1z6c: Difference between revisions

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New page: left|200px<br /> <applet load="1z6c" size="450" color="white" frame="true" align="right" spinBox="true" caption="1z6c" /> '''Solution structure of an EGF pair (EGF34) f...
 
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[[Image:1z6c.gif|left|200px]]<br />
[[Image:1z6c.gif|left|200px]]<br /><applet load="1z6c" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1z6c" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1z6c" />
caption="1z6c" />
'''Solution structure of an EGF pair (EGF34) from vitamin K-dependent protein S'''<br />
'''Solution structure of an EGF pair (EGF34) from vitamin K-dependent protein S'''<br />


==Overview==
==Overview==
Vitamin K-dependent protein S is a cofactor of activated protein C, a, serine protease that regulates blood coagulation. Deficiency of protein S, can cause venous thrombosis. Protein S has four EGF domains in tandem;, domains 2-4 bind calcium with high affinity whereas domains 1-2 mediate, interaction with activated protein C. We have now solved the solution, structure of the EGF3-4 fragment of protein S. The linker between the two, domains is similar to what has been observed in other calcium-binding EGF, domains where it provides an extended conformation. Interestingly, a, disagreement between NOE and RDC data revealed a conformational, heterogeneity within EGF3 due to a hinge-like motion around Glu186 in the, Cys-Glu-Cys sequence, the only point in the domain where flexibility is, allowed. The dominant, bent conformation of EGF3 in the pair has no, precedent among calcium-binding EGF domains. It is characterized by a, change in the psi angle of Glu186 from 160 degrees +/- 40 degrees , as, seen in ten other EGF domains, to approximately 0 degrees +/- 15 degrees ., NOESY data suggest that Tyr193, a residue not conserved in other, calcium-binding EGF domains (except in the homologue Gas6), induces the, unique fold of EGF3. However, SAXS data, obtained on EGF1-4 and EGF2-4, showed a dominant, extended conformation in these fragments. This may be, due to a counterproductive domain-domain interaction between EGF2 and EGF4, if EGF3 is in a bent conformation. We speculate that the ability of EGF3, to adopt different conformations may be of functional significance in, protein-protein interactions involving protein S.
Vitamin K-dependent protein S is a cofactor of activated protein C, a serine protease that regulates blood coagulation. Deficiency of protein S can cause venous thrombosis. Protein S has four EGF domains in tandem; domains 2-4 bind calcium with high affinity whereas domains 1-2 mediate interaction with activated protein C. We have now solved the solution structure of the EGF3-4 fragment of protein S. The linker between the two domains is similar to what has been observed in other calcium-binding EGF domains where it provides an extended conformation. Interestingly, a disagreement between NOE and RDC data revealed a conformational heterogeneity within EGF3 due to a hinge-like motion around Glu186 in the Cys-Glu-Cys sequence, the only point in the domain where flexibility is allowed. The dominant, bent conformation of EGF3 in the pair has no precedent among calcium-binding EGF domains. It is characterized by a change in the psi angle of Glu186 from 160 degrees +/- 40 degrees , as seen in ten other EGF domains, to approximately 0 degrees +/- 15 degrees . NOESY data suggest that Tyr193, a residue not conserved in other calcium-binding EGF domains (except in the homologue Gas6), induces the unique fold of EGF3. However, SAXS data, obtained on EGF1-4 and EGF2-4, showed a dominant, extended conformation in these fragments. This may be due to a counterproductive domain-domain interaction between EGF2 and EGF4 if EGF3 is in a bent conformation. We speculate that the ability of EGF3 to adopt different conformations may be of functional significance in protein-protein interactions involving protein S.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1Z6C is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with CA as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Z6C OCA].  
1Z6C is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CA:'>CA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Z6C OCA].  


==Reference==
==Reference==
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[[Category: Muranyi, A.]]
[[Category: Muranyi, A.]]
[[Category: Stenflo, J.]]
[[Category: Stenflo, J.]]
[[Category: Thamlitz, A.M.]]
[[Category: Thamlitz, A M.]]
[[Category: Thulin, E.]]
[[Category: Thulin, E.]]
[[Category: CA]]
[[Category: CA]]
[[Category: egf module]]
[[Category: egf module]]


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