Literature DB >> 3670397

Vitamin K-dependent blood coagulation proteins form hetero-dimers.

K Harlos1, S K Holland, C W Boys, A I Burgess, M P Esnouf, C C Blake.   

Abstract

The later stages of the blood coagulation cascade are characterized by the presence of vitamin K-dependent proteins and their involvement in membrane-bound, multi-protein converting complexes with an essential requirement for calcium ions. Specific interactions between zymogens and activating enzymes have not yet been identified. Here we describe a crystallographic study of prothrombin fragment 1 (residues 1-156 of prothrombin) which indicates that vitamin K-dependent coagulation proteins have specific association sites that allow them to form hetero-dimers. The calcium-induced formation of a hetero-dimer between fragment 1 and factor X is demonstrated by cross-linking. Such hetero-dimers of vitamin K-dependent proteins could be significant in the coagulation system.

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Year:  1987        PMID: 3670397     DOI: 10.1038/330082a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  12 in total

1.  Prothrombin kringle 1 domain interacts with factor Va during the assembly of prothrombinase complex.

Authors:  H Deguchi; H Takeya; E C Gabazza; J Nishioka; K Suzuki
Journal:  Biochem J       Date:  1997-02-01       Impact factor: 3.857

2.  Prothrombin structure: unanticipated features and opportunities.

Authors:  Nicola Pozzi; Enrico Di Cera
Journal:  Expert Rev Proteomics       Date:  2014-10-18       Impact factor: 3.940

3.  A dimeric form of prothrombin on membrane surfaces.

Authors:  P J Anderson
Journal:  Biochem J       Date:  1998-12-15       Impact factor: 3.857

4.  Solution conformations of the gamma-carboxyglutamic acid domain of bovine prothrombin fragment 1, residues 1-65.

Authors:  P S Charifson; T Darden; A Tulinsky; J L Hughey; R G Hiskey; L G Pedersen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-15       Impact factor: 11.205

5.  The association of human coagulation factors VIII, IXa and X with phospholipid vesicles involves both electrostatic and hydrophobic interactions.

Authors:  J S Atkins; P R Ganz
Journal:  Mol Cell Biochem       Date:  1992-05-13       Impact factor: 3.396

6.  Interference of blood-coagulation vitamin K-dependent proteins in the activation of human protein C. Involvement of the 4-carboxyglutamic acid domain in two distinct interactions with the thrombin-thrombomodulin complex and with phospholipids.

Authors:  J M Freyssinet; A Beretz; C Klein-Soyer; J Gauchy; S Schuhler; J P Cazenave
Journal:  Biochem J       Date:  1988-12-01       Impact factor: 3.857

7.  The linker connecting the two kringles plays a key role in prothrombin activation.

Authors:  Nicola Pozzi; Zhiwei Chen; Leslie A Pelc; Daniel B Shropshire; Enrico Di Cera
Journal:  Proc Natl Acad Sci U S A       Date:  2014-05-12       Impact factor: 11.205

8.  How the Linker Connecting the Two Kringles Influences Activation and Conformational Plasticity of Prothrombin.

Authors:  Nicola Pozzi; Zhiwei Chen; Enrico Di Cera
Journal:  J Biol Chem       Date:  2016-01-12       Impact factor: 5.157

9.  Molecular pathology of haemophilia B.

Authors:  P M Green; D R Bentley; R S Mibashan; I M Nilsson; F Giannelli
Journal:  EMBO J       Date:  1989-04       Impact factor: 11.598

10.  Mechanism of protein-z-mediated inhibition of coagulation factor xa by z-protein-dependent inhibitor: a molecular dynamic approach.

Authors:  Mohammad Reza Dayer; Omid Ghayour; Mohammad Saaid Dayer
Journal:  ISRN Hematol       Date:  2012-03-20
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