5jcb | pdb_00005jcb

Microtubule depolymerizing agent podophyllotoxin derivative YJTSF1

spinqualitylabelsall models 5jcb, resolution 2.30Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5jcb is a 6 chain structure with sequence from [1] and Sus scrofa. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: ACP, CA, GDP, GOL, GTP, IMD, MES, MG, NA, NV4, PEG Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function [TBA1B_PIG] Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain. [F2Z5B2_PIG] Tubulin is the major constituent of microtubules. It binds two moles of GTP, one at an exchangeable site on the beta chain and one at a non-exchangeable site on the alpha chain.[RuleBase:RU003505] Publication Abstract from PubMed The colchicine domain is widely recognized as the binding site of microtubule depolymerization agents for anticancer drug design. Almost all of the drugs targeting the colchicine domain have been confirmed to bind to the tubulin beta-subunit. Here we studied a crystal structure (2.3 A) of the complex between tubulin and 4beta-(1,2,4-triazol-3-ylthio)-4-deoxypodophyllotoxin (compound 1S) with superior antitumor activity, which was designed on the basis of the colchicine domain and synthesized in our previous work. A distinct binding model of the colchicine domain was found in the complexes of tubulin with compound 1S. From a comparison of the crystal structures of tubulin-compound 1S and tubulin-colchicine complexes, the side chains of the T7 loop of beta-tubulin flip outward and the T5 loop of alpha-tubulin changes its conformation. It has been shown that the beta-subunit T7 loop reversibly participates in resistance to straightening that opposes microtubule assembly by flipping in and out. Together with the biochemical results from compound 1S, the structural data highlight the main contributors in the alpha-subunits and the colchicine domain beta-subunits: the dual-target binding sites in the alpha-T7 loop and beta-H7-T7 loop of tubulin. Compound 1S can synchronously bind to alphabeta-tubulin. The structures also highlight common features for the design and development of novel potent microtubule destabilizing agents. Structural Insights into the Inhibition of Tubulin by the Antitumor Agent 4beta-(1,2,4-triazol-3-ylthio)-4-deoxypodophyllotoxin.,Zhao W, Zhou C, Guan ZY, Yin P, Chen F, Tang YJ ACS Chem Biol. 2017 Mar 17;12(3):746-752. doi: 10.1021/acschembio.6b00842. Epub, 2017 Jan 25. PMID:28035796 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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