Abl kinase domain in complex with PD180970. Determined by X-ray diffraction at 1.7 Å resolution. Released 16 Jan 2007.
Explore 2HZI in 3D Show helices and sheets RCSB PDB PDBe
2HZI contains 44 α-helices and 30 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 | 236 | 1 | 1 |
| α-helix | 239-241 | 3 | |
| β-strand | 242-247 | 6 | 1 |
| α-helix | 249-251 | 3 | |
| β-strand | 256-261 | 6 | 1 |
| α-helix | 262-264 | 3 | |
| β-strand | 266-272 | 7 | 1 |
| α-helix | 280-290 | 11 | |
| β-strand | 298 | 1 | 2 |
| α-helix | 299-300 | 2 | |
| β-strand | 301-305 | 5 | 1 |
| α-helix | 311 | 1 | |
| β-strand | 312-316 | 5 | 1 |
| α-helix | 317-318 | 2 | |
| β-strand | 321-322 | 2 | 2 |
| α-helix | 323-329 | 7 | |
| α-helix | 337-356 | 20 | |
| β-strand | 359-360 | 2 | 3 |
| α-helix | 366-368 | 3 | |
| β-strand | 369-371 | 3 | 2 |
| α-helix | 373-375 | 3 | |
| β-strand | 377-379 | 3 | 2 |
| β-strand | 385-386 | 2 | 3 |
| β-strand | 389 | 1 | 4 |
| β-strand | 391 | 1 | 4 |
| β-strand | 393-394 | 2 | 5 |
| α-helix | 395-396 | 2 | |
| α-helix | 403-405 | 3 | |
| α-helix | 408-413 | 6 | |
| β-strand | 415-416 | 2 | 5 |
| α-helix | 418-433 | 16 | |
| α-helix | 437-438 | 2 | |
| α-helix | 445-447 | 3 | |
| α-helix | 448-453 | 6 | |
| α-helix | 458-461 | 4 | |
| α-helix | 466-475 | 10 | |
| α-helix | 480-482 | 3 | |
| α-helix | 484-485 | 2 | |
| α-helix | 486-499 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 236 | 1 | 6 |
| α-helix | 239-241 | 3 | |
| β-strand | 242-247 | 6 | 6 |
| α-helix | 249-251 | 3 | |
| β-strand | 256-261 | 6 | 6 |
| α-helix | 262-264 | 3 | |
| β-strand | 266-272 | 7 | 6 |
| α-helix | 280-292 | 13 | |
| β-strand | 298 | 1 | 7 |
| α-helix | 299-300 | 2 | |
| β-strand | 301-305 | 5 | 6 |
| α-helix | 311 | 1 | |
| β-strand | 312-316 | 5 | 6 |
| β-strand | 322 | 1 | 7 |
| α-helix | 323-329 | 7 | |
| α-helix | 337-356 | 20 | |
| β-strand | 359-360 | 2 | 8 |
| α-helix | 366-368 | 3 | |
| β-strand | 369-371 | 3 | 7 |
| α-helix | 373-375 | 3 | |
| β-strand | 377-379 | 3 | 7 |
| β-strand | 385-386 | 2 | 8 |
| β-strand | 393-394 | 2 | 9 |
| α-helix | 395-396 | 2 | |
| α-helix | 403-405 | 3 | |
| α-helix | 408-413 | 6 | |
| β-strand | 415-416 | 2 | 9 |
| α-helix | 418-433 | 16 | |
| α-helix | 437-438 | 2 | |
| α-helix | 445-453 | 9 | |
| α-helix | 458-461 | 4 | |
| α-helix | 466-475 | 10 | |
| α-helix | 480-482 | 3 | |
| α-helix | 484-485 | 2 | |
| α-helix | 486-499 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Proto-oncogene tyrosine-protein kinase ABL1 | A, B | protein | 277 | Homo sapiens | P00519 (AlphaFold model) |
>2HZI_1 Proto-oncogene tyrosine-protein kinase ABL1 (chains A, B) GAMDPSPNYDKWEMERTDITMKHKLGGGQYGEVYEGVWKKYSLTVAVKTLKEDTMEVEEF LKEAAVMKEIKHPNLVQLLGVCTREPPFYIITEFMTYGNLLDYLRECNRQEVNAVVLLYM ATQISSAMEYLEKKNFIHRDLAARNCLVGENHLVKVADFGLSRLMTGDTYTAHAGAKFPI KWTAPESLAYNKFSIKSDVWAFGVLLWEIATYGMSPYPGIDLSQVYELLEKDYRMERPEG CPEKVYELMRACWQWNPSDRPSFAEIHQAFETMFQES
| ID | Name | Formula | Copies |
|---|---|---|---|
| JIN | 6-(2,6-dichlorophenyl)-2-[(4-fluoro-3-methylphenyl)amino]-8-METHYLPYRIDO[2,3-D]… | C21 H15 Cl2 F N4 O | 2 |
Structural biology contributions to the discovery of drugs to treat chronic myelogenous leukaemia. Cowan-Jacob, S.W., Fendrich, G., Floersheimer, A. et al. Acta Crystallogr D Biol Crystallogr (2007) 63:80-93. DOI 10.1107/S0907444906047287 · PubMed
Other PDB entries of the same protein (UniProt P00519 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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