2kls: Difference between revisions

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==Apo-form of the second Ca2+ binding domain of NCX1.4==
==Apo-form of the second Ca2+ binding domain of NCX1.4==
<StructureSection load='2kls' size='340' side='right' caption='[[2kls]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''>
<StructureSection load='2kls' size='340' side='right'caption='[[2kls]]' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2kls]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Canlf Canlf]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KLS OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2KLS FirstGlance]. <br>
<table><tr><td colspan='2'>[[2kls]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Canis_lupus_familiaris Canis lupus familiaris]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KLS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KLS FirstGlance]. <br>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2klt|2klt]]</td></tr>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">SLC8A1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9615 CANLF])</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2kls FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kls OCA], [https://pdbe.org/2kls PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kls RCSB], [https://www.ebi.ac.uk/pdbsum/2kls PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kls ProSAT]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2kls FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kls OCA], [http://pdbe.org/2kls PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2kls RCSB], [http://www.ebi.ac.uk/pdbsum/2kls PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2kls ProSAT]</span></td></tr>
</table>
</table>
== Evolutionary Conservation ==
== Evolutionary Conservation ==
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Canlf]]
[[Category: Canis lupus familiaris]]
[[Category: Aelen, J]]
[[Category: Large Structures]]
[[Category: Foarce, A]]
[[Category: Aelen J]]
[[Category: Hilge, M]]
[[Category: Foarce A]]
[[Category: Perrakis, A]]
[[Category: Hilge M]]
[[Category: Vuister, G W]]
[[Category: Perrakis A]]
[[Category: Ca2+ regulation]]
[[Category: Vuister GW]]
[[Category: Ca2+ sensor]]
[[Category: Electrostatic switch]]
[[Category: Metal binding protein]]
[[Category: Sodium calcium exchanger]]

Latest revision as of 12:40, 22 May 2024

Apo-form of the second Ca2+ binding domain of NCX1.4Apo-form of the second Ca2+ binding domain of NCX1.4

Structural highlights

2kls is a 1 chain structure with sequence from Canis lupus familiaris. Full experimental information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:Solution NMR
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

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 PubMed

Regulation of ion-transport in the Na(+)/Ca(2+) exchanger (NCX) occurs via its cytoplasmic Ca(2+)-binding domains, CBD1 and CBD2. Here, we present a mechanism for NCX activation and inactivation based on data obtained using NMR, isothermal titration calorimetry (ITC) and small-angle X-ray scattering (SAXS). We initially determined the structure of the Ca(2+)-free form of CBD2-AD and the structure of CBD2-BD that represent the two major splice variant classes in NCX1. Although the apo-form of CBD2-AD displays partially disordered Ca(2+)-binding sites, those of CBD2-BD are entirely unstructured even in an excess of Ca(2+). Striking differences in the electrostatic potential between the Ca(2+)-bound and -free forms strongly suggest that Ca(2+)-binding sites in CBD1 and CBD2 form electrostatic switches analogous to C(2)-domains. SAXS analysis of a construct containing CBD1 and CBD2 reveals a conformational change mediated by Ca(2+)-binding to CBD1. We propose that the electrostatic switch in CBD1 and the associated conformational change are necessary for exchanger activation. The response of the CBD1 switch to intracellular Ca(2+) is influenced by the closely located cassette exons. We further propose that Ca(2+)-binding to CBD2 induces a second electrostatic switch, required to alleviate Na(+)-dependent inactivation of Na(+)/Ca(2+) exchange. In contrast to CBD1, the electrostatic switch in CBD2 is isoform- and splice variant-specific and allows for tailored exchange activities.

Ca2+ regulation in the Na+/Ca2+ exchanger features a dual electrostatic switch mechanism.,Hilge M, Aelen J, Foarce A, Perrakis A, Vuister GW Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14333-8. Epub 2009 Aug 10. PMID:19667209[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Hilge M, Aelen J, Foarce A, Perrakis A, Vuister GW. Ca2+ regulation in the Na+/Ca2+ exchanger features a dual electrostatic switch mechanism. Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14333-8. Epub 2009 Aug 10. PMID:19667209
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