2kul: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2kul]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KUL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KUL FirstGlance]. <br> | <table><tr><td colspan='2'>[[2kul]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2KUL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2KUL 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=2kul FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kul OCA], [https://pdbe.org/2kul PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kul RCSB], [https://www.ebi.ac.uk/pdbsum/2kul PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kul ProSAT]</span></td></tr> | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2kul FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2kul OCA], [https://pdbe.org/2kul PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2kul RCSB], [https://www.ebi.ac.uk/pdbsum/2kul PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2kul ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Disease == | == Disease == |
Latest revision as of 08:36, 15 May 2024
Structural highlights
DiseaseVRK1_HUMAN Pontocerebellar hypoplasia type 1. The disease is caused by mutations affecting the gene represented in this entry. FunctionVRK1_HUMAN Serine/threonine kinase involved in Golgi disassembly during the cell cycle: following phosphorylation by PLK3 during mitosis, required to induce Golgi fragmentation. Acts by mediating phosphorylation of downstream target protein. Phosphorylates 'Thr-18' of p53/TP53 and may thereby prevent the interaction between p53/TP53 and MDM2. Phosphorylates casein and histone H3. Phosphorylates BANF1: disrupts its ability to bind DNA, reduces its binding to LEM domain-containing proteins and causes its relocalization from the nucleus to the cytoplasm. Phosphorylates ATF2 which activates its transcriptional activity.[1] [2] [3] [4] [5] [6] See AlsoReferences
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