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| | <StructureSection load='7a06' size='340' side='right'caption='[[7a06]], [[Resolution|resolution]] 1.80Å' scene=''> | | <StructureSection load='7a06' size='340' side='right'caption='[[7a06]], [[Resolution|resolution]] 1.80Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[7a06]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7A06 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=7A06 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7a06]] 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=7A06 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7A06 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=QTH:1-[(4-phenylphenyl)methyl]-4-pyrrolidin-1-yl-pyridine'>QTH</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8Å</td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CHKA, CHK, CKI ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=QTH:1-[(4-phenylphenyl)methyl]-4-pyrrolidin-1-yl-pyridine'>QTH</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=7a06 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7a06 OCA], [http://pdbe.org/7a06 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=7a06 RCSB], [http://www.ebi.ac.uk/pdbsum/7a06 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=7a06 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=7a06 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7a06 OCA], [https://pdbe.org/7a06 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7a06 RCSB], [https://www.ebi.ac.uk/pdbsum/7a06 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7a06 ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/CHKA_HUMAN CHKA_HUMAN]] Has a key role in phospholipid biosynthesis and may contribute to tumor cell growth. Catalyzes the first step in phosphatidylcholine biosynthesis. Contributes to phosphatidylethanolamine biosynthesis. Phosphorylates choline and ethanolamine. Has higher activity with choline.<ref>PMID:19915674</ref> | + | [https://www.uniprot.org/uniprot/CHKA_HUMAN CHKA_HUMAN] Has a key role in phospholipid biosynthesis and may contribute to tumor cell growth. Catalyzes the first step in phosphatidylcholine biosynthesis. Contributes to phosphatidylethanolamine biosynthesis. Phosphorylates choline and ethanolamine. Has higher activity with choline.<ref>PMID:19915674</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 7a06" style="background-color:#fffaf0;"></div> | | <div class="pdbe-citations 7a06" style="background-color:#fffaf0;"></div> |
| | + | |
| | + | ==See Also== |
| | + | *[[Choline kinase 3D structures|Choline kinase 3D structures]] |
| | == References == | | == References == |
| | <references/> | | <references/> |
| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Human]] | + | [[Category: Homo sapiens]] |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Ballarotto, M]] | + | [[Category: Ballarotto M]] |
| - | [[Category: Carrasco-Jimenez, M P]] | + | [[Category: Carrasco-Jimenez MP]] |
| - | [[Category: Hurtado-Guerrero, R]] | + | [[Category: Castro Navas FC]] |
| - | [[Category: Lopez-Cara, L C]] | + | [[Category: Hurtado-Guerrero R]] |
| - | [[Category: Macchiarulo, A]] | + | [[Category: Lopez-Cara LC]] |
| - | [[Category: Marco, C]] | + | [[Category: Macchiarulo A]] |
| - | [[Category: Mariotto, E]] | + | [[Category: Marco C]] |
| - | [[Category: Navas, F C.Castro]]
| + | [[Category: Mariotto E]] |
| - | [[Category: Rubbini, G]] | + | [[Category: Rubbini G]] |
| - | [[Category: Serran-Aguilera, L]] | + | [[Category: Serran-Aguilera L]] |
| - | [[Category: Viola, G]] | + | [[Category: Viola G]] |
| - | [[Category: Anti proliferative effect]]
| + | |
| - | [[Category: Cancer]]
| + | |
| - | [[Category: Choline kinase]]
| + | |
| - | [[Category: Drug]]
| + | |
| - | [[Category: Half molecule]]
| + | |
| - | [[Category: Transferase]]
| + | |
| Structural highlights
Function
CHKA_HUMAN Has a key role in phospholipid biosynthesis and may contribute to tumor cell growth. Catalyzes the first step in phosphatidylcholine biosynthesis. Contributes to phosphatidylethanolamine biosynthesis. Phosphorylates choline and ethanolamine. Has higher activity with choline.[1]
Publication Abstract from PubMed
Seeking for new anticancer drugs with strong antiproliferative activity and simple molecular structure, we designed a novel series of compounds based on our previous reported pharmacophore model composed of five moieties. Antiproliferative assays on four tumoral cell lines and evaluation of Human Choline Kinase CKalpha1 enzymatic activity was performed for these compounds. Among tested molecules, those ones with biphenyl spacer showed betters enzymatic and antiproliferative activities (n-v). Docking and crystallization studies validate the hypothesis and confirm the results. The most active compound (t) induces a significant arrest of the cell cycle in G0/G1 phase that ultimately lead to apoptosis, following the mitochondrial pathway, as demonstrated for other choline kinase inhibitors. However additional assays reveal that the inhibition of choline uptake could also be involved in the antiproliferative outcome of this class of compounds.
Synthesis, biological evaluation, in silico modeling and crystallization of novel small monocationic molecules with potent antiproliferative activity by dual mechanism.,Serran-Aguilera L, Mariotto E, Rubbini G, Castro Navas FF, Marco C, Carrasco-Jimenez MP, Ballarotto M, Macchiarulo A, Hurtado-Guerrero R, Viola G, Lopez-Cara LC Eur J Med Chem. 2020 Sep 6;207:112797. doi: 10.1016/j.ejmech.2020.112797. PMID:32977218[2]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Gallego-Ortega D, Ramirez de Molina A, Ramos MA, Valdes-Mora F, Barderas MG, Sarmentero-Estrada J, Lacal JC. Differential role of human choline kinase alpha and beta enzymes in lipid metabolism: implications in cancer onset and treatment. PLoS One. 2009 Nov 12;4(11):e7819. doi: 10.1371/journal.pone.0007819. PMID:19915674 doi:10.1371/journal.pone.0007819
- ↑ Serran-Aguilera L, Mariotto E, Rubbini G, Castro Navas FF, Marco C, Carrasco-Jimenez MP, Ballarotto M, Macchiarulo A, Hurtado-Guerrero R, Viola G, Lopez-Cara LC. Synthesis, biological evaluation, in silico modeling and crystallization of novel small monocationic molecules with potent antiproliferative activity by dual mechanism. Eur J Med Chem. 2020 Sep 6;207:112797. doi: 10.1016/j.ejmech.2020.112797. PMID:32977218 doi:http://dx.doi.org/10.1016/j.ejmech.2020.112797
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