http://smart.embl.de/smart/do_annotation.pl?DOMAIN=SM00504 WebPoint mutations and deletion of the amino (N)-terminal RING finger domain of Siah-1 abrogated its ability to promote DCC proteolysis. In the course of defining Siah-1 sequences required for DCC degradation, we found that Siah-1 is itself rapidly degraded via the proteasome pathway, and RING domain mutations stabilized the Siah-1 protein.
79836 - Gene ResultLONRF3 LON peptidase N-terminal domain …
Web10 nov. 2024 · The ability of the TRIM32 RING domain to self-associate is both necessary and sufficient for its catalytic activity: the deletion of the N- and C-terminal helices produces a monomeric form of the protein, whose NMR solution structure has been determined (PDB: 2CT2), and which lacks any detectable E3 ligase activity . Web23 nov. 2024 · They are characterised by a conserved N-terminal tripartite motif comprising a RING, B-box domains, and a coiled-coil region, with C-terminal domains often mediating substrate recruitment ... Macromolecules Find similar proteins by: (by identity cutoff) 3D Structure Small Molecules Experimental Data & Validation Experimental Data sugar grove elementary school houston
BRCA1/BARD1 site-specific ubiquitylation of nucleosomal H2A is
http://smart.embl.de/smart/do_annotation.pl?DOMAIN=SM00184 WebThe data indicate that the Siah-1 N-terminal RING domain is required for its proteolysis function, while the C-terminal sequences regulate oligomerization and binding to target … Web1 jan. 1999 · Siah-1 N-terminal RING domain is required for proteolysis function, and C-terminal sequences regulate oligomerization and binding to target proteins. G Hu … paint thinner in general mills cereal