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The Crystal Structure of the Second PDZ Domain of Human DLG3The Crystal Structure of the Second PDZ Domain of Human DLG3
Structural highlights
Disease[DLG3_HUMAN] Defects in DLG3 are the cause of mental retardation X-linked type 90 (MRX90) [MIM:300850]. Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.[1] Function[DLG3_HUMAN] Required for learning most likely through its role in synaptic plasticity following NMDA receptor signaling. Evolutionary Conservation![]() Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. References
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OCACategories:
- Homo sapiens
- Arrowsmith, C.
- Berridge, G.
- Bray, J.
- Bunkoczi, G.
- Colebrook, S.
- Debreczeni, J.
- Delft, F von.
- Doyle, D.
- Edwards, A.
- Elkins, J.
- Gorrec, F.
- Phillips, C.
- SGC, Structural Genomics Consortium.
- Salah, E.
- Savitsky, P.
- Schoch, G.
- Smee, C.
- Sundstrom, M.
- Turnbull, A.
- Ugochukwu, E.
- Weigelt, J.
- Dlg3
- Human
- Pdz domain
- Sgc
- Structural genomic
- Structural genomics consortium
- Structural protein