ELM
The Eukaryotic Linear Motif resource for
Functional Sites in Proteins

MOD_PIKK_1

Accession:
Functional site class:
PIKK phosphorylation site
Functional site description:
The phosphoinositide-3-OH-kinase related kinases (PIKKs) are atypical protein kinases exclusive to eukaryotes. The PIKK members are large proteins with Ser/Thr kinase activity serving important roles in DNA repair and DNA damage checkpoints. The three PIKK proteins with repair and checkpoint functions in mammalian cells are: DNA-PK (DNA-dependent protein kinase), ATM (ataxia telangiectasia mutated), and ATR (ATM and Rad3 related).
ELM Description:
The PIKK family member proteins specifically phosphorylate the (ST)Q motif in their substrates. The glutamine adjacent to the target serine-threonine is critical for the substrate recognition.
Pattern: ...([ST])Q..
Pattern Probability: 0.0092301
Present in taxon: Eukaryota
Interaction Domain:
PI3_PI4_kinase (PF00454) Phosphatidylinositol 3- and 4-kinase (Stochiometry: 1 : 1)
o See 48 Instances for MOD_PIKK_1
The PIKKs are a group of ancient eukaryotic protein kinases including ATM, ATR and DNA-PK. These proteins are characterized by their large size (>200 KDa) and by the presence of a highly conserved phosphoinositide 3-kinase-like catalytic domain. They appear to function principally as protein kinases, however (Yang,2004). PIKKs are the principal components of the DNA damage checkpoint pathway and are probably present in all eukaryotes. The common phosphorylation site for PIKKs is a serine or threonine followed by a glutamine residue, a motif commonly dubbed ...[S/T]Q... (Kim,1999). Often substrate regions are characterized by high local density of SQ/TQ motifs that have been termed "SCDs" (SQ/TQ cluster domains). While sharing the same substrate specificity, the PIKK family members are activated by different checkpoint responses. ATM is involved in the checkpoint response to ionizing radiation, DNA double strand breaks and in V(D)J recombination, while ATR seems