4P5Q: Human EphA3 Kinase domain

Human EphA3 Kinase domain in complex with quinoxaline derivatives. Determined by X-ray diffraction at 1.35 Å resolution. Released 13 Aug 2014.

Method
X-ray diffraction
Resolution
1.35 Å
Organism
Homo sapiens
Chains
1
Atoms
2,542
Mol. weight
40.88 kDa
Ligands
Q0B
Released
13 Aug 2014

Explore 4P5Q in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4P5Q 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
α-helix6141
β-strand61511
α-helix616-6172
α-helix618-6203
β-strand621-62991
β-strand634-64181
β-strand647-65481
α-helix655-6562
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-helix788-7903
α-helix793-7986
α-helix803-81816
α-helix822-8232
α-helix830-8389
β-strand841-84223
α-helix843-8464
β-strand85014
α-helix851-86010
α-helix865-8673
α-helix869-8702
α-helix871-88313
α-helix885-8895
β-strand89114
β-strand902-90323

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ephrin type-A receptor 3Aprotein361Homo sapiensP29320 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>4P5Q_1 Ephrin type-A receptor 3 (chains A)
MGSSHHHHHHSSGLVPRGSTQTVHEFAKELDATNISIDKVVGAGEFGEVCSGRLKLPSKK
EISVAIKTLKVGYTEKQRRDFLGEASIMGQFDHPNIIRLEGVVTKSKPVMIVTEYMENGS
LDSFLRKHDAQFTVIQLVGMLRGIASGMKYLSDMGYVHRDLAARNILINSNLVCKVSDFG
LSRVLEDDPEAAYTTRGGKIPIRWTSPEAIAYRKFTSASDVWSYGIVLWEVMSYGERPYW
EMSNQDVIKAVDEGYRLPPPMDCPAALYQLMLDCWQKDRNNRPKFEQIVSILDKLIRNPG
SLKIITSAAARPSNLLLDQSNVDITTFRTTGDWLNGVWTAHCKEIFTGVEYSSCDTIAKI
S

Ligands and cofactors

IDNameFormulaCopies
Q0B2-amino-1-(2-chlorophenyl)-N-(3-ethoxypropyl)-1H-pyrrolo[2,3-b]quinoxaline-3-ca…C22 H22 Cl N5 O21

Primary citation

Pyrrolo[3,2-b]quinoxaline Derivatives as Types I1/2 and II Eph Tyrosine Kinase Inhibitors: Structure-Based Design, Synthesis, and in Vivo Validation. Unzue, A., Dong, J., Lafleur, K. et al. J Med Chem (2014) 57:6834. DOI 10.1021/jm5009242 · 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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