The Synthesis of N-Terminal Acetylpeptides of Ovalbumin and Mammalian Heart Cytochrome c
- 1 February 1965
- journal article
- research article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 38 (2) , 215-220
- https://doi.org/10.1246/bcsj.38.215
Abstract
In previous studies acetylglycylserine and acetylglycylaspartylalylglutamic acid had been isolated from the enzymatic digests of ovalbumin and cytochromes c of bovine and equine hearts respectively. Here, in order to confirm the structures of the acetylpeptides isolated, acetylglycyl-L-serine and acetylglycyl-L-aspartyl-L-valyl-L-glutamic acid have been synthesized. It has been proved that the natural acetylpeptides are identical with the synthetic ones in every respect examined. Some troubles encountered during the synthesis of the acetyltetrapeptide have been discussed.Keywords
This publication has 4 references indexed in Scilit:
- N-Terminal Sequence in OvalbuminThe Journal of Biochemistry, 1962
- Amino-Acid Sequence of Horse Heart Cytochrome C : The Complete Amino-acid SequenceNature, 1961
- Studies on Serine Peptides. I. Optical Resolution of O-Benzyl-Dl-serine and Synthesis of Dl-Serine PeptidesBulletin of the Chemical Society of Japan, 1956
- Titration of Acids in Nonaqueous SolventsAnalytical Chemistry, 1951