1AUJ

BOVINE TRYPSIN COMPLEXED TO META-CYANO-BENZYLIC INHIBITOR

Summary for 1AUJ

• Entry DOI: 10.2210/pdb1auj/pdb
• Descriptor: TRYPSIN, CALCIUM ION, 1-{[1-(2-AMINO-3-PHENYL-PROPIONYL)-PYRROLIDINE-2-CARBONYL]-AMINO}-2-(3-CYANO-PHENYL)-ETHANEBORONIC ACID, ... (4 entities in total)
• Functional Keywords: hydrolase, serine proteinase
• Biological source: Bos taurus (cattle)
• Cellular location: Secreted, extracellular space: P00760
• Total number of polymer chains: 1
• Total formula weight: 23798.66

Authors

Alexander, R.,Smallwood, A.,Kettner, C. (deposition date: 1997-08-28, release date: 1998-10-14, Last modification date: 2024-11-13)

Primary citation

Lee, S.L.,Alexander, R.S.,Smallwood, A.,Trievel, R.,Mersinger, L.,Weber, P.C.,Kettner, C.
New inhibitors of thrombin and other trypsin-like proteases: hydrogen bonding of an aromatic cyano group with a backbone amide of the P1 binding site replaces binding of a basic side chain.
Biochemistry, 36:13180-13186, 1997

PubMed Abstract: Highly effective thrombin inhibitors have been obtained by preparing boronic acid analogues of m-cyano-substituted phenylalanine and its incorporation into peptides. The cyano group enhances binding by several orders of magnitude. For example, Ac-(D)Phe-Pro-boroPheOH binds to thrombin with a Ki of 320 nM and the Ki of Ac-(D)Phe-Pro-boroPhe(m-CN)-OH is 0.79 nM. Protein crystal structure determination of trypsin complexed to H-(D)Phe-Pro-boroPhe(m-CN)-OH indicates that the aromatic side chain is bound in the P1 binding site and that the cyano group can act as a H-bond acceptor for the amide proton of Gly219. Enhanced binding for inhibitors containing the m-cyano group was observed for coagulation factor Xa and for the factor VIIa.tissue factor complex [Ki values of Ac-(D)Phe-Pro-boroPhe(mCN)-OH are 760 and 3.3 nM, respectively]. This result is consistent with the sequence homology of these two enzymes in the P1 binding site. Two enzymes lacking the strict homology in the P1 binding site, pancreatic kallikrein and chymotrypsin, did not exhibit significantly enhanced binding.

PubMed: 9341205
DOI: 10.1021/bi970912m

Experimental method

X-RAY DIFFRACTION (2.1 Å)