Gorilla gorilla      Atypical/PIKK


※ PIKK family introduction

    Phosphatidylinositol-3 kinase-related kinases (PIKKs) belong to atypical protein kinase group, which share little similarity of kinase catalytic domain. PIKKs family contains six members which are involved in responding to various stresses, including DNA damage, blocks in DNA replication, availability of nutrients and errors in mRNA splicing. The protein kinase domain of PIKKS, located in C-terminus, is always flanked by two conserved domain, known as FAT and FATC domain, which may interact and participate in kinase regulation (1). ATM, one of family member, is involved in responding to a specific type of DNA damage, such as DNA double strand breaks, and controls the cell-cycle progression by phosphorylates multiple substrates including p53 and Chk2. In addition, ATM also locates in cytoplasmic especially in neuronal or neuron-like cells (2). Ataxia telangiectasia and Rad3-related protein (ATR) acts as a DNA damage sensor. Activated by DNA lesions including base adducts, crosslinks, DSBs, and compounds that directly promote replication stress such as hydroxyurea and aphidicolin and phosphorylates multiple substrates to control the DNA replication and mitosis (3). mTOR is a serine/threonine protein kinase which is a central regulator of cellular metabolism, growth and survival in response to hormones, growth factors, nutrients, energy and stress signals. mTOR is regulated by dynamic changes in cellular localization (3). Transformation/transcription domain-associated protein (TRRAP) is also structurally related to the PIKK family. TRRAP proteins (Tra1 in budding yeast) are common components of many histone acetyltransferase (HAT) complexes, and mediate a variety of cellular processes by recruiting HAT complexes to chromatin (4).

Reference
1. Lempiainen, H. and Halazonetis, T.D. (2009) Emerging common themes in regulation of PIKKs and PI3Ks. EMBO J, 28, 3067-3073. PMID: 19779456
2. Yang, D.Q., Halaby, M.J., Li, Y., Hibma, J.C. and Burn, P. (2011) Cytoplasmic ATM protein kinase: an emerging therapeutic target for diabetes, cancer and neuronal degeneration. Drug Discov Today, 16, 332-338. PMID: 21315178
3. Lovejoy, C.A. and Cortez, D. (2009) Common mechanisms of PIKK regulation. DNA Repair (Amst), 8, 1004-1008. PMID: 19464237
4. Kanoh, J. and Yanagida, M. (2007) Tel2: a common partner of PIK-related kinases and a link between DNA checkpoint and nutritional response? Genes Cells, 12, 1301-1304. PMID: 18076567


There are 15 genes.  Reviewed (0 or Unreviewed (15

No.StatusiEKPD IDEnsemble Gene IDUniProt AccessionGene Name
1
iEKPD-Gog-0222
ENSGGOG00000010057.3
G3R3L1
2
iEKPD-Gog-g008
ENSGGOG00000001355.3
A0A2I2Z6X7
3
iEKPD-Gog-0226
ENSGGOG00000010362.3
G3R4E3
ATM
4
iEKPD-Gog-0185
ENSGGOG00000008083.3
A0A2I2YTG6
ATR
5
iEKPD-Gog-0233
ENSGGOG00000010597.3
G3R506
MTOR
6
iEKPD-Gog-0364
ENSGGOG00000015153.3
A0A2I2YXD3
PI4KB
7
iEKPD-Gog-0251
ENSGGOG00000011040.3
G3RRS8
PIK3C2A
8
iEKPD-Gog-0416
ENSGGOG00000017159.3
A0A2I2Z7Z4
PIK3C2G
9
iEKPD-Gog-0372
ENSGGOG00000015471.3
A0A2I2YN96
PIK3C3
10
iEKPD-Gog-0206
ENSGGOG00000009365.3
G3R1S6
PIK3CA
11
iEKPD-Gog-0210
ENSGGOG00000009579.3
G3R2C2
PIK3CB
12
iEKPD-Gog-0289
ENSGGOG00000012386.3
G3R9L0
PIK3CD
13
iEKPD-Gog-0354
ENSGGOG00000014735.3
G3S7D1
PIK3CG
14
iEKPD-Gog-0129
ENSGGOG00000006036.3
G3QTD2
PRKDC
15
iEKPD-Gog-0064
ENSGGOG00000002928.3
A0A2I2Z877
TRRAP