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'''Unreleased structure'''


The entry 8xxs is ON HOLD  until Paper Publication
==Crystal structure of PDE4D catalytic domain complexed with L11==
 
<StructureSection load='8xxs' size='340' side='right'caption='[[8xxs]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
Authors: Wu, D., Huang, Y.-Y., Luo, H.-B.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[8xxs]] 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=8XXS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8XXS FirstGlance]. <br>
Description: Crystal structure of PDE4D catalytic domain complexed with L11
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.1000094&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1D5M:2-[4-[bis(fluoranyl)methoxy]-3-(cyclopropylmethoxy)phenyl]-1-benzofuran-6-ol'>A1D5M</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
[[Category: Luo, H.-B]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8xxs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8xxs OCA], [https://pdbe.org/8xxs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8xxs RCSB], [https://www.ebi.ac.uk/pdbsum/8xxs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8xxs ProSAT]</span></td></tr>
[[Category: Wu, D]]
</table>
[[Category: Huang, Y.-Y]]
== Disease ==
[https://www.uniprot.org/uniprot/PDE4D_HUMAN PDE4D_HUMAN] Note=Genetic variations in PDE4D might be associated with susceptibility to stroke. PubMed:17006457 states that association with stroke has to be considered with caution.  Defects in PDE4D are the cause of acrodysostosis type 2, with or without hormone resistance (ACRDYS2) [MIM:[https://omim.org/entry/614613 614613]. ACRDYS2 is a pleiotropic disorder characterized by skeletal, endocrine, and neurological abnormalities. Skeletal features include brachycephaly, midface hypoplasia with a small upturned nose, brachydactyly, and lumbar spinal stenosis. Endocrine abnormalities include hypothyroidism and hypogonadism in males and irregular menses in females. Developmental disability is a common finding but is variable in severity and can be associated with significant behavioral problems.<ref>PMID:22464250</ref>
== Function ==
[https://www.uniprot.org/uniprot/PDE4D_HUMAN PDE4D_HUMAN] Hydrolyzes the second messenger cAMP, which is a key regulator of many important physiological processes.<ref>PMID:15260978</ref> <ref>PMID:15576036</ref>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Huang Y-Y]]
[[Category: Luo H-B]]
[[Category: Wu D]]
Retrieved from "https://proteopedia.org/8xxs"