Design of peptidase-resistant peptide inhibitors of myosin light chain kinase

Author:

Khapchaev Asker Y.1,Kazakova Olga A.1,Samsonov Mikhail V.1,Sidorova Maria V.1,Bushuev Valery N.1,Vilitkevich Elena L.1,Az'muko Andrey A.1,Molokoedov Alexander S.1,Bespalova Zhanna D.1,Shirinsky Vladimir P.1

Affiliation:

1. Russian Cardiology Research and Production Center; 3rd Cherepkovskaya St., 15a Moscow 121552 Russia

Funder

Ministry of Education and Science of the Russian Federation

Russian Foundation for Basic Research

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference39 articles.

1. Non-muscle myosin light chain kinase isoform is a viable molecular target in acute inflammatory lung injury;Mirzapoiazova;Am. J. Respir. Cell Mol. Biol.,2011

2. Protein kinase involved in lung injury susceptibility: evidence from enzyme isoform genetic knockout and in vivo inhibitor treatment;Wainwright;Proc. Natl. Acad. Sci. U. S. A.,2003

3. The calmodulin binding domain of chicken smooth muscle myosin light chain kinase contains a pseudosubstrate sequence;Kemp;J. Biol. Chem.,1987

4. Use of DNA sequence and mutant analyses and antisense oligodeoxynucleotides to examine the molecular basis of nonmuscle myosin light chain kinase autoinhibition, calmodulin recognition, and activity;Shoemaker;J. Cell Biol.,1990

5. Proteolysis of smooth muscle myosin light chain kinase. Formation of inactive and calmodulin-independent fragments;Ikebe;J. Biol. Chem.,1987

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