2fn5
From Proteopedia
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| - | [[Image:2fn5.gif|left|200px]] | + | [[Image:2fn5.gif|left|200px]] |
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| - | '''NMR Structure of the Neurabin PDZ domain (502-594)''' | + | {{Structure |
| + | |PDB= 2fn5 |SIZE=350|CAPTION= <scene name='initialview01'>2fn5</scene> | ||
| + | |SITE= | ||
| + | |LIGAND= | ||
| + | |ACTIVITY= | ||
| + | |GENE= Ppp1r9a ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10116 Rattus norvegicus]) | ||
| + | }} | ||
| + | |||
| + | '''NMR Structure of the Neurabin PDZ domain (502-594)''' | ||
| + | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 2FN5 is a [ | + | 2FN5 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Rattus_norvegicus Rattus norvegicus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FN5 OCA]. |
==Reference== | ==Reference== | ||
| - | Structural basis for spinophilin-neurabin receptor interaction., Kelker MS, Dancheck B, Ju T, Kessler RP, Hudak J, Nairn AC, Peti W, Biochemistry. 2007 Mar 6;46(9):2333-44. Epub 2007 Feb 6. PMID:[http:// | + | Structural basis for spinophilin-neurabin receptor interaction., Kelker MS, Dancheck B, Ju T, Kessler RP, Hudak J, Nairn AC, Peti W, Biochemistry. 2007 Mar 6;46(9):2333-44. Epub 2007 Feb 6. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17279777 17279777] |
[[Category: Rattus norvegicus]] | [[Category: Rattus norvegicus]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: pdz]] | [[Category: pdz]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:54:29 2008'' |
Revision as of 14:54, 20 March 2008
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| Gene: | Ppp1r9a (Rattus norvegicus) | ||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||
NMR Structure of the Neurabin PDZ domain (502-594)
Overview
Neurabin and spinophilin are neuronal scaffolding proteins that play important roles in the regulation of synaptic transmission through their ability to target protein phosphatase 1 (PP1) to dendritic spines where PP1 dephosphorylates and inactivates glutamate receptors. However, thus far, it is still unknown how neurabin and spinophilin themselves are targeted to these membrane receptors. Spinophilin and neurabin contain a single PDZ domain, a common protein-protein interaction recognition motif, which are 86% identical in sequence. We report the structures of both the neurabin and spinophilin PDZ domains determined using biomolecular NMR spectroscopy. These proteins form the canonical PDZ domain fold. However, despite their high degree of sequence identity, there are distinct and significant structural differences between them, especially between the peptide binding pockets. Using two-dimensional 1H-15N HSQC NMR analysis, we demonstrate that C-terminal peptide ligands derived from glutamatergic AMPA and NMDA receptors and cytosolic proteins directly and differentially bind spinophilin and neurabin PDZ domains. This peptide binding data also allowed us to classify the neurabin and spinophilin PDZ domains as the first identified neuronal hybrid class V PDZ domains, which are capable of binding both class I and II peptides. Finally, the ability to bind to glutamate receptor subunits suggests that the PDZ domains of neurabin and spinophilin are important for targeting PP1 to C-terminal phosphorylation sites in AMPA and NMDA receptor subunits.
About this Structure
2FN5 is a Single protein structure of sequence from Rattus norvegicus. Full crystallographic information is available from OCA.
Reference
Structural basis for spinophilin-neurabin receptor interaction., Kelker MS, Dancheck B, Ju T, Kessler RP, Hudak J, Nairn AC, Peti W, Biochemistry. 2007 Mar 6;46(9):2333-44. Epub 2007 Feb 6. PMID:17279777
Page seeded by OCA on Thu Mar 20 16:54:29 2008
