| 词条 | Ankyrin-G binding motif of KCNQ2-3 |
| 释义 |
| Symbol = KCNQC3-Ank-G_bd | Name = Ankyrin-G binding motif of KCNQ2-3 | image = | width = | caption = | Pfam = PF11956 | Pfam_clan = | InterPro = IPR020969 | SMART = | PROSITE = | MEROPS = | SCOP = | TCDB = | OPM family = | OPM protein = | CAZy = | CDD = }} In molecular biology, the ankyrin-G binding motif of KCNQ2-3 is a protein motif found in the potassium channels KCNQ2 and KCNQ3. Interactions with ankyrin-G (ankyrin-3) are crucial to the localisation of voltage-gated sodium channels (VGSCs) at the axon initial segment and for neurons to initiate action potentials. This conserved 9-amino acid motif ((V/A)P(I/L)AXXE(S/D)D) is required for ankyrin-G binding and functions to localise sodium channels to a variety of 'excitable' membrane domains both inside and outside of the nervous system.[1] This motif has also been identified in the potassium channel 6TM proteins KCNQ2 and KCNQ3 [2] that correspond to the M channels that exert a crucial influence over neuronal excitability. KCNQ2/KCNQ3 channels are preferentially localised to the surface of axons both at the axonal initial segment and more distally, and this axonal initial segment targeting of surface KCNQ channels is mediated by these ankyrin-G binding motifs of KCNQ2 and KCNQ3.[3] KCNQ3 is a major determinant of M channel localisation to the AIS, rather than KCNQ2.[4] Phylogenetic analysis reveals that anchor motifs evolved sequentially in chordates (NaV channel) and jawed vertebrates (KCNQ2/3).[5] References1. ^{{cite journal |vauthors=Lemaillet G, Walker B, Lambert S | title = Identification of a conserved ankyrin-binding motif in the family of sodium channel alpha subunits | journal = J. Biol. Chem. | volume = 278 | issue = 30 | pages = 27333–9 |date=July 2003 | pmid = 12716895 | doi = 10.1074/jbc.M303327200 | url = }} {{InterPro content|IPR020969}}2. ^{{cite journal |vauthors=Pan Z, Kao T, Horvath Z, Lemos J, Sul JY, Cranstoun SD, Bennett V, Scherer SS, Cooper EC | title = A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon | journal = J. Neurosci. | volume = 26 | issue = 10 | pages = 2599–613 |date=March 2006 | pmid = 16525039 | doi = 10.1523/JNEUROSCI.4314-05.2006 | url = }} 3. ^{{cite journal |vauthors=Chung HJ, Jan YN, Jan LY | title = Polarized axonal surface expression of neuronal KCNQ channels is mediated by multiple signals in the KCNQ2 and KCNQ3 C-terminal domains | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 103 | issue = 23 | pages = 8870–5 |date=June 2006 | pmid = 16735477 | pmc = 1472242 | doi = 10.1073/pnas.0603376103 | url = }} 4. ^{{cite journal |vauthors=Rasmussen HB, Frøkjaer-Jensen C, Jensen CS, Jensen HS, Jørgensen NK, Misonou H, Trimmer JS, Olesen SP, Schmitt N | title = Requirement of subunit co-assembly and ankyrin-G for M-channel localization at the axon initial segment | journal = J. Cell Sci. | volume = 120 | issue = Pt 6 | pages = 953–63 |date=March 2007 | pmid = 17311847 | doi = 10.1242/jcs.03396 | url = }} 5. ^{{cite journal |vauthors=Hill AS, Nishino A, Nakajo K, Zhang G, Fineman JR, Selzer ME, Okamura Y, Cooper EC | title = Ion channel clustering at the axon initial segment and node of Ranvier evolved sequentially in early chordates | journal = PLoS Genet. | volume = 4 | issue = 12 | pages = e1000317 |date=December 2008 | pmid = 19112491 | pmc = 2597720 | doi = 10.1371/journal.pgen.1000317 | url = }} 1 : Molecular biology |
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