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Journal Abstract Search

878 related items for PubMed ID: 1304349

  • 41. Hirunorms are true hirudin mimetics. The crystal structure of human alpha-thrombin-hirunorm V complex.
    De Simone G, Lombardi A, Galdiero S, Nastri F, Della Morte R, Staiano N, Pedone C, Bolognesi M, Pavone V.
    Protein Sci; 1998 Feb; 7(2):243-53. PubMed ID: 9521099
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  • 42. Changes in interactions in complexes of hirudin derivatives and human alpha-thrombin due to different crystal forms.
    Priestle JP, Rahuel J, Rink H, Tones M, Grütter MG.
    Protein Sci; 1993 Oct; 2(10):1630-42. PubMed ID: 8251938
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  • 47. Immobilization of the irreversible thrombin inhibitor D-Phe-Pro-Arg-chloromethylketone: a concept for hemocompatible surfaces?
    Maitz MF, Sperling C, Werner C.
    J Biomed Mater Res A; 2010 Sep 01; 94(3):905-12. PubMed ID: 20730927
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  • 48. Synthesis, structure, and structure-activity relationships of divalent thrombin inhibitors containing an alpha-keto-amide transition-state mimetic.
    Krishnan R, Tulinsky A, Vlasuk GP, Pearson D, Vallar P, Bergum P, Brunck TK, Ripka WC.
    Protein Sci; 1996 Mar 01; 5(3):422-33. PubMed ID: 8868478
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  • 49. A player of many parts: the spotlight falls on thrombin's structure.
    Stubbs MT, Bode W.
    Thromb Res; 1993 Jan 01; 69(1):1-58. PubMed ID: 8465268
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  • 50. Thermal shift assay to probe melting of thrombin, fibrinogen, fibrin monomer, and fibrin: Gly-Pro-Arg-Pro induces a fibrin monomer-like state in fibrinogen.
    Crossen J, Diamond SL.
    Biochim Biophys Acta Gen Subj; 2021 Feb 01; 1865(2):129805. PubMed ID: 33276061
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  • 53. Structure of the hirulog 3-thrombin complex and nature of the S' subsites of substrates and inhibitors.
    Qiu X, Padmanabhan KP, Carperos VE, Tulinsky A, Kline T, Maraganore JM, Fenton JW.
    Biochemistry; 1992 Dec 01; 31(47):11689-97. PubMed ID: 1445905
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  • 54. Bovine thrombin complexed with an uncleavable analog of residues 7-19 of fibrinogen A alpha: geometry of the catalytic triad and interactions of the P1', P2', and P3' substrate residues.
    Martin PD, Malkowski MG, DiMaio J, Konishi Y, Ni F, Edwards BF.
    Biochemistry; 1996 Oct 08; 35(40):13030-9. PubMed ID: 8855938
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  • 55. Structural comparison of two serine proteinase-protein inhibitor complexes: eglin-c-subtilisin Carlsberg and CI-2-subtilisin Novo.
    McPhalen CA, James MN.
    Biochemistry; 1988 Aug 23; 27(17):6582-98. PubMed ID: 3064813
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  • 56. Crystal structure of a peptidyl pyridinium methyl ketone inhibitor with thrombin.
    Rehse PH, Steinmetzer T, Li Y, Konishi Y, Cygler M.
    Biochemistry; 1995 Sep 12; 34(36):11537-44. PubMed ID: 7547884
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  • 57. Electrostatic steering and ionic tethering in the formation of thrombin-hirudin complexes: the role of the thrombin anion-binding exosite-I.
    Myles T, Le Bonniec BF, Betz A, Stone SR.
    Biochemistry; 2001 Apr 24; 40(16):4972-9. PubMed ID: 11305913
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  • 58. Crystal structure of an oligomer of proteolytic zymogens: detailed conformational analysis of the bovine ternary complex and implications for their activation.
    Gomis-Rüth FX, Gómez-Ortiz M, Vendrell J, Ventura S, Bode W, Huber R, Avilés FX.
    J Mol Biol; 1997 Jun 27; 269(5):861-80. PubMed ID: 9223647
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  • 59. X-ray analysis at 2.0 A resolution of mouse submaxillary renin complexed with a decapeptide inhibitor CH-66, based on the 4-16 fragment of rat angiotensinogen.
    Dealwis CG, Frazao C, Badasso M, Cooper JB, Tickle IJ, Driessen H, Blundell TL, Murakami K, Miyazaki H, Sueiras-Diaz J.
    J Mol Biol; 1994 Feb 11; 236(1):342-60. PubMed ID: 8107115
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  • 60. Crystal structure of a Kunitz-type trypsin inhibitor from Erythrina caffra seeds.
    Onesti S, Brick P, Blow DM.
    J Mol Biol; 1991 Jan 05; 217(1):153-76. PubMed ID: 1988676
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