50
>5.0e+4±n/a nM
Citation
 Magiera, KTomala, MKubica, KDe Cesare, VTrost, MZieba, BJKachamakova-Trojanowska, NLes, MDubin, GHolak, TASkalniak, L Lithocholic Acid Hydroxyamide Destabilizes Cyclin D1 and Induces G0/G1 Arrest by Inhibiting Deubiquitinase USP2a. Cell Chem Biol 24:458-470 (2017) [PubMed]  Article 
Target
Name:
Ubiquitin carboxyl-terminal hydrolase 2 [258-605]
Synonyms:
UBP2_HUMAN | UBP41 | USP2 | Ubiquitin-specific peptidase 2a (USP2a)
Type:
Enzyme
Mol. Mass.:
40094.16
Organism:
Homo sapiens (Human)
Description:
Hman USP2a (258-605 aa)
Residue:
348
Sequence:
MNSKSAQGLAGLRNLGNTCFMNSILQCLSNTRELRDYCLQRLYMRDLHHGSNAHTALVEEFAKLIQTIWTSSPNDVVSPSEFKTQIQRYAPRFVGYNQQDAQEFLRFLLDGLHNEVNRVTLRPKSNPENLDHLPDDEKGRQMWRKYLEREDSRIGDLFVGQLKSSLTCTDCGYCSTVFDPFWDLSLPIAKRGYPEVTLMDCMRLFTKEDVLDGDEKPTCCRCRGRKRCIKKFSIQRFPKILVLHLKRFSESRIRTSKLTTFVNFPLRDLDLREFASENTNHAVYNLYAVSNHSGTTMGGHYTAYCRSPGTGEWHTFNDSSVTPMSSSQVRTSDAYLLFYELASPPSRM
  
Inhibitor
Name:
BDBM223978
Synonyms:
NSC 632839
Type:
Small organic molecule
Emp. Form.:
C21H21NO
Mol. Mass.:
303.3975
SMILES:
Cc1ccc(\C=C2/CNC\C(=C/c3ccc(C)cc3)C2=O)cc1
Structure:
Search PDB for entries with ligand similarity: