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N-terminal amino acid sequencing of EDP208 conjugative pili

Authors :
Frost, L S
Armstrong, G D
Finlay, B B
Edwards, B F
Paranchych, W
Source :
Journal of Bacteriology; February 1983, Vol. 153 Issue: 2 p950-954, 5p
Publication Year :
1983

Abstract

EDP208 conjugative pili contain a single polypeptide subunit of 11,500 daltons with a blocked N-terminus. This N-terminal blocking moiety was identified as an N-acetyl group by 1H nuclear magnetic resonance analysis of an N-terminal tripeptide isolated from pronase digests of EDP208 pilin. Limited acid hydrolysis of the tripeptide allowed its sequence to be determined as acetyl-NH-Thr-Asp-Leu. Trypsin digestion of EDP208 pilin resulted in the quantitative release of a fragment containing 12 residues from the N-terminus of the protein. The sequence of this dodecapeptide was determined to be acetyl-NH-Thr-Asp-Leu-Leu-Ala-Gly-Gly-Lys-Asp-Val-Asp-Lys.

Details

Language :
English
ISSN :
00219193 and 10985530
Volume :
153
Issue :
2
Database :
Supplemental Index
Journal :
Journal of Bacteriology
Publication Type :
Periodical
Accession number :
ejs57602918
Full Text :
https://doi.org/10.1128/jb.153.2.950-954.1983