Isolation and sequence analysis of a cDNA clone encoding the entire catalytic subunit of phosphorylase kinase.

Abstract:

:Synthetic oligonucleotides have been used to isolate a 1.85 kb clone containing the full length coding sequence for the catalytic subunit of rabbit skeletal muscle phosphorylase kinase from a cDNA library constructed in lambda gt10. Sequence analysis of the clone predicted an amino acid sequence in agreement with a published primary structure. Inspection of the codon usage revealed a strong preference for G or C nucleotides at the third codon position as found for several other skeletal muscle proteins. This cDNA clone should facilitate identification of functional domains, including the calmodulin-binding site, and investigation of the molecular basis of X-linked phosphorylase kinase deficiencies.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

da Cruz e Silva EF,Cohen PT

doi

10.1016/0014-5793(87)80871-2

subject

Has Abstract

pub_date

1987-08-10 00:00:00

pages

36-42

issue

1

eissn

0014-5793

issn

1873-3468

pii

0014-5793(87)80871-2

journal_volume

220

pub_type

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