2K3W
NMR structure of VPS4A-MIT-CHMP6
Summary for 2K3W
Entry DOI | 10.2210/pdb2k3w/pdb |
Descriptor | Vacuolar protein sorting-associating protein 4A, Charged multivesicular body protein 6 (2 entities in total) |
Functional Keywords | esrct-iii, chmp6, mit, atp-binding, membrane, nucleotide-binding, protein transport, transport, coiled coil, endosome, lipoprotein, myristate |
Biological source | Homo sapiens (human) More |
Cellular location | Prevacuolar compartment membrane; Peripheral membrane protein: Q9UN37 Endomembrane system: Q96FZ7 |
Total number of polymer chains | 2 |
Total formula weight | 11700.34 |
Authors | Kieffer, C.,Skalicky, J.J.,Morita, E.,De Domini, I.,Ward, D.M.,Kaplan, J.,Sundquist, W.I. (deposition date: 2008-05-19, release date: 2008-10-28, Last modification date: 2024-05-29) |
Primary citation | Kieffer, C.,Skalicky, J.J.,Morita, E.,De Domenico, I.,Ward, D.M.,Kaplan, J.,Sundquist, W.I. Two distinct modes of ESCRT-III recognition are required for VPS4 functions in lysosomal protein targeting and HIV-1 budding Dev.Cell, 15:62-73, 2008 Cited by PubMed Abstract: The ESCRT pathway mediates membrane remodeling during enveloped virus budding, cytokinesis, and intralumenal endosomal vesicle formation. Late in the pathway, a subset of membrane-associated ESCRT-III proteins display terminal amphipathic "MIM1" helices that bind and recruit VPS4 ATPases via their MIT domains. We now report that VPS4 MIT domains also bind a second, "MIM2" motif found in a different subset of ESCRT-III subunits. The solution structure of the VPS4 MIT-CHMP6 MIM2 complex revealed that MIM2 elements bind in extended conformations along the groove between the first and third helices of the MIT domain. Mutations that block VPS4 MIT-MIM2 interactions inhibit VPS4 recruitment, lysosomal protein targeting, and HIV-1 budding. MIT-MIM2 interactions appear to be common throughout the ESCRT pathway and possibly elsewhere, and we suggest how these interactions could contribute to a mechanism in which VPS4 and ESCRT-III proteins function together to constrict the necks of budding vesicles. PubMed: 18606141DOI: 10.1016/j.devcel.2008.05.014 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
Download full validation report