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4E53

Calmodulin and Nm peptide complex

Summary for 4E53
Entry DOI10.2210/pdb4e53/pdb
Related4E50
DescriptorCalmodulin, Linker, IQ motif of Neuromodulin (2 entities in total)
Functional Keywordscalmodulin (cam), intrinsically unstructured proteins, protein kinase c (pkc), neuromodulin, growth associated protein -43 (gap-43), long term potentiation (ltp), long term depression (ltd), iq motif, protein binding
Biological sourceMus musculus (mouse)
More
Cellular locationCell membrane; Peripheral membrane protein; Cytoplasmic side: P06837
Total number of polymer chains2
Total formula weight41486.13
Authors
Kumar, V.,Sivaraman, J. (deposition date: 2012-03-13, release date: 2013-03-20, Last modification date: 2024-03-20)
Primary citationKumar, V.,Chichili, V.P.R.,Zhong, L.,Tang, X.,Velazquez-Campoy, A.,Sheu, F.-S.,Seetharaman, J.,Gerges, N.Z.,Sivaraman, J.
Structural basis for the interaction of unstructured neuron specific substrates neuromodulin and neurogranin with calmodulin
Sci Rep, 3:1392-1392, 2013
Cited by
PubMed Abstract: Neuromodulin (Nm) and neurogranin (Ng) are neuron-specific substrates of protein kinase C (PKC). Their interactions with Calmodulin (CaM) are crucial for learning and memory formation in neurons. Here, we report the structure of IQ peptides (24aa) of Nm/Ng complexed with CaM and their functional studies with full-length proteins. Nm/Ng and their respective IQ peptides are intrinsically unstructured; however, upon binding with CaM, IQ motifs adopt a helical conformation. Ser41 (Ser36) of Nm (Ng) is located in a negatively charged pocket in the apo CaM and, when phosphorylated, it will repel Nm/Ng from CaM. These observations explain the mechanism by which PKC-induced Ser phosphorylation blocks the association of Nm/Ng with CaM and interrupts several learning- and memory-associated functions. Moreover, the present study identified Arg as a key CaM interacting residue from Nm/Ng. This residue is crucial for CaM-mediated function, as evidenced by the inability of the Ng mutant (Arg-to-Ala) to potentiate synaptic transmission in CA1 hippocampal neurons.
PubMed: 23462742
DOI: 10.1038/srep01392
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.69 Å)
Structure validation

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