Kinetics and regioselectivity of peptide-to-heterocycle conversions by microcin B17 synthetase
- 1 July 1998
- journal article
- Published by Elsevier in Chemistry & Biology
- Vol. 5 (7) , 373-384
- https://doi.org/10.1016/s1074-5521(98)90071-0
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Role of the microcin B17 propeptide in substrate recognition: solution structure and mutational analysis of McbA1−26Chemistry & Biology, 1998
- Mutational Analysis of Posttranslational Heterocycle Biosynthesis in the Gyrase Inhibitor Microcin B17: Distance Dependence from Propeptide and Tolerance for Substitution in a GSCG Cyclizable SequenceBiochemistry, 1998
- The leader peptide is essential for the post‐translational modification of the DNA‐gyrase inhibitor microcin B17Molecular Microbiology, 1997
- From Peptide Precursors to Oxazole and Thiazole-Containing Peptide Antibiotics: Microcin B17 SynthaseScience, 1996
- Post‐Translational Heterocyclic Backbone Modifications in the 43‐Peptide Antibiotic Microcin B17European Journal of Biochemistry, 1995
- High-resolution tandem FT mass spectrometry above 10 kDaAccounts of Chemical Research, 1994
- The maturation pathway of microcin B17, a peptide inhibitor of DNA gyraseMolecular Microbiology, 1993
- Site-directed mutagenesis of virtually any plasmid by eliminating a unique siteAnalytical Biochemistry, 1992
- Two Acyclic Analogues of 2-b-D-Ribofuranosylthiazole-4-carboxamide (Tiazofurin)HETEROCYCLES, 1987
- 194. Chemistry of micrococcin P. Part IIIJournal of the Chemical Society, 1960