CNKSR2

Last updated
CNKSR2
Protein CNKSR2 PDB 2EAN.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases CNKSR2 , CNK2, KSR2, MAGUIN, connector enhancer of kinase suppressor of Ras 2, MRXSHG
External IDs OMIM: 300724 MGI: 2661175 HomoloGene: 8956 GeneCards: CNKSR2
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_177751
NM_001310719
NM_001374835

RefSeq (protein)

NP_001297648
NP_808419
NP_001361764

Location (UCSC) Chr X: 21.37 – 21.65 Mb Chr X: 156.6 – 156.83 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Connector enhancer of kinase suppressor of ras 2, also known as CNK homolog protein 2 (CNK2) or MAGUIN (membrane-associated guanylate kinase-interacting protein), is an enzyme that in humans is encoded by the CNKSR2 gene. [5]

Contents

Function

CNKSR2 is a multidomain protein that functions as a scaffold protein to mediate the mitogen-activated protein kinase pathways downstream from Ras. This gene product is induced by vitamin D and inhibits apoptosis in certain cancer cells. It may also play a role in ternary complex assembly of synaptic proteins at the postsynaptic membrane and coupling of signal transduction to membrane/cytoskeletal remodeling. [5]

Mechanism of action

It is the mammalian homolog of the Drosophila gene Cnk, which is known to bind Raf, and is implicated in ras signalling. It has been shown that CNKSR2 is also a Raf binding protein, and is assumed to function in bringing together the Ras signalling complex at the post synaptic density. [6]

It is known to have two isoforms, one of which binds PSD95 and S-SCAM (synaptic scaffolding molecule) through its PDZ domain, and another which does not. Both of the isoforms are, however, known to be synaptically localized, and it is understood that this is mediated by the Pleckstrin homology domain. It's synaptic localization is not known to be affected by NMDA receptor activation. Overexpression of MAGUIN's C-terminal PDZ domain is known to repress synaptic localization of PSD95. In cultures, MAGUIN colocalizes with PSD95 and synaptophysin at puncta in neurites, and these puncta are first visible at 6DIV.

Proteomic work done on binding partners of Ksr2 suggests that the CNKSR2/KSR2 complex may play a role in mediating crosstalk between the MAPK, Pi3K and insulin pathways. [7] It was found to form a complex with MEK1 (Erk2, p38), MEK2, cdk4, PI3k, the phosphatases PP2A and PP^, and also various translational, ribosomal, transport and structural proteins. It remains to be established how many of these are affected by CNKSR2, and whether this remains true for Ksr2 in the nervous system.

Densin-180 is another important synaptic protein found to interact with CNKSR2. It is known to bind at its C-terminal PDZ domain. In transfected cells, no association could be found between PSD95 and Densin-180 without the presence of CNKSR2. [8] This brings it into a complex with CamKII and β-catenin, and further to the binding partners of CNKSR2 suggest that CNKSR2 may have a role in dendritic branching.

Mutation

Deletions of this gene on the X-chromosome of males leads to intellectual disability and epileptic seizures. [9]

Related Research Articles

<span class="mw-page-title-main">DLG4</span> Mammalian protein found in Homo sapiens

PSD-95 also known as SAP-90 is a protein that in humans is encoded by the DLG4 gene.

<span class="mw-page-title-main">DLG1</span> Protein-coding gene in the species Homo sapiens

Discs large homolog 1 (DLG1), also known as synapse-associated protein 97 or SAP97, is a scaffold protein that in humans is encoded by the SAP97 gene.

<span class="mw-page-title-main">CASK</span> Protein-coding gene in humans

Peripheral plasma membrane protein CASK is a protein that in humans is encoded by the CASK gene. This gene is also known by several other names: CMG 2, calcium/calmodulin-dependent serine protein kinase 3 and membrane-associated guanylate kinase 2. CASK gene mutations are the cause of XL-ID with or without nystagmus and MICPCH, an X-linked neurological disorder.

<span class="mw-page-title-main">DLG3</span> Protein-coding gene in humans

Disks large homolog 3 (DLG3) also known as neuroendocrine-DLG or synapse-associated protein 102 (SAP-102) is a protein that in humans is encoded by the DLG3 gene. DLG3 is a member of the membrane-associated guanylate kinase (MAGUK) superfamily of proteins.

<span class="mw-page-title-main">DLG2</span> Protein-coding gene in the species Homo sapiens

Disks large homolog 2 (DLG2) also known as channel-associated protein of synapse-110 (chapsyn-110) or postsynaptic density protein 93 (PSD-93) is a protein that in humans is encoded by the DLG2 gene.

<span class="mw-page-title-main">KCNA4</span> Protein-coding gene in the species Homo sapiens

Potassium voltage-gated channel subfamily A member 4 also known as Kv1.4 is a protein that in humans is encoded by the KCNA4 gene. It contributes to the cardiac transient outward potassium current (Ito1), the main contributing current to the repolarizing phase 1 of the cardiac action potential.

<span class="mw-page-title-main">DLG5</span> Protein-coding gene in the species Homo sapiens

Disks large homolog 5 is a protein that in humans is encoded by the DLG5 gene.

