blastp_kegg |
lcl|vvi:100250198
|
5 |
761 |
+ |
757 |
Gaps:30 |
24.59 |
2956 |
88.86 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|mdm:103438130
|
5 |
761 |
+ |
757 |
Gaps:30 |
80.96 |
898 |
87.21 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|cic:CICLE_v10018427mg
|
5 |
761 |
+ |
757 |
Gaps:30 |
24.83 |
2928 |
86.93 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102620162
|
5 |
761 |
+ |
757 |
Gaps:30 |
24.00 |
3029 |
86.93 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa000124mg
|
5 |
761 |
+ |
757 |
Gaps:30 |
42.22 |
1722 |
86.80 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_1510550
|
4 |
761 |
+ |
758 |
Gaps:30 |
24.64 |
2954 |
86.54 |
0.0 |
ataxia telangiectasia mutated putative (EC:2.7.11.1)
|
blastp_kegg |
lcl|gmx:100788458
|
5 |
761 |
+ |
757 |
Gaps:30 |
23.97 |
3033 |
85.14 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|cam:101498080
|
5 |
761 |
+ |
757 |
Gaps:30 |
24.61 |
2954 |
85.14 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|csv:101208785
|
8 |
761 |
+ |
754 |
Gaps:30 |
24.25 |
2985 |
85.91 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_kegg |
lcl|fve:101295891
|
5 |
761 |
+ |
757 |
Gaps:41 |
23.34 |
3068 |
86.45 |
0.0 |
serine/threonine-protein kinase ATM-like
|
blastp_pdb |
2y3a_A
|
568 |
723 |
+ |
156 |
Gaps:26 |
13.37 |
1092 |
36.99 |
1e-10 |
mol:protein length:1092 PHOSPHATIDYLINOSITOL-4 5-BISPHOSPHATE 3-KINAS
|
blastp_pdb |
1e90_A
|
439 |
669 |
+ |
231 |
Gaps:45 |
20.81 |
961 |
27.00 |
6e-07 |
mol:protein length:961 PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUN
|
blastp_pdb |
1e8x_A
|
439 |
669 |
+ |
231 |
Gaps:45 |
20.81 |
961 |
27.00 |
6e-07 |
mol:protein length:961 PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUN
|
blastp_pdb |
1e8w_A
|
439 |
669 |
+ |
231 |
Gaps:45 |
20.81 |
961 |
27.00 |
6e-07 |
mol:protein length:961 PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUN
|
blastp_pdb |
1e7v_A
|
439 |
669 |
+ |
231 |
Gaps:45 |
20.81 |
961 |
27.00 |
6e-07 |
mol:protein length:961 PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUN
|
blastp_pdb |
1e7u_A
|
439 |
669 |
+ |
231 |
Gaps:45 |
20.81 |
961 |
27.00 |
6e-07 |
mol:protein length:961 PHOSPHATIDYLINOSITOL 3-KINASE CATALYTIC SUBUN
|
blastp_uniprot_sprot |
sp|Q9M3G7|ATM_ARATH
|
7 |
761 |
+ |
755 |
Gaps:31 |
18.83 |
3856 |
80.17 |
0.0 |
Serine/threonine-protein kinase ATM OS Arabidopsis thaliana GN ATM PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q13315|ATM_HUMAN
|
5 |
761 |
+ |
757 |
Gaps:112 |
24.64 |
3056 |
42.76 |
9e-170 |
Serine-protein kinase ATM OS Homo sapiens GN ATM PE 1 SV 4
|
blastp_uniprot_sprot |
sp|Q62388|ATM_MOUSE
|
27 |
761 |
+ |
735 |
Gaps:80 |
23.52 |
3066 |
43.13 |
5e-169 |
Serine-protein kinase ATM OS Mus musculus GN Atm PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q6PQD5|ATM_PIG
|
5 |
761 |
+ |
757 |
Gaps:112 |
24.63 |
3057 |
42.10 |
1e-165 |
Serine-protein kinase ATM OS Sus scrofa GN ATM PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q4WVM7|ATM_ASPFU
|
33 |
760 |
+ |
728 |
Gaps:84 |
24.32 |
2796 |
38.53 |
6e-121 |
Serine/threonine-protein kinase tel1 OS Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN tel1 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q7RZT9|ATM_NEUCR
|
144 |
760 |
+ |
617 |
Gaps:55 |
20.89 |
2939 |
38.60 |
5e-119 |
Serine/threonine-protein kinase tel1 OS Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN mus-21 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q5EAK6|ATM_DROME
|
156 |
761 |
+ |
606 |
Gaps:48 |
21.25 |
2767 |
39.29 |
2e-117 |
Serine/threonine-protein kinase ATM OS Drosophila melanogaster GN tefu PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O74630|ATM_SCHPO
|
176 |
760 |
+ |
585 |
Gaps:56 |
20.66 |
2812 |
38.55 |
1e-116 |
Serine/threonine-protein kinase tel1 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN tel1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q4IB89|ATM_GIBZE
|
144 |
760 |
+ |
617 |
Gaps:64 |
21.79 |
2813 |
38.83 |
2e-116 |
Serine/threonine-protein kinase TEL1 OS Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN TEL1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q2U639|ATM_ASPOR
|
176 |
760 |
+ |
585 |
Gaps:49 |
19.62 |
2925 |
40.07 |
5e-116 |
Serine/threonine-protein kinase tel1 OS Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN tel1 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|119431
