Summary for 5WDE
| Entry DOI | 10.2210/pdb5wde/pdb |
| Descriptor | Kinesin-like protein KIFC3, ADENOSINE-5'-DIPHOSPHATE, MAGNESIUM ION, ... (5 entities in total) |
| Functional Keywords | kinesin, motor domain, adp, structural genomics, structur al genomics consortium, sgc, structural genomics consortium, motor protein |
| Biological source | Homo sapiens (Human) |
| Cellular location | Cell junction, adherens junction : Q9BVG8 |
| Total number of polymer chains | 1 |
| Total formula weight | 36673.03 |
| Authors | Shen, Y.,Tempel, W.,Landry, R.,Arrowsmith, C.H.,Edwards, A.M.,Park, H.,Structural Genomics Consortium (SGC) (deposition date: 2017-07-05, release date: 2017-08-09, Last modification date: 2023-10-04) |
| Primary citation | Park, H.W.,Ma, Z.,Zhu, H.,Jiang, S.,Robinson, R.C.,Endow, S.A. Structural basis of small molecule ATPase inhibition of a human mitotic kinesin motor protein. Sci Rep, 7:15121-15121, 2017 Cited by PubMed Abstract: Kinesin microtubule motor proteins play essential roles in division, including attaching chromosomes to spindles and crosslinking microtubules for spindle assembly. Human kinesin-14 KIFC1 is unique in that cancer cells with amplified centrosomes are dependent on the motor for viable division because of its ability to cluster centrosomes and form bipolar spindles, but it is not required for division in almost all normal cells. Screens for small molecule inhibitors of KIFC1 have yielded several candidates for further development, but obtaining structural data to determine their sites of binding has been difficult. Here we compare a previously unreported KIFC1 crystal structure with new structures of two closely related kinesin-14 proteins, Ncd and KIFC3, to determine the potential binding site of a known KIFC1 ATPase inhibitor, AZ82. We analyze the previously identified kinesin inhibitor binding sites and identify features of AZ82 that favor binding to one of the sites, the α4/α6 site. This selectivity can be explained by unique structural features of the KIFC1 α4/α6 binding site. These features may help improve the drug-like properties of AZ82 and other specific KIFC1 inhibitors. PubMed: 29123223DOI: 10.1038/s41598-017-14754-6 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.85 Å) |
Structure validation
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