Ternary complex structure - BTK cIAP compound 17. Determined by X-ray diffraction at 2.17 Å resolution. Released 18 Nov 2020.
Explore 6W7O in 3D Show helices and sheets RCSB PDB PDBe
6W7O contains 46 α-helices and 28 β-strands across 4 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 |
|---|---|---|---|
| α-helix | 399-401 | 3 | |
| β-strand | 406-409 | 4 | 1 |
| β-strand | 416-420 | 5 | 1 |
| β-strand | 426-431 | 6 | 1 |
| β-strand | 437 | 1 | 2 |
| α-helix | 439-449 | 11 | |
| β-strand | 457 | 1 | 3 |
| β-strand | 460-464 | 5 | 1 |
| α-helix | 470 | 1 | |
| β-strand | 471-475 | 5 | 1 |
| β-strand | 481 | 1 | 3 |
| α-helix | 482-487 | 6 | |
| α-helix | 489-491 | 3 | |
| α-helix | 495-514 | 20 | |
| α-helix | 524-526 | 3 | |
| β-strand | 527-529 | 3 | 3 |
| β-strand | 535-537 | 3 | 3 |
| α-helix | 542-545 | 4 | |
| β-strand | 546 | 1 | 2 |
| α-helix | 549-552 | 4 | |
| α-helix | 561-563 | 3 | |
| α-helix | 566-571 | 6 | |
| α-helix | 576-591 | 16 | |
| α-helix | 595-596 | 2 | |
| α-helix | 603-611 | 9 | |
| α-helix | 624-632 | 9 | |
| α-helix | 638-640 | 3 | |
| α-helix | 644-653 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 399-401 | 3 | |
| β-strand | 402-411 | 10 | 4 |
| β-strand | 414-421 | 8 | 4 |
| β-strand | 425-432 | 8 | 4 |
| β-strand | 437 | 1 | 5 |
| α-helix | 439-449 | 11 | |
| β-strand | 457 | 1 | 6 |
| β-strand | 460-464 | 5 | 4 |
| β-strand | 470-475 | 6 | 4 |
| β-strand | 481 | 1 | 6 |
| α-helix | 482-487 | 6 | |
| α-helix | 489-491 | 3 | |
| α-helix | 495-514 | 20 | |
| α-helix | 524-526 | 3 | |
| β-strand | 527-529 | 3 | 6 |
| β-strand | 535-537 | 3 | 6 |
| α-helix | 542-545 | 4 | |
| β-strand | 546 | 1 | 5 |
| α-helix | 549-552 | 4 | |
| α-helix | 561-563 | 3 | |
| α-helix | 566-571 | 6 | |
| α-helix | 576-591 | 16 | |
| α-helix | 595-596 | 2 | |
| α-helix | 603-611 | 9 | |
| α-helix | 616-619 | 4 | |
| α-helix | 624-632 | 9 | |
| α-helix | 638-640 | 3 | |
| α-helix | 644-653 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 264-266 | 3 | |
| α-helix | 269-274 | 6 | |
| α-helix | 275-278 | 4 | |
| α-helix | 287-292 | 6 | |
| β-strand | 295-297 | 3 | 7 |
| β-strand | 304-306 | 3 | 7 |
| β-strand | 312-313 | 2 | 7 |
| α-helix | 322-329 | 8 | |
| α-helix | 334-349 | 16 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 264-266 | 3 | |
| α-helix | 269-274 | 6 | |
| α-helix | 275-278 | 4 | |
| α-helix | 287-292 | 6 | |
| β-strand | 295-297 | 3 | 8 |
| β-strand | 304-306 | 3 | 8 |
| β-strand | 312-313 | 2 | 8 |
| α-helix | 322-329 | 8 | |
| α-helix | 334-348 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | A, B | protein | 277 | Homo sapiens | Q06187 (AlphaFold model) |
| Baculoviral IAP repeat-containing protein 2 | C, D | protein | 99 | Homo sapiens | Q13490 (AlphaFold model) |
>6W7O_1 Tyrosine-protein kinase BTK (chains A, B) SAPSTAGLGYGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEF IEEAKVMMNLSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMC KDVCEAMEYLESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVR WSPPEVLMYSKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLA SEKVYTIMYSCWHEKADERPTFKILLSNILDVMDEES
>6W7O_2 Baculoviral IAP repeat-containing protein 2 (chains C, D) GSGPGSSISNLSMQTHAARMRTFMYWPSSVPVQPEQLASAGFYYVGRNDDVKCFCCDGGL RCWESGDDPWVEHAKWFPRCEFLIRMKGQEFVDEIQGRY
| ID | Name | Formula | Copies |
|---|---|---|---|
| TL7 | [5-({[(3S)-2-(N-methyl-L-alanyl-3-methyl-L-valyl)-3-{[(1R)-1,2,3,4-tetrahydrona… | C58 H65 F2 N11 O8 | 2 |
| ZN | Zinc ion | Zn | 2 |
Structural Characterization of BTK:PROTAC:cIAP Ternary Complexes: From Snapshots to Ensembles. Calabrese, M.F., Schiemer, J.S., Horst, R. et al. Nat Chem Biol (2020).
Other PDB entries of the same protein (UniProt Q06187 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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