Literature DB >> 18398003

Morphing peptide backbones into heterocycles.

Christopher T Walsh1, Elizabeth M Nolan.   

Abstract

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Year:  2008        PMID： 18398003      PMCID： PMC2311349          DOI： 10.1073/pnas.0802300105

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  16 in total

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4.  The structure of thiostrepton.

Authors:  B Anderson; D C Hodgkin; M A Viswamitra
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5.  From peptide precursors to oxazole and thiazole-containing peptide antibiotics: microcin B17 synthase.

Authors:  Y M Li; J C Milne; L L Madison; R Kolter; C T Walsh
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6.  Revised structure of the antibiotic GE 2270A.

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8.  Oxidase domains in epothilone and bleomycin biosynthesis: thiazoline to thiazole oxidation during chain elongation.

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9.  Cofactor requirements and reconstitution of microcin B17 synthetase: a multienzyme complex that catalyzes the formation of oxazoles and thiazoles in the antibiotic microcin B17.

Authors:  J C Milne; R S Roy; A C Eliot; N L Kelleher; A Wokhlu; B Nickels; C T Walsh
Journal:  Biochemistry       Date:  1999-04-13       Impact factor: 3.162

10.  ATP/GTP hydrolysis is required for oxazole and thiazole biosynthesis in the peptide antibiotic microcin B17.

Authors:  J C Milne; A C Eliot; N L Kelleher; C T Walsh
Journal:  Biochemistry       Date:  1998-09-22       Impact factor: 3.162
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2.  Insights into heterocyclization from two highly similar enzymes.

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3.  Structural elements of an NRPS cyclization domain and its intermodule docking domain.

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