Journal article
A serine in the first transmembrane domain of the human E3 ubiquitin ligase MARCH9 is critical for down-regulation of its protein substrates
C Tan, EFX Byrne, C Ah-Cann, MJ Call, ME Call
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2019
Abstract
The membrane-associated RING-CH (MARCH) family of membrane-bound E3 ubiquitin ligases regulates the levels of cell-surface membrane proteins, many of which are involved in immune responses. Although their role in ubiquitin-dependent endocytosis and degradation of cell-surface proteins is extensively documented, the features of MARCH proteins and their substrates that drive the molecular recognition events leading to ubiquitin transfer remain poorly defined. In this study, we sought to determine the features of human MARCH9 that are required for regulating the surface levels of its substrate proteins. Consistent with previous studies of other MARCH proteins, we found that susceptibility to MA..
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Awarded by University of Melbourne
Funding Acknowledgements
[ "This work was supported in part by Australian National Health and Medical Research Council Grant GNT1030902 and IRIISS Infrastructure Support and Human Frontier Science Program Grant RGP0064/2011. The authors declare that they have no conflicts of interest with the contents of this article.", "Supported by Melbourne Research and Fee Remission Scholarships (University of Melbourne).", "Supported by Australian Research Council Future Fellowship FT120100145.", "Supported by QEII Fellowship DP110104369 from the Australian Research Council." ]