1pvb: Difference between revisions
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==X-RAY STRUCTURE OF A NEW CRYSTAL FORM OF PIKE 4.10 PARVALBUMIN== | ==X-RAY STRUCTURE OF A NEW CRYSTAL FORM OF PIKE 4.10 PARVALBUMIN== | ||
<StructureSection load='1pvb' size='340' side='right' caption='[[1pvb]], [[Resolution|resolution]] 1.75Å' scene=''> | <StructureSection load='1pvb' size='340' side='right'caption='[[1pvb]], [[Resolution|resolution]] 1.75Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1pvb]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Esolu Esolu]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PVB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1PVB FirstGlance]. <br> | <table><tr><td colspan='2'>[[1pvb]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Esolu Esolu]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PVB OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1PVB FirstGlance]. <br> | ||
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</div> | </div> | ||
<div class="pdbe-citations 1pvb" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 1pvb" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Parvalbumin|Parvalbumin]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Esolu]] | [[Category: Esolu]] | ||
[[Category: Large Structures]] | |||
[[Category: Declercq, J P]] | [[Category: Declercq, J P]] | ||
[[Category: Parello, J]] | [[Category: Parello, J]] | ||
[[Category: Tinant, B]] | [[Category: Tinant, B]] | ||
[[Category: Calcium binding protein]] | [[Category: Calcium binding protein]] | ||
Revision as of 13:19, 27 November 2019
X-RAY STRUCTURE OF A NEW CRYSTAL FORM OF PIKE 4.10 PARVALBUMINX-RAY STRUCTURE OF A NEW CRYSTAL FORM OF PIKE 4.10 PARVALBUMIN
Structural highlights
Function[PRVB_ESOLU] In muscle, parvalbumin is thought to be involved in relaxation after contraction. It binds two calcium ions. Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. Publication Abstract from PubMedA new crystal form of pike (pI 4.10) parvalbumin has been crystallized in presence of EDTA at pH 8.0. The crystals are orthorhombic, space group P2(1)2(1)2(1), with a = 51.84, b = 49.95, c = 34.96 A. Diffractometer data were collected to 1.75 A. The structure was solved by molecular replacement and refined to R = 0.168 for 7774 observed reflections [I>/= 2sigma(I)] in the range 8.0-1.75 A. In spite of the presence of EDTA, calcium ions are present in both primary binding sites. As compared to the previously reported structures, the main differences concern the conformation of the N-terminal residues and the packing in the unit cell. X-ray structure of a new crystal form of pike 4.10 beta parvalbumin.,Declercq JP, Tinant B, Parello J Acta Crystallogr D Biol Crystallogr. 1996 Jan 1;52(Pt 1):165-9. PMID:15299738[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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