RPS6KB1

(Preusmjereno sa S6K)

Ribosomna protein S6 kinaza beta-1 (S6K1), znana i kao p70S6 kinaza (p70S6K, p70-S6K), je enzim (preciznije protein-kinaza) koji je kod ljudi kodiran genom RPS6KB1.[5][6] To je serin / treonin kinaza koja djeluje nizvodno od PIP3 i fosfoinozitid-ovisne kinaze-1 u PI3 kinaznom putu.[7] Kao što i samo ime govori, njegov cilj supstrat je ribosomski protein S6.[8] Sintezu proteina na ribosomu nducira fosforilacija S6.

RPS6KB1
Dostupne strukture
PDBPretraga ortologa: PDBe RCSB
Spisak PDB ID kodova

3A60, 3A61, 3A62, 3WE4, 3WF5, 3WF6, 3WF7, 3WF8, 3WF9, 4L3J, 4L3L, 4L42, 4L43, 4L44, 4L45, 4L46, 4RLO, 4RLP

Identifikatori
AliasiRPS6KB1
Vanjski ID-jeviOMIM: 608938 MGI: 1270849 HomoloGene: 81703 GeneCards: RPS6KB1
Lokacija gena (čovjek)
Hromosom 17 (čovjek)
Hrom.Hromosom 17 (čovjek)[1]
Hromosom 17 (čovjek)
Genomska lokacija za RPS6KB1
Genomska lokacija za RPS6KB1
Bend17q23.1Početak59,893,046 bp[1]
Kraj59,950,574 bp[1]
Lokacija gena (miš)
Hromosom 11 (miš)
Hrom.Hromosom 11 (miš)[2]
Hromosom 11 (miš)
Genomska lokacija za RPS6KB1
Genomska lokacija za RPS6KB1
Bend11|11 CPočetak86,498,871 bp[2]
Kraj86,544,805 bp[2]
Obrazac RNK ekspresije


Više referentnih podataka o ekspresiji
Ontologija gena
Molekularna funkcija aktivnost sa transferazom
protein kinase activity
nucleotide binding
peptide binding
GO:0001948, GO:0016582 vezivanje za proteine
vezivanje identičnih proteina
protein serine/threonine/tyrosine kinase activity
ATP binding
kinase activity
protein serine/threonine kinase activity
ribosomal protein S6 kinase activity
PDZ domain binding
protein phosphatase 2A binding
Ćelijska komponenta citoplazma
citosol
membrana
sinapsa
nukleoplazma
cell surface
mitochondrial outer membrane
međućelijske veze
mitohondrija
perinuklearno područje citoplazme
neuron projection
jedro
Biološki proces germ cell development
response to amino acid
response to glucagon
GO:1904578 response to organic cyclic compound
protein kinase B signaling
response to nutrient
Fosforilacija
regulation of glucose import
response to testosterone
negative regulation of extrinsic apoptotic signaling pathway
cellular response to growth factor stimulus
skeletal muscle contraction
response to mechanical stimulus
GO:0010260 starenje
response to leucine
GO:1904579 cellular response to organic cyclic compound
positive regulation of mitotic cell cycle
negative regulation of apoptotic process
response to heat
response to glucocorticoid
response to glucose
response to peptide hormone
behavioral fear response
positive regulation of translation
response to organic substance
positive regulation of smooth muscle cell migration
response to tumor necrosis factor
response to insulin
response to lipopolysaccharide
GO:1903105 negative regulation of insulin receptor signaling pathway
cellular response to hormone stimulus
Dugoročno pamćenje
response to wounding
response to organonitrogen compound
response to electrical stimulus involved in regulation of muscle adaptation
skeletal muscle atrophy
ćelijski ciklus
response to ethanol
positive regulation of translational initiation
Ćelijska migracija
response to toxic substance
positive regulation of skeletal muscle tissue growth
regulation of translation
phosphatidylinositol-mediated signaling
GO:0072468 Transdukcija signala
positive regulation of smooth muscle cell proliferation
GO:0097285 apoptoza
protein phosphorylation
cellular response to dexamethasone stimulus
cellular response to insulin stimulus
G1/S transition of mitotic cell cycle
GO:0035404 peptidyl-serine phosphorylation
TOR signaling
cellular response to interferon-gamma
long-chain fatty acid import into cell
GO:0007243 intracellular signal transduction
response to nutrient levels
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)

NM_001272042
NM_001272043
NM_001272044
NM_001272060
NM_003161

NM_001114334
NM_028259
NM_001363162

RefSeq (bjelančevina)
NP_001258971
NP_001258972
NP_001258973
NP_001258989
NP_003152

NP_001356598
NP_001356599
NP_001356600
NP_001356601
NP_001356602
NP_001356603
NP_001356604
NP_001356605
NP_001356606
NP_001356607
NP_001356608

NP_001107806
NP_082535
NP_001350091

Lokacija (UCSC)Chr 17: 59.89 – 59.95 MbChr 11: 86.5 – 86.54 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš

Fosforilacija p70S6K na treoninu 389 korištena je kao obilježje aktivacije od mTOR i u korelaciji je s inhibicijom autofagija u različitim situacijama. Međutim, nekoliko nedavnih studija sugerira da aktivnost p70S6K ima pozitivniju ulogu u porastu autofagije.[9][10]

Aminokiselinska sekvenca

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Dužina polipeptidnog lanca je 525 aminokiselina, a molekulska težina 59.140 Da.[11].

