3HPN: Ligand Recognition By A-Class Eph Receptors: Crystal Structures Of The Epha2 Ligand-Binding Domain And The Epha2EPHRIN-A1 Complex

Ephrin (Eph) receptor tyrosine kinases fall into two subclasses (A and B) according to preferences for their ephrin ligands. All published structural studies of Eph receptor/ephrin complexes involve B-class receptors. Here, we present the crystal structures of an A-class complex between EphA2 and ephrin-A1 and of unbound EphA2. Although these structures are similar overall to their B-class counterparts, they reveal important differences that define subclass specificity. The structures suggest that the A-class Eph receptor/ephrin interactions involve smaller rearrangements in the interacting partners, better described by a 'lock-and-key'-type binding mechanism, in contrast to the 'induced fit' mechanism defining the B-class molecules. This model is supported by structure-based mutagenesis and by differential requirements for ligand oligomerization by the two subclasses in cell-based Eph receptor activation assays. Finally, the structure of the unligated receptor reveals a homodimer assembly that might represent EphA2-specific homotypic cell adhesion interactions.
PDB ID: 3HPNDownload
MMDB ID: 75020
PDB Deposition Date: 2009/6/4
Updated in MMDB: 2012/09
Experimental Method:
x-ray diffraction
Resolution: 2.52  Å
Source Organism:
Similar Structures:
Biological Unit for 3HPN: monomeric; determined by author
Molecular Components in 3HPN
Label Count Molecule
Protein (1 molecule)
Ephrin Type-a Receptor 2(Gene symbol: EPHA2)
Molecule annotation
* Click molecule labels to explore molecular sequence information.

Citing MMDB