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6POK

Crystal structure of the Robo3 FN2-3 domains

Summary for 6POK
Entry DOI10.2210/pdb6pok/pdb
Related6POG
DescriptorRoundabout homolog 3, GLYCEROL (3 entities in total)
Functional Keywordsaxon guidance, nervous system, cell surface receptor, fibronectin type iii domains, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight22586.43
Authors
Wang, J.,Pak, J.S.,Ozkan, E. (deposition date: 2019-07-04, release date: 2020-05-06, Last modification date: 2023-10-11)
Primary citationPak, J.S.,DeLoughery, Z.J.,Wang, J.,Acharya, N.,Park, Y.,Jaworski, A.,Ozkan, E.
NELL2-Robo3 complex structure reveals mechanisms of receptor activation for axon guidance.
Nat Commun, 11:1489-1489, 2020
Cited by
PubMed Abstract: Axon pathfinding is critical for nervous system development, and it is orchestrated by molecular cues that activate receptors on the axonal growth cone. Robo family receptors bind Slit guidance cues to mediate axon repulsion. In mammals, the divergent family member Robo3 does not bind Slits, but instead signals axon repulsion from its own ligand, NELL2. Conversely, canonical Robos do not mediate NELL2 signaling. Here, we present the structures of NELL-Robo3 complexes, identifying a mode of ligand engagement for Robos that is orthogonal to Slit binding. We elucidate the structural basis for differential binding between NELL and Robo family members and show that NELL2 repulsive activity is a function of its Robo3 affinity and is enhanced by ligand trimerization. Our results reveal a mechanism of oligomerization-induced Robo activation for axon guidance and shed light on Robo family member ligand binding specificity, conformational variability, divergent modes of signaling, and evolution.
PubMed: 32198364
DOI: 10.1038/s41467-020-15211-1
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.796 Å)
Structure validation

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