4FOC: Human anaplastic lymphoma kinase

Crystal structure of human anaplastic lymphoma kinase in complex with acyliminobenzimidazole inhibitor 2. Determined by X-ray diffraction at 1.7 Å resolution. Released 11 Jul 2012.

Method
X-ray diffraction
Resolution
1.7 Å
Organism
Homo sapiens
Chains
1
Atoms
2,686
Mol. weight
40.53 kDa
Ligands
0UU
Released
11 Jul 2012

Explore 4FOC in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4FOC contains 20 α-helices and 14 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: 20 helices, 14 β-strands

ElementResiduesLengthSheet
β-strand1096-109831
β-strand1101-110331
α-helix1105-11073
β-strand111012
α-helix1111-11122
α-helix1113-11153
β-strand1116-112492
β-strand1129-113572
α-helix11441
β-strand1145-115172
α-helix1158-117316
β-strand117913
β-strand1182-118652
β-strand1193-119752
β-strand1202-120323
α-helix1204-12107
β-strand121414
β-strand121714
α-helix1223-124220
α-helix1252-12543
β-strand1255-125733
β-strand1266-126833
α-helix1272-12787
α-helix1293-12953
α-helix1298-13036
α-helix1308-132316
α-helix1327-13282
α-helix1335-13439
α-helix1348-13514
α-helix1356-136510
α-helix1370-13723
α-helix1376-138813
α-helix1390-13934
α-helix1395-14017

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
ALK tyrosine kinase receptorAprotein353Homo sapiensQ9UM73 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4FOC_1 ALK tyrosine kinase receptor (chains A)
VYRRKHQELQAMQMELQSPEYKLSKLRTSTIMTDYNPNYSFAGKTSSISDLKEVPRKNIT
LIRGLGHGAFGEVYEGQVSGMPNDPSPLQVAVKTLPEVCSEQDELDFLMEALIISKFNHQ
NIVRCIGVSLQSLPRFILLELMAGGDLKSFLRETRPRPSQPSSLAMLDLLHVARDIACGC
QYLEENHFIHRDIAARNCLLTCPGPGRVAKIGDFGMARDIYRASYYRKGGCAMLPVKWMP
PEAFMEGIFTSKTDTWSFGVLLWEIFSLGYMPYPSKSNQEVLEFVTSGGRMDPPKNCPGP
VYRIMTQCWQHQPEDRPNFAIILERIEYCTQDPDVINTALPIEYGPLVEEEEK

Ligands and cofactors

IDNameFormulaCopies
0UUmethyl cis-4-[2-(benzoylamino)-6-(piperidin-1-ylmethyl)-1H-benzimidazol-1-yl]cy…C28 H34 N4 O31

Primary citation

The Discovery and Optimization of a Novel Class of Potent, Selective, and Orally Bioavailable Anaplastic Lymphoma Kinase (ALK) Inhibitors with Potential Utility for the Treatment of Cancer. Lewis, R.T., Bode, C.M., Choquette, D.M. et al. J Med Chem (2012) 55:6523-6540. DOI 10.1021/jm3005866 · PubMed

Other PDB entries of the same protein (UniProt Q9UM73 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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