to play a primary role in checkpoints induced by UV irradiation or DNA replication blocks. DNA-PK, which has essential functions in V(D)J recombination as well as in non-homologous end joining, is also associated with the checkpoint response (Yang,2004). In general it is often found that the same substrate is phosphorylated by both ATM and ATR in a cell cycle and time dependent manner.
o 15 selected references:


o 6 GO-Terms:
Biological Process:
Dna Damage Induced Protein Phosphorylation (also annotated in these classes: LIG_BRCT_BRCA1_1 LIG_BRCT_BRCA1_2 LIG_BRCT_MDC1_1 )
Dna Damage Checkpoint (also annotated in these classes: LIG_BRCT_BRCA1_1 LIG_BRCT_BRCA1_2 )
Somatic Recombination Of Antibody Genes (also annotated in class: )
Cellular Compartment:
Cytosol (also annotated in these classes: CLV_C14_Caspase3-7 CLV_Separin_Fungi CLV_Separin_Metazoa DEG_APCC_DBOX_1 DEG_APCC_KENBOX_2 DEG_APCC_TPR_1 DEG_Cend_DCAF12_1 DEG_Cend_FEM1AC_1 DEG_Cend_FEM1B_2 DEG_Cend_KLHDC2_1 DEG_Cend_TRIM7_1 DEG_COP1_1 DEG_CRBN_cyclicCter_1 DEG_Kelch_actinfilin_1 DEG_Kelch_Keap1_1 DEG_Kelch_Keap1_2 DEG_Kelch_KLHL12_1 DEG_Kelch_KLHL3_1 DEG_MDM2_SWIB_1 DEG_Nend_Nbox_1 DEG_Nend_UBRbox_1 DEG_Nend_UBRbox_2 DEG_Nend_UBRbox_3 DEG_Nend_UBRbox_4 DEG_ODPH_VHL_1 DEG_SCF_FBW7_1 DEG_SCF_FBW7_2 DEG_SCF_FBXO31_1 DEG_SCF_SKP2-CKS1_1 DEG_SCF_TRCP1_1 DEG_SIAH_1 DOC_AGCK_PIF_1 DOC_AGCK_PIF_2 DOC_AGCK_PIF_3 DOC_ANK_TNKS_1 DOC_CDC14_PxL_1 DOC_CKS1_1 DOC_CYCLIN_D_Helix_1 DOC_CYCLIN_RevRxL_6 DOC_CYCLIN_RxL_1 DOC_CYCLIN_yClb1_LxF_4 DOC_CYCLIN_yClb3_PxF_3 DOC_CYCLIN_yCln2_LP_2 DOC_GSK3_Axin_1 DOC_MAPK_DCC_7 DOC_MAPK_FxFP_2 DOC_MAPK_gen_1 DOC_MAPK_GRA24_9 DOC_MAPK_HePTP_8 DOC_MAPK_JIP1_4 DOC_MAPK_MEF2A_6 DOC_MAPK_NFAT4_5 DOC_MAPK_RevD_3 DOC_MIT_MIM_1 DOC_PP1_MyPhoNE_1 DOC_PP1_RVXF_1 DOC_PP1_SILK_1 DOC_PP2A_B56_1 DOC_PP2A_KARD_1 DOC_PP2B_LxvP_1 DOC_PP2B_PxIxIT_1 DOC_PUB_PIM_1 DOC_RSK_DDVF_1 DOC_SPAK_OSR1_1 DOC_TBK1_STING_1 DOC_WD40_RPTOR_TOS_1 DOC_WW_Pin1_4 LIG_14-3-3_CanoR_1 LIG_14-3-3_ChREBP_3 LIG_14-3-3_CterR_2 LIG_ActinCP_CPI_1 