2qyk: Difference between revisions

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[[Image:2qyk.png|left|200px]]


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==Crystal structure of PDE4A10 in complex with inhibitor NPV==
The line below this paragraph, containing "STRUCTURE_2qyk", creates the "Structure Box" on the page.
<StructureSection load='2qyk' size='340' side='right'caption='[[2qyk]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[2qyk]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2QYK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2QYK FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1&#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=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=NPV:4-[8-(3-NITROPHENYL)-1,7-NAPHTHYRIDIN-6-YL]BENZOIC+ACID'>NPV</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
{{STRUCTURE_2qyk| PDB=2qyk |  SCENE= }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2qyk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2qyk OCA], [https://pdbe.org/2qyk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2qyk RCSB], [https://www.ebi.ac.uk/pdbsum/2qyk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2qyk ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/PDE4A_HUMAN PDE4A_HUMAN] Hydrolyzes the second messenger cAMP, which is a key regulator of many important physiological processes.<ref>PMID:11566027</ref> <ref>PMID:17727341</ref>
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/qy/2qyk_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </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/main_output.php?pdb_ID=2qyk ConSurf].
<div style="clear:both"></div>


===Crystal structure of PDE4A10 in complex with inhibitor NPV===
==See Also==
 
*[[Phosphodiesterase 3D structures|Phosphodiesterase 3D structures]]
 
== References ==
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The line below this paragraph, {{ABSTRACT_PUBMED_17727341}}, adds the Publication Abstract to the page
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(as it appears on PubMed at http://www.pubmed.gov), where 17727341 is the PubMed ID number.
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{{ABSTRACT_PUBMED_17727341}}
 
==About this Structure==
2QYK is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2QYK OCA].
 
==Reference==
<ref group="xtra">PMID:17727341</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Chen, Y.]]
[[Category: Large Structures]]
[[Category: Geng, J.]]
[[Category: Chen Y]]
[[Category: Houslay, M.]]
[[Category: Geng J]]
[[Category: Peng, M.]]
[[Category: Houslay M]]
[[Category: Robinson, H.]]
[[Category: Peng M]]
[[Category: Wang, H.]]
[[Category: Robinson H]]
[[Category: Hydrolase]]
[[Category: Wang H]]
[[Category: Pde4 inhibitor]]
[[Category: Subfamily inhibitor selectivity]]
 
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