1. The primary structure of skeletal muscle myosin heavy chain: I. Sequence of the amino-terminal 23 kDa fragment
- Author
-
Tetsuo Maita, Masaki Hayashida, and Genji Matsuda
- Subjects
Myosin light-chain kinase ,Molecular Sequence Data ,Sequence alignment ,macromolecular substances ,Biology ,Myosins ,Biochemistry ,chemistry.chemical_compound ,Sequence Homology, Nucleic Acid ,Myosin ,Consensus sequence ,Animals ,Amino Acid Sequence ,Amino Acids ,Molecular Biology ,chemistry.chemical_classification ,Muscles ,Protein primary structure ,Myosin Subfragments ,General Medicine ,Amino acid ,Molecular Weight ,chemistry ,Organ Specificity ,MYH7 ,Cyanogen bromide ,Chickens - Abstract
Subfragment-1 was prepared from adult chicken pectoralis myosin by limited digestion with alpha-chymotrypsin, and an amino-terminal 23 kDa fragment of the heavy chain was obtained by digesting the subfragment-1 with trypsin. The 205-residue sequence of the fragment was determined by sequencing its cyanogen bromide, tryptic, and chymotryptic peptides. The amino-terminal alpha-amino group of the fragment was acetylated, and two methylated lysines; epsilon-N-monomethyllysine and epsilon-N-trimethyllysine were recognized at the 35th and 130th positions, respectively, as in rabbit skeletal myosin. Comparing the 205-residue sequence of the skeletal myosin with those of cardiac, and gizzard myosins from chicken, considerable differences are recognized, especially in the amino-terminal region, but strong homologies are observed around the reactive lysine residue, around the epsilon-N-trimethyllysine residue, and around the consensus sequence of GXXGXGKT for nucleotide-binding proteins. On the other hand, only 12 amino acid substitutions are recognized between adult and embryonic skeletal myosins, allowing for the post-translational methylation.
- Published
- 1991