X-ray structure of mitotic kinesin-5 (KSP, KIF11, Eg5)in complex with the hexahydro-2H-pyrano[3,2-c]quinoline EMD 534085. Determined by X-ray diffraction at 2.0 Å resolution. Released 2 Mar 2010.
Explore 3L9H in 3D Show helices and sheets RCSB PDB PDBe
3L9H contains 39 α-helices and 40 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 17-18 | 2 | 1 |
| α-helix | 19 | 1 | |
| β-strand | 20-25 | 6 | 2 |
| α-helix | 30-33 | 4 | |
| α-helix | 37-38 | 2 | |
| β-strand | 39 | 1 | 3 |
| β-strand | 41-44 | 4 | 4 |
| β-strand | 49-56 | 8 | 4 |
| β-strand | 61-67 | 7 | 4 |
| β-strand | 70-72 | 3 | 2 |
| α-helix | 78-81 | 4 | |
| α-helix | 82-86 | 5 | |
| α-helix | 87-94 | 8 | |
| β-strand | 98-105 | 8 | 2 |
| α-helix | 111-115 | 5 | |
| β-strand | 117 | 1 | 5 |
| α-helix | 119-120 | 2 | |
| α-helix | 121-123 | 3 | |
| β-strand | 133 | 1 | 5 |
| α-helix | 135-146 | 12 | |
| β-strand | 153-164 | 12 | 2 |
| β-strand | 167-170 | 4 | 2 |
| β-strand | 181-182 | 2 | 2 |
| β-strand | 183-186 | 4 | 6 |
| β-strand | 194-197 | 4 | 6 |
| β-strand | 202-203 | 2 | 2 |
| α-helix | 207-209 | 3 | |
| α-helix | 210-227 | 18 | |
| α-helix | 231-234 | 4 | |
| β-strand | 236-248 | 13 | 2 |
| β-strand | 254-265 | 12 | 2 |
| α-helix | 266-268 | 3 | |
| α-helix | 290-303 | 14 | |
| α-helix | 311-313 | 3 | |
| α-helix | 315-319 | 5 | |
| α-helix | 321-323 | 3 | |
| β-strand | 329-336 | 8 | 2 |
| β-strand | 339 | 1 | 3 |
| α-helix | 340-342 | 3 | |
| α-helix | 343-356 | 14 | |
| β-strand | 360-361 | 2 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 17 | 1 | |
| β-strand | 18 | 1 | 7 |
| α-helix | 19 | 1 | |
| β-strand | 20-25 | 6 | 8 |
| α-helix | 26-28 | 3 | |
| α-helix | 30-34 | 5 | |
| β-strand | 41-44 | 4 | 9 |
| β-strand | 49-56 | 8 | 9 |
| β-strand | 61-67 | 7 | 9 |
| β-strand | 70-72 | 3 | 8 |
| α-helix | 78-81 | 4 | |
| α-helix | 82-86 | 5 | |
| α-helix | 87-94 | 8 | |
| β-strand | 98-104 | 7 | 8 |
| α-helix | 111-115 | 5 | |
| β-strand | 117 | 1 | 10 |
| α-helix | 127-129 | 3 | |
| β-strand | 133 | 1 | 10 |
| α-helix | 135-146 | 12 | |
| β-strand | 152-164 | 13 | 8 |
| β-strand | 167-170 | 4 | 8 |
| β-strand | 182 | 1 | 8 |
| β-strand | 183-186 | 4 | 11 |
| β-strand | 194-197 | 4 | 11 |
| β-strand | 202-204 | 3 | 8 |
| α-helix | 210-227 | 18 | |
| α-helix | 231-234 | 4 | |
| β-strand | 236-248 | 13 | 8 |
| β-strand | 254-265 | 12 | 8 |
| α-helix | 266-268 | 3 | |
| α-helix | 290-304 | 15 | |
| α-helix | 311-313 | 3 | |
| α-helix | 315-319 | 5 | |
| α-helix | 321-323 | 3 | |
| β-strand | 329-336 | 8 | 8 |
| α-helix | 340-342 | 3 | |
| α-helix | 343-356 | 14 | |
| β-strand | 360 | 1 | 7 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Kinesin-like protein KIF11 | A, B | protein | 368 | Homo sapiens | P52732 (AlphaFold model) |
>3L9H_1 Kinesin-like protein KIF11 (chains A, B) MASQPNSSAKKKEEKGKNIQVVVRCRPFNLAERKASAHSIVECDPVRKEVSVRTGGLADK SSRKTYTFDMVFGASTKQIDVYRSVVCPILDEVIMGYNCTIFAYGQTGTGKTFTMEGERS PNEEYTWEEDPLAGIIPRTLHQIFEKLTDNGTEFSVKVSLLEIYNEELFDLLNPSSDVSE RLQMFDDPRNKRGVIIKGLEEITVHNKDEVYQILEKGAAKRTTAATLMNAYSSRSHSVFS VTIHMKETTIDGEELVKIGKLNLVDLAGSENIGRSGAVDKRAREAGNINQSLLTLGRVIT ALVERTPHVPYRESKLTRILQDSLGGRTRTSIIATISPASLNLEETLSTLEYAHRAKNIL NKPEVNQK
| ID | Name | Formula | Copies |
|---|---|---|---|
| ADP | Adenosine-5'-diphosphate | C10 H15 N5 O10 P2 | 2 |
| EMQ | 1-[2-(dimethylamino)ethyl]-3-{[(2R,4aS,5R,10bS)-5-phenyl-9-(trifluoromethyl)-3,… | C25 H31 F3 N4 O2 | 2 |
The discovery and optimization of hexahydro-2H-pyrano[3,2-c]quinolines (HHPQs) as potent and selective inhibitors of the mitotic kinesin-5. Schiemann, K., Finsinger, D., Zenke, F. et al. Bioorg Med Chem Lett (2010) 20:1491-1495. DOI 10.1016/j.bmcl.2010.01.110 · PubMed
Other PDB entries of the same protein (UniProt P52732 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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