4jln: Difference between revisions
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{{STRUCTURE_4jln| PDB=4jln | SCENE= }} | |||
===Human dCK C4S-S74E mutant in complex with UDP and the F2.4.1 inhibitor (2-[({2-[3-(2-FLUOROETHOXY)-4-METHOXYPHENYL]-5-PROPYL-1,3-THIAZOL-4-YL}METHYL)SULFANYL]PYRIMIDINE-4,6-DIAMINE)=== | |||
==Function== | |||
[[http://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> | |||
==About this Structure== | |||
[[4jln]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4JLN OCA]. | |||
==Reference== | |||
<references group="xtra"/><references/> | |||
[[Category: Deoxycytidine kinase]] | |||
[[Category: Lavie, A.]] | |||
[[Category: Nomme, J.]] | |||
[[Category: Kinase]] | |||
[[Category: Phosphoryl transfer]] | |||
[[Category: Phosphorylation]] | |||
[[Category: Transferase-transferase inhibitor complex]] | |||