4TWN: Human EphA3 Kinase domain

Human EphA3 Kinase domain in complex with Birb796. Determined by X-ray diffraction at 1.71 Å resolution. Released 13 May 2015.

Method
X-ray diffraction
Resolution
1.71 Å
Organism
Homo sapiens
Chains
1
Atoms
2,346
Mol. weight
40.99 kDa
Ligands
B96
Released
13 May 2015

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

Secondary structure: helices and β-sheets

4TWN contains 22 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: 22 helices, 14 β-strands

ElementResiduesLengthSheet
α-helix609-6113
α-helix6141
β-strand61511
α-helix616-6172
α-helix618-6203
β-strand621-62991
β-strand633-64191
β-strand647-65591
α-helix6561
α-helix661-67414
β-strand68212
α-helix683-6842
β-strand685-68951
β-strand696-70051
β-strand70612
α-helix707-7126
α-helix720-73920
α-helix749-7513
β-strand752-75432
β-strand760-76232
α-helix765-7684
α-helix788-7903
α-helix793-7986
α-helix803-81816
α-helix822-8232
α-helix830-83910
β-strand84213
α-helix843-8464
β-strand85014
α-helix851-86010
α-helix865-8673
α-helix869-8702
α-helix871-88313
α-helix885-8895
β-strand89114
β-strand90213

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ephrin type-A receptor 3Aprotein361Homo sapiensP29320 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4TWN_1 Ephrin type-A receptor 3 (chains A)
MGSSHHHHHHSSGLVPRGSTQTVHEFAKELDATNISIDKVVGAGEFGEVCSGRLKLPSKK
EISVAIKTLKVGYTEKQRRDFLGEASIMGQFDHPNIIRLEGVVTKSKPVMIVTEYMENGS
LDSFLRKHDAQFTVIQLVGMLRGIASGMKYLSDMGYVHRDLAARNILINSNLVCKVSDFG
LSRVLEDDPEAAYTTRGGKIPIRWTSPEAIAYRKFTSASDVWSYGIVLWEVMSYGERPYW
EMSNQDVIKAVDEGYRLPPPMDCPAALYQLMLDCWQKDRNNRPKFEQIVSILDKLIRNPG
SLKIITSAAARPSNLLLDQSNVDITTFRTTGDWLNGVWTAHCKEIFTGVEYSSCDTIAKI
S

Ligands and cofactors

IDNameFormulaCopies
B961-(5-tert-butyl-2-P-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)-napht…C31 H37 N5 O31

Primary citation

Structural Analysis of the Binding of Type I, I1/2, and II Inhibitors to Eph Tyrosine Kinases. Dong, J., Zhao, H., Zhou, T. et al. ACS Med Chem Lett (2015) 6:79-83. DOI 10.1021/ml500355x · PubMed

Other PDB entries of the same protein (UniProt P29320 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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