2VWV: EphB4 kinase domain inhibitor complex

ephB4 kinase domain inhibitor complex. Determined by X-ray diffraction at 1.9 Å resolution. Released 8 Jul 2008.

Method
X-ray diffraction
Resolution
1.9 Å
Organism
HOMO SAPIENS
Chains
1
Atoms
2,127
Mol. weight
34.35 kDa
Ligands
7X3
Released
8 Jul 2008

Explore 2VWV in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2VWV contains 17 α-helices and 10 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: 17 helices, 10 β-strands

ElementResiduesLengthSheet
β-strand60911
α-helix612-6143
β-strand615-62391
β-strand628-63471
α-helix640-6412
β-strand642-64871
α-helix655-66814
β-strand67612
β-strand679-68351
β-strand690-69451
β-strand70012
α-helix701-7077
α-helix714-73320
α-helix743-7453
β-strand746-74832
β-strand754-75632
α-helix784-7863
α-helix789-7946
α-helix799-81416
α-helix818-8192
α-helix826-8349
α-helix839-8424
α-helix847-85610
α-helix861-8633
α-helix865-8662
α-helix867-87913
α-helix881-8844

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Ephrin type-B receptor 4Aprotein302HOMO SAPIENSP54760 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>2VWV_1 EPHRIN TYPE-B RECEPTOR 4 (chains A)
DPNEAVREFAKEIDVSYVKIEEVIGAGEFGEVCRGRLKAPGKKESCVAIKTLKGGYTERQ
RREFLSEASIMGQFEHPNIIRLEGVVTNSMPVMILTEFMENGALDSFLRLNDGQFTVIQL
VGMLRGIASGMRYLAEMSYVHRDLAARNILVNSNLVCKVSDFGLSRFLEENSSDPTETSS
LGGKIPIRWTAPEAIAFRKFTSASDAWSYGIVMWEVMSFGERPYWDMSNQDVINAIEQDY
RLPPPPDCPTSLHQLMLDCWQKDRNARPRFPQVVSALDKMIRNPASLKIVARENGGASHP
LL

Ligands and cofactors

IDNameFormulaCopies
7X3N'-(3-chloro-4-methoxy-phenyl)-N-(3,4,5-trimethoxyphenyl)-1,3,5-triazine-2,4-di…C19 H20 Cl N5 O41

Primary citation

Inhibitors of the Tyrosine Kinase Ephb4. Part 1: Structure-Based Design and Optimization of a Series of 2,4-Bis-Anilinopyrimidines. Bardelle, C., Cross, D., Davenport, S. et al. Bioorg Med Chem Lett (2008) 18:2776. DOI 10.1016/J.BMCL.2008.04.015 · PubMed

Other PDB entries of the same protein (UniProt P54760 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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