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Furthermore, alphaSNAP-deficient mutant animals displayed reduced formation of lysozyme granules in small intestinal crypts and decreased expression of lysozyme and defensins in the intestinal mucosa, which is indicative of defects in Paneth cell differentiation. By contrast, development of Goblet cells, enteroendocrine cells, and assembly of enterocyte apical junctions was not altered in hyh mutant mice. Our data reve...
AMPK (zeige PRKAA1 Proteine) associates with alpha-SNAP, an adapter that enables disassembly of cis (zeige CISH Proteine)-SNARE (zeige VTI1B Proteine) complexes formed during membrane fusion.
analysis of alpha- and betaSNAP deletion mutant neurons shows that the two N-Ethylmaleimide-Sensitive Factor (zeige NSF Proteine) cofactors support synaptic vesicle priming by determining the availability of free SNARE (zeige VTI1B Proteine) components
Study indicate that the genotyping method enhances the potentiality of hyh mouse as a unique in vivo model to study the role of membrane trafficking in different developmental and physiological processes.
The hyh mutation uncovers roles for alpha Snap in apical protein localization and control of neural cell fate.
data implicates beta1 integrin, FAK (zeige PTK2 Proteine), and paxillin (zeige PXN Proteine) in mediating the observed pro-adhesive effects of alphaSNAP. These results reveal novel roles for alphaSNAP in regulating ECM (zeige MMRN1 Proteine) adhesion and motility of epithelial cells.
Study revealed a novel role for alphaSNAP as a negative regulator of autophagy that acts by enhancing mTOR (zeige FRAP1 Proteine) signaling and regulating the integrity of the Golgi complex.
The most N-terminal part of BKV agnoprotein is involved in the interaction with alpha-SNAP
a novel role for alphaSNAP in promoting epithelial cell survival by unique mechanisms involving regulation of Bcl-2 (zeige BCL2 Proteine) expression and Golgi biogenesis
Results suggest that the combinational SNARE proteins VAMP8 and Vti1b mediate the fusion of antimicrobial and canonical autophagosomes with lysosomes, an essential event for autophagic degradation.
alpha-SNAP plays a key role in the acrosome reaction.
G alpha12 interaction with alphaSNAP induces VE-cadherin (zeige CDH5 Proteine) localization at endothelial junctions and regulates barrier function
alpha-SNAP destabilized the linker domain (LD) of the SNARE complex but stabilized its C-terminal domain.
This gene encodes a member of the soluble NSF attachment protein (SNAP) family. SNAP proteins play a critical role in the docking and fusion of vesicles to target membranes as part of the 20S NSF-SNAP-SNARE complex. The encoded protein plays a role in the completion of membrane fusion by mediating the interaction of N-ethylmaleimide-sensitive factor (NSF) with the vesicle-associated and membrane-associated SNAP receptor (SNARE) complex, and stimulating the ATPase activity of NSF. Alternatively spliced transcript variants have been observed for this gene.
, alpha-soluble NSF attachment protein
, N-ethylmaleimide-sensitive factor attachment protein, beta
, N-ethylmaleimide sensitive fusion protein attachment protein alpha
, N-ethylmaleimide-sensitive factor attachment protein alpha
, N-ethylmaleimide-sensitive factor attachment protein, alpha
, hydrocephaly with hop gait