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3. Role of disulfide bridges in the folding, structure and biological activity of omega-conotoxin GVIA. Flinn JP; Pallaghy PK; Lew MJ; Murphy R; Angus JA; Norton RS Biochim Biophys Acta; 1999 Sep; 1434(1):177-90. PubMed ID: 10556572 [TBL] [Abstract][Full Text] [Related]
4. Tyr13 is essential for the activity of omega-conotoxin MVIIA and GVIA, specific N-type calcium channel blockers. Kim JI; Takahashi M; Ohtake A; Wakamiya A; Sato K Biochem Biophys Res Commun; 1995 Jan; 206(2):449-54. PubMed ID: 7826361 [TBL] [Abstract][Full Text] [Related]
8. Circular dichroism spectra of calcium channel antagonist omega-conotoxins. Kim JI; Ohtake A; Sato K Biochem Biophys Res Commun; 1997 Jan; 230(1):133-5. PubMed ID: 9020029 [TBL] [Abstract][Full Text] [Related]
9. Hydroxyl group of Tyr13 is essential for the activity of omega-conotoxin GVIA, a peptide toxin for N-type calcium channel. Kim JI; Takahashi M; Ogura A; Kohno T; Kudo Y; Sato K J Biol Chem; 1994 Sep; 269(39):23876-8. PubMed ID: 7929033 [TBL] [Abstract][Full Text] [Related]
10. Effects of N-, P- and Q-type neuronal calcium channel antagonists on mammalian peripheral neurotransmission. Wright CE; Angus JA Br J Pharmacol; 1996 Sep; 119(1):49-56. PubMed ID: 8872356 [TBL] [Abstract][Full Text] [Related]
11. The cyclic contryphan motif CPxXPXC, a robust scaffold potentially useful as an omega-conotoxin mimic. Pallaghy PK; Norton RS Biopolymers; 2000 Sep; 54(3):173-9. PubMed ID: 10861378 [TBL] [Abstract][Full Text] [Related]
12. Solution structure of omega-conotoxin MVIIA using 2D NMR spectroscopy. Basus VJ; Nadasdi L; Ramachandran J; Miljanich GP FEBS Lett; 1995 Aug; 370(3):163-9. PubMed ID: 7656969 [TBL] [Abstract][Full Text] [Related]
13. Solution structure of the calcium channel antagonist omega-conotoxin GVIA. Skalicky JJ; Metzler WJ; Ciesla DJ; Galdes A; Pardi A Protein Sci; 1993 Oct; 2(10):1591-603. PubMed ID: 8251934 [TBL] [Abstract][Full Text] [Related]
14. Three-dimensional solution structure of omega-conotoxin TxVII, an L-type calcium channel blocker. Kobayashi K; Sasaki T; Sato K; Kohno T Biochemistry; 2000 Dec; 39(48):14761-7. PubMed ID: 11101291 [TBL] [Abstract][Full Text] [Related]
16. Synthesis and biological characterization of a series of analogues of omega-conotoxin GVIA. Flinn JP; Murphy R; Boublik JH; Lew MJ; Wright CE; Angus JA J Pept Sci; 1995; 1(6):379-84. PubMed ID: 9223017 [TBL] [Abstract][Full Text] [Related]
17. Role of basic residues for the binding of omega-conotoxin GVIA to N-type calcium channels. Sato K; Park NG; Kohno T; Maeda T; Kim JI; Kato R; Takahashi M Biochem Biophys Res Commun; 1993 Aug; 194(3):1292-6. PubMed ID: 8394704 [TBL] [Abstract][Full Text] [Related]
18. Roles of individual disulfide bonds in the stability and folding of an omega-conotoxin. Price-Carter M; Hull MS; Goldenberg DP Biochemistry; 1998 Jul; 37(27):9851-61. PubMed ID: 9657699 [TBL] [Abstract][Full Text] [Related]
19. Pharmacological evidence that tetraethylammonium-sensitive, iberiotoxin-insensitive K+ channels function as a negative feedback element for sympathetic neurotransmission by suppressing omega-conotoxin-GVIA-insensitive Ca2+ channels in the relaxation of rabbit facial vein. Tanaka Y; Akutsu A; Tanaka H; Horinouchi T; Tsuru H; Koike K; Shigenobu K Naunyn Schmiedebergs Arch Pharmacol; 2003 Jan; 367(1):35-42. PubMed ID: 12616339 [TBL] [Abstract][Full Text] [Related]
20. Solution structure determination by two-dimensional 1H NMR of omega-conotoxin MVIID, a calcium channel blocker peptide. Civera C; Vázquez A; Sevilla JM; Bruix M; Gago F; García AG; Sevilla P Biochem Biophys Res Commun; 1999 Jan; 254(1):32-5. PubMed ID: 9920728 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]