186 related articles for article (PubMed ID: 24613487)
1. Lytic water dynamics reveal evolutionarily conserved mechanisms of ATP hydrolysis by TIP49 AAA+ ATPases.
Afanasyeva A; Hirtreiter A; Schreiber A; Grohmann D; Pobegalov G; McKay AR; Tsaneva I; Petukhov M; Käs E; Grigoriev M; Werner F
Structure; 2014 Apr; 22(4):549-59. PubMed ID: 24613487
[TBL] [Abstract][Full Text] [Related]
2. Large-scale conformational flexibility determines the properties of AAA+ TIP49 ATPases.
Petukhov M; Dagkessamanskaja A; Bommer M; Barrett T; Tsaneva I; Yakimov A; Quéval R; Shvetsov A; Khodorkovskiy M; Käs E; Grigoriev M
Structure; 2012 Aug; 20(8):1321-31. PubMed ID: 22748767
[TBL] [Abstract][Full Text] [Related]
3. Insights into the evolutionary conserved regulation of Rio ATPase activity.
Knüppel R; Christensen RH; Gray FC; Esser D; Strauß D; Medenbach J; Siebers B; MacNeill SA; LaRonde N; Ferreira-Cerca S
Nucleic Acids Res; 2018 Feb; 46(3):1441-1456. PubMed ID: 29237037
[TBL] [Abstract][Full Text] [Related]
4. A notable example of an evolutionary conserved gene: studies on a putative DNA helicase TIP49.
Kurokawa Y; Kanemaki M; Makino Y; Tamura TA
DNA Seq; 1999; 10(1):37-42. PubMed ID: 10565543
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Conserved motifs involved in ATP hydrolysis by MalT, a signal transduction ATPase with numerous domains from Escherichia coli.
Marquenet E; Richet E
J Bacteriol; 2010 Oct; 192(19):5181-91. PubMed ID: 20693326
[TBL] [Abstract][Full Text] [Related]
7. The thermosome from Methanopyrus kandleri possesses an NH4+-dependent ATPase activity.
Andrä S; Frey G; Jaenicke R; Stetter KO
Eur J Biochem; 1998 Jul; 255(1):93-9. PubMed ID: 9692906
[TBL] [Abstract][Full Text] [Related]
8. Elements in nucleotide sensing and hydrolysis of the AAA+ disaggregation machine ClpB: a structure-based mechanistic dissection of a molecular motor.
Zeymer C; Barends TR; Werbeck ND; Schlichting I; Reinstein J
Acta Crystallogr D Biol Crystallogr; 2014 Feb; 70(Pt 2):582-95. PubMed ID: 24531492
[TBL] [Abstract][Full Text] [Related]
9. Dissecting the role of a conserved motif (the second region of homology) in the AAA family of ATPases. Site-directed mutagenesis of the ATP-dependent protease FtsH.
Karata K; Inagawa T; Wilkinson AJ; Tatsuta T; Ogura T
J Biol Chem; 1999 Sep; 274(37):26225-32. PubMed ID: 10473576
[TBL] [Abstract][Full Text] [Related]
10. The first crystal structure of the peptidase domain of the U32 peptidase family.
Schacherl M; Montada AA; Brunstein E; Baumann U
Acta Crystallogr D Biol Crystallogr; 2015 Dec; 71(Pt 12):2505-12. PubMed ID: 26627657
[TBL] [Abstract][Full Text] [Related]
11. The promiscuous phosphomonoestearase activity of Archaeoglobus fulgidus CopA, a thermophilic Cu+ transport ATPase.
Bredeston LM; González Flecha FL
Biochim Biophys Acta; 2016 Jul; 1858(7 Pt A):1471-8. PubMed ID: 27086711
[TBL] [Abstract][Full Text] [Related]
12. Dodecameric structure and ATPase activity of the human TIP48/TIP49 complex.
Puri T; Wendler P; Sigala B; Saibil H; Tsaneva IR
J Mol Biol; 2007 Feb; 366(1):179-92. PubMed ID: 17157868
[TBL] [Abstract][Full Text] [Related]
13. Conserved arginine residues implicated in ATP hydrolysis, nucleotide-sensing, and inter-subunit interactions in AAA and AAA+ ATPases.
Ogura T; Whiteheart SW; Wilkinson AJ
J Struct Biol; 2004; 146(1-2):106-12. PubMed ID: 15095758
[TBL] [Abstract][Full Text] [Related]
14. Direct evidence that a conserved arginine in RuvB AAA+ ATPase acts as an allosteric effector for the ATPase activity of the adjacent subunit in a hexamer.
Hishida T; Han YW; Fujimoto S; Iwasaki H; Shinagawa H
Proc Natl Acad Sci U S A; 2004 Jun; 101(26):9573-7. PubMed ID: 15210950
[TBL] [Abstract][Full Text] [Related]
15. Insights into FlaI functions in archaeal motor assembly and motility from structures, conformations, and genetics.
Reindl S; Ghosh A; Williams GJ; Lassak K; Neiner T; Henche AL; Albers SV; Tainer JA
Mol Cell; 2013 Mar; 49(6):1069-82. PubMed ID: 23416110
[TBL] [Abstract][Full Text] [Related]
16. ATPase site architecture is required for self-assembly and remodeling activity of a hexameric AAA+ transcriptional activator.
Joly N; Zhang N; Buck M
Mol Cell; 2012 Aug; 47(3):484-90. PubMed ID: 22789710
[TBL] [Abstract][Full Text] [Related]
17. The stimulating role of subunit F in ATPase activity inside the A1-complex of the Methanosarcina mazei Gö1 A1AO ATP synthase.
Singh D; Sielaff H; Sundararaman L; Bhushan S; Grüber G
Biochim Biophys Acta; 2016 Feb; 1857(2):177-187. PubMed ID: 26682760
[TBL] [Abstract][Full Text] [Related]
18. VAT, the thermoplasma homolog of mammalian p97/VCP, is an N domain-regulated protein unfoldase.
Gerega A; Rockel B; Peters J; Tamura T; Baumeister W; Zwickl P
J Biol Chem; 2005 Dec; 280(52):42856-62. PubMed ID: 16236712
[TBL] [Abstract][Full Text] [Related]
19. The RadA protein from a hyperthermophilic archaeon Pyrobaculum islandicum is a DNA-dependent ATPase that exhibits two disparate catalytic modes, with a transition temperature at 75 degrees C.
Spies M; Kil Y; Masui R; Kato R; Kujo C; Ohshima T; Kuramitsu S; Lanzov V
Eur J Biochem; 2000 Feb; 267(4):1125-37. PubMed ID: 10672022
[TBL] [Abstract][Full Text] [Related]
20. Two-way communication between SecY and SecA suggests a Brownian ratchet mechanism for protein translocation.
Allen WJ; Corey RA; Oatley P; Sessions RB; Baldwin SA; Radford SE; Tuma R; Collinson I
Elife; 2016 May; 5():. PubMed ID: 27183269
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]