7zi5: Difference between revisions
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New page: '''Unreleased structure''' The entry 7zi5 is ON HOLD Authors: Saez-Ayala, M., Ben-Yaala, K., Betzi, S., Rebuffet, E., Morelli, X. Description: Crystal structure of dCK C4S-S74E mutant ... |
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==Crystal structure of dCK C4S-S74E mutant in complex with UDP and the OR0274 inhibitor== | |||
<StructureSection load='7zi5' size='340' side='right'caption='[[7zi5]], [[Resolution|resolution]] 2.00Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[7zi5]] is a 1 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=7ZI5 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7ZI5 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]] 2Å</td></tr> | |||
[[Category: | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=J9I:4-(4-azanylpyrimidin-2-yl)-N-[2-methyl-5-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]phenyl]-1,3-thiazol-2-amine'>J9I</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=UDP:URIDINE-5-DIPHOSPHATE'>UDP</scene></td></tr> | ||
[[Category: | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7zi5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7zi5 OCA], [https://pdbe.org/7zi5 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7zi5 RCSB], [https://www.ebi.ac.uk/pdbsum/7zi5 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7zi5 ProSAT]</span></td></tr> | ||
[[Category: Betzi | </table> | ||
[[Category: | == Function == | ||
[[Category: | [https://www.uniprot.org/uniprot/DCK_HUMAN DCK_HUMAN] Required for the phosphorylation of the deoxyribonucleosides deoxycytidine (dC), deoxyguanosine (dG) and deoxyadenosine (dA). Has broad substrate specificity, and does not display selectivity based on the chirality of the substrate. It is also an essential enzyme for the phosphorylation of numerous nucleoside analogs widely employed as antiviral and chemotherapeutic agents.<ref>PMID:18377927</ref> <ref>PMID:20614893</ref> | ||
[[Category: | == References == | ||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Large Structures]] | |||
[[Category: Ben-Yaala K]] | |||
[[Category: Betzi S]] | |||
[[Category: Morelli X]] | |||
[[Category: Rebuffet E]] | |||
[[Category: Saez-Ayala M]] | |||
Latest revision as of 08:03, 7 February 2024
Crystal structure of dCK C4S-S74E mutant in complex with UDP and the OR0274 inhibitor
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