2F3N
Crystal Structure of the native Shank SAM domain.
Summary for 2F3N
| Entry DOI | 10.2210/pdb2f3n/pdb |
| Descriptor | SH3 and multiple ankyrin repeat domains 3 (2 entities in total) |
| Functional Keywords | postsynaptic density, sam domain, shank, scaffolding protein, structural protein |
| Biological source | Rattus norvegicus (Norway rat) |
| Cellular location | Cytoplasm: Q9JLU4 |
| Total number of polymer chains | 3 |
| Total formula weight | 27276.31 |
| Authors | Baron, M.K.,Bowie, J.U.,Faham, S. (deposition date: 2005-11-22, release date: 2006-02-07, Last modification date: 2024-02-14) |
| Primary citation | Baron, M.K.,Boeckers, T.M.,Vaida, B.,Faham, S.,Gingery, M.,Sawaya, M.R.,Salyer, D.,Gundelfinger, E.D.,Bowie, J.U. An architectural framework that may lie at the core of the postsynaptic density. Science, 311:531-535, 2006 Cited by PubMed Abstract: The postsynaptic density (PSD) is a complex assembly of proteins associated with the postsynaptic membrane that organizes neurotransmitter receptors, signaling pathways, and regulatory elements within a cytoskeletal matrix. Here we show that the sterile alpha motif domain of rat Shank3/ProSAP2, a master scaffolding protein located deep within the PSD, can form large sheets composed of helical fibers stacked side by side. Zn2+, which is found in high concentrations in the PSD, binds tightly to Shank3 and may regulate assembly. Sheets of the Shank protein could form a platform for the construction of the PSD complex. PubMed: 16439662DOI: 10.1126/science.1118995 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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