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Kv channel interacting protein 1
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| PDB rendering based on 1s1e. | |||||||||||
| Available structures: 1s1e, 1s6c, 2i2r, 2nz0 | |||||||||||
| Identifiers | |||||||||||
| Symbols | KCNIP1; KCHIP1; MGC95; VABP | ||||||||||
| External IDs | OMIM: 604660 MGI: 1917607 HomoloGene: 22824 | ||||||||||
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| RNA expression pattern | |||||||||||
| Orthologs | |||||||||||
| Human | Mouse | ||||||||||
| Entrez | 30820 | 70357 | |||||||||
| Ensembl | ENSG00000182132 | ENSMUSG00000053519 | |||||||||
| Uniprot | Q9NZI2 | Q3YAB4 | |||||||||
| Refseq | NM_001034837 (mRNA) NP_001030009 (protein) |
NM_027398 (mRNA) NP_081674 (protein) |
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| Location | Chr 5: 169.71 - 170.1 Mb | Chr 11: 33.53 - 33.89 Mb | |||||||||
| Pubmed search | [1] | [2] | |||||||||
Kv channel interacting protein 1, also known as KCNIP1, is a human gene.[1]
This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have EF-hand-like domains, and differ from each other in the N-terminus. They are integral subunit components of native Kv4 channel complexes. They may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. Alternative splicing results in multiple transcript variant encoding different isoforms.[1]
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References
See also
Further reading
- An WF, Bowlby MR, Betty M, et al. (2000). "Modulation of A-type potassium channels by a family of calcium sensors.". Nature 403 (6769): 553–6. doi:. PMID 10676964.
- Bähring R, Dannenberg J, Peters HC, et al. (2001). "Conserved Kv4 N-terminal domain critical for effects of Kv channel-interacting protein 2.2 on channel expression and gating.". J. Biol. Chem. 276 (26): 23888–94. doi:. PMID 11287421.
- Nakamura TY, Nandi S, Pountney DJ, et al. (2001). "Different effects of the Ca(2+)-binding protein, KChIP1, on two Kv4 subfamily members, Kv4.1 and Kv4.2.". FEBS Lett. 499 (3): 205–9. PMID 11423117.
- Kutsenko AS, Gizatullin RZ, Al-Amin AN, et al. (2002). "NotI flanking sequences: a tool for gene discovery and verification of the human genome.". Nucleic Acids Res. 30 (14): 3163–70. PMID 12136098.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:. PMID 12477932.
- Shibata R, Misonou H, Campomanes CR, et al. (2003). "A fundamental role for KChIPs in determining the molecular properties and trafficking of Kv4.2 potassium channels.". J. Biol. Chem. 278 (38): 36445–54. doi:. PMID 12829703.
- Van Hoorick D, Raes A, Keysers W, et al. (2004). "Differential modulation of Kv4 kinetics by KCHIP1 splice variants.". Mol. Cell. Neurosci. 24 (2): 357–66. PMID 14572458.
- Scannevin RH, Wang K, Jow F, et al. (2004). "Two N-terminal domains of Kv4 K(+) channels regulate binding to and modulation by KChIP1.". Neuron 41 (4): 587–98. PMID 14980207.
- Lin YL, Lin SR, Wu TT, Chang LS (2004). "Evidence showing an intermolecular interaction between KChIP proteins and Taiwan cobra cardiotoxins.". Biochem. Biophys. Res. Commun. 319 (3): 720–4. doi:. PMID 15184042.
- Lin YL, Chen CY, Cheng CP, Chang LS (2004). "Protein-protein interactions of KChIP proteins and Kv4.2.". Biochem. Biophys. Res. Commun. 321 (3): 606–10. doi:. PMID 15358149.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:. PMID 15489334.
- Pruunsild P, Timmusk T (2005). "Structure, alternative splicing, and expression of the human and mouse KCNIP gene family.". Genomics 86 (5): 581–93. doi:. PMID 16112838.
- Pioletti M, Findeisen F, Hura GL, Minor DL (2007). "Three-dimensional structure of the KChIP1-Kv4.3 T1 complex reveals a cross-shaped octamer.". Nat. Struct. Mol. Biol. 13 (11): 987–95. doi:. PMID 17057713.
External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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Wikipedia content modification information:
- This page was last modified on 10 July 2008, at 11:16.
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