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TargetThermolysin
LigandBDBM50035236
Substrate/Competitorn/a
Meas. Tech.ChEMBL_210393 (CHEMBL814123)
IC50 1900±n/a nM
Citation Bihovsky, RLevinson, BLLoewi, RCErhardt, PWPolokoff, MA Hydroxamic acids as potent inhibitors of endothelin-converting enzyme from human bronchiolar smooth muscle. J Med Chem38:2119-29 (1995) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Thermolysin
Name:Thermolysin
Synonyms:THER_BACTH | npr
Type:PROTEIN
Mol. Mass.:60097.54
Organism:Bacillus thermoproteolyticus
Description:ChEMBL_1468794
Residue:548
Sequence:
MKMKMKLASFGLAAGLAAQVFLPYNALASTEHVTWNQQFQTPQFISGDLLKVNGTSPEEL
VYQYVEKNENKFKFHENAKDTLQLKEKKNDNLGFTFMRFQQTYKGIPVFGAVVTSHVKDG
TLTALSGTLIPNLDTKGSLKSGKKLSEKQARDIAEKDLVANVTKEVPEYEQGKDTEFVVY
VNGDEASLAYVVNLNFLTPEPGNWLYIIDAVDGKILNKFNQLDAAKPGDVKSITGTSTVG
VGRGVLGDQKNINTTYSTYYYLQDNTRGNGIFTYDAKYRTTLPGSLWADADNQFFASYDA
PAVDAHYYAGVTYDYYKNVHNRLSYDGNNAAIRSSVHYSQGYNNAFWNGSQMVYGDGDGQ
TFIPLSGGIDVVAHELTHAVTDYTAGLIYQNESGAINEAISDIFGTLVEFYANKNPDWEI
GEDVYTPGISGDSLRSMSDPAKYGDPDHYSKRYTGTQDNGGVHINSGIINKAAYLISQGG
THYGVSVVGIGRDKLGKIFYRALTQYLTPTSNFSQLRAAAVQSATDLYGSTSQEVASVKQ
AFDAVGVK
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  Blast E-value cutoff:
BDBM50035236
n/a
NameBDBM50035236
Synonyms:3-(2-Hydroxycarbamoyl-3-methyl-butyrylamino)-propionic acid | CHEMBL66284
TypeSmall organic molecule
Emp. Form.C9H16N2O5
Mol. Mass.232.2337
SMILESCC(C)C(C(=O)NO)C(=O)NCCC(O)=O
Structure
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