Ontology highlight
ABSTRACT:
SUBMITTER: Mandal K
PROVIDER: S-EPMC2774425 | biostudies-literature | 2009 Jun
REPOSITORIES: biostudies-literature
Mandal Kalyaneswar K Pentelute Brad L BL Tereshko Valentina V Thammavongsa Vilasak V Schneewind Olaf O Kossiakoff Anthony A AA Kent Stephen B H SB
Protein science : a publication of the Protein Society 20090601 6
We describe the use of racemic crystallography to determine the X-ray structure of the natural product plectasin, a potent antimicrobial protein recently isolated from fungus. The protein enantiomers L-plectasin and D-plectasin were prepared by total chemical synthesis; interestingly, L-plectasin showed the expected antimicrobial activity, while D-plectasin was devoid of such activity. The mirror image proteins were then used for racemic crystallization. Synchrotron X-ray diffraction data were c ...[more]