1j35: Difference between revisions

Revision as of 14:25, 1 July 2008

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File:1j35.png

Template:STRUCTURE 1j35

Crystal Structure of Ca(II)-bound Gla Domain of Factor IX Complexed with Binding ProteinCrystal Structure of Ca(II)-bound Gla Domain of Factor IX Complexed with Binding Protein

Template:ABSTRACT PUBMED 12695512

About this StructureAbout this Structure

1J35 is a Protein complex structure of sequences from Bos taurus and Trimeresurus flavoviridis. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of Mg2+- and Ca2+-bound Gla domain of factor IX complexed with binding protein., Shikamoto Y, Morita T, Fujimoto Z, Mizuno H, J Biol Chem. 2003 Jun 27;278(26):24090-4. Epub 2003 Apr 14. PMID:12695512

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OCA

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-'''Crystal Structure of Ca(II)-bound Gla Domain of Factor IX Complexed with Binding Protein'''
+===Crystal Structure of Ca(II)-bound Gla Domain of Factor IX Complexed with Binding Protein===
-==Overview==
+<!--
-Factor IX is an indispensable protein required in the blood coagulation cascade. It binds to the surface of phospholipid membrane by means of a gamma-carboxyglutamic acid (Gla) domain situated at the N terminus. Recently, we showed that physiological concentrations of Mg2+ ions affect the native conformation of the Gla domain and in doing so augment the biological activity of factor IXa and binding affinity with its binding protein even in the presence of Ca2+ ions. Here we report on the crystal structures of the Mg2+/Ca2+-bound and Ca2+-bound (Mg2+-free) factor IX Gla domain (IXGD1-46) in complex with its binding protein (IX-bp) at 1.55 and 1.80 A resolutions, respectively. Three Mg2+ and five Ca2+ ions were bound in the Mg2+/Ca2+-bound IXGD1-46, and the Mg2+ ions were replaced by Ca2+ ions in Mg2+-free IXGD1-46. Comparison of Mg2+/Ca2+-bound with Ca2+-bound structures of the complexes showed that Mg2+ ion, which formed a bridge between IXGD1-46 and IX-bp, forced IXGD1-46 to rotate 4 degrees relative to IX-bp and hence might be the cause of a more tight interaction between the molecules than in the case of the Mg2+-free structure. The results clearly suggest that Mg2+ ions are required to maintain native conformation and in vivo function of factor IX Gla domain during blood coagulation.
+The line below this paragraph, {{ABSTRACT_PUBMED_12695512}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 12695512 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_12695512}}
 ==About this Structure==
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 [[Category: Gla domain]]
 [[Category: Magnesium ion]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 20:44:56 2008''
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