1020304050
MRRRRRRDGFYPAPDFRDREAEDMAGVFDIDLDQPEDAGSEDELEEGGQL
NESMDHGGVGPYELGMEHCEKFEISETSVNRGPEKIRPECFELLRVLGKG
GYGKVFQVRKVTGANTGKIFAMKVLKKAMIVRNAKDTAHTKAERNILEEV
KHPFIVDLIYAFQTGGKLYLILEYLSGGELFMQLEREGIFMEDTACFYLA
EISMALGHLHQKGIIYRDLKPENIMLNHQGHVKLTDFGLCKESIHDGTVT
HTFCGTIEYMAPEILMRSGHNRAVDWWSLGALMYDMLTGAPPFTGENRKK
TIDKILKCKLNLPPYLTQEARDLLKKLLKRNAASRLGAGPGDAGEVQAHP
FFRHINWEELLARKVEPPFKPLLQSEEDVSQFDSKFTRQTPVDSPDDSTL
SESANQVFLGFTYVAPSVLESVKEKFSFEPKIRSPRRFIGSPRTPVSPVK
FSPGDFWGRGASASTANPQTPVEYPMETSGIEQMDVTMSGEASAPLPIRQ
PNSGPYKKQAFPMISKRPEHLRMNL
Simboli

Funkcija

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Ovaj gen kodira člana RSK porodice serin / treonin kinaza. Ova kinaza sadrži dva neidentična katalitska domena kinaze i fosforilira nekoliko ostataka ribosomskog proteina S6. Aktivnost kinaze ovog proteina dovodi do povećanja sinteze proteina i proliferacije ćelija. Pojačanje regije DNK koja kodira ovaj gen i prekomerna ekspresija ove kinaze uočene su u nekim ćelijskim linijama karcinoma dojke. Opisana su alternativna mjesta translacije i varijante prerađenih transkripata, ali nisu detaljno okarakterizirana.

P70S6 kinaza je nizvodna meta signalizacije mTOR (cilj sisarskog rapamicina), posebno mTORC1, kompleksa koji sadrži mTOR, a karakterizira se uključivanjem Raptora, a ne Riktora (mTORC2). mTOR se može aktivirati putem mehanizma sličnog AND-vratima u lizosomu, integrirajući signale o faktorima rasta i bioraspoloživosti važnih molekula. Naprimjer, aminokiseline poput arginina i leucina mogu podstaknuti lizosomsko regrutiranje mTORC1. Kada se nađe u lizosomu, mTOR može aktivirati Rheb, malu GTPazu, koja se nalazi u lizosomu, u svom stanju vezanom za GTP. Aktivnost reb GTPaze stimulira (i samim tim smanjuje kapacitet za aktiviranje mTOR) uzvodnim TSC kompleksom, koji je inhibiran IGF signalizacijom. Stoga se AND ulaz sastoji od pravilne lokalizacije dovoljnom količinom aminokiselina i aktivacije faktorima rasta. Jednom kada je mTOR pravilno lokaliziran i aktiviran, može fosforilirati nizvodne ciljeve kao što su p70S6K, 4EBP i ULK1, koji su važni za regulaciju anaboličke/ kataboličke ravnoteže proteina. Fizička vježba aktivira sintezu proteina, fosforilacijom (aktivacijom) p70S6K na putu koji ovisi o mTOR, konkretno mTORC1. To je dokazano upotrebom inhibitora mTOR-a, rapamicina, za blokiranje povećanja mišićne mase, uprkos povećanom opterećenju (npr. vježbanjem). Pokazalo se da vježba povećava nivo IGF-1 u mišićima, indukujući tako signalni put IGF-1/PI3K/Akt/p70S6K, a samim tim povećanu sintezu proteina potrebnih za izgradnju mišića.

Klinički značaj

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Inhibicija proteina S6K1, ili njegov nedostatak, usporava proizvodnju masnih ćelija, ometanjem i usporavanjem početne "faze posvećenosti" njihovom formiranju. Studija bi mogla imati implikacije na liječenje gojaznosti.[12]

Amplifikacija regije DNK koja kodira ovaj gen i prekomerna ekspresija ove kinaze uočena je kod nekih karcinoma dojke u ćelijskim linijama.

Sljedeći put, za koji je P70 predložio njegovosudjelovanje, produžuje i rast mišića. P70 se fosforilira pasivnim istezanjem u mišićima. Ovo je možda jedna od mnogih proteinskih kinaza uključenih u izgradnju mišića.[13]

U svom neaktivnom stanju, S6K1 je vezan za eIF3 i odvaja se nakon fosforilacije, pomoću mTOR/Raptor-a. Slobodni S6K1 tada može fosforilirati svoje brojne ciljeve, uključujući eIF4B.[14]

Interakcije

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Pokazano je da P70-S6 kinaza 1 komunicira sa:

Također pogledajte

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Reference

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000108443 - Ensembl, maj 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000020516 - Ensembl, maj 2017
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Vanjski linkovi

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