LIG_ActinCP_TwfCPI_2 LIG_Actin_RPEL_3 LIG_Actin_WH2_1 LIG_Actin_WH2_2 LIG_ANK_PxLPxL_1 LIG_AP2alpha_1 LIG_AP2alpha_2 LIG_APCC_ABBA_1 LIG_APCC_Cbox_1 LIG_APCC_Cbox_2 LIG_AP_GAE_1 LIG_Arc_Nlobe_1 LIG_ARL_BART_1 LIG_BH_BH3_1 LIG_BIR_II_1 LIG_BIR_III_1 LIG_BIR_III_2 LIG_BIR_III_3 LIG_BIR_III_4 LIG_CaM_1-14-15-16_REV_1 LIG_CaM_1-26_7 LIG_CaM_1-5-10-14_3 LIG_CaM_1-8-14_4 LIG_CaM_1-8-9-10_5 LIG_CaM_1-8_REV_2 LIG_CaM_IQ_9 LIG_CaMK_CASK_1 LIG_CaM_NSCaTE_8 LIG_CAP-Gly_1 LIG_CAP-Gly_2 LIG_Clathr_ClatBox_1 LIG_Clathr_ClatBox_2 LIG_CNOT1_NIM_1 LIG_CSK_EPIYA_1 LIG_CtBP_PxDLS_1 LIG_deltaCOP1_diTrp_1 LIG_DLG_GKlike_1 LIG_Dynein_DLC8_1 LIG_EABR_CEP55_1 LIG_EF_ALG2_ABM_1 LIG_EF_ALG2_ABM_2 LIG_EH_1 LIG_eIF4E_1 LIG_eIF4E_2 LIG_EVH1_1 LIG_EVH1_2 LIG_EVH1_3 LIG_FAT_LD_1 LIG_FERM_MyoX_1 LIG_FZD_DVL_PDZ LIG_G3BP_FGDF_1 LIG_GBD_Chelix_1 LIG_GBD_WASP_1 LIG_GSK3_LRP6_1 LIG_GYF LIG_IBAR_NPY_1 LIG_IRF7_LxLS_2 LIG_IRFs_LxIS_1 LIG_KLC1_WD_1 LIG_KLC1_Yacidic_2 LIG_LIR_Apic_2 LIG_LIR_Gen_1 LIG_LIR_LC3C_4 LIG_LIR_Nem_3 LIG_LYPXL_L_2 LIG_LYPXL_S_1 LIG_LYPXL_yS_3 LIG_MYND_3 LIG_OCRL_FandH_1 LIG_PAM2_1 LIG_PAM2_2 LIG_PDZ_Class_1 LIG_PDZ_Class_2 LIG_PDZ_Class_3 LIG_PDZ_Wminus1_1 LIG_Pex14_1 LIG_Pex14_2 LIG_Pex14_3 LIG_Pex14_4 LIG_Pex3_1 LIG_PIP2_ANTH_1 LIG_PIP2_ENTH_1 LIG_PROFILIN_1 LIG_PTAP_UEV_1 LIG_PTB_Apo_2 LIG_PTB_Phospho_1 LIG_SH2_CRK LIG_SH2_GRB2like LIG_SH2_NCK_1 LIG_SH2_PTP2 LIG_SH2_SFK_2 LIG_SH2_SFK_CTail_3 LIG_SH2_STAT3 LIG_SH2_STAT5 LIG_SH2_STAT6 LIG_SH3_1 LIG_SH3_2 LIG_SH3_3 LIG_SH3_4 LIG_SH3_CIN85_PxpxPR_1 LIG_SH3_PxRPPK_7 LIG_SH3_PxxDY_5 LIG_SH3_PxxPPRxxK_8 LIG_SH3_PxxxRxxKP_6 LIG_SPRY_1 LIG_SUFU_1 LIG_SxIP_EBH_1 LIG_TPR LIG_TRAF2like_MATH_loPxQ_2 LIG_TRAF2like_MATH_shPxQ_1 LIG_TRAF3_MATH_PxP_3 LIG_TRAF4_MATH_1 LIG_TRAF6_MATH_1 LIG_TYR_ITAM LIG_TYR_ITIM LIG_TYR_ITSM LIG_UFM1_UFIM_1 LIG_VCP_SHPBox_1 LIG_VCP_VBM_3 LIG_VCP_VIM_2 LIG_Vh1_VBS_1 LIG_WH1 LIG_WRC_WIRS_1 LIG_WW_1 LIG_WW_2 LIG_WW_3 MOD_AAK1BIKe_LxxQxTG_1 MOD_CAAXbox MOD_CDC14_SPxK_1 MOD_CDK_SPK_2 MOD_CDK_SPxK_1 MOD_CDK_SPxxK_3 MOD_CK1_1 MOD_CK2_1 