7xbb
From Proteopedia
(Difference between revisions)
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==Crystal structure of PDE4D catalytic domain complexed with compound 23a== | ==Crystal structure of PDE4D catalytic domain complexed with compound 23a== | ||
| - | <StructureSection load='7xbb' size='340' side='right'caption='[[7xbb]]' scene=''> | + | <StructureSection load='7xbb' size='340' side='right'caption='[[7xbb]], [[Resolution|resolution]] 2.10Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7XBB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7XBB FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7xbb]] 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=7XBB OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7XBB FirstGlance]. <br> |
| - | </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=7xbb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xbb OCA], [https://pdbe.org/7xbb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xbb RCSB], [https://www.ebi.ac.uk/pdbsum/7xbb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xbb ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=B6V:(2~{R},4~{S})-6-ethyl-2-[(2~{E})-2-hydroxyiminoethyl]-2,8-dimethyl-4-(2-methylprop-1-enyl)-3,4-dihydropyrano[3,2-c][1,8]naphthyridin-5-one'>B6V</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=7xbb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xbb OCA], [https://pdbe.org/7xbb PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xbb RCSB], [https://www.ebi.ac.uk/pdbsum/7xbb PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xbb ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == 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__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Huang Y-Y]] | [[Category: Huang Y-Y]] | ||
[[Category: Luo H-B]] | [[Category: Luo H-B]] | ||
Revision as of 06:49, 8 September 2022
Crystal structure of PDE4D catalytic domain complexed with compound 23a
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