Crystal structure of the mitotic kinesin eg5 (ksp) in complex with mg-adp and (r)-4-(3-hydroxyphenyl)-n,n,7,8-tetramethyl-3,4-dihydroisoquinoline-2(1h)-carboxamide. Determined by X-ray diffraction at 2.1 Å resolution. Released 18 Apr 2006.
Explore 2FME in 3D Show helices and sheets RCSB PDB PDBe
2FME contains 42 α-helices and 42 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 | 18 | 1 | 1 |
| β-strand | 20-25 | 6 | 2 |
| α-helix | 26-28 | 3 | |
| α-helix | 30-32 | 3 | |
| β-strand | 39 | 1 | 3 |
| β-strand | 41-44 | 4 | 4 |
| β-strand | 49-53 | 5 | 4 |
| β-strand | 62-67 | 6 | 4 |
| β-strand | 70-72 | 3 | 2 |
| α-helix | 78-81 | 4 | |
| α-helix | 82-86 | 5 | |
| α-helix | 87-94 | 8 | |
| β-strand | 98-104 | 7 | 2 |
| α-helix | 111-115 | 5 | |
| β-strand | 117 | 1 | 5 |
| α-helix | 119-120 | 2 | |
| α-helix | 121-123 | 3 | |
| α-helix | 127-129 | 3 | |
| β-strand | 133 | 1 | 5 |
| α-helix | 135-146 | 12 | |
| β-strand | 154-164 | 11 | 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 | 236-245 | 10 | 2 |
| β-strand | 258-265 | 8 | 2 |
| α-helix | 266-268 | 3 | |
| α-helix | 269-271 | 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 | 2 |
| β-strand | 339 | 1 | 3 |
| α-helix | 340-342 | 3 | |
| α-helix | 343-356 | 14 | |
| β-strand | 360 | 1 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 18 | 1 | 7 |
| β-strand | 20-25 | 6 | 8 |
| α-helix | 26-28 | 3 | |
| α-helix | 30-32 | 3 | |
| β-strand | 39 | 1 | 9 |
| β-strand | 41-44 | 4 | 4 |
| β-strand | 49-55 | 7 | 4 |
| β-strand | 62-67 | 6 | 4 |
| 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 | 119-120 | 2 | |
| α-helix | 121-123 | 3 | |
| α-helix | 127-129 | 3 | |
| β-strand | 133 | 1 | 10 |
| α-helix | 135-146 | 12 | |
| β-strand | 154-164 | 11 | 8 |
| β-strand | 167-170 | 4 | 8 |
| β-strand | 181-182 | 2 | 8 |
| β-strand | 183-186 | 4 | 11 |
| β-strand | 194-197 | 4 | 11 |
| β-strand | 202-203 | 2 | 8 |
| α-helix | 207-209 | 3 | |
| 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 | 269-271 | 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 |
| β-strand | 339 | 1 | 9 |
| 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) |
>2FME_1 Kinesin-like protein KIF11 (chains A, B) MASQPNSSAKKKEEKGKNIQVVVRCRPFNLAERKASAHSIVECDPVRKEVSVRTGGLADK SSRKTYTFDMVFGASTKQIDVYRSVVCPILDEVIMGYNCTIFAYGQTGTGKTFTMEGERS PNEEYTWEEDPLAGIIPRTLHQIFEKLTDNGTEFSVKVSLLEIYNEELFDLLNPSSDVSE RLQMFDDPRNKRGVIIKGLEEITVHNKDEVYQILEKGAAKRTTAATLMNAYSSRSHSVFS VTIHMKETTIDGEELVKIGKLNLVDLAGSENIGRSGAVDKRAREAGNINQSLLTLGRVIT ALVERTPHVPYRESKLTRILQDSLGGRTRTSIIATISPASLNLEETLSTLEYAHRAKNIL NKPEVNQK
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 2 |
| 3QC | (4R)-4-(3-hydroxyphenyl)-N,N,7,8-tetramethyl-3,4-dihydroisoquinoline-2(1H)-carb… | C20 H24 N2 O2 | 2 |
| ADP | Adenosine-5'-diphosphate | C10 H15 N5 O10 P2 | 2 |
Inhibitors of human mitotic kinesin Eg5: Characterization of the 4-phenyl-tetrahydroisoquinoline lead series. Tarby, C.M., Kaltenbach III, R.F., Huynh, T. et al. Bioorg Med Chem Lett (2006) 16:2095-2100. DOI 10.1016/j.bmcl.2006.01.056 · PubMed
Other PDB entries of the same protein (UniProt P52732 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 2FME directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.