MOD_DYRK1A_RPxSP_1 MOD_GSK3_1 MOD_LATS_1 MOD_LOK_YxT_1 MOD_NEK2_1 MOD_NEK2_2 MOD_NMyristoyl MOD_PK_1 MOD_PKA_1 MOD_PKA_2 MOD_PKB_1 MOD_PLK MOD_Plk_1 MOD_Plk_2-3 MOD_Plk_4 MOD_PRMT_GGRGG_1 MOD_ProDKin_1 MOD_SPalmitoyl_2 MOD_SPalmitoyl_4 MOD_TYR_CSK MOD_TYR_DYR ELM:old_LIG_14-3-3_1 ELM:old_LIG_14-3-3_2 ELM:old_LIG_14-3-3_3 TRG_AP2beta_CARGO_1 TRG_Cilium_Arf4_1 TRG_Cilium_RVxP_2 TRG_DiLeu_BaEn_1 TRG_DiLeu_BaEn_2 TRG_DiLeu_BaEn_3 TRG_DiLeu_BaEn_4 TRG_DiLeu_BaLyEn_6 TRG_DiLeu_LyEn_5 TRG_ENDOCYTIC_2 TRG_ER_diArg_1 TRG_ER_diLys_1 TRG_ER_FFAT_1 TRG_ER_FFAT_2 TRG_Golgi_diPhe_1 TRG_LysEnd_APsAcLL_1 TRG_LysEnd_APsAcLL_3 TRG_LysEnd_GGAAcLL_1 TRG_LysEnd_GGAAcLL_2 TRG_NES_CRM1_1 TRG_NESrev_CRM1_2 TRG_PTS1 TRG_PTS2 )
Nucleus (also annotated in these classes: CLV_C14_Caspase3-7 CLV_Separin_Fungi CLV_Separin_Metazoa CLV_TASPASE1 DEG_APCC_DBOX_1 DEG_APCC_KENBOX_2 DEG_APCC_TPR_1 DEG_Cend_DCAF12_1 DEG_Cend_FEM1AC_1 DEG_Cend_FEM1B_2 DEG_Cend_KLHDC2_1 DEG_Cend_TRIM7_1 DEG_COP1 DEG_COP1_1 DEG_CRL4_CDT2_1 DEG_CRL4_CDT2_2 DEG_Kelch_Keap1_1 DEG_Kelch_Keap1_2 DEG_MDM2_SWIB_1 DEG_ODPH_VHL_1 DEG_SCF_COI1_1 DEG_SCF_FBW7_1 DEG_SCF_FBW7_2 DEG_SCF_FBXO31_1 DEG_SCF_SKP2-CKS1_1 DEG_SCF_TIR1_1 DEG_SCF_TRCP1_1 DEG_SIAH_1 DEG_SPOP_SBC_1 DOC_ANK_TNKS_1 DOC_CDC14_PxL_1 DOC_CKS1_1 DOC_CYCLIN_D_Helix_1 DOC_CYCLIN_RevRxL_6 DOC_CYCLIN_RxL_1 DOC_CYCLIN_yClb1_LxF_4 DOC_CYCLIN_yClb3_PxF_3 DOC_CYCLIN_yClb5_NLxxxL_5 DOC_CYCLIN_yCln2_LP_2 DOC_MAPK_DCC_7 DOC_MAPK_FxFP_2 DOC_MAPK_gen_1 DOC_MAPK_GRA24_9 DOC_MAPK_HePTP_8 DOC_MAPK_JIP1_4 DOC_MAPK_MEF2A_6 DOC_MAPK_NFAT4_5 DOC_MAPK_RevD_3 DOC_PIKK_1 DOC_PP1_MyPhoNE_1 DOC_PP1_RVXF_1 DOC_PP1_SILK_1 DOC_PP2A_B56_1 DOC_PP2A_KARD_1 DOC_PP2B_LxvP_1 DOC_PP2B_PxIxIT_1 DOC_PP4_FxxP_1 DOC_PP4_MxPP_1 DOC_USP7_MATH_1 DOC_USP7_MATH_2 DOC_USP7_UBL2_3 DOC_WW_Pin1_4 LIG_14-3-3_CanoR_1 LIG_14-3-3_ChREBP_3 LIG_14-3-3_CterR_2 LIG_ANK_PxLPxL_1 LIG_APCC_ABBA_1 LIG_APCC_Cbox_1 LIG_APCC_Cbox_2 LIG_ARL_BART_1 LIG_ARS2_EDGEI_1 LIG_BRCT_BRCA1_1 LIG_BRCT_BRCA1_2 LIG_BRCT_MDC1_1 LIG_CaM_1-14-15-16_REV_1 