Literature DB >> 1541261

Natural protein proteinase inhibitors and their interaction with proteinases.

W Bode1, R Huber.   

Abstract

The substrate-like 'canonical' inhibition by the 'small' serine proteinase inhibitors and the product-like inhibition by the carboxypeptidase inhibitor have provided the only atomic models of protein inhibitor--proteinase interactions for about 15 years. The recently published structures of cystatin/stefin--papain complexes and of hirudin--thrombin complexes reveal novel non-substrate-like interactions. In addition, the structure of pro-carboxypeptidase shows a model of inactivation which bears resemblance to proteinase/protein inhibitor systems. Considerable progress in understanding the transition between native and cleaved states of the serpins has also been made by several recent structural studies.

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Year:  1992        PMID: 1541261     DOI: 10.1111/j.1432-1033.1992.tb16654.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  157 in total

1.  The structure of the human betaII-tryptase tetramer: fo(u)r better or worse.

Authors:  C P Sommerhoff; W Bode; P J Pereira; M T Stubbs; J Stürzebecher; G P Piechottka; G Matschiner; A Bergner
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

2.  New structural motifs on the chymotrypsin fold and their potential roles in complement factor B.

Authors:  H Jing; Y Xu; M Carson; D Moore; K J Macon; J E Volanakis; S V Narayana
Journal:  EMBO J       Date:  2000-01-17       Impact factor: 11.598

3.  The involvement of cysteine proteases and protease inhibitor genes in the regulation of programmed cell death in plants.

Authors:  M Solomon; B Belenghi; M Delledonne; E Menachem; A Levine
Journal:  Plant Cell       Date:  1999-03       Impact factor: 11.277

4.  Crystal structure of MHC class II-associated p41 Ii fragment bound to cathepsin L reveals the structural basis for differentiation between cathepsins L and S.

Authors:  G Guncar; G Pungercic; I Klemencic; V Turk; D Turk
Journal:  EMBO J       Date:  1999-02-15       Impact factor: 11.598

5.  Pyramidalization of backbone carbonyl carbon atoms in proteins.

Authors:  L Esposito; L Vitagliano; A Zagari; L Mazzarella
Journal:  Protein Sci       Date:  2000-10       Impact factor: 6.725

6.  Modulation of protein-protein interactions by synthetic receptors: design of molecules that disrupt serine protease-proteinaceous inhibitor interaction.

Authors:  Hyung Soon Park; Qing Lin; Andrew D Hamilton
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

7.  Proteins of circularly permuted sequence present within the same organism: the major serine proteinase inhibitor from Capsicum annuum seeds.

Authors:  N Antcheva; A Pintar; A Patthy; A Simoncsits; E Barta; B Tchorbanov; S Pongor
Journal:  Protein Sci       Date:  2001-11       Impact factor: 6.725

8.  Amino-acid substitutions at the fully exposed P1 site of bovine pancreatic trypsin inhibitor affect its stability.

Authors:  D Krowarsch; J Otlewski
Journal:  Protein Sci       Date:  2001-04       Impact factor: 6.725

9.  High affinity small protein inhibitors of human chymotrypsin C (CTRC) selected by phage display reveal unusual preference for P4' acidic residues.

Authors:  András Szabó; Dávid Héja; Dávid Szakács; Katalin Zboray; Katalin A Kékesi; Evette S Radisky; Miklós Sahin-Tóth; Gábor Pál
Journal:  J Biol Chem       Date:  2011-04-22       Impact factor: 5.157

10.  A structure-derived snap-trap mechanism of a multispecific serpin from the dysbiotic human oral microbiome.

Authors:  Theodoros Goulas; Miroslaw Ksiazek; Irene Garcia-Ferrer; Alicja M Sochaj-Gregorczyk; Irena Waligorska; Marcin Wasylewski; Jan Potempa; F Xavier Gomis-Rüth
Journal:  J Biol Chem       Date:  2017-05-16       Impact factor: 5.157

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