3snl: Difference between revisions

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[[Image:3snl.png|left|200px]]


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==Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors==
The line below this paragraph, containing "STRUCTURE_3snl", creates the "Structure Box" on the page.
<StructureSection load='3snl' size='340' side='right'caption='[[3snl]], [[Resolution|resolution]] 2.40&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'>[[3snl]] 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=3SNL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SNL 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]] 2.4&#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=548:6-CHLORO-3,4-DIMETHYL-1-(3-METHYLPYRIDIN-4-YL)-8-(TRIFLUOROMETHYL)IMIDAZO[1,5-A]QUINOXALINE'>548</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
{{STRUCTURE_3snl|  PDB=3snl  |  SCENE= }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3snl FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3snl OCA], [https://pdbe.org/3snl PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3snl RCSB], [https://www.ebi.ac.uk/pdbsum/3snl PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3snl ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/PDE10_HUMAN PDE10_HUMAN] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. Can hydrolyze both cAMP and cGMP, but has higher affinity for cAMP and is more efficient with cAMP as substrate.<ref>PMID:17389385</ref>


===Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors===
==See Also==
 
*[[Phosphodiesterase 3D structures|Phosphodiesterase 3D structures]]
 
== References ==
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(as it appears on PubMed at http://www.pubmed.gov), where 21988093 is the PubMed ID number.
</StructureSection>
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{{ABSTRACT_PUBMED_21988093}}
 
==About this Structure==
[[3snl]] is a 2 chain structure with sequence 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=3SNL OCA].
 
==Reference==
<ref group="xtra">PMID:021988093</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Brandon, N J.]]
[[Category: Large Structures]]
[[Category: Brennan, J.]]
[[Category: Brandon NJ]]
[[Category: Egerland, U.]]
[[Category: Brennan J]]
[[Category: Erdei, J.]]
[[Category: Egerland U]]
[[Category: Fan, K Y.]]
[[Category: Erdei J]]
[[Category: Graf, R.]]
[[Category: Fan KY]]
[[Category: Grauer, S]]
[[Category: Graf R]]
[[Category: Grunwald, C]]
[[Category: Grauer S]]
[[Category: Hage, T.]]
[[Category: Grunwald C]]
[[Category: Harrison, B L.]]
[[Category: Hage T]]
[[Category: Hofgen, N.]]
[[Category: Harrison BL]]
[[Category: Kronbach, T.]]
[[Category: Hofgen N]]
[[Category: Langen, B.]]
[[Category: Kronbach T]]
[[Category: Lankau, H J.]]
[[Category: Langen B]]
[[Category: Malamas, M S.]]
[[Category: Lankau H-J]]
[[Category: Marquis, K L.]]
[[Category: Malamas MS]]
[[Category: Navarra, R.]]
[[Category: Marquis KL]]
[[Category: Ni, Y.]]
[[Category: Navarra R]]
[[Category: Pangalos, M.]]
[[Category: Ni Y]]
[[Category: Parris, K D.]]
[[Category: Pangalos M]]
[[Category: Robichaud, A.]]
[[Category: Parris KD]]
[[Category: Schindler, R.]]
[[Category: Robichaud A]]
[[Category: Stange, H.]]
[[Category: Schindler R]]
[[Category: Hydrolase]]
[[Category: Stange H]]
[[Category: Hydrolase inhibitor]]
[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: Zn binding]]

Latest revision as of 09:52, 1 March 2024

Highly Potent, Selective, and Orally Active Phosphodiestarase 10A Inhibitors

3snl, resolution 2.40Å

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