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TargetCathepsin K
LigandBDBM50042850
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1444643 (CHEMBL3376641)
IC50>100000±n/a nM
Citation Grosche, PSirockin, FMac Sweeney, ARamage, PErbel, PMelkko, SBernardi, AHughes, NEllis, DCombrink, KDJarousse, NAltmann, E Structure-based design and optimization of potent inhibitors of the adenoviral protease. Bioorg Med Chem Lett25:438-43 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Cathepsin K
Name:Cathepsin K
Synonyms:CATK_HUMAN | CTSK | CTSO | CTSO2 | Cathepsin O | Cathepsin O2 | Cathepsin X
Type:Enzyme
Mol. Mass.:36975.68
Organism:Homo sapiens (Human)
Description:P43235
Residue:329
Sequence:
MWGLKVLLLPVVSFALYPEEILDTHWELWKKTHRKQYNNKVDEISRRLIWEKNLKYISIH
NLEASLGVHTYELAMNHLGDMTSEEVVQKMTGLKVPLSHSRSNDTLYIPEWEGRAPDSVD
YRKKGYVTPVKNQGQCGSCWAFSSVGALEGQLKKKTGKLLNLSPQNLVDCVSENDGCGGG
YMTNAFQYVQKNRGIDSEDAYPYVGQEESCMYNPTGKAAKCRGYREIPEGNEKALKRAVA
RVGPVSVAIDASLTSFQFYSKGVYYDESCNSDNLNHAVLAVGYGIQKGNKHWIIKNSWGE
NWGNKGYILMARNKNNACGIANLASFPKM
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50042850
n/a
NameBDBM50042850
Synonyms:CHEMBL3354492
TypeSmall organic molecule
Emp. Form.C22H21Cl2N3O4
Mol. Mass.462.326
SMILESCOc1ccc(cc1C(=O)C(C)(C)c1cc(Cl)cc(Cl)c1)C(=O)NCC(=O)NCC#N
Structure
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