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The AAA ATPase spastin links microtubule severing to membrane modelling
AbstractIn 1999, mutations in the gene encoding the microtubule severing AAA ATPase spastin were identified as a major cause of a gene
Coupling and Dynamics of Subunits in the Hexameric AAA+ Chaperone ClpB
AbstractThe bacterial AAA+ protein ClpB and its eukaryotic homologue Hsp104 ensure thermotolerance of their respective organisms by re
The major-effect quantitative trait locus CsARN6.1 encodes an AAA ATPase domain-containing prote
In plants, the formation of hypocotyl-derived adventitious roots (ARs) is an important morphological acclimation to waterlogging stres
Regulation of the co-evolved HrpR and HrpS AAA+ proteins required for Pseudomonas syringae patho
The bacterial AAA+ enhancer-binding proteins (EBPs) HrpR and HrpS (HrpRS) of Pseudomonas syringae (Ps) activate σ(54)-dependent trans
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic p
Autosomal dominant hereditary spastic paraplegia (AD-HSP) is a genetically heterogeneous neurodegenerative disorder characterized by p
A Conserved Unfoldase Activity for the p97 AAA-ATPase in Proteasomal Degradation
AbstractThe multifunctional AAA-ATPase p97 is one of the most abundant and conserved proteins in eukaryotic cells. The p97/Npl4/Ufd1 c
Reconstitution of the 26S proteasome reveals functional asymmetries in its AAA+ unfoldase.
The 26S proteasome is the major eukaryotic ATP-dependent protease, yet the detailed mechanisms used by the proteasomal heterohexameric
The Pex1/Pex6 Complex Is a Heterohexameric AAA + Motor with Alternating and Highly Coordinated S
AbstractPex1 and Pex6 are Type-2 AAA+ ATPases required for the de novo biogenesis of peroxisomes. Mutations in Pex1 and Pex6 account f
The N-end rule pathway: From recognition by N-recognins, to destruction by AAA + proteases
AbstractIntracellular proteolysis is a tightly regulated process responsible for the targeted removal of unwanted or damaged proteins.
Structure of the AAA ATPase p97
Abstract p97, an abundant hexameric ATPase of the AAA family, is involved in homotypic membrane fusion. It is thought to disassem
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