LIG_CaMK_CASK_1 LIG_CORNRBOX LIG_CSL_BTD_1 LIG_CtBP_PxDLS_1 LIG_CtBP_RRT_2 LIG_DCNL_PONY_1 LIG_EF_ALG2_ABM_1 LIG_EF_ALG2_ABM_2 LIG_EH1_1 LIG_FHA_1 LIG_FHA_2 LIG_GLEBS_BUB3_1 LIG_HCF-1_HBM_1 LIG_HOMEOBOX LIG_HP1_1 LIG_IRF7_LxLS_2 LIG_IRFs_LxIS_1 LIG_KEPE_1 LIG_KEPE_2 LIG_KEPE_3 LIG_LEDGF_IBM_1 LIG_LSD1_SNAG_1 LIG_MAD2 LIG_Menin_MBM1_1 LIG_MLH1_MIPbox_1 LIG_MSH2_SHIPbox_1 LIG_MTR4_AIM_1 LIG_Mtr4_Air2_1 LIG_Mtr4_Trf4_1 LIG_Mtr4_Trf4_2 LIG_MYND_1 LIG_MYND_2 LIG_MYND_3 LIG_NBox_RRM_1 LIG_NRBOX LIG_Nrd1CID_NIM_1 LIG_PALB2_WD40_1 LIG_PCNA_APIM_2 LIG_PCNA_PIPBox_1 LIG_PCNA_TLS_4 LIG_PCNA_yPIPBox_3 LIG_PTAP_UEV_1 LIG_RBL1_LxSxE_2 LIG_RB_LxCxE_1 LIG_RB_pABgroove_1 LIG_REV1ctd_RIR_1 LIG_RPA_C_Plants LIG_RPA_C_Vert LIG_RRM_PRI_1 LIG_Rrp6Rrp47_Mtr4_1 LIG_Sin3_1 LIG_Sin3_2 LIG_Sin3_3 LIG_SUFU_1 LIG_SUMO_SIM_anti_2 LIG_SUMO_SIM_par_1 LIG_TPR LIG_Trf4_IWRxY_1 LIG_TRFH_1 LIG_UBA3_1 LIG_ULM_U2AF65_1 LIG_VCP_SHPBox_1 LIG_VCP_VBM_3 LIG_VCP_VIM_2 LIG_WD40_WDR5_VDV_1 LIG_WD40_WDR5_VDV_2 LIG_WD40_WDR5_WIN_1 LIG_WD40_WDR5_WIN_2 LIG_WD40_WDR5_WIN_3 LIG_WRPW_1 LIG_WRPW_2 LIG_WW_2 MOD_AAK1BIKe_LxxQxTG_1 MOD_CDC14_SPxK_1 MOD_CDK_SPK_2 MOD_CDK_SPxK_1 MOD_CDK_SPxxK_3 MOD_CK1_1 MOD_CK2_1 MOD_DYRK1A_RPxSP_1 MOD_GSK3_1 MOD_NEK2_1 MOD_NEK2_2 MOD_PKA_1 MOD_PKA_2 MOD_PKB_1 MOD_PLK MOD_Plk_1 MOD_Plk_2-3 MOD_Plk_4 MOD_PRMT_GGRGG_1 MOD_ProDKin_1 MOD_SUMO_for_1 MOD_SUMO_rev_2 ELM:old_LIG_14-3-3_1 ELM:old_LIG_14-3-3_2 ELM:old_LIG_14-3-3_3 TRG_NES_CRM1_1 TRG_NESrev_CRM1_2 TRG_NLS_Bipartite_1 TRG_NLS_MonoCore_2 TRG_NLS_MonoExtC_3 TRG_NLS_MonoExtN_4 )
Molecular Function:
Protein Serine/Threonine Kinase (also annotated in these classes: DOC_AGCK_PIF_1 DOC_AGCK_PIF_2 DOC_AGCK_PIF_3 DOC_MAPK_DCC_7 DOC_MAPK_HePTP_8 DOC_MAPK_MEF2A_6 MOD_AAK1BIKe_LxxQxTG_1 MOD_DYRK1A_RPxSP_1 MOD_GSK3_1 MOD_LOK_YxT_1 MOD_NEK2_1 MOD_NEK2_2 MOD_TYR_DYR )


o 48 Instances for MOD_PIKK_1
(click table headers for sorting; Notes column: =Number of Switches, =Number of Interactions)
Acc., Gene-, NameStartEndSubsequenceLogic#Ev.OrganismNotes
Q5H924 HUWE1
