Amino acid sequence comparison as an aid to determining evolutionary origins
β Scribed by Russell F. Doolittle
- Book ID
- 105274073
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 101 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1573-4943
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The aminolysis of products of sequential degradation of proteins and peptides by methylamine is an alternative method of conversion of the unstable 5-alkyl-2-anilino-4-thiazolinones into the stable methyl amides of N alpha-phenylthiocarbamoyl amino acids. The volatility of methylamine permits use in
Boron trifluoride-etherate (BF,), one of the Lewis acids, was found to be an efficient acid in the Edman sequencing method, affording the retention of the N-terminal amino acid configuration at the cyclization/ cleavage reaction from peptides. Examples for the sequencing of o-ku-Gly and L-Pro-L-ku a