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Journal Abstract Search

109 related items for PubMed ID: 1868168

  • 1. Effects of proline ring conformation on theoretical pi-pi* absorption and CD spectra of helical poly(L-proline) forms I and II.
    Thomasson KA, Applequist J.
    Biopolymers; 1991 Apr; 31(5):529-35. PubMed ID: 1868168
    [Abstract] [Full Text] [Related]

  • 2. Circular dichroism spectrum of peptides in the poly(Pro)II conformation.
    Woody RW.
    J Am Chem Soc; 2009 Jun 17; 131(23):8234-45. PubMed ID: 19462996
    [Abstract] [Full Text] [Related]

  • 3. Theoretical CD studies of polypeptide helices: examination of important electronic and geometric factors.
    Manning MC, Woody RW.
    Biopolymers; 1991 Apr 17; 31(5):569-86. PubMed ID: 1868170
    [Abstract] [Full Text] [Related]

  • 4. Reassessment of the random coil conformation: vibrational CD study of proline oligopeptides and related polypeptides.
    Dukor RK, Keiderling TA.
    Biopolymers; 1991 Dec 17; 31(14):1747-61. PubMed ID: 1793813
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  • 5. CD investigations on conformation of H-X-(Pro)n-Y-OH peptides (X = Trp, Tyr; Y = Tyr, Met); models for intramolecular long range electron transfer.
    Wierzchowski KL, Majcher K, Poznański J.
    Acta Biochim Pol; 1995 Dec 17; 42(2):259-68. PubMed ID: 8588474
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  • 7. Theoretical UV circular dichroism of cyclo(L-Proline-L-Proline).
    Carlson KL, Lowe SL, Hoffmann MR, Thomasson KA.
    J Phys Chem A; 2006 Feb 09; 110(5):1925-33. PubMed ID: 16451026
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  • 9. Delineation of an active fragment and poly(L-proline) II conformation for candidacidal activity of bactenecin 5.
    Raj PA, Marcus E, Edgerton M.
    Biochemistry; 1996 Apr 09; 35(14):4314-25. PubMed ID: 8605180
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  • 10. [Left-helical (PPII-PPII) type of globular protein structure: the level of the left helical type of poly-L-proline II in Kunitz trypsin inhibitor is no less than 43%. Experimental Reper spectrum of the extended left helix].
    Bazhulina NP, Korolev SV, Morozov NIu, Rogulenkova VN, Esipova NG.
    Biofizika; 1994 Apr 09; 39(4):746-8. PubMed ID: 7981285
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  • 12. The structure of tri-proline in water probed by polarized Raman, Fourier transform infrared, vibrational circular dichroism, and electric ultraviolet circular dichroism spectroscopy.
    Schweitzer-Stenner R, Eker F, Perez A, Griebenow K, Cao X, Nafie LA.
    Biopolymers; 2003 Apr 09; 71(5):558-68. PubMed ID: 14635096
    [Abstract] [Full Text] [Related]

  • 13. Bond-optimized ring closure for proline: comparison of conformations and semiempirical energies with small molecule X-ray structures.
    Thomasson KA, Applequist J.
    Biopolymers; 1990 Apr 09; 30(3-4):437-50. PubMed ID: 2279073
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  • 14. Examination of structural characteristics of the potent oxytocin antagonists [dPen1,Pen6]-OT and [dPen1,Pen6, 5-tBuPro7]-OT by NMR, Raman, CD spectroscopy and molecular modeling.
    Bélec L, Blankenship JW, Lubell WD.
    J Pept Sci; 2005 Jul 09; 11(7):365-78. PubMed ID: 15641022
    [Abstract] [Full Text] [Related]

  • 15. Short sequences of non-proline residues can adopt the polyproline II helical conformation.
    Chellgren BW, Creamer TP.
    Biochemistry; 2004 May 18; 43(19):5864-9. PubMed ID: 15134460
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  • 16. Dipole interaction model predicted pi-pi* circular dichroism of cyclo(L-Pro)3 using structures created by semi-empirical, ab initio, and molecular mechanics methods.
    Lowe SL, Pandey RR, Czlapinski J, Kie-Adams G, Hoffmann MR, Thomasson KA, Pierce KS.
    J Pept Res; 2003 Apr 18; 61(4):189-201. PubMed ID: 12605604
    [Abstract] [Full Text] [Related]

  • 17. 1H- and 13C-NMR investigations on cis-trans isomerization of proline peptide bonds and conformation of aromatic side chains in H-Trp-(Pro)n-Tyr-OH peptides.
    Poznański J, Ejchart A, Wierzchowski KL, Ciurak M.
    Biopolymers; 1993 May 18; 33(5):781-95. PubMed ID: 8393714
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  • 19. Conformational preferences of proline analogues with different ring size.
    Jhon JS, Kang YK.
    J Phys Chem B; 2007 Apr 05; 111(13):3496-507. PubMed ID: 17388495
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