Q5H924_HUMAN
1407 1413 IVSRSGEDESQEDVLMDEAP TP 1 Homo sapiens (Human)
A0A024R7R0 RAP80
A0A024R7R0_HUMAN
98 104 SEQEAREVNSQEEEEEELLR TP 1 Homo sapiens (Human)
A8K964 Pinin
A8K964_HUMAN
378 384 VRESEKQQDSQPEEVMDVLE TP 1 Homo sapiens (Human)
A6NNK5 TP53BP1
A6NNK5_HUMAN
582 588 PAQDGEVQLSQNDDKTKGDD TP 1 Homo sapiens (Human)
A0A0A0MTR7 RNF213
A0A0A0MTR7_HUMAN
214 220 SIPSGGRGLSQEGTGPPTSA TP 1 Homo sapiens (Human)
X5DRB1 XPC
X5DRB1_HUMAN
348 354 DPGGSSETSSQVLENHTKPK TP 1 Homo sapiens (Human)
A6NNK5 TP53BP1
A6NNK5_HUMAN
833 839 ETEPVEQDSSQPSLPLVRAD TP 1 Homo sapiens (Human)
P17096 HMGA1
HMGA1_HUMAN
41 47 VSPGTALVGSQKEPSEVPTP TP 1 Homo sapiens (Human)
Q9UQ35 SRRM2
SRRM2_HUMAN
1230 1236 EQNSALPTSSQDEELMEVVE TP 1 Homo sapiens (Human)
A0A0C4DG07 NBN
A0A0C4DG07_HUMAN
258 264 KTTTPGPSLSQGVSVDEKLM TP 1 Homo sapiens (Human)
Q6PK95 TOP1
Q6PK95_HUMAN
7 13 MSGDHLHNDSQIEADFRLND TP 1 Homo sapiens (Human)
A6NNK5 TP53BP1
A6NNK5_HUMAN
1070 1076 RGNLLHFPSSQGEEEKEKLE TP 1 Homo sapiens (Human)
B7Z7Z8 peptidylprolyl isomerase
B7Z7Z8_HUMAN
263 269 GVTNEKGTDSQAMEEEKPEG TP 1 Homo sapiens (Human)
Q14566 MCM6
MCM6_HUMAN
10 16 AAAAEPGAGSQHLEVRDEVA TP 1 Homo sapiens (Human)
Q9BVJ6-3 UTP14A
UT14A_HUMAN
398 404 GSQETKDSGSQEVLSELRVL TP 1 Homo sapiens (Human)
Q9BVJ6-3 UTP14A
UT14A_HUMAN
390 396 LSQDAEPAGSQETKDSGSQE TP 1 Homo sapiens (Human)
S4R3H4 ACIN1
S4R3H4_HUMAN
182 188 ARAAKLSEGSQPAEEEEDQE TP 1 Homo sapiens (Human)
Q3LRH8 BRCA1
Q3LRH8_HUMAN
1521 1527 GSLQNRNYPSQEELIKVVDV TP 1 Homo sapiens (Human)
Q03164 MLL
MLL1_HUMAN
513 519 PEVHPPLPISQSPENESNDR TP 3 Homo sapiens (Human)
Q00987 MDM2
MDM2_HUMAN
404 410 STSSSIIYSSQEDVKEFERE TP 3 Homo sapiens (Human)
O15151 MDM4
MDM4_HUMAN
400 406 FLDLAHSSESQETISSMGEQ TP 5 Homo sapiens (Human)
O14757 CHEK1
CHK1_HUMAN
314 320 SEENVKYSSSQPEPRTGLSL TP 3 Homo sapiens (Human)
O14757 CHEK1
CHK1_HUMAN
342 348 DKLVQGISFSQPTCPDHMLL TP 2 Homo sapiens (Human)
P18887 XRCC1
XRCC1_HUMAN
368 374 CAFANTPKYSQVLGLGGRIV TP 1 Homo sapiens (Human)
P04911 HTA1
H2A1_YEAST
