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SHMT2 and the BRCC36/BRISC deubiquitinase regulate HIV-1 Tat K63-ubiquitylation and destruction by autophagy.
Xu, Muyu; Moresco, James J; Chang, Max; Mukim, Amey; Smith, Davey; Diedrich, Jolene K; Yates, John R; Jones, Katherine A.
Affiliation
  • Xu M; Regulatory Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA, United States of America.
  • Moresco JJ; Mass Spectrometry Core for Proteomics and Metabolomics, The Salk Institute for Biological Studies, La Jolla, CA, United States of America.
  • Chang M; Razavi Newman Integrative Genomics and Bioinformatics Core, The Salk Institute for Biological Studies, La Jolla, CA, United States of America.
  • Mukim A; Division of Infectious Diseases, University of California San Diego School of Medicine, La Jolla, CA, United States of America.
  • Smith D; Division of Infectious Diseases, University of California San Diego School of Medicine, La Jolla, CA, United States of America.
  • Diedrich JK; Mass Spectrometry Core for Proteomics and Metabolomics, The Salk Institute for Biological Studies, La Jolla, CA, United States of America.
  • Yates JR; Department of Molecular Medicine, Scripps Research Institute, La Jolla, CA, United States of America.
  • Jones KA; Department of Molecular Medicine, Scripps Research Institute, La Jolla, CA, United States of America.
PLoS Pathog ; 14(5): e1007071, 2018 05.
Article in En | MEDLINE | ID: mdl-29791506

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycine Hydroxymethyltransferase / Tat Gene Products, Human Immunodeficiency Virus / Deubiquitinating Enzymes / Aminopyridines / Hydrazones / Membrane Proteins Type of study: Prognostic_studies Limits: Humans Language: En Journal: PLoS Pathog Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycine Hydroxymethyltransferase / Tat Gene Products, Human Immunodeficiency Virus / Deubiquitinating Enzymes / Aminopyridines / Hydrazones / Membrane Proteins Type of study: Prognostic_studies Limits: Humans Language: En Journal: PLoS Pathog Year: 2018 Document type: Article Affiliation country: United States Country of publication: United States