The ER membrane protein complex interacts cotranslationally to enable biogenesis of multipass membrane proteins.

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Bibliographic Details
Title: The ER membrane protein complex interacts cotranslationally to enable biogenesis of multipass membrane proteins.
Authors: Shurtleff MJ; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Itzhak DN; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany., Hussmann JA; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Schirle Oakdale NT; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States.; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United States., Costa EA; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Jonikas M; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Weibezahn J; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Popova KD; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Jan CH; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States., Sinitcyn P; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany., Vembar SS; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, United States., Hernandez H; Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, United States., Cox J; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany., Burlingame AL; Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, United States., Brodsky JL; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, United States., Frost A; Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, United States.; Chan Zuckerberg Biohub, San Francisco, United States., Borner GH; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany., Weissman JS; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, United States.; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, United States.
Source: ELife [Elife] 2018 May 29; Vol. 7. Date of Electronic Publication: 2018 May 29.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: eLife Sciences Publications, Ltd Country of Publication: England NLM ID: 101579614 Publication Model: Electronic Cited Medium: Internet ISSN: 2050-084X (Electronic) Linking ISSN: 2050084X NLM ISO Abbreviation: Elife Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2050-084X
DOI:10.7554/eLife.37018