Član 1 potporodice H kanala sa kalijskim naponom jest protein koji je kod ljudi kodiran genom KCNH1 sa hromosoma 1.[5][6][7]

KCNH1
Dostupne strukture
PDBPretraga ortologa: PDBe RCSB
Spisak PDB ID kodova

5J7E

Identifikatori
AliasiKCNH1
Vanjski ID-jeviOMIM: 603305 MGI: 1341721 HomoloGene: 68242 GeneCards: KCNH1
Lokacija gena (čovjek)
Hromosom 1 (čovjek)
Hrom.Hromosom 1 (čovjek)[1]
Hromosom 1 (čovjek)
Genomska lokacija za KCNH1
Genomska lokacija za KCNH1
Bend1q32.2Početak210,676,823 bp[1]
Kraj211,134,165 bp[1]
Lokacija gena (miš)
Hromosom 1 (miš)
Hrom.Hromosom 1 (miš)[2]
Hromosom 1 (miš)
Genomska lokacija za KCNH1
Genomska lokacija za KCNH1
Bend1|1 H6Početak191,873,082 bp[2]
Kraj192,192,467 bp[2]
Obrazac RNK ekspresije
Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija phosphorelay sensor kinase activity
voltage-gated potassium channel activity
calmodulin binding
cyclic nucleotide binding
ion channel activity
potassium channel activity
voltage-gated ion channel activity
GO:0001948, GO:0016582 vezivanje za proteine
lipid binding
phosphatidylinositol bisphosphate binding
delayed rectifier potassium channel activity
vezivanje identičnih proteina
protein kinase binding
transmembrane transporter binding
protein heterodimerization activity
14-3-3 protein binding
Ćelijska komponenta sinapsa
integral component of membrane
jedro
Akson
nuclear inner membrane
presynaptic membrane
membrana
early endosome membrane
dendrit
ćelijska membrana
endozom
voltage-gated potassium channel complex
GO:0097483, GO:0097481 postsynaptic density
međućelijske veze
projekcija ćelije
perikaryon
intracellular membrane-bounded organelle
postsynaptic membrane
integral component of plasma membrane
cell surface
axolemma
potassium channel complex
soma
perinuklearno područje citoplazme
integral component of presynaptic membrane
Biološki proces transmembrane transport
regulation of cell population proliferation
potassium ion transport
GO:0072468 Transdukcija signala
phosphorelay signal transduction system
regulation of ion transmembrane transport
ion transport
potassium ion transmembrane transport
myoblast fusion
regulation of membrane potential
phosphatidylinositol-mediated signaling
startle response
ion transmembrane transport
cellular response to calcium ion
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)

NM_002238
NM_172362

NM_001038607
NM_010600

RefSeq (bjelančevina)

NP_002229
NP_758872

NP_001033696
NP_034730

Lokacija (UCSC)Chr 1: 210.68 – 211.13 MbChr 1: 191.87 – 192.19 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Aminokiselinska sekvenca

uredi

Dužina polipeptidnog lanca je 989 aminokiselina, a molekulska težina 111.423 Da.[8]

1020304050
MTMAGGRRGLVAPQNTFLENIVRRSNDTNFVLGNAQIVDWPIVYSNDGFC
KLSGYHRAEVMQKSSTCSFMYGELTDKDTIEKVRQTFENYEMNSFEILMY
KKNRTPVWFFVKIAPIRNEQDKVVLFLCTFSDITAFKQPIEDDSCKGWGK
FARLTRALTSSRGVLQQLAPSVQKGENVHKHSRLAEVLQLGSDILPQYKQ
EAPKTPPHIILHYCVFKTTWDWIILILTFYTAILVPYNVSFKTRQNNVAW
LVVDSIVDVIFLVDIVLNFHTTFVGPAGEVISDPKLIRMNYLKTWFVIDL
LSCLPYDVINAFENVDEVSAFMGDPGKIGFADQIPPPLEGRESQGISSLF
SSLKVVRLLRLGRVARKLDHYIEYGAAVLVLLVCVFGLAAHWMACIWYSI
GDYEIFDEDTKTIRNNSWLYQLAMDIGTPYQFNGSGSGKWEGGPSKNSVY
ISSLYFTMTSLTSVGFGNIAPSTDIEKIFAVAIMMIGSLLYATIFGNVTT
IFQQMYANTNRYHEMLNSVRDFLKLYQVPKGLSERVMDYIVSTWSMSRGI
DTEKVLQICPKDMRADICVHLNRKVFKEHPAFRLASDGCLRALAMEFQTV
HCAPGDLIYHAGESVDSLCFVVSGSLEVIQDDEVVAILGKGDVFGDVFWK
EATLAQSCANVRALTYCDLHVIKRDALQKVLEFYTAFSHSFSRNLILTYN
LRKRIVFRKISDVKREEEERMKRKNEAPLILPPDHPVRRLFQRFRQQKEA
RLAAERGGRDLDDLDVEKGNVLTEHASANHSLVKASVVTVRESPATPVSF
QAASTSGVPDHAKLQAPGSECLGPKGGGGDCAKRKSWARFKDACGKSEDW
NKVSKAESMETLPERTKASGEATLKKTDSCDSGITKSDLRLDNVGEARSP
QDRSPILAEVKHSFYPIPEQTLQATVLEVRHELKEDIKALNAKMTNIEKQ
LSEILRILTSRRSSQSPQELFEISRPQSPESERDIFGAS

