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PMID: 2012809 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Definition of the inhibitory domain of smooth muscle myosin light chain kinase by site-directed mutagenesis.

Biochemistry ·Vol. 30 ·No. 14 ·1991-04-09 ·Pages 3498-503

Ito M, Guerriero V, Chen XM, Hartshorne DJ

Abstract

Site-directed mutagenesis of smooth muscle myosin light chain kinase was applied to define its autoinhibitory domain. Mutants were all initiated at Leu-447 but contained varying lengths of C-terminal sequence. Those containing the complete C-terminal sequence to Glu-972 possessed kinase activities that were calmodulin-dependent. Removal of the putative inhibitory domain by truncation to Thr-778 resulted in generation of a constitutively active (calmodulin-independent) species. Thus, the inhibitory domain lies to the C-terminal side of Thr-778. Truncation to Lys-793 and to Trp-800 also resulted in constitutively active mutants, although the specific activity of the latter was less than the other mutants. None of the truncated mutants bound calmodulin. For each mutant, the Km values with respect to ATP and to the 20,000-dalton light chain were similar to values obtained with the native enzyme. The presence of the inhibitory domain was detected by activation of kinase activity following limited proteolysis with trypsin. Using this procedure, it was determined that the inhibitory domain was manifest only in the mutant truncated to Trp-800 and was absent from that ending at Lys-793. These results indicate that a critical region of the inhibitory domain is contained within the sequence Tyr-794 to Trp-800. This region overlaps with the calmodulin-binding site for five residues. Our assignment of the inhibitory sequence is consistent with autoinhibition via a pseudosubstrate domain.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Enzyme Activation/drug effects Gizzard, Avian/enzymology Hydrolysis Molecular Sequence Data Muscle, Smooth/drug effects,enzymology Mutagenesis, Site-Directed Myosin-Light-Chain Kinase/genetics,metabolism Structure-Activity Relationship Substrate Specificity Trypsin/pharmacology Turkeys
Chemicals
Myosin-Light-Chain Kinase Trypsin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ito M
First Medical Clinic, Mie University Hospital, Mieken, Japan.
Guerriero V
Chen X M
Hartshorne D J
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1991-04-09
Pages
3498-503
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NHLBI NIH HHS · HL-23615 · United States
NHLBI NIH HHS · HL-43651 · United States
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