126 132 IHQNLLPKKSAKATKASQEL TP 2 Saccharomyces cerevisiae (Baker"s yeast)
Q8AY27 rad1
Q8AY27_XENLA
2 8 MPFLTQPEADDDQYVLTCSL TP 2 Xenopus laevis (African clawed frog)
P54132 BLM
BLM_HUMAN
119 125 QTPKEVVCTTQNTPTVKKSR TP 2 Homo sapiens (Human)
P54132 BLM
BLM_HUMAN
96 102 FKNAPAGQETQRGGSKSLLP TP 2 Homo sapiens (Human)
P23025 XPA
XPA_HUMAN
193 199 VKRSLEVWGSQEALEEAKEV TP 2 Homo sapiens (Human)
Q01094 E2F1
E2F1_HUMAN
28 34 AGALRLLDSSQIVIISAAQD TP 1 Homo sapiens (Human)
P07900 HSP90AA1
HS90A_HUMAN
4 10 MPEETQTQDQPMEEEEVETF TP 1 Homo sapiens (Human)
P07900 HSP90AA1
HS90A_HUMAN
2 8 MPEETQTQDQPMEEEEVETF TP 1 Homo sapiens (Human)
P49736 MCM2
MCM2_HUMAN
105 111 DEDVEELTASQREAAERAMR TP 2 Homo sapiens (Human)
P05412 JUN
JUN_HUMAN
246 252 PPLSPIDMESQERIKAERKR TP 1 Homo sapiens (Human)
P38398 BRCA1
BRCA1_HUMAN
1521 1527 GSLQNRNYPSQEELIKVVDV TP 1 Homo sapiens (Human)
P38398 BRCA1
BRCA1_HUMAN
1420 1426 LEAVLEQHGSQPSNSYPSII TP 1 Homo sapiens (Human)
P38398 BRCA1
BRCA1_HUMAN
1384 1390 VSEDCSGLSSQSDILTTQQR TP 1 Homo sapiens (Human)
P06536 Nr3c1
GCR_RAT
524 530 GIQQATAGVSQDTSENPNKT TP 2 Rattus norvegicus (Norway rat)
P11831 SRF
SRF_HUMAN
443 449 APSTMQVSHSQVQEPGGVPQ TP 2 Homo sapiens (Human)
P11831 SRF
SRF_HUMAN
432 438 GSLTVLNAFSQAPSTMQVSH TP 2 Homo sapiens (Human)
Q62622 Eif4ebp1
4EBP1_RAT
108 114 HSSPEDKRAGGEESQFEMDI TP 1 Rattus norvegicus (Norway rat)
P54274 TERF1
TERF1_HUMAN
216 222 FKSKLLMIISQKDTFHSFFQ TP 4 Homo sapiens (Human)
O96017 CHEK2
CHK2_HUMAN
65 71 TLSSLETVSTQELYSIPEDQ TP 6 Homo sapiens (Human)
Q00987 MDM2
MDM2_HUMAN
392 398 SQSQESEDYSQPSTSSSIIY TP 4 Homo sapiens (Human)
P27661 H2afx
H2AX_MOUSE
137 143 TVGPKAPAVGKKASQASQEY TP 1 Mus musculus (House mouse)
O60934 NBN
NBN_HUMAN
340 346 KTTTPGPSLSQGVSVDEKLM TP 3 Homo sapiens (Human)
P00520 Abl1
ABL1_MOUSE
443 449 MSPYPGIDLSQVYELLEKDY TP 3 Mus musculus (House mouse)
P04637 TP53
P53_HUMAN
12 18 SDPSVEPPLSQETFSDLWKL TP 3 Homo sapiens (Human)
Please cite: ELM-the Eukaryotic Linear Motif resource-2024 update. (PMID:37962385)

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