4fcb: Difference between revisions
From Proteopedia
Jump to navigationJump to search
m Protected "4fcb" [edit=sysop:move=sysop] |
No edit summary |
||
| (7 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
==Potent and Selective Phosphodiesterase 10A Inhibitors== | |||
<StructureSection load='4fcb' size='340' side='right'caption='[[4fcb]], [[Resolution|resolution]] 2.10Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[4fcb]] 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=4FCB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4FCB FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1Å</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0T7:3,4-DIMETHYL-1-PROPYL-7-(QUINOLIN-2-YLMETHOXY)IMIDAZO[1,5-A]QUINOXALINE'>0T7</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4fcb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4fcb OCA], [https://pdbe.org/4fcb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4fcb RCSB], [https://www.ebi.ac.uk/pdbsum/4fcb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4fcb 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> | |||
==See Also== | |||
*[[Phosphodiesterase 3D structures|Phosphodiesterase 3D structures]] | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Parris KD]] | |||
Latest revision as of 11:13, 1 March 2024
Potent and Selective Phosphodiesterase 10A Inhibitors
| ||||||||||||
