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5OJK

Crystal structure of the human neuroligin 1 cholinesterase domain containing spliced sequence B (SSB) (NL1(-A+B))

Summary for 5OJK
Entry DOI10.2210/pdb5ojk/pdb
DescriptorNeuroligin-1,Neuroligin-1, 2-acetamido-2-deoxy-beta-D-glucopyranose, TRIETHYLENE GLYCOL, ... (4 entities in total)
Functional Keywordsneuroligin-neurexin, synaptic organizer protein, spliced sequence b, cell adhesion
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight132162.05
Authors
Elegheert, J.,Aricescu, A.R. (deposition date: 2017-07-21, release date: 2017-08-23, Last modification date: 2024-10-23)
Primary citationElegheert, J.,Cvetkovska, V.,Clayton, A.J.,Heroven, C.,Vennekens, K.M.,Smukowski, S.N.,Regan, M.C.,Jia, W.,Smith, A.C.,Furukawa, H.,Savas, J.N.,de Wit, J.,Begbie, J.,Craig, A.M.,Aricescu, A.R.
Structural Mechanism for Modulation of Synaptic Neuroligin-Neurexin Signaling by MDGA Proteins.
Neuron, 95:896-913.e10, 2017
Cited by
PubMed Abstract: Neuroligin-neurexin (NL-NRX) complexes are fundamental synaptic organizers in the central nervous system. An accurate spatial and temporal control of NL-NRX signaling is crucial to balance excitatory and inhibitory neurotransmission, and perturbations are linked with neurodevelopmental and psychiatric disorders. MDGA proteins bind NLs and control their function and interaction with NRXs via unknown mechanisms. Here, we report crystal structures of MDGA1, the NL1-MDGA1 complex, and a spliced NL1 isoform. Two large, multi-domain MDGA molecules fold into rigid triangular structures, cradling a dimeric NL to prevent NRX binding. Structural analyses guided the discovery of a broad, splicing-modulated interaction network between MDGA and NL family members and helped rationalize the impact of autism-linked mutations. We demonstrate that expression levels largely determine whether MDGAs act selectively or suppress the synapse organizing function of multiple NLs. These results illustrate a potentially brain-wide regulatory mechanism for NL-NRX signaling modulation.
PubMed: 28817804
DOI: 10.1016/j.neuron.2017.07.040
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.55 Å)
Structure validation

226707

数据于2024-10-30公开中

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