The structural basis for substrate versatility of chloramphenicol acetyltransferase CATI-Reference-Cited by-同舟云学术

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The structural basis for substrate versatility of chloramphenicol acetyltransferase CATI

Published:2012-03-06 Issue:4 Volume:21 Page:520-530
ISSN:0961-8368
Container-title:Protein Science
language:en
Short-container-title:Protein Science

Author:

Biswas Tapan,Houghton Jacob L.,Garneau-Tsodikova Sylvie,Tsodikov Oleg V.

Funder

Life Sciences Institute

College of Pharmacy (University of Michigan)

Cellular Biotechnology Training Program (CBTP)

American Foundation of Pharmaceutical Education (AFPE) Fellowship

Rackham Merit Fellowship at the University of Michigan

National Institutes of Health (NIH)

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pro.2036/fullpdf

Reference54 articles.

1. Chloromycetin and streptothricin;Carter;Science,1948

2. Molecular basis of chloramphenicol and thiamphenicol toxicity to DNA in vitro;Skolimowski;J Antimicrob Chemother,1983

3. Is chloramphenicol making a comeback?;Nitzan;Isr Med Assoc,2010

4. Structures of the Escherichia coli ribosome with antibiotics bound near the peptidyl transferase center explain spectra of drug action;Dunkle;Proc Natl Acad Sci USA,2010

5. Revisiting the structures of several antibiotics bound to the bacterial ribosome;Bulkley;Proc Natl Acad Sci USA,2010

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