BTK complex with compound 13. Determined by X-ray diffraction at 1.3 Å resolution. Released 7 Nov 2018.
Explore 6BLN in 3D Show helices and sheets RCSB PDB PDBe
6BLN contains 19 α-helices and 12 β-strands across 1 chain. 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 | 396 | 1 | 1 |
| α-helix | 399-401 | 3 | |
| β-strand | 402-411 | 10 | 1 |
| β-strand | 414-421 | 8 | 1 |
| β-strand | 425-431 | 7 | 1 |
| β-strand | 437 | 1 | 2 |
| α-helix | 439-444 | 6 | |
| α-helix | 446-450 | 5 | |
| β-strand | 457 | 1 | 3 |
| α-helix | 458-459 | 2 | |
| β-strand | 460-464 | 5 | 1 |
| β-strand | 471-475 | 5 | 1 |
| β-strand | 481 | 1 | 3 |
| α-helix | 482-488 | 7 | |
| 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 | 616-619 | 4 | |
| α-helix | 624-632 | 9 | |
| α-helix | 638-640 | 3 | |
| α-helix | 642-643 | 2 | |
| α-helix | 644-657 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | A | protein | 287 | Homo sapiens | Q06187 (AlphaFold model) |
>6BLN_1 Tyrosine-protein kinase BTK (chains A) MGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMN LSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEY LESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMY SKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMY SCWHEKADERPTFKILLSNILDVMDENLYFQGEEYMPTEHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| DY4 | N-(3-{5-[(1,5-dimethyl-1H-pyrazol-3-yl)amino]-6-oxo-1,6-dihydropyridazin-3-yl}-… | C24 H22 F2 N6 O2 S | 1 |
Water and common crystallization additives (SO4, GOL) are not listed.
Water molecules in protein-ligand interfaces. Evaluation of software tools and SAR comparison. Nittinger, E., Gibbons, P., Eigenbrot, C. et al. J Comput Aided Mol Des (2019) 33:307-330. DOI 10.1007/s10822-019-00187-y · PubMed
Other PDB entries of the same protein (UniProt Q06187 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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