2a1d: Difference between revisions

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New page: left|200px<br /><applet load="2a1d" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a1d, resolution 3.50Å" /> '''Staphylocoagulase bo...
 
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[[Image:2a1d.gif|left|200px]]<br /><applet load="2a1d" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2a1d.gif|left|200px]]<br /><applet load="2a1d" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2a1d, resolution 3.50&Aring;" />
caption="2a1d, resolution 3.50&Aring;" />
'''Staphylocoagulase bound to bovine thrombin'''<br />
'''Staphylocoagulase bound to bovine thrombin'''<br />


==Overview==
==Overview==
Staphylocoagulase (SC) is a protein secreted by the human pathogen, Staphylococcus aureus, that activates human prothrombin (ProT) by inducing, a conformational change. SC-bound ProT efficiently clots fibrinogen, thus, bypassing the physiological blood coagulation pathway. The crystal, structure of a fully active SC fragment, SC-(1-325), bound to human, prethrombin 2 showed that the SC-(1-325) N terminus inserts into the, Ile(16) pocket of prethrombin 2, thereby inducing expression of a, functional catalytic site in the cognate zymogen without peptide bond, cleavage. As shown here, SC-(1-325) binds to bovine and human ProT with, similar affinity but activates the bovine zymogen only very poorly. By, contrast to the approximately 2-fold difference in chromogenic substrate, kinetic constants between human thrombin and the SC-(1-325).human, (pro)thrombin complexes, SC-(1-325).bovine ProT shows a 3,500-fold lower, k(cat)/K(m) compared with free bovine thrombin, because of a 47-fold, increase in K(m) and a 67-fold decrease in k(cat). The SC-(1-325).bovine, ProT complex is approximately 5,800-fold less active compared with its, human counterpart. Comparison of human and bovine fibrinogen as substrates, of human and bovine thrombin and the SC-(1-325).(pro)thrombin complexes, indicates that the species specificity of SC-(1-325) cofactor activity is, determined primarily by differences in conformational activation of bound, ProT. These results suggest that the catalytic site in the, SC-(1-325).bovine ProT complex is incompletely formed. The current crystal, structure of SC-(1-325).bovine thrombin reveals that SC would dock, similarly to the bovine proenzyme, whereas the bovine, (pro)thrombin-characteristic residues Arg(144) and Arg(145) would likely, interfere with insertion of the SC N terminus, thus explaining the greatly, reduced activation of bovine ProT.
Staphylocoagulase (SC) is a protein secreted by the human pathogen, Staphylococcus aureus, that activates human prothrombin (ProT) by inducing a conformational change. SC-bound ProT efficiently clots fibrinogen, thus bypassing the physiological blood coagulation pathway. The crystal structure of a fully active SC fragment, SC-(1-325), bound to human prethrombin 2 showed that the SC-(1-325) N terminus inserts into the Ile(16) pocket of prethrombin 2, thereby inducing expression of a functional catalytic site in the cognate zymogen without peptide bond cleavage. As shown here, SC-(1-325) binds to bovine and human ProT with similar affinity but activates the bovine zymogen only very poorly. By contrast to the approximately 2-fold difference in chromogenic substrate kinetic constants between human thrombin and the SC-(1-325).human (pro)thrombin complexes, SC-(1-325).bovine ProT shows a 3,500-fold lower k(cat)/K(m) compared with free bovine thrombin, because of a 47-fold increase in K(m) and a 67-fold decrease in k(cat). The SC-(1-325).bovine ProT complex is approximately 5,800-fold less active compared with its human counterpart. Comparison of human and bovine fibrinogen as substrates of human and bovine thrombin and the SC-(1-325).(pro)thrombin complexes indicates that the species specificity of SC-(1-325) cofactor activity is determined primarily by differences in conformational activation of bound ProT. These results suggest that the catalytic site in the SC-(1-325).bovine ProT complex is incompletely formed. The current crystal structure of SC-(1-325).bovine thrombin reveals that SC would dock similarly to the bovine proenzyme, whereas the bovine (pro)thrombin-characteristic residues Arg(144) and Arg(145) would likely interfere with insertion of the SC N terminus, thus explaining the greatly reduced activation of bovine ProT.


==About this Structure==
==About this Structure==
2A1D is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus] with NDG and NA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2A1D OCA].  
2A1D is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus] and [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus] with <scene name='pdbligand=NDG:'>NDG</scene> and <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2A1D OCA].  


==Reference==
==Reference==
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[[Category: Staphylococcus aureus]]
[[Category: Staphylococcus aureus]]
[[Category: Thrombin]]
[[Category: Thrombin]]
[[Category: Bock, P.E.]]
[[Category: Bock, P E.]]
[[Category: Bode, W.]]
[[Category: Bode, W.]]
[[Category: Friedrich, R.]]
[[Category: Friedrich, R.]]
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[[Category: prothrombin activator]]
[[Category: prothrombin activator]]


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