BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

219 related articles for article (PubMed ID: 7640281)

  • 1. Three-dimensional structure in solution of the calcium channel blocker omega-conotoxin MVIIA.
    Kohno T; Kim JI; Kobayashi K; Kodera Y; Maeda T; Sato K
    Biochemistry; 1995 Aug; 34(32):10256-65. PubMed ID: 7640281
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Three-dimensional solution structure of the calcium channel antagonist omega-agatoxin IVA: consensus molecular folding of calcium channel blockers.
    Kim JI; Konishi S; Iwai H; Kohno T; Gouda H; Shimada I; Sato K; Arata Y
    J Mol Biol; 1995 Jul; 250(5):659-71. PubMed ID: 7623383
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Three-dimensional solution structure of the sodium channel agonist/antagonist delta-conotoxin TxVIA.
    Kohno T; Sasaki T; Kobayashi K; Fainzilber M; Sato K
    J Biol Chem; 2002 Sep; 277(39):36387-91. PubMed ID: 12145313
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Solution structure of omega-conotoxin MVIIC, a high affinity ligand of P-type calcium channels, using 1H NMR spectroscopy and complete relaxation matrix analysis.
    Farr-Jones S; Miljanich GP; Nadasdi L; Ramachandran J; Basus VJ
    J Mol Biol; 1995 Apr; 248(1):106-24. PubMed ID: 7731037
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Three-dimensional structure in solution of the calcium channel blocker omega-conotoxin.
    Pallaghy PK; Duggan BM; Pennington MW; Norton RS
    J Mol Biol; 1993 Nov; 234(2):405-20. PubMed ID: 8230223
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Structure-activity relationships of omega-conotoxins MVIIA, MVIIC and 14 loop splice hybrids at N and P/Q-type calcium channels.
    Nielsen KJ; Adams D; Thomas L; Bond T; Alewood PF; Craik DJ; Lewis RJ
    J Mol Biol; 1999 Jun; 289(5):1405-21. PubMed ID: 10373375
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Solution structure of omega-conotoxin MVIIC determined by NMR.
    Nemoto N; Kubo S; Yoshida T; Chino N; Kimura T; Sakakibara S; Kyogoku Y; Kobayashi Y
    Biochem Biophys Res Commun; 1995 Feb; 207(2):695-700. PubMed ID: 7864862
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Conotoxin TVIIA, a novel peptide from the venom of Conus tulipa 2. Three-dimensional solution structure.
    Hill JM; Alewood PF; Craik DJ
    Eur J Biochem; 2000 Aug; 267(15):4649-57. PubMed ID: 10903497
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Folding of omega-conotoxins. 2. Influence of precursor sequences and protein disulfide isomerase.
    Price-Carter M; Gray WR; Goldenberg DP
    Biochemistry; 1996 Dec; 35(48):15547-57. PubMed ID: 8952509
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Folding of omega-conotoxins. 1. Efficient disulfide-coupled folding of mature sequences in vitro.
    Price-Carter M; Gray WR; Goldenberg DP
    Biochemistry; 1996 Dec; 35(48):15537-46. PubMed ID: 8952508
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Residue Gly1326 of the N-type calcium channel alpha 1B subunit controls reversibility of omega-conotoxin GVIA and MVIIA block.
    Feng ZP; Hamid J; Doering C; Bosey GM; Snutch TP; Zamponi GW
    J Biol Chem; 2001 May; 276(19):15728-35. PubMed ID: 11279062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Solution structure and backbone dynamics of an omega-conotoxin precursor.
    Goldenberg DP; Koehn RE; Gilbert DE; Wagner G
    Protein Sci; 2001 Mar; 10(3):538-50. PubMed ID: 11344322
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A consensus structure for omega-conotoxins with different selectivities for voltage-sensitive calcium channel subtypes: comparison of MVIIA, SVIB and SNX-202.
    Nielsen KJ; Thomas L; Lewis RJ; Alewood PF; Craik DJ
    J Mol Biol; 1996 Oct; 263(2):297-310. PubMed ID: 8913308
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three-dimensional solution structure of conotoxin psi-PIIIE, an acetylcholine gated ion channel antagonist.
    Mitchell SS; Shon KJ; Foster MP; Davis DR; Olivera BM; Ireland CM
    Biochemistry; 1998 Feb; 37(5):1215-20. PubMed ID: 9477946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.