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6POG

Crystal structure of the NELL2 EGF1-6-Robo3 FN1 complex

Summary for 6POG
Entry DOI10.2210/pdb6pog/pdb
DescriptorRoundabout homolog 3, Protein kinase C-binding protein NELL2, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
Functional Keywordsaxon guidance, nervous system, heterodimeric complex, glycoprotein, signaling protein
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight40542.66
Authors
Wang, J.,Pak, J.S.,Ozkan, E. (deposition date: 2019-07-03, release date: 2020-05-06, Last modification date: 2020-07-29)
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 (2.755 Å)
Structure validation

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数据于2024-11-13公开中

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