| Literature DB >> 2065774 |
S Pfeffer1, W Höhne, S Branner, K Wilson, C Betzel.
Abstract
Bacitracins are a group of widely used peptide antibiotics. There has been interest in determining the three-dimensional structure of the bacitracins. However, solution studies indicate significant flexibility in their structure and to date native bacitracins have resisted attempts at crystallisation despite considerable efforts over a number of years by several groups. Here we report the first three-dimensional X-ray structure of a bacitracin, complexed to a subtilisin proteinase. X-Ray diffraction data were collected using synchrotron radiation in combination with the Image Plate Scanner system. The complex structure including two enzymes, two bacitracins, 220 water molecules and two Ca2+ ions was refined by restrained least-squares to a crystallographic R factor ( = sigma [[Fo-Fc]]/sigma [Fo]]) of 16.3% at 2.0 A.Entities:
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Year: 1991 PMID: 2065774 DOI: 10.1016/0014-5793(91)80738-o
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124