6HET: Ephrin type-A receptor 2

Crystal Structure of Ephrin A2 (EphA2) Receptor Protein Kinase with the NVP-BHG712 derivative AT055. Determined by X-ray diffraction at 1.21 Å resolution. Released 28 Aug 2019.

Method
X-ray diffraction
Resolution
1.21 Å
Organism
Homo sapiens
Chains
1
Atoms
2,506
Mol. weight
34.93 kDa
Ligands
G0Q
Released
28 Aug 2019

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

Secondary structure: helices and β-sheets

6HET 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-strand60711
α-helix610-6123
β-strand613-622101
β-strand625-63281
β-strand641-64881
α-helix654-66916
β-strand67512
α-helix676-6772
β-strand678-68251
β-strand688-69361
β-strand69912
α-helix700-7067
α-helix713-73220
α-helix742-7443
β-strand745-74732
β-strand753-75532
α-helix781-7833
α-helix786-7916
α-helix796-81116
α-helix815-8162
α-helix823-8319
α-helix836-8394
β-strand84313
α-helix844-85310
α-helix858-8603
α-helix862-8632
α-helix864-87613
α-helix878-8825
β-strand88413
α-helix885-8873

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ephrin type-A receptor 2Aprotein306Homo sapiensP29317 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6HET_1 Ephrin type-A receptor 2 (chains A)
GDPNQAVLKFTTEIHPSCVTRQKVIGAGEFGEVYKGMLKTSSGKKEVPVAIKTLKAGYTE
KQRVDFLGEAGIMGQFSHHNIIRLEGVISKYKPMMIITEYMENGALDKFLREKDGEFSVL
QLVGMLRGIAAGMKYLANMNYVHRDLAARNILVNSNLVCKVSDFGLSRVLEDDPEATYTT
SGGKIPIRWTAPEAISYRKFTSASDVWSFGIVMWEVMTYGERPYWELSNHEVMKAINDGF
RLPTPMDCPSAIYQLMMQCWQQERARRPKFADIVSILDKLIRAPDSLKTLADFDPRVSIR
LPSTSG

Ligands and cofactors

IDNameFormulaCopies
G0Q~{N}-(3-chlorophenyl)-4-methyl-3-[(1-methyl-6-pyridin-3-yl-pyrazolo[3,4-d]pyrim…C25 H20 Cl N7 O1

Primary citation

Effects of NVP-BHG712 chemical modifications on EPHA2 binding and affinity. Troester, A., Kudlinzki, D., Saxena, K. et al. To be published.

Other PDB entries of the same protein (UniProt P29317 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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