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Publication : Hybrid structural model of the complete human ESCRT-0 complex.

First Author  Ren X Year  2009
Journal  Structure Volume  17
Issue  3 Pages  406-16
PubMed ID  19278655 Mgi Jnum  J:245341
Mgi Id  MGI:5918198 Doi  10.1016/j.str.2009.01.012
Citation  Ren X, et al. (2009) Hybrid structural model of the complete human ESCRT-0 complex. Structure 17(3):406-16
abstractText  The human Hrs and STAM proteins comprise the ESCRT-0 complex, which sorts ubiquitinated cell surface receptors to lysosomes for degradation. Here we report a model for the complete ESCRT-0 complex based on the crystal structure of the Hrs-STAM core complex, previously solved domain structures, hydrodynamic measurements, and Monte Carlo simulations. ESCRT-0 expressed in insect cells has a hydrodynamic radius of RH = 7.9 nm and is a 1:1 heterodimer. The 2.3 Angstroms crystal structure of the ESCRT-0 core complex reveals two domain-swapped GAT domains and an antiparallel two-stranded coiled-coil, similar to yeast ESCRT-0. ESCRT-0 typifies a class of biomolecular assemblies that combine structured and unstructured elements, and have dynamic and open conformations to ensure versatility in target recognition. Coarse-grained Monte Carlo simulations constrained by experimental RH values for ESCRT-0 reveal a dynamic ensemble of conformations well suited for diverse functions.
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