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TargetMyeloblastin
LigandBDBM50270031
Substrate/Competitorn/a
Meas. Tech.ChEMBL_508159 (CHEMBL1008217)
IC50 150±n/a nM
Citation Méthot, NRubin, JGuay, DBeaulieu, CEthier, DReddy, TJRiendeau, DPercival, MD Inhibition of the activation of multiple serine proteases with a cathepsin C inhibitor requires sustained exposure to prevent pro-enzyme processing. J Biol Chem282:20836-46 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Myeloblastin
Name:Myeloblastin
Synonyms:PRTN3_MOUSE | Prtn3
Type:PROTEIN
Mol. Mass.:27628.93
Organism:Mus musculus
Description:ChEMBL_508159
Residue:254
Sequence:
MSGSYPSPKGIHPFLLLALVVGGAVQASKIVGGHEARPHSRPYVASLQLSRFPGSHFCGG
TLIHPRFVLTAAHCLQDISWQLVTVVLGAHDLLSSEPEQQKFTISQVFQNNYNPEENLND
VLLLQLNRTASLGKEVAVASLPQQDQTLSQGTQCLAMGWGRLGTQAPTPRVLQELNVTVV
TFLCREHNVCTLVPRRAAGICFGDSGGPLICNGILHGVDSFVIRECASLQFPDFFARVSM
YVDWIQNVLRGAEP
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  Blast E-value cutoff:
BDBM50270031
n/a
NameBDBM50270031
Synonyms:1-((1R,2R)-1-cyano-2-phenylcyclopropylamino)-3-(3-fluorothiophen-2-yl)-1-oxopropan-2-aminium 2,2,2-trifluoroacetate | CHEMBL515494
TypeSmall organic molecule
Emp. Form.C17H17FN3OS
Mol. Mass.330.399
SMILES[NH3+]C(Cc1sccc1F)C(=O)N[C@@]1(C[C@@H]1c1ccccc1)C#N |r|
Structure
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