Inozitol-trisfosfat 3-kinaza A jest enzim koji je kod ljudi kodiran genom ITPKA.[5][6][7]

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

1W2C, 1W2D, 1W2F, 4UPU

Identifikatori
AliasiITPKA
Vanjski ID-jeviOMIM: 147521 MGI: 1333822 HomoloGene: 1671 GeneCards: ITPKA
Lokacija gena (čovjek)
Hromosom 15 (čovjek)
Hrom.Hromosom 15 (čovjek)[1]
Hromosom 15 (čovjek)
Genomska lokacija za ITPKA
Genomska lokacija za ITPKA
Bend15q15.1Početak41,493,393 bp[1]
Kraj41,503,551 bp[1]
Lokacija gena (miš)
Hromosom 2 (miš)
Hrom.Hromosom 2 (miš)[2]
Hromosom 2 (miš)
Genomska lokacija za ITPKA
Genomska lokacija za ITPKA
Bend2|2 E5Početak119,572,818 bp[2]
Kraj119,581,744 bp[2]
Obrazac RNK ekspresije
Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija calmodulin-dependent protein kinase activity
aktivnost sa transferazom
nucleotide binding
inositol-1,4,5-trisphosphate 3-kinase activity
ATP binding
calmodulin binding
kinase activity
Ćelijska komponenta citosol
dendritična kičma
Biološki proces dendritic spine maintenance
protein phosphorylation
inositol phosphate metabolic process
positive regulation of dendritic spine morphogenesis
actin cytoskeleton organization
inositol metabolic process
Fosforilacija
GO:0072468 Transdukcija signala
regulation of synaptic plasticity
inositol phosphate biosynthetic process
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)

NM_002220

NM_146125

RefSeq (bjelančevina)

NP_002211

NP_666237

Lokacija (UCSC)Chr 15: 41.49 – 41.5 MbChr 2: 119.57 – 119.58 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Aminokiselinska sekvenca uredi

Dužina polipeptidnog lanca je 461 aminokiselina, a molekulska težina 51.009 Da.[8].

1020304050
MTLPGGPTGMARPGGARPCSPGLERAPRRSVGELRLLFEARCAAVAAAAA
AGEPRARGAKRRGGQVPNGLPRAPPAPVIPQLTVTAEEPDVPPTSPGPPE
RERDCLPAAGSSHLQQPRRLSTSSVSSTGSSSLLEDSEDDLLSDSESRSR
GNVQLEAGEDVGQKNHWQKIRTMVNLPVISPFKKRYAWVQLAGHTGSFKA
AGTSGLILKRCSEPERYCLARLMADALRGCVPAFHGVVERDGESYLQLQD
LLDGFDGPCVLDCKMGVRTYLEEELTKARERPKLRKDMYKKMLAVDPEAP
TEEEHAQRAVTKPRYMQWREGISSSTTLGFRIEGIKKADGSCSTDFKTTR
SREQVLRVFEEFVQGDEEVLRRYLNRLQQIRDTLEVSEFFRRHEVIGSSL
LFVHDHCHRAGVWLIDFGKTTPLPDGQILDHRRPWEEGNREDGYLLGLDN
LIGILASLAER
Simboli

Struktura uredi

ITPKA je jedan od tri gena inozitol-trisfosfat 3-kinaze (ITP3K) kod ljudi. ITP3K proteini reguliraju metabolizam inozitol-fosfata, fosforilacijom drugog prenosnika inozitol 1,4,5-trisfosfata, dajući Ins (1,3 , 4,5) P4, što se ponekad skraćuje kao IP4. Strukturno, ITPKA pripada porodici inozitol-polifosfat kinaza (IPK). Aktivnost inozitol 1,4,5-trisfosfat 3-kinaze odgovorna je za regulaciju nivoa velikog broja inozitol-polifosfata, koji su važni u ćelijskoj signalizaciji, ponajviše inozitol-trifosfat, koji je jedini enzimska podloga. I mehanizmi fosforilacije kalcija/ kalmodulina i proteina kontroliraju njegovu aktivnost. Takođe je supstrat za cikličnu protein-kinazu koja zavisi od AMP, Ca2 + / protein-kinaza ovisna od kalcija kalmodulina i protein-kinaza C in vitro. ITPKA i ITPKB su 68% identični u C-terminalnoj regiji. Amino-terminalni region ITPKA veže filamentni aktin. Ovo svojstvo lokalizira ITPKA na dendritsku kičmu u glavnim neuronima.[9][10][11] ITPKA se fiziološki eksprimira u neuronima, ali ponekad i u ćelijama karcinoma i može doprinijeti procesima metastaziranja.[12]

Fiziološka funkcija uredi

ITPKA učestvuje u procesima učenja i pamćenja u neuronima.[13][14]

Uloge u ljudskim bolestima uredi

Iako se ITPKA fiziološki eksprimira u neuronima i sjemenicima, ponekad se izražava i u ćelijama karcinoma, a ekspresija čini karcinom agresivnijim.[12][15]

Odnos sa F-traktinom uredi

F-traktin obuhvata pacovske ITPKA aminokiseline 9-52. Kasnije je utvrđeno da su aminokiseline 9-40 dovoljne za vezivanje nitastih aktina.[16][17] Kada se stopi sa reporterom, kao što je zeleni fluorescentni protein, koristan je za vizualizaciju dinamike aktina u živim ćelijama.[18][19]

