Ontology highlight
ABSTRACT:
SUBMITTER: Lentz CS
PROVIDER: S-EPMC6202179 | biostudies-literature | 2018 Jun
REPOSITORIES: biostudies-literature
Lentz Christian S CS Sheldon Jessica R JR Crawford Lisa A LA Cooper Rachel R Garland Megan M Amieva Manuel R MR Weerapana Eranthie E Skaar Eric P EP Bogyo Matthew M
Nature chemical biology 20180516 6
Serine hydrolases play diverse roles in regulating host-pathogen interactions in a number of organisms, yet few have been characterized in the human pathogen Staphylococcus aureus. Here we describe a chemical proteomic screen that identified ten previously uncharacterized S. aureus serine hydrolases that mostly lack human homologs. We termed these enzymes fluorophosphonate-binding hydrolases (FphA-J). One hydrolase, FphB, can process short fatty acid esters, exhibits increased activity in respon ...[more]