3evg
From Proteopedia
(Difference between revisions)
Line 2: | Line 2: | ||
<StructureSection load='3evg' size='340' side='right' caption='[[3evg]], [[Resolution|resolution]] 2.20Å' scene=''> | <StructureSection load='3evg' size='340' side='right' caption='[[3evg]], [[Resolution|resolution]] 2.20Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[3evg]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[3evg]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Den27 Den27]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3EVG OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3EVG FirstGlance]. <br> |
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | ||
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3eva|3eva]], [[3evb|3evb]], [[3evc|3evc]], [[3evd|3evd]], [[3eve|3eve]], [[3evf|3evf]]</td></tr> | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3eva|3eva]], [[3evb|3evb]], [[3evc|3evc]], [[3evd|3evd]], [[3eve|3eve]], [[3evf|3evf]]</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=3evg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3evg OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3evg RCSB], [http://www.ebi.ac.uk/pdbsum/3evg PDBsum]</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=3evg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3evg OCA], [http://pdbe.org/3evg PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3evg RCSB], [http://www.ebi.ac.uk/pdbsum/3evg PDBsum]</span></td></tr> |
</table> | </table> | ||
== Function == | == Function == | ||
Line 17: | Line 17: | ||
<text>to colour the structure by Evolutionary Conservation</text> | <text>to colour the structure by Evolutionary Conservation</text> | ||
</jmolCheckbox> | </jmolCheckbox> | ||
- | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/ | + | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=3evg ConSurf]. |
<div style="clear:both"></div> | <div style="clear:both"></div> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
Line 27: | Line 27: | ||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
+ | <div class="pdbe-citations 3evg" style="background-color:#fffaf0;"></div> | ||
==See Also== | ==See Also== | ||
Line 34: | Line 35: | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Den27]] |
[[Category: Geiss, B J]] | [[Category: Geiss, B J]] | ||
[[Category: Peersen, O B]] | [[Category: Peersen, O B]] |
Revision as of 20:16, 9 February 2016
Crystal structure of Dengue-2 virus methyltransferase complexed with S-adenosyl-L-homocysteine
|
Categories: Den27 | Geiss, B J | Peersen, O B | Thompson, A A | Atp-binding | Capsid protein | Cleavage on pair of basic residue | Dengue virus | Endoplasmic reticulum | Envelope protein | Flavivirus | Glycoprotein | Helicase | Hydrolase | Membrane | Metal-binding | Multifunctional enzyme | Ns5 methyltransferase | Nucleotide-binding | Nucleotidyltransferase | Nucleus | Phosphoprotein | Protease | Ribonucleoprotein | Rna cap binding | Rna replication | Rna-binding | Rna-directed rna polymerase | Secreted | Serine protease | Transcription | Transcription regulation | Transferase | Transmembrane | Viral nucleoprotein | Virion