Human Eg5 motor domain bound to Mg-ADP and monastrol. Determined by X-ray diffraction at 1.8 Å resolution. Released 15 Nov 2005.
Explore 1X88 in 3D Show helices and sheets RCSB PDB PDBe
1X88 contains 42 α-helices and 36 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 | 20-25 | 6 | 1 |
| α-helix | 26-29 | 4 | |
| α-helix | 30-34 | 5 | |
| β-strand | 41-44 | 4 | 2 |
| β-strand | 49-57 | 9 | 2 |
| β-strand | 60-67 | 8 | 2 |
| β-strand | 70-72 | 3 | 1 |
| α-helix | 78-81 | 4 | |
| α-helix | 82-86 | 5 | |
| α-helix | 87-94 | 8 | |
| β-strand | 98-105 | 8 | 1 |
| α-helix | 111-115 | 5 | |
| β-strand | 117 | 1 | 3 |
| α-helix | 119-120 | 2 | |
| α-helix | 121-123 | 3 | |
| α-helix | 127-129 | 3 | |
| β-strand | 133 | 1 | 3 |
| α-helix | 135-146 | 12 | |
| β-strand | 152-164 | 13 | 1 |
| β-strand | 167-170 | 4 | 1 |
| α-helix | 180-181 | 2 | |
| β-strand | 182 | 1 | 1 |
| β-strand | 183-187 | 5 | 4 |
| β-strand | 190-197 | 8 | 4 |
| β-strand | 202-204 | 3 | 1 |
| α-helix | 207-209 | 3 | |
| α-helix | 210-227 | 18 | |
| α-helix | 231-234 | 4 | |
| β-strand | 236-248 | 13 | 1 |
| β-strand | 254-265 | 12 | 1 |
| 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 | 1 |
| α-helix | 340-342 | 3 | |
| α-helix | 343-356 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 18 | 1 | 5 |
| α-helix | 19 | 1 | |
| β-strand | 20-25 | 6 | 6 |
| α-helix | 26-28 | 3 | |
| α-helix | 30-34 | 5 | |
| β-strand | 41-44 | 4 | 7 |
| β-strand | 49-53 | 5 | 7 |
| β-strand | 63-67 | 5 | 7 |
| β-strand | 70-72 | 3 | 6 |
| α-helix | 78-81 | 4 | |
| α-helix | 82-86 | 5 | |
| α-helix | 87-94 | 8 | |
| β-strand | 98-105 | 8 | 6 |
| α-helix | 111-115 | 5 | |
| β-strand | 117 | 1 | 8 |
| α-helix | 119-120 | 2 | |
| α-helix | 121-123 | 3 | |
| α-helix | 127-129 | 3 | |
| β-strand | 133 | 1 | 8 |
| α-helix | 135-147 | 13 | |
| β-strand | 152-164 | 13 | 6 |
| β-strand | 167-170 | 4 | 6 |
| β-strand | 182 | 1 | 6 |
| β-strand | 183-186 | 4 | 9 |
| β-strand | 194-197 | 4 | 9 |
| β-strand | 202-204 | 3 | 6 |
| α-helix | 207-209 | 3 | |
| α-helix | 210-227 | 18 | |
| α-helix | 231-234 | 4 | |
| β-strand | 236-248 | 13 | 6 |
| β-strand | 254-265 | 12 | 6 |
| 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 | 6 |
| α-helix | 340-342 | 3 | |
| α-helix | 343-356 | 14 | |
| β-strand | 360 | 1 | 5 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Kinesin-like protein KIF11 | A, B | protein | 359 | Homo sapiens | P52732 (AlphaFold model) |
>1X88_1 Kinesin-like protein KIF11 (chains A, B) KKKEEKGKNIQVVVRCRPFNLAERKASAHSIVECDPVRKEVSVRTGGLADKSSRKTYTFD MVFGASTKQIDVYRSVVCPILDEVIMGYNCTIFAYGQTGTGKTFTMEGERSPNEEYTWEE DPLAGIIPRTLHQIFEKLTDNGTEFSVKVSLLEIYNEELFDLLNPSSDVSERLQMFDDPR NKRGVIIKGLEEITVHNKDEVYQILEKGAAKRTTAATLMNAYSSRSHSVFSVTIHMKETT IDGEELVKIGKLNLVDLAGSENIGRSGAVDKRAREAGNINQSLLTLGRVITALVERTPHV PYRESKLTRILQDSLGGRTRTSIIATISPASLNLEETLSTLEYAHRAKNILNKPEVNQK
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAT | Ethyl 4-(3-hydroxyphenyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carb… | C14 H16 N2 O3 S | 2 |
| ADP | Adenosine-5'-diphosphate | C10 H15 N5 O10 P2 | 2 |
| MG | Magnesium ion | Mg | 2 |
Structural Basis of Eg5 Inhibition by Monastrol. Maliga, Z., Mitchison, T.J. To be published.
Other PDB entries of the same protein (UniProt P52732 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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