307 related articles for article (PubMed ID: 16219770)
21. The Hsp110 molecular chaperone stabilizes apolipoprotein B from endoplasmic reticulum-associated degradation (ERAD).
Hrizo SL; Gusarova V; Habiel DM; Goeckeler JL; Fisher EA; Brodsky JL
J Biol Chem; 2007 Nov; 282(45):32665-75. PubMed ID: 17823116
[TBL] [Abstract][Full Text] [Related]
22. The hsp110 and Grp1 70 stress proteins: newly recognized relatives of the Hsp70s.
Easton DP; Kaneko Y; Subjeck JR
Cell Stress Chaperones; 2000 Oct; 5(4):276-90. PubMed ID: 11048651
[TBL] [Abstract][Full Text] [Related]
23. Overexpression of yeast Hsp110 homolog Sse1p suppresses ydj1-151 thermosensitivity and restores Hsp90-dependent activity.
Goeckeler JL; Stephens A; Lee P; Caplan AJ; Brodsky JL
Mol Biol Cell; 2002 Aug; 13(8):2760-70. PubMed ID: 12181344
[TBL] [Abstract][Full Text] [Related]
24. Human and yeast Hsp110 chaperones exhibit functional differences.
Raviol H; Bukau B; Mayer MP
FEBS Lett; 2006 Jan; 580(1):168-74. PubMed ID: 16364315
[TBL] [Abstract][Full Text] [Related]
25. The mammalian disaggregase machinery: Hsp110 synergizes with Hsp70 and Hsp40 to catalyze protein disaggregation and reactivation in a cell-free system.
Shorter J
PLoS One; 2011; 6(10):e26319. PubMed ID: 22022600
[TBL] [Abstract][Full Text] [Related]
26. The endoplasmic reticulum Grp170 acts as a nucleotide exchange factor of Hsp70 via a mechanism similar to that of the cytosolic Hsp110.
Andréasson C; Rampelt H; Fiaux J; Druffel-Augustin S; Bukau B
J Biol Chem; 2010 Apr; 285(16):12445-53. PubMed ID: 20177057
[TBL] [Abstract][Full Text] [Related]
27. The biochemical properties of the ATPase activity of a 70-kDa heat shock protein (Hsp70) are governed by the C-terminal domains.
Lopez-Buesa P; Pfund C; Craig EA
Proc Natl Acad Sci U S A; 1998 Dec; 95(26):15253-8. PubMed ID: 9860955
[TBL] [Abstract][Full Text] [Related]
28. Insights into the structural dynamics of the Hsp110-Hsp70 interaction reveal the mechanism for nucleotide exchange activity.
Andréasson C; Fiaux J; Rampelt H; Druffel-Augustin S; Bukau B
Proc Natl Acad Sci U S A; 2008 Oct; 105(43):16519-24. PubMed ID: 18948593
[TBL] [Abstract][Full Text] [Related]
29. Differential regulation of Hsp70 subfamilies by the eukaryotic DnaJ homologue YDJ1.
Cyr DM; Douglas MG
J Biol Chem; 1994 Apr; 269(13):9798-804. PubMed ID: 8144572
[TBL] [Abstract][Full Text] [Related]
30. Interdomain communication suppressing high intrinsic ATPase activity of Sse1 is essential for its co-disaggregase activity with Ssa1.
Kumar V; Peter JJ; Sagar A; Ray A; Jha MP; Rebeaud ME; Tiwari S; Goloubinoff P; Ashish F; Mapa K
FEBS J; 2020 Feb; 287(4):671-694. PubMed ID: 31423733
[TBL] [Abstract][Full Text] [Related]
31. Mutational analysis of Sse1 (Hsp110) suggests an integral role for this chaperone in yeast prion propagation in vivo.
Moran C; Kinsella GK; Zhang ZR; Perrett S; Jones GW
G3 (Bethesda); 2013 Aug; 3(8):1409-18. PubMed ID: 23797105
[TBL] [Abstract][Full Text] [Related]
32. Roles of cytosolic Hsp70 and Hsp40 molecular chaperones in post-translational translocation of presecretory proteins into the endoplasmic reticulum.
Ngosuwan J; Wang NM; Fung KL; Chirico WJ
J Biol Chem; 2003 Feb; 278(9):7034-42. PubMed ID: 12493732
[TBL] [Abstract][Full Text] [Related]
33. Hsp70 nucleotide exchange factor Fes1 is essential for ubiquitin-dependent degradation of misfolded cytosolic proteins.
Gowda NK; Kandasamy G; Froehlich MS; Dohmen RJ; Andréasson C
Proc Natl Acad Sci U S A; 2013 Apr; 110(15):5975-80. PubMed ID: 23530227
[TBL] [Abstract][Full Text] [Related]
34. Two chaperones locked in an embrace: structure and function of the ribosome-associated complex RAC.
Zhang Y; Sinning I; Rospert S
Nat Struct Mol Biol; 2017 Aug; 24(8):611-619. PubMed ID: 28771464
[TBL] [Abstract][Full Text] [Related]
35. The molecular chaperone Ssb from Saccharomyces cerevisiae is a component of the ribosome-nascent chain complex.
Pfund C; Lopez-Hoyo N; Ziegelhoffer T; Schilke BA; Lopez-Buesa P; Walter WA; Wiedmann M; Craig EA
EMBO J; 1998 Jul; 17(14):3981-9. PubMed ID: 9670014
[TBL] [Abstract][Full Text] [Related]
36. Hsp110 is required for spindle length control.
Makhnevych T; Wong P; Pogoutse O; Vizeacoumar FJ; Greenblatt JF; Emili A; Houry WA
J Cell Biol; 2012 Aug; 198(4):623-36. PubMed ID: 22908312
[TBL] [Abstract][Full Text] [Related]
37. Divergent functional properties of the ribosome-associated molecular chaperone Ssb compared with other Hsp70s.
Pfund C; Huang P; Lopez-Hoyo N; Craig EA
Mol Biol Cell; 2001 Dec; 12(12):3773-82. PubMed ID: 11739779
[TBL] [Abstract][Full Text] [Related]
38. Profiling Ssb-Nascent Chain Interactions Reveals Principles of Hsp70-Assisted Folding.
Döring K; Ahmed N; Riemer T; Suresh HG; Vainshtein Y; Habich M; Riemer J; Mayer MP; O'Brien EP; Kramer G; Bukau B
Cell; 2017 Jul; 170(2):298-311.e20. PubMed ID: 28708998
[TBL] [Abstract][Full Text] [Related]
39. The Hsp110 protein chaperone Sse1 is required for yeast cell wall integrity and morphogenesis.
Shaner L; Gibney PA; Morano KA
Curr Genet; 2008 Jul; 54(1):1-11. PubMed ID: 18478233
[TBL] [Abstract][Full Text] [Related]
40. Prediction of novel Bag-1 homologs based on structure/function analysis identifies Snl1p as an Hsp70 co-chaperone in Saccharomyces cerevisiae.
Sondermann H; Ho AK; Listenberger LL; Siegers K; Moarefi I; Wente SR; Hartl FU; Young JC
J Biol Chem; 2002 Sep; 277(36):33220-7. PubMed ID: 12105220
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