Reference uredi

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000137825 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027296 - 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. ^ Erneux C, Roeckel N, Takazawa K, Mailleux P, Vassart G, Mattei MG (oktobar 1992). "Localization of the genes for human inositol 1,4,5-trisphosphate 3-kinase A (ITPKA) and B (ITPKB) to chromosome regions 15q14-q21 and 1q41-q43, respectively, by in situ hybridization". Genomics. 14 (2): 546–7. doi:10.1016/S0888-7543(05)80265-4. PMID 1330886.
  6. ^ Takazawa K, Perret J, Dumont JE, Erneux C (decembar 1990). "Human brain inositol 1,4,5-trisphosphate 3-kinase cDNA sequence". Nucleic Acids Research. 18 (23): 7141. doi:10.1093/nar/18.23.7141. PMC 332787. PMID 2175886.
  7. ^ name="entrez""Entrez Gene: ITPKA inositol 1,4,5-trisphosphate 3-kinase A".
  8. ^ "UniProt, P23677". Pristupljeno 15. 7. 2021.
  9. ^ Yamada M, Kakita A, Mizuguchi M, Rhee SG, Kim SU, Ikuta F (mart 1993). "Specific expression of inositol 1,4,5-trisphosphate 3-kinase in dendritic spines". Brain Research. 606 (2): 335–40. doi:10.1016/0006-8993(93)91004-C. PMID 8387863.
  10. ^ Schell MJ, Erneux C, Irvine RF (oktobar 2001). "Inositol 1,4,5-trisphosphate 3-kinase A associates with F-actin and dendritic spines via its N terminus". The Journal of Biological Chemistry. 276 (40): 37537–46. doi:10.1074/jbc.M104101200. PMID 11468283.
  11. ^ Windhorst S, Minge D, Bähring R, Hüser S, Schob C, Blechner C, Lin HY, Mayr GW, Kindler S (mart 2012). "Inositol-1,4,5-trisphosphate 3-kinase A regulates dendritic morphology and shapes synaptic Ca2+ transients". Cellular Signalling. 24 (3): 750–7. doi:10.1016/j.cellsig.2011.11.010. PMID 22120525.
  12. ^ a b Windhorst S, Fliegert R, Blechner C, Möllmann K, Hosseini Z, Günther T, Eiben M, Chang L, Lin HY, Fanick W, Schumacher U, Brandt B, Mayr GW (februar 2010). "Inositol 1,4,5-trisphosphate 3-kinase-A is a new cell motility-promoting protein that increases the metastatic potential of tumor cells by two functional activities". The Journal of Biological Chemistry. 285 (8): 5541–54. doi:10.1074/jbc.M109.047050. PMC 2820782. PMID 20022963.
  13. ^ Chung S, Kim IH, Lee D, Park K, Kim JY, Lee YK, Kim EJ, Lee HW, Choi JS, Son GH, Sun W, Shin KS, Kim H (april 2016). "The role of inositol 1,4,5-trisphosphate 3-kinase A in regulating emotional behavior and amygdala function". Scientific Reports. 6: 23757. doi:10.1038/srep23757. PMC 4823716. PMID 27053114.
  14. ^ Choi B, Lee HW, Mo S, Kim JY, Kim HW, Rhyu IJ, Hong E, Lee YK, Choi JS, Kim CH, Kim H (2018). "Inositol 1,4,5-trisphosphate 3-kinase A overexpressed in mouse forebrain modulates synaptic transmission and mGluR-LTD of CA1 pyramidal neurons". PLOS One. 13 (4): e0193859. doi:10.1371/journal.pone.0193859. PMC 5884490. PMID 29617377.
  15. ^ Windhorst S, Song K, Gazdar AF (august 2017). "Inositol-1,4,5-trisphosphate 3-kinase-A (ITPKA) is frequently over-expressed and functions as an oncogene in several tumor types". Biochemical Pharmacology. 137: 1–9. doi:10.1016/j.bcp.2017.03.023. PMC 5555585. PMID 28377279.
  16. ^ Johnson HW, Schell MJ (decembar 2009). "Neuronal IP3 3-kinase is an F-actin-bundling protein: role in dendritic targeting and regulation of spine morphology". Molecular Biology of the Cell. 20 (24): 5166–80. doi:10.1091/mbc.E09-01-0083. PMC 2793293. PMID 19846664.
  17. ^ Yi J, Wu XS, Crites T, Hammer JA (mart 2012). "Actin retrograde flow and actomyosin II arc contraction drive receptor cluster dynamics at the immunological synapse in Jurkat T cells". Molecular Biology of the Cell. 23 (5): 834–52. doi:10.1091/mbc.E11-08-0731. PMC 3290643. PMID 22219382.
  18. ^ Belin BJ, Goins LM, Mullins RD (2014). "Comparative analysis of tools for live cell imaging of actin network architecture". Bioarchitecture. 4 (6): 189–202. doi:10.1080/19490992.2014.1047714. PMC 4914014. PMID 26317264.
  19. ^ Melak M, Plessner M, Grosse R (februar 2017). "Actin visualization at a glance". Journal of Cell Science. 130 (3): 525–530. doi:10.1242/jcs.189068. PMID 28082420.

Dopunska literatura uredi