1XKK: EGFR kinase domain

EGFR kinase domain complexed with a quinazoline inhibitor- GW572016. Determined by X-ray diffraction at 2.4 Å resolution. Released 7 Dec 2004.

Method
X-ray diffraction
Resolution
2.4 Å
Organism
Homo sapiens
Chains
1
Atoms
2,376
Mol. weight
41.1 kDa
Ligands
PO4, FMM
Released
7 Dec 2004

Explore 1XKK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1XKK contains 18 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: 18 helices, 12 β-strands

ElementResiduesLengthSheet
β-strand705-70621
β-strand712-72091
β-strand724-73181
β-strand740-74781
α-helix756-76813
β-strand77412
β-strand777-78261
β-strand786-79161
β-strand79712
α-helix798-8047
α-helix811-83020
α-helix840-8423
β-strand843-84752
β-strand850-85342
α-helix858-8614
α-helix883-8886
α-helix893-90816
α-helix912-9132
α-helix920-9223
α-helix923-9297
α-helix933-9364
β-strand93913
α-helix941-95010
α-helix955-9573
α-helix959-9602
α-helix961-97313
α-helix975-9784
β-strand97913
α-helix996-10027
α-helix1013-10164

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Epidermal growth factor receptorAprotein352Homo sapiensP00533 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>1XKK_1 Epidermal growth factor receptor (chains A)
MKKGHHHHHHDYDIPTTENLYFQGSGEAPNQALLRILKETEFKKIKVLGSGAFGTVYKGL
WIPEGEKVKIPVAIKELREATSPKANKEILDEAYVMASVDNPHVCRLLGICLTSTVQLIT
QLMPFGCLLDYVREHKDNIGSQYLLNWCVQIAKGMNYLEDRRLVHRDLAARNVLVKTPQH
VKITDFGLAKLLGAEEKEYHAEGGKVPIKWMALESILHRIYTHQSDVWSYGVTVWELMTF
GSKPYDGIPASEISSILEKGERLPQPPICTIDVYMIMVKCWMIDADSRPKFRELIIEFSK
MARDPQRYLVIQGDERMHLPSPTDSNFYRALMDEEDMDDVVDADEYLIPQQG

Ligands and cofactors

IDNameFormulaCopies
PO4Phosphate ionO4 P2
FMMN-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-[5-({[2-(methylsulfonyl)ethyl]amin…C29 H26 Cl F N4 O4 S1

Primary citation

A unique structure for epidermal growth factor receptor bound to GW572016 (Lapatinib): relationships among protein conformation, inhibitor off-rate, and receptor activity in tumor cells. Wood, E.R., Truesdale, A.T., McDonald, O.B. et al. Cancer Res (2004) 64:6652-6659. DOI 10.1158/0008-5472.CAN-04-1168 · PubMed

Other PDB entries of the same protein (UniProt P00533 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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1XKK is part of these collections:

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