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Journal Abstract Search

430 related items for PubMed ID: 9398179

  • 41. Viscous drag as the source of active site perturbation during protease translocation: insights into how inhibitory processes are controlled by serpin metastability.
    Shin JS, Yu MH.
    J Mol Biol; 2006 Jun 02; 359(2):378-89. PubMed ID: 16626735
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  • 42. Contributions of basic amino acids in the autolysis loop of factor XIa to serpin specificity.
    Rezaie AR, Sun MF, Gailani D.
    Biochemistry; 2006 Aug 08; 45(31):9427-33. PubMed ID: 16878977
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  • 43. Rational design of complex formation between plasminogen activator inhibitor-1 and its target proteinases.
    Aertgeerts K, De Ranter CJ, Booth NA, Declerck PJ.
    J Struct Biol; 1997 Apr 08; 118(3):236-42. PubMed ID: 9169233
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  • 47. Modeling of serpin-protease complexes: antithrombin-thrombin, alpha 1-antitrypsin (358Met-->Arg)-thrombin, alpha 1-antitrypsin (358Met-->Arg)-trypsin, and antitrypsin-elastase.
    Whisstock J, Lesk AM, Carrell R.
    Proteins; 1996 Nov 08; 26(3):288-303. PubMed ID: 8953650
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  • 48. Interscaffolding additivity. Association of P1 variants of eglin c and of turkey ovomucoid third domain with serine proteinases.
    Qasim MA, Ganz PJ, Saunders CW, Bateman KS, James MN, Laskowski M.
    Biochemistry; 1997 Feb 18; 36(7):1598-607. PubMed ID: 9048543
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  • 49. Specificity and reactive loop length requirements for crmA inhibition of serine proteases.
    Tesch LD, Raghavendra MP, Bedsted-Faarvang T, Gettins PG, Olson ST.
    Protein Sci; 2005 Feb 18; 14(2):533-42. PubMed ID: 15632287
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  • 50. Identification of serpin determinants of specificity and selectivity for furin inhibition through studies of α1PDX (α1-protease inhibitor Portland)-serpin B8 and furin active-site loop chimeras.
    Izaguirre G, Qi L, Lima M, Olson ST.
    J Biol Chem; 2013 Jul 26; 288(30):21802-14. PubMed ID: 23744066
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  • 53. Roles of the P1, P2, and P3 residues in determining inhibitory specificity of kallistatin toward human tissue kallikrein.
    Chen VC, Chao L, Chao J.
    J Biol Chem; 2000 Dec 08; 275(49):38457-66. PubMed ID: 10993887
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  • 56. Pigment epithelium-derived factor behaves like a noninhibitory serpin. Neurotrophic activity does not require the serpin reactive loop.
    Becerra SP, Sagasti A, Spinella P, Notario V.
    J Biol Chem; 1995 Oct 27; 270(43):25992-9. PubMed ID: 7592790
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  • 57. Structural basis of latency in plasminogen activator inhibitor-1.
    Mottonen J, Strand A, Symersky J, Sweet RM, Danley DE, Geoghegan KF, Gerard RD, Goldsmith EJ.
    Nature; 1992 Jan 16; 355(6357):270-3. PubMed ID: 1731226
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  • 58. Heterogeneity in serpin-protease complexes as demonstrated by differences in the mechanism of complex breakdown.
    Plotnick MI, Samakur M, Wang ZM, Liu X, Rubin H, Schechter NM, Selwood T.
    Biochemistry; 2002 Jan 08; 41(1):334-42. PubMed ID: 11772033
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  • 59. Alpha 1-proteinase inhibitor variant T345R. Influence of P14 residue on substrate and inhibitory pathways.
    Hood DB, Huntington JA, Gettins PG.
    Biochemistry; 1994 Jul 19; 33(28):8538-47. PubMed ID: 8031789
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  • 60. Predicting serpin/protease interactions.
    Song J, Matthews AY, Reboul CF, Kaiserman D, Pike RN, Bird PI, Whisstock JC.
    Methods Enzymol; 2011 Jul 19; 501():237-73. PubMed ID: 22078538
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