6co7: Difference between revisions
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<StructureSection load='6co7' size='340' side='right' caption='[[6co7]], [[Resolution|resolution]] 3.07Å' scene=''> | <StructureSection load='6co7' size='340' side='right' caption='[[6co7]], [[Resolution|resolution]] 3.07Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6co7]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CO7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CO7 FirstGlance]. <br> | <table><tr><td colspan='2'>[[6co7]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Nemve Nemve]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CO7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CO7 FirstGlance]. <br> | ||
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CLR:CHOLESTEROL'>CLR</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=POV:(2S)-3-(HEXADECANOYLOXY)-2-[(9Z)-OCTADEC-9-ENOYLOXY]PROPYL+2-(TRIMETHYLAMMONIO)ETHYL+PHOSPHATE'>POV</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CLR:CHOLESTEROL'>CLR</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=POV:(2S)-3-(HEXADECANOYLOXY)-2-[(9Z)-OCTADEC-9-ENOYLOXY]PROPYL+2-(TRIMETHYLAMMONIO)ETHYL+PHOSPHATE'>POV</scene></td></tr> | ||
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">v1g248535 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=45351 NEMVE])</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=6co7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6co7 OCA], [http://pdbe.org/6co7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6co7 RCSB], [http://www.ebi.ac.uk/pdbsum/6co7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6co7 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=6co7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6co7 OCA], [http://pdbe.org/6co7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6co7 RCSB], [http://www.ebi.ac.uk/pdbsum/6co7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6co7 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Transient Receptor Potential Melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channel required for immune cell activation, insulin secretion, and body heat control. TRPM2 is activated by cytosolic Ca(2+), phosphatidyl-inositol-4,5-bisphosphate and ADP ribose. Here we present the ~3A resolution electron cryo-microscopy structure of TRPM2 from Nematostella vectensis, 63% similar in sequence to human TRPM2, in the Ca(2+)-bound closed state. Compared to other TRPM channels, TRPM2 exhibits unique structural features that correlate with its function. The pore is larger and more negatively charged, consistent with its high Ca(2+) selectivity and larger conductance. The intracellular Ca(2+) binding sites are connected to the pore and cytosol, explaining the unusual dependence of TRPM2 activity on intra- and extracellular Ca(2+). In addition, the absence of a post-filter motif is likely the cause of the rapid inactivation of human TRPM2. Together, our cryo-EM and electrophysiology studies provide a molecular understanding of the unique gating mechanism of TRPM2. | |||
Structure of a TRPM2 channel in complex with Ca(2+) explains unique gating regulation.,Zhang Z, Toth B, Szollosi A, Chen J, Csanady L Elife. 2018 May 10;7. pii: 36409. doi: 10.7554/eLife.36409. PMID:29745897<ref>PMID:29745897</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
</div> | |||
<div class="pdbe-citations 6co7" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Nemve]] | |||
[[Category: Chen, J]] | [[Category: Chen, J]] | ||
[[Category: Csanady, L]] | [[Category: Csanady, L]] | ||
Revision as of 10:47, 23 May 2018
Structure of the nvTRPM2 channel in complex with Ca2+Structure of the nvTRPM2 channel in complex with Ca2+
Structural highlights
Publication Abstract from PubMedTransient Receptor Potential Melastatin 2 (TRPM2) is a Ca(2+)-permeable cation channel required for immune cell activation, insulin secretion, and body heat control. TRPM2 is activated by cytosolic Ca(2+), phosphatidyl-inositol-4,5-bisphosphate and ADP ribose. Here we present the ~3A resolution electron cryo-microscopy structure of TRPM2 from Nematostella vectensis, 63% similar in sequence to human TRPM2, in the Ca(2+)-bound closed state. Compared to other TRPM channels, TRPM2 exhibits unique structural features that correlate with its function. The pore is larger and more negatively charged, consistent with its high Ca(2+) selectivity and larger conductance. The intracellular Ca(2+) binding sites are connected to the pore and cytosol, explaining the unusual dependence of TRPM2 activity on intra- and extracellular Ca(2+). In addition, the absence of a post-filter motif is likely the cause of the rapid inactivation of human TRPM2. Together, our cryo-EM and electrophysiology studies provide a molecular understanding of the unique gating mechanism of TRPM2. Structure of a TRPM2 channel in complex with Ca(2+) explains unique gating regulation.,Zhang Z, Toth B, Szollosi A, Chen J, Csanady L Elife. 2018 May 10;7. pii: 36409. doi: 10.7554/eLife.36409. PMID:29745897[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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