5JR2: EphA4 LBD

Crystal structure of the EphA4 LBD in complex with APYd3 peptide inhibitor. Determined by X-ray diffraction at 1.75 Å resolution. Released 6 Jul 2016.

Method
X-ray diffraction
Resolution
1.75 Å
Organisms
Homo sapiens, synthetic construct
Chains
8
Atoms
7,210
Mol. weight
89.02 kDa
Ligands
HEZ
Released
6 Jul 2016

Explore 5JR2 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5JR2 contains 20 α-helices and 66 β-strands across 8 chains. 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: 4 helices, 13 β-strands

ElementResiduesLengthSheet
α-helix27-293
β-strand30-3561
α-helix36-383
β-strand46-4832
β-strand55-6061
β-strand66-7381
β-strand82-8542
β-strand89-9022
β-strand97-10591
α-helix108-1103
β-strand121-12992
α-helix139-1413
β-strand143-14972
β-strand154-15851
β-strand163-173111
β-strand180-18782
β-strand191-202121
Chain B: 4 helices, 15 β-strands
ElementResiduesLengthSheet
α-helix27-293
β-strand30-3563
α-helix36-383
β-strand46-4834
β-strand55-6063
β-strand66-7383
β-strand82-8544
β-strand89-9024
β-strand97-10593
α-helix108-1103
β-strand11915
β-strand121-12994
α-helix139-1413
β-strand143-14974
β-strand154-15853
β-strand163-173113
β-strand180-18784
β-strand19015
β-strand191-202123
Chain C: 6 helices, 15 β-strands
ElementResiduesLengthSheet
α-helix27-293
β-strand30-3566
α-helix36-383
α-helix451
β-strand46-4837
β-strand55-6066
α-helix651
β-strand66-7276
β-strand82-8547
β-strand89-9027
β-strand97-10596
α-helix108-1103
β-strand11918
β-strand121-12997
α-helix139-1413
β-strand143-14977
β-strand154-15856
β-strand163-173116
β-strand180-18787
β-strand19018
β-strand192-202116
Chain D: 6 helices, 15 β-strands
ElementResiduesLengthSheet
α-helix27-293
β-strand30-3569
α-helix36-383
β-strand46-48310
β-strand55-5959
α-helix65-662
β-strand67-7269
β-strand82-85410
α-helix86-883
β-strand89-90210
β-strand97-10599
α-helix108-1103
β-strand119111
β-strand121-129910
α-helix139-1413
β-strand143-149710
β-strand154-15859
β-strand163-173119
β-strand180-187810
β-strand190111
β-strand192-202119
Chains E, F, G and H: 0 helices, 2 β-strands
ElementResiduesLengthSheet
β-strand5-6212
β-strand10-11212

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ephrin type-A receptor 4A, B, C, Dprotein179Homo sapiensP54764 (AlphaFold model)
APYd3 peptideE, F, G, Hprotein13synthetic construct
Sequence of entity 1 (A, B, C, D), FASTA
>5JR2_1 Ephrin type-A receptor 4 (chains A, B, C, D)
GPGNEVTLLDSRSVQGELGWIASPLEGGWEEVSIMDEKNTPIRTYQVCNVMEPSQNNWLR
TDWITREGAQRVYIEIKFTLRDCNSLPGVMGTCKETFNLYYYESDNDKERFIRENQFVKI
DTIAADESFTQVDIGDRIMKLNTEIRDVGPLSKKGFYLAFQDVGACIALVSVRVFYKKA
Sequence of entity 2 (E, F, G, H), FASTA
>5JR2_2 APYd3 peptide (chains E, F, G, H)
XPYCVYRXSWSCX

Ligands and cofactors

IDNameFormulaCopies
HEZHexane-1,6-diolC6 H14 O26

Water and common crystallization additives (GOL) are not listed.

Primary citation

Modifications of a Nanomolar Cyclic Peptide Antagonist for the EphA4 Receptor To Achieve High Plasma Stability. Olson, E.J., Lechtenberg, B.C., Zhao, C. et al. ACS Med Chem Lett (2016) 7:841-846. DOI 10.1021/acsmedchemlett.6b00132 · PubMed

Other PDB entries of the same protein (UniProt P54764 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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