Ubiquitination of MHC Class I Heavy Chains Is Essential for Dislocation by Human Cytomegalovirus-encoded US2 but Not US11
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference72 articles.
1. The major substrates for TAP in vivo are derived from newly synthesized proteins
2. Making sense of mass destruction: quantitating MHC class I antigen presentation
3. Sec6l-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction
4. The Human Cytomegalovirus US11 Gene Product Dislocates MHC Class I Heavy Chains from the Endoplasmic Reticulum to the Cytosol
5. Dislocation of Type I Membrane Proteins from the ER to the Cytosol Is Sensitive to Changes in Redox Potential
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