5e1n

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(New page: '''Unreleased structure''' The entry 5e1n is ON HOLD Authors: Lin, J., van den Bedem, H., Brunger, A.T., Wilson, M.A. Description: Selenomethionine Ca2+-Calmodulin from Paramecium tetr...)
Current revision (06:09, 5 July 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5e1n is ON HOLD
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==Selenomethionine Ca2+-Calmodulin from Paramecium tetraurelia qFit disorder model==
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<StructureSection load='5e1n' size='340' side='right'caption='[[5e1n]], [[Resolution|resolution]] 1.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5e1n]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Paramecium_tetraurelia Paramecium tetraurelia]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5E1N OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5E1N FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=MPD:(4S)-2-METHYL-2,4-PENTANEDIOL'>MPD</scene>, <scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5e1n FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5e1n OCA], [https://pdbe.org/5e1n PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5e1n RCSB], [https://www.ebi.ac.uk/pdbsum/5e1n PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5e1n ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/CALM_PARTE CALM_PARTE] Calmodulin mediates the control of a large number of enzymes, ion channels and other proteins by Ca(2+). Among the enzymes to be stimulated by the calmodulin-Ca(2+) complex are a number of protein kinases and phosphatases.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Calmodulin (CaM) is the primary calcium signaling protein in eukaryotes and has been extensively studied using various biophysical techniques. Prior crystal structures have noted the presence of ambiguous electron density in both hydrophobic binding pockets of Ca(2+)-CaM, but no assignment of these features has been made. In addition, Ca(2+)-CaM samples many conformational substates in the crystal and accurately modeling the full range of this functionally important disorder is challenging. In order to characterize these features in a minimally biased manner, a 1.0 A resolution single-wavelength anomalous diffraction data set was measured for selenomethionine-substituted Ca(2+)-CaM. Density-modified electron-density maps enabled the accurate assignment of Ca(2+)-CaM main-chain and side-chain disorder. These experimental maps also substantiate complex disorder models that were automatically built using low-contour features of model-phased electron density. Furthermore, experimental electron-density maps reveal that 2-methyl-2,4-pentanediol (MPD) is present in the C-terminal domain, mediates a lattice contact between N-terminal domains and may occupy the N-terminal binding pocket. The majority of the crystal structures of target-free Ca(2+)-CaM have been derived from crystals grown using MPD as a precipitant, and thus MPD is likely to be bound in functionally critical regions of Ca(2+)-CaM in most of these structures. The adventitious binding of MPD helps to explain differences between the Ca(2+)-CaM crystal and solution structures and is likely to favor more open conformations of the EF-hands in the crystal.
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Authors: Lin, J., van den Bedem, H., Brunger, A.T., Wilson, M.A.
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Atomic resolution experimental phase information reveals extensive disorder and bound 2-methyl-2,4-pentanediol in Ca(2+)-calmodulin.,Lin J, van den Bedem H, Brunger AT, Wilson MA Acta Crystallogr D Struct Biol. 2016 Jan;72(Pt 1):83-92. doi:, 10.1107/S2059798315021609. Epub 2016 Jan 1. PMID:26894537<ref>PMID:26894537</ref>
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Description: Selenomethionine Ca2+-Calmodulin from Paramecium tetraurelia qFit disorder model
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Wilson, M.A]]
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<div class="pdbe-citations 5e1n" style="background-color:#fffaf0;"></div>
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[[Category: Van Den Bedem, H]]
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[[Category: Brunger, A.T]]
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==See Also==
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[[Category: Lin, J]]
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*[[Calmodulin 3D structures|Calmodulin 3D structures]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Paramecium tetraurelia]]
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[[Category: Brunger AT]]
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[[Category: Lin J]]
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[[Category: Wilson MA]]
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[[Category: Van den Bedem H]]

Current revision

Selenomethionine Ca2+-Calmodulin from Paramecium tetraurelia qFit disorder model

PDB ID 5e1n

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