Ontology highlight
ABSTRACT:
SUBMITTER: Stegmann M
PROVIDER: S-EPMC7163605 | biostudies-literature | 2013 Jan
REPOSITORIES: biostudies-literature
Stegmann Monika M Metcalfe Clive C Barclay A Neil AN
European journal of immunology 20130101 1
Selected disulfide bonds in membrane proteins are labile and are thus susceptible to changes in redox potential and/or the presence of thiol isomerase enzymes. Modification of these disulfide bonds can lead to conformational changes of the protein that in turn may alter protein activity and function. This occurs in the entry of several enveloped viruses into their host cells, e.g. HIV, hepatitis C virus and Newcastle disease virus. Labile disulfide bonds are also important in platelet activation ...[more]