Papio anubis      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 16 genes.  Reviewed (0 or Unreviewed (16

No.StatusiEKPD IDEnsemble Gene IDUniProt AccessionGene Name
1
iEKPD-Paa-0307
ENSPANG00000020399.3
A0A2I3LIL3
2
iEKPD-Paa-0282
ENSPANG00000019174.2
A0A096NCH4
ATM
3
iEKPD-Paa-0062
ENSPANG00000005574.2
A0A096NG15
ATR
4
iEKPD-Paa-0055
ENSPANG00000005055.2
A0A096NRV8
MTOR
5
iEKPD-Paa-g010
ENSPANG00000026010.2
A0A2I3N996
PI4KA
6
iEKPD-Paa-0202
ENSPANG00000015538.2
A0A2I3NGB5
PIK3C2A
7
iEKPD-Paa-g003
ENSPANG00000012285.2
A0A096N2T8
PIK3C2B
8
iEKPD-Paa-0140
ENSPANG00000010277.2
A0A096N515
PIK3C2G
9
iEKPD-Paa-0098
ENSPANG00000007681.2
A0A2I3MY56
PIK3C3
10
iEKPD-Paa-0379
ENSPANG00000023166.2
A0A096MY63
PIK3CA
11
iEKPD-Paa-0125
ENSPANG00000009667.2
A0A2I3MD87
PIK3CB
12
iEKPD-Paa-0258
ENSPANG00000018295.3
A0A096NPP4
PIK3CD
13
iEKPD-Paa-0084
ENSPANG00000007066.2
A0A096NGU7
PIK3CG
14
iEKPD-Paa-0449
ENSPANG00000025864.3
A0A096NQQ5
PRKDC
15
iEKPD-Paa-0079
ENSPANG00000006900.2
A0A096NRG0
SMG1
16
iEKPD-Paa-0082
ENSPANG00000006931.2
A0A2I3N9K6
TRRAP