Thymidine kinase
From Proteopedia
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</StructureSection> | </StructureSection> | ||
| - | == 3D Structures of thymidine kinase == | ||
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| - | *'''Thymidine kinase''' | ||
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| - | **[[1e2h]] – HsvTK – Herpes simplex virus 1<BR /> | ||
| - | **[[3e2i]] – TK – ''Staphylococcus aureus''<BR /> | ||
| - | **[[2qpo]] – TmTK – ''Thermotoga maritima'' | ||
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| - | *Thymidine kinase complex with reactants or products | ||
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| - | **[[1e2i]] - HsvTK 46-376 + hydroxypropyladenine<BR /> | ||
| - | **[[1e2j]] - HsvTK (mutant) + THM<BR /> | ||
| - | **[[1kim]] - HsvTK + THM<BR /> | ||
| - | **[[1vtk]] - HsvTK + THMP + ADP<BR /> | ||
| - | **[[2vtk]] - HsvTK + THM + ADP<BR /> | ||
| - | **[[3vtk]] - HsvTK + substrate analog + ADP<BR /> | ||
| - | **[[3f0t]], [[1of1]], [[4jby]], [[4jbx]], [[4ivr]], [[4ivq]], [[4ivp]] – HsvTK residues 45-376 + thymine derivative <BR /> | ||
| - | **[[3rdp]] - HsvTK residues 45-376 + pyrimidine derivative<br /> | ||
| - | **[[4oql]], [[4oqm]], [[4oqn]], [[4oqx]] - HsvTK residues 45-376 + uridine derivative<br /> | ||
| - | **[[1qhi]], [[1ki3]], [[1ki2]], [[1ki4]] - HsvTK + inhibitor<BR /> | ||
| - | **[[1e2p]], [[1e2m]], [[1e2n]], [[1e2k]], [[1e2l]], [[1ki6]], [[1ki7]], [[1ki8]] – HsvTK + substrate analog<BR /> | ||
| - | **[[1osn]] – TK + inhibitor + ADP - Human Herpes virus 3<BR /> | ||
| - | **[[4uxh]], [[4uxi]], [[4uxj]] – TK + thymidine derivative – ''Leishmania major''<br /> | ||
| - | **[[1p6x]] – EhvTK 23-352 + THM – Equine Herpes virus 4<BR /> | ||
| - | **[[1p72]] - EhvTK + THM + ADP<BR /> | ||
| - | **[[2qqe]] – TmTK + THM<BR /> | ||
| - | **[[2qq0]] – TmTK + THM + ADP + THMP + ANP<BR /> | ||
| - | **[[2b8t]] - TK + THM – ''Ureaplasma parvum''<BR /> | ||
| - | **[[2j9r]] – TK + THM – ''Bacillus anthracis''<BR /> | ||
| - | **[[1xx6]] – TK + ADP – ''Clostridium acetobutylicum''<br /> | ||
| - | **[[5fuv]] – TbTK catalytic domain 204-383 + THM – ''Trypanosoma brucei''<br /> | ||
| - | **[[5fuw]] – TbTK catalytic domain + THM + DTMP<br /> | ||
| - | **[[5fux]], [[5fuy]] – TbTK catalytic domain (mutation) + DTMP<br /> | ||
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| - | *Thymidine kinase complex with feed-back inhibitor | ||
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| - | **[[2j87]] – TK + TTP – Vaccinia virus<BR /> | ||
| - | **[[2uz3]] – TK (mutant) + TTP – ''Ureaplasma urealyticum''<BR /> | ||
| - | **[[2ja1]] – TK + TTP – ''Bacillus cereus'' | ||
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| - | *Thymidine kinase complex with bisubstrate inhibitor | ||
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| - | **[[1p7c]] – HsvTK + TP5A<BR /> | ||
| - | **[[1p73]] - EhvTK + TP4A<BR /> | ||
| - | **[[1p75]] - EhvTK + TP5A<BR /> | ||
| - | **[[2orw]] – TmTK + TP4A<BR /> | ||
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| - | **[[2ki5]] – HsvTK + aciclovir | ||
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| - | *'''Thymidine kinase 1''' | ||
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| - | **[[1xbt]] - hTK1 residues 1-193 – human<BR /> | ||
| - | **[[2wvj]] – hTK1 residues 1-193 (mutant) + TTP<BR /> | ||
| - | **[[2orv]] – hTK1 (mutant) + TP4A<BR /> | ||
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| - | *'''Thymidine kinase 2''' | ||
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| - | **[[1w4r]] – hTK2 + TTP | ||
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== References == | == References == | ||
<references/> | <references/> | ||
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[[Category:Topic Page]] | [[Category:Topic Page]] | ||
Revision as of 08:37, 24 April 2022
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References
- ↑ Perez-Perez MJ, Priego EM, Hernandez AI, Familiar O, Camarasa MJ, Negri A, Gago F, Balzarini J. Structure, physiological role, and specific inhibitors of human thymidine kinase 2 (TK2): present and future. Med Res Rev. 2008 Sep;28(5):797-820. doi: 10.1002/med.20124. PMID:18459168 doi:http://dx.doi.org/10.1002/med.20124
- ↑ He Q, Zhang P, Zou L, Li H, Wang X, Zhou S, Fornander T, Skog S. Concentration of thymidine kinase 1 in serum (S-TK1) is a more sensitive proliferation marker in human solid tumors than its activity. Oncol Rep. 2005 Oct;14(4):1013-9. PMID:16142366
- ↑ Saada A, Shaag A, Mandel H, Nevo Y, Eriksson S, Elpeleg O. Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy. Nat Genet. 2001 Nov;29(3):342-4. PMID:11687801 doi:http://dx.doi.org/10.1038/ng751
- ↑ Kosinska U, Carnrot C, Sandrini MP, Clausen AR, Wang L, Piskur J, Eriksson S, Eklund H. Structural studies of thymidine kinases from Bacillus anthracis and Bacillus cereus provide insights into quaternary structure and conformational changes upon substrate binding. FEBS J. 2007 Feb;274(3):727-37. PMID:17288553 doi:10.1111/j.1742-4658.2006.05617.x
