These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
111 related articles for article (PubMed ID: 15613467)
41. The R6A-1 peptide binds to switch II of Galphai1 but is not a GDP-dissociation inhibitor. Willard FS; Siderovski DP Biochem Biophys Res Commun; 2006 Jan; 339(4):1107-12. PubMed ID: 16338227 [TBL] [Abstract][Full Text] [Related]
42. Helix dipole movement and conformational variability contribute to allosteric GDP release in Galphai subunits. Preininger AM; Funk MA; Oldham WM; Meier SM; Johnston CA; Adhikary S; Kimple AJ; Siderovski DP; Hamm HE; Iverson TM Biochemistry; 2009 Mar; 48(12):2630-42. PubMed ID: 19222191 [TBL] [Abstract][Full Text] [Related]
43. Detection of adenylyl cyclase activity using a fluorescent ATP substrate and capillary electrophoresis. Cunliffe JM; Sunahara RK; Kennedy RT Anal Chem; 2006 Mar; 78(6):1731-8. PubMed ID: 16536404 [TBL] [Abstract][Full Text] [Related]
44. The GAPs, GEFs, and GDIs of heterotrimeric G-protein alpha subunits. Siderovski DP; Willard FS Int J Biol Sci; 2005; 1(2):51-66. PubMed ID: 15951850 [TBL] [Abstract][Full Text] [Related]
45. Is there a rate-limiting step before GTP cleavage by H-ras p21? Rensland H; Lautwein A; Wittinghofer A; Goody RS Biochemistry; 1991 Nov; 30(46):11181-5. PubMed ID: 1932038 [TBL] [Abstract][Full Text] [Related]
46. Two RGS proteins that inhibit Galpha(o) and Galpha(q) signaling in C. elegans neurons require a Gbeta(5)-like subunit for function. Chase DL; Patikoglou GA; Koelle MR Curr Biol; 2001 Feb; 11(4):222-31. PubMed ID: 11250150 [TBL] [Abstract][Full Text] [Related]
47. The human delta opioid receptor activates G(i1)alpha more efficiently than G(o1)alpha. Moon HE; Cavalli A; Bahia DS; Hoffmann M; Massotte D; Milligan G J Neurochem; 2001 Mar; 76(6):1805-13. PubMed ID: 11259498 [TBL] [Abstract][Full Text] [Related]
48. Roles of G(o)alpha tryptophans in GTP hydrolysis, GDP release, and fluorescence signals. Lan KL; Remmers AE; Neubig RR Biochemistry; 1998 Jan; 37(3):837-43. PubMed ID: 9454573 [TBL] [Abstract][Full Text] [Related]
49. Thermodynamic characterization of the binding of activator of G protein signaling 3 (AGS3) and peptides derived from AGS3 with G alpha i1. Adhikari A; Sprang SR J Biol Chem; 2003 Dec; 278(51):51825-32. PubMed ID: 14530282 [TBL] [Abstract][Full Text] [Related]
50. Identification of a novel site within G protein alpha subunits important for specificity of receptor-G protein interaction. Heydorn A; Ward RJ; Jorgensen R; Rosenkilde MM; Frimurer TM; Milligan G; Kostenis E Mol Pharmacol; 2004 Aug; 66(2):250-9. PubMed ID: 15266015 [TBL] [Abstract][Full Text] [Related]
51. Structure of RGS4 bound to AlF4--activated G(i alpha1): stabilization of the transition state for GTP hydrolysis. Tesmer JJ; Berman DM; Gilman AG; Sprang SR Cell; 1997 Apr; 89(2):251-61. PubMed ID: 9108480 [TBL] [Abstract][Full Text] [Related]
52. Measurement of GTP-binding and GTPase activity of heterotrimeric Gα proteins. Choudhury SR; Westfall CS; Hackenberg D; Pandey S Methods Mol Biol; 2013; 1043():13-20. PubMed ID: 23913031 [TBL] [Abstract][Full Text] [Related]
53. Role of palmitoylation in RGS protein function. Jones TL Methods Enzymol; 2004; 389():33-55. PubMed ID: 15313558 [TBL] [Abstract][Full Text] [Related]
54. Palmitoylation regulates GDP/GTP exchange of G protein by affecting the GTP-binding activity of Goalpha. Cao Y; Huang Y Int J Biochem Cell Biol; 2005 Mar; 37(3):637-44. PubMed ID: 15618020 [TBL] [Abstract][Full Text] [Related]
55. Regulators of G-protein signaling accelerate GPCR signaling kinetics and govern sensitivity solely by accelerating GTPase activity. Lambert NA; Johnston CA; Cappell SD; Kuravi S; Kimple AJ; Willard FS; Siderovski DP Proc Natl Acad Sci U S A; 2010 Apr; 107(15):7066-71. PubMed ID: 20351284 [TBL] [Abstract][Full Text] [Related]
56. Mechanism of the intrinsic arginine finger in heterotrimeric G proteins. Mann D; Teuber C; Tennigkeit SA; Schröter G; Gerwert K; Kötting C Proc Natl Acad Sci U S A; 2016 Dec; 113(50):E8041-E8050. PubMed ID: 27911799 [TBL] [Abstract][Full Text] [Related]
57. RGS7 is palmitoylated and exists as biochemically distinct forms. Rose JJ; Taylor JB; Shi J; Cockett MI; Jones PG; Hepler JR J Neurochem; 2000 Nov; 75(5):2103-12. PubMed ID: 11032900 [TBL] [Abstract][Full Text] [Related]
58. YjeQ, an essential, conserved, uncharacterized protein from Escherichia coli, is an unusual GTPase with circularly permuted G-motifs and marked burst kinetics. Daigle DM; Rossi L; Berghuis AM; Aravind L; Koonin EV; Brown ED Biochemistry; 2002 Sep; 41(37):11109-17. PubMed ID: 12220175 [TBL] [Abstract][Full Text] [Related]
59. Rapid irreversible G protein alpha subunit misfolding due to intramolecular kinetic bottleneck that precedes Mg2+ "lock" after GTP/GDP exchange. Zelent B; Veklich Y; Murray J; Parkes JH; Gibson S; Liebman PA Biochemistry; 2001 Aug; 40(32):9647-56. PubMed ID: 11583165 [TBL] [Abstract][Full Text] [Related]
60. Functional coupling with Galpha(q) and Galpha(i1) protein subunits promotes high-affinity agonist binding to the neurotensin receptor NTS-1 expressed in Escherichia coli. Grisshammer R; Hermans E FEBS Lett; 2001 Mar; 493(2-3):101-5. PubMed ID: 11287004 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]