6BLN: BTK complex with compound 13

BTK complex with compound 13. Determined by X-ray diffraction at 1.3 Å resolution. Released 7 Nov 2018.

Method
X-ray diffraction
Resolution
1.3 Å
Organism
Homo sapiens
Chains
1
Atoms
2,489
Mol. weight
34.76 kDa
Ligands
DY4
Released
7 Nov 2018

Explore 6BLN in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 19 helices, 12 β-strands

ElementResiduesLengthSheet
β-strand39611
α-helix399-4013
β-strand402-411101
β-strand414-42181
β-strand425-43171
β-strand43712
α-helix439-4446
α-helix446-4505
β-strand45713
α-helix458-4592
β-strand460-46451
β-strand471-47551
β-strand48113
α-helix482-4887
α-helix495-51420
α-helix524-5263
β-strand527-52933
β-strand535-53733
α-helix542-5454
β-strand54612
α-helix549-5524
α-helix561-5633
α-helix566-5716
α-helix576-59116
α-helix595-5962
α-helix603-6119
α-helix616-6194
α-helix624-6329
α-helix638-6403
α-helix642-6432
α-helix644-65714

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Tyrosine-protein kinase BTKAprotein287Homo sapiensQ06187 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6BLN_1 Tyrosine-protein kinase BTK (chains A)
MGSWEIDPKDLTFLKELGTGQFGVVKYGKWRGQYDVAIKMIKEGSMSEDEFIEEAKVMMN
LSHEKLVQLYGVCTKQRPIFIITEYMANGCLLNYLREMRHRFQTQQLLEMCKDVCEAMEY
LESKQFLHRDLAARNCLVNDQGVVKVSDFGLSRYVLDDEYTSSVGSKFPVRWSPPEVLMY
SKFSSKSDIWAFGVLMWEIYSLGKMPYERFTNSETAEHIAQGLRLYRPHLASEKVYTIMY
SCWHEKADERPTFKILLSNILDVMDENLYFQGEEYMPTEHHHHHHHH

Ligands and cofactors

IDNameFormulaCopies
DY4N-(3-{5-[(1,5-dimethyl-1H-pyrazol-3-yl)amino]-6-oxo-1,6-dihydropyridazin-3-yl}-…C24 H22 F2 N6 O2 S1

Water and common crystallization additives (SO4, GOL) are not listed.

Primary citation

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:

Browse structure collections

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