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Studies on cytochrome c. Part III. Synthesis of the protected heneicosapeptide (sequence 24–44) of Baker's yeast iso‐1‐cytochrome c
Author(s) -
Moroder Luis,
Borin Gianfranco,
Marchiori Fernando,
Scoffone Ernesto
Publication year - 1973
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1973.360120305
Subject(s) - chemistry , yeast , sequence (biology) , cytochrome c , azide , stereochemistry , cytochrome , biochemistry , organic chemistry , enzyme , mitochondrion
Syntheses are described for two N ‐benzyloxycarbonylpeptide tert ‐butoxycarbonylhydrazides which correspond to positions 24–34 and 35–44, respectively, of the primary structure of baker's yeast iso‐1‐cytochrome c. The two peptide derivatives were coupled via the azide procedure to form the N ‐benzyloxycarbonylheneicosapeptide tert ‐butoxycarbonylhydrazide (sequence 24–44).