<span class="mw-page-title-main">MPP5</span> Protein-coding gene in the species Homo sapiens

MAGUK p55 subfamily member 5 is a protein that in humans is encoded by the MPP5 gene. Members of the peripheral membrane-associated guanylate kinase (MAGUK) family function in tumor suppression and receptor clustering by forming multiprotein complexes containing distinct sets of transmembrane, cytoskeletal, and cytoplasmic signaling proteins. All MAGUKs contain a PDZ-SH3-GUK core and are divided into 4 subfamilies, DLG-like, ZO1-like, p55-like, and LIN2-like, based on their size and the presence of additional domains. MPP5 is a member of the p55-like MAGUK subfamily.[supplied by OMIM]

<span class="mw-page-title-main">MAGI1</span> Protein-coding gene in the species Homo sapiens

Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 is an enzyme that in humans is encoded by the MAGI1 gene.

<span class="mw-page-title-main">DLGAP1</span> Protein-coding gene in the species Homo sapiens

Disks large-associated protein 1 (DAP-1), also known as guanylate kinase-associated protein (GKAP), is a protein that in humans is encoded by the DLGAP1 gene. DAP-1 is known to be highly enriched in synaptosomal preparations of the brain, and present in the post-synaptic density.

<span class="mw-page-title-main">MAGI2</span> Protein-coding gene in the species Homo sapiens

Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 also known as membrane-associated guanylate kinase inverted 2 (MAGI-2) and atrophin-1-interacting protein 1 (AIP-1) is an enzyme that in humans is encoded by the MAGI2 gene.

<span class="mw-page-title-main">MPP1</span> Protein-coding gene in the species Homo sapiens

55 kDa erythrocyte membrane protein is a protein that in humans is encoded by the MPP1 gene.

<span class="mw-page-title-main">DLGAP4</span> Protein-coding gene in the species Homo sapiens

Disks large-associated protein 4 (DAP-4) also known as SAP90/PSD-95-associated protein 4 (SAPAP-4) is a protein that in humans is encoded by the DLGAP4 gene.

<span class="mw-page-title-main">DLGAP2</span> Protein-coding gene in the species Homo sapiens

Disks large-associated protein 2 is a protein that in humans is encoded by the DLGAP2 gene.

<span class="mw-page-title-main">NRXN2</span> Protein-coding gene in the species Homo sapiens

Neurexin-2-alpha is a protein that in humans is encoded by the NRXN2 gene.

<span class="mw-page-title-main">LRRC7</span> Protein-coding gene in the species Homo sapiens

Leucine rich repeat containing 7 also known as LRRC7, Densin-180, or LAP1 is a protein which in humans is encoded by the LRRC7 gene.

<span class="mw-page-title-main">NRXN3</span> Protein-coding gene in the species Homo sapiens

Neurexin-3-alpha is a protein that in humans is encoded by the NRXN3 gene.

<span class="mw-page-title-main">MAGI3</span> Protein-coding gene in the species Homo sapiens

Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 is an enzyme that in humans is encoded by the MAGI3 gene.

<span class="mw-page-title-main">RAPGEF2</span> Protein-coding gene in the species Homo sapiens

Rap guanine nucleotide exchange factor 2 is a protein that in humans is encoded by the RAPGEF2 gene.

<span class="mw-page-title-main">SNTG1</span> Protein-coding gene in the species Homo sapiens

Gamma-1-syntrophin is a protein that in humans is encoded by the SNTG1 gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000149970 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000025658 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 "Entrez Gene: CNKSR2 connector enhancer of kinase suppressor of Ras 2".
  6. Iida J, Nishimura W, Yao I, Hata Y (May 2002). "Synaptic localization of membrane-associated guanylate kinase-interacting protein mediated by the pleckstrin homology domain". Eur. J. Neurosci. 15 (9): 1493–8. doi:10.1046/j.1460-9568.2002.01987.x. PMID   12028359. S2CID   32653086.
  7. Liu L, Channavajhala PL, Rao VR, Moutsatsos I, Wu L, Zhang Y, et al. (October 2009). "Proteomic characterization of the dynamic KSR-2 interactome, a signaling scaffold complex in MAPK pathway". Biochim. Biophys. Acta. 1794 (10): 1485–95. doi:10.1016/j.bbapap.2009.06.016. PMID   19563921.
  8. Yao I, Hata Y, Ide N, Hirao K, Deguchi M, Nishioka H, et al. (April 1999). "MAGUIN, a novel neuronal membrane-associated guanylate kinase-interacting protein". J. Biol. Chem. 274 (17): 11889–96. doi: 10.1074/jbc.274.17.11889 . PMID   10207009.
  9. Higa LA, Wardley J, Wardley C, Singh S, Foster T, Shen JJ (2021). "CNKSR2-related neurodevelopmental and epilepsy disorder: A cohort of 13 new families and literature review indicating a predominance of loss of function pathogenic variants". BMC Medical Genomics. 14 (1): 186. doi: 10.1186/s12920-021-01033-7 . PMC   8281706 . PMID   34266427.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.