Funkcija

uredi

Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit of a voltage-gated non-inactivating delayed rectifier potassium channel. It is activated at the onset of myoblast differentiation. The gene is highly expressed in brain and in myoblasts. Overexpression of the gene may confer a growth advantage to cancer cells and favor tumor cell proliferation. Alternative splicing of this gene results in two transcript variants encoding distinct isoforms.[7]

Interakcije

uredi

Pokazalo se da KCNH1 ima interakcije sa KCNB1.[9]

Klinički značaj

uredi

Nedavna studija je pokazala da misens mutacije de novo u genu KCNH1 rezultiraju štetnim povećanjem funkcije, što rezultira multisistemskim razvojnim poremećajem poznatim kao Temple-Baraitserov sindrom ( TBS). TBS je kategoriziran prema intelektualnim teškoćama, epilepsiji i aplaziji noktiju. Simons et al. sugerirali su da je mutacijski mozaicizam prisutan kod majki nekih probanada odgovoran za fenotip TBS njihove djece. Ovo je još jedan dokaz uloge koju genetički mozaicizam ima u etiologiji neuroloških poremećaja.[10]

Također pogledajte

uredi

Reference

uredi
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000143473 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000058248 - Ensembl, maj 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. ^ Occhiodoro T, Bernheim L, Liu JH, Bijlenga P, Sinnreich M, Bader CR, Fischer-Lougheed J (Sep 1998). "Cloning of a human ether-a-go-go potassium channel expressed in myoblasts at the onset of fusion". FEBS Lett. 434 (1–2): 177–82. doi:10.1016/S0014-5793(98)00973-9. PMID 9738473.
  6. ^ Gutman GA, Chandy KG, Grissmer S, Lazdunski M, McKinnon D, Pardo LA, Robertson GA, Rudy B, Sanguinetti MC, Stuhmer W, Wang X (Dec 2005). "International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels". Pharmacol Rev. 57 (4): 473–508. doi:10.1124/pr.57.4.10. PMID 16382104. S2CID 219195192.
  7. ^ a b "Entrez Gene: KCNH1 potassium voltage-gated channel, subfamily H (eag-related), member 1".
  8. ^ "UniProt, O95259" (jezik: engleski). Pristupljeno 13. 12. 2021.
  9. ^ Ottschytsch, N; Raes A; Van Hoorick D; Snyders D J (Jun 2002). "Obligatory heterotetramerization of three previously uncharacterized Kv channel α-subunits identified in the human genome". Proc. Natl. Acad. Sci. U.S.A. 99 (12): 7986–91. Bibcode:2002PNAS...99.7986O. doi:10.1073/pnas.122617999. ISSN 0027-8424. PMC 123007. PMID 12060745.
  10. ^ Simons, Cas; Rash, Lachlan D.; Crawford, Joanna; Ma, Linlin; Cristofori-Armstrong, Ben; Miller, David; Ru, Kelin; Baillie, Gregory J.; Alanay, Yasemin (januar 2015). "Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy". Nature Genetics (jezik: engleski). 47 (1): 73–77. doi:10.1038/ng.3153. ISSN 1061-4036. PMID 25420144. S2CID 52799681.

Dopunska literatura

uredi

Vanjski linkovi

uredi

Ovaj članak uključuje tekst iz Nacionalne medicinske biblioteke Sjedinjenih Država, koji je u javnom vlasništvu.