|
401 |
678 |
+ |
278 |
Gaps:9 |
100.00 |
279 |
63.80 |
1e-143 |
cd05171 PIKKc_ATM Ataxia telangiectasia mutated (ATM) catalytic domain The ATM catalytic domain subfamily is part of a larger superfamily that includes the catalytic domains of other kinases such as the typical serine/threonine/tyrosine protein kinases (PKs) aminoglycoside phosphotransferase choline kinase and RIO kinases. ATM is a member of the phosphoinositide 3-kinase-related protein kinase (PIKK) subfamily. PIKKs have intrinsic serine/threonine kinase activity and are distinguished from other PKs by their unique catalytic domain similar to that of lipid PI3K and their large molecular weight (240-470 kDa). ATM contains a FAT (FRAP ATM and TRRAP) domain a catalytic domain and a FATC domain at the C-terminus. ATM is critical in the response to DNA double strand breaks (DSBs) caused by radiation. It is activated at the site of a DSB and phosphorylates key substrates that trigger pathways that regulate DNA repair and cell cycle checkpoints at the G1/S S phase and G2/M transition. Patients with the human genetic disorder Ataxia telangiectasia (A-T) caused by truncating mutations in ATM show genome instability increased cancer risk immunodeficiency compromised mobility and neurodegeneration. A-T displays clinical heterogeneity which is correlated to the degree of retained ATM activity..
|
rpsblast_cdd |
gnl|CDD|119418
|
401 |
676 |
+ |
276 |
Gaps:41 |
99.16 |
237 |
48.51 |
4e-76 |
cd00892 PIKKc_ATR ATR (Ataxia telangiectasia and Rad3-related) catalytic domain The ATR catalytic domain subfamily is part of a larger superfamily that includes the catalytic domains of other kinases such as the typical serine/threonine/tyrosine protein kinases (PKs) aminoglycoside phosphotransferase choline kinase and RIO kinases. ATR is also referred to as Mei-41 (Drosophila) Esr1/Mec1p (Saccharomyces cerevisiae) Rad3 (Schizosaccharomyces pombe) and FRAP-related protein (human). ATR is a member of the phosphoinositide 3-kinase-related protein kinase (PIKK) subfamily. PIKKs have intrinsic serine/threonine kinase activity and are distinguished from other PKs by their unique catalytic domain similar to that of lipid PI3K and their large molecular weight (240-470 kDa). ATR contains a UME domain of unknown function a FAT (FRAP ATM and TRRAP) domain a catalytic domain and a FATC domain at the C-terminus. Together with its downstream effector kinase Chk1 ATR plays a central role in regulating the replication checkpoint. ATR stabilizes replication forks by promoting the association of DNA polymerases with the fork. Preventing fork collapse is essential in preserving genomic integrity. ATR plays a role in normal cell growth and in response to DNA damage..
|
rpsblast_cdd |
gnl|CDD|119424
|
403 |
671 |
+ |
269 |
Gaps:49 |
99.10 |
222 |
49.55 |
1e-71 |
cd05164 PIKKc Phosphoinositide 3-kinase-related protein kinase (PIKK) subfamily catalytic domain The PIKK catalytic domain subfamily is part of a larger superfamily that includes the catalytic domains of other kinases such as the typical serine/threonine/tyrosine protein kinases (PKs) aminoglycoside phosphotransferase choline kinase and RIO kinases. Members include ATM (Ataxia telangiectasia mutated) ATR (Ataxia telangiectasia and Rad3-related) TOR (Target of rapamycin) SMG-1 (Suppressor of morphogenetic effect on genitalia-1) and DNA-PK (DNA-dependent protein kinase). PIKKs have intrinsic serine/threonine kinase activity and are distinguished from other PKs by their unique catalytic domain similar to that of lipid PI3K and their large molecular weight (240-470 kDa). They show strong preference for phosphorylating serine/threonine residues followed by a glutamine and are also referred to as (S/T)-Q-directed kinases. They all contain a FATC (FRAP ATM and TRRAP C-terminal) domain. PIKKs have diverse functions including cell-cycle checkpoints genome surveillance mRNA surveillance and translation control..
|
rpsblast_cdd |
gnl|CDD|34637
|
241 |
761 |
+ |
521 |
Gaps:59 |
22.42 |
2105 |
31.36 |
6e-68 |
COG5032 TEL1 Phosphatidylinositol kinase and protein kinases of the PI-3 kinase family [Signal transduction mechanisms / Cell division and chromosome partitioning / Chromatin structure and dynamics / DNA replication recombination and repair / Intracellular trafficking and secretion].
|