7a4s
From Proteopedia
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<StructureSection load='7a4s' size='340' side='right'caption='[[7a4s]], [[Resolution|resolution]] 3.10Å' scene=''> | <StructureSection load='7a4s' size='340' side='right'caption='[[7a4s]], [[Resolution|resolution]] 3.10Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'> | + | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7A4S OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7A4S FirstGlance]. <br> |
| - | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.1Å</td></tr> |
| - | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PTR:O-PHOSPHOTYROSINE'>PTR</scene>, <scene name='pdbligand=QYE:7-chlorothieno[3,2-c]pyridin-4-amine'>QYE</scene>, <scene name='pdbligand=SEP:PHOSPHOSERINE'>SEP</scene></td></tr> |
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7a4s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7a4s OCA], [https://pdbe.org/7a4s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7a4s RCSB], [https://www.ebi.ac.uk/pdbsum/7a4s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7a4s ProSAT]</span></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=7a4s FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7a4s OCA], [https://pdbe.org/7a4s PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7a4s RCSB], [https://www.ebi.ac.uk/pdbsum/7a4s PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7a4s ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| - | == Disease == | ||
| - | [[https://www.uniprot.org/uniprot/DYR1A_HUMAN DYR1A_HUMAN]] Defects in DYRK1A are the cause of mental retardation autosomal dominant type 7 (MRD7) [MIM:[https://omim.org/entry/614104 614104]]. A disease characterized by primary microcephaly, severe mental retardation without speech, anxious autistic behavior, and dysmorphic features, including bitemporal narrowing, deep-set eyes, large simple ears, and a pointed nasal tip. Mental retardation is characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period.<ref>PMID:21294719</ref> | ||
| - | == Function == | ||
| - | [[https://www.uniprot.org/uniprot/DYR1A_HUMAN DYR1A_HUMAN]] May play a role in a signaling pathway regulating nuclear functions of cell proliferation. Phosphorylates serine, threonine and tyrosine residues in its sequence and in exogenous substrates.<ref>PMID:8769099</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 7a4s" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 7a4s" style="background-color:#fffaf0;"></div> | ||
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| - | ==See Also== | ||
| - | *[[Dual specificity tyrosine-phosphorylation-regulated kinase|Dual specificity tyrosine-phosphorylation-regulated kinase]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: Dual-specificity kinase]] | ||
| - | [[Category: Human]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Dokurno | + | [[Category: Dokurno P]] |
| - | [[Category: Hubbard | + | [[Category: Hubbard RE]] |
| - | [[Category: Surgenor | + | [[Category: Surgenor AE]] |
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Current revision
Structure of DYRK1A in complex with compound 2
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