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282 related items for PubMed ID: 8643443

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  • 3. Structure and function in rhodopsin: correct folding and misfolding in two point mutants in the intradiscal domain of rhodopsin identified in retinitis pigmentosa.
    Liu X, Garriga P, Khorana HG.
    Proc Natl Acad Sci U S A; 1996 May 14; 93(10):4554-9. PubMed ID: 8643442
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  • 5. Structure and function in rhodopsin: further elucidation of the role of the intradiscal cysteines, Cys-110, -185, and -187, in rhodopsin folding and function.
    Hwa J, Reeves PJ, Klein-Seetharaman J, Davidson F, Khorana HG.
    Proc Natl Acad Sci U S A; 1999 Mar 02; 96(5):1932-5. PubMed ID: 10051572
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  • 8. Altered functionality in rhodopsin point mutants associated with retinitis pigmentosa.
    Andrés A, Garriga P, Manyosa J.
    Biochem Biophys Res Commun; 2003 Mar 28; 303(1):294-301. PubMed ID: 12646201
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  • 9. Molecular mechanisms of rhodopsin retinitis pigmentosa and the efficacy of pharmacological rescue.
    Krebs MP, Holden DC, Joshi P, Clark CL, Lee AH, Kaushal S.
    J Mol Biol; 2010 Feb 05; 395(5):1063-78. PubMed ID: 19913029
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  • 10. Retinitis pigmentosa rhodopsin mutations L125R and A164V perturb critical interhelical interactions: new insights through compensatory mutations and crystal structure analysis.
    Stojanovic A, Hwang I, Khorana HG, Hwa J.
    J Biol Chem; 2003 Oct 03; 278(40):39020-8. PubMed ID: 12871954
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  • 11. Structure and function in rhodopsin. Separation and characterization of the correctly folded and misfolded opsins produced on expression of an opsin mutant gene containing only the native intradiscal cysteine codons.
    Ridge KD, Lu Z, Liu X, Khorana HG.
    Biochemistry; 1995 Mar 14; 34(10):3261-7. PubMed ID: 7880821
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  • 14. Mutations at position 125 in transmembrane helix III of rhodopsin affect the structure and signalling of the receptor.
    Andrés A, Kosoy A, Garriga P, Manyosa J.
    Eur J Biochem; 2001 Nov 14; 268(22):5696-704. PubMed ID: 11722553
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  • 15. Misfolded rhodopsin mutants display variable aggregation properties.
    Gragg M, Park PS.
    Biochim Biophys Acta Mol Basis Dis; 2018 Sep 14; 1864(9 Pt B):2938-2948. PubMed ID: 29890221
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  • 16. Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration.
    Colley NJ, Cassill JA, Baker EK, Zuker CS.
    Proc Natl Acad Sci U S A; 1995 Mar 28; 92(7):3070-4. PubMed ID: 7708777
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  • 17. Unusual thermal and conformational properties of the rhodopsin congenital night blindness mutant Thr-94 --> Ile.
    Ramon E, del Valle LJ, Garriga P.
    J Biol Chem; 2003 Feb 21; 278(8):6427-32. PubMed ID: 12466267
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  • 19. Opsin stability and folding: the role of Cys185 and abnormal disulfide bond formation in the intradiscal domain.
    McKibbin C, Toye AM, Reeves PJ, Khorana HG, Edwards PC, Villa C, Booth PJ.
    J Mol Biol; 2007 Dec 14; 374(5):1309-18. PubMed ID: 17988684
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  • 20. Role of the intradiscal domain in rhodopsin assembly and function.
    Doi T, Molday RS, Khorana HG.
    Proc Natl Acad Sci U S A; 1990 Jul 14; 87(13):4991-5. PubMed ID: 2367520
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