blastp_kegg |
lcl|pper:PRUPE_ppa017676mg
|
14 |
918 |
+ |
905 |
Gaps:20 |
98.49 |
925 |
76.07 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pop:POPTR_0001s18290g
|
13 |
918 |
+ |
906 |
Gaps:19 |
99.89 |
918 |
73.94 |
0.0 |
POPTRDRAFT_797535 hypothetical protein
|
blastp_kegg |
lcl|pmum:103327938
|
14 |
918 |
+ |
905 |
Gaps:44 |
98.44 |
899 |
76.95 |
0.0 |
probable ATP-dependent RNA helicase DDX11
|
blastp_kegg |
lcl|pxb:103944873
|
13 |
918 |
+ |
906 |
Gaps:20 |
79.06 |
1151 |
75.60 |
0.0 |
probable ATP-dependent RNA helicase DDX11
|
blastp_kegg |
lcl|mdm:103443822
|
13 |
918 |
+ |
906 |
Gaps:20 |
98.38 |
925 |
75.27 |
0.0 |
probable ATP-dependent RNA helicase DDX11
|
blastp_kegg |
lcl|fve:101301420
|
1 |
918 |
+ |
918 |
Gaps:40 |
77.74 |
1168 |
74.12 |
0.0 |
probable ATP-dependent RNA helicase DDX11-like
|
blastp_kegg |
lcl|vvi:100265299
|
13 |
918 |
+ |
906 |
Gaps:34 |
92.61 |
961 |
76.74 |
0.0 |
probable ATP-dependent RNA helicase DDX11-like
|
blastp_kegg |
lcl|tcc:TCM_028743
|
7 |
918 |
+ |
912 |
Gaps:19 |
99.89 |
912 |
74.09 |
0.0 |
RAD3-like DNA-binding helicase protein isoform 1
|
blastp_kegg |
lcl|cit:102611409
|
1 |
918 |
+ |
918 |
Gaps:21 |
99.89 |
930 |
72.01 |
0.0 |
probable ATP-dependent RNA helicase DDX11-like
|
blastp_kegg |
lcl|cic:CICLE_v10024822mg
|
14 |
916 |
+ |
903 |
Gaps:16 |
98.38 |
928 |
72.40 |
0.0 |
hypothetical protein
|
blastp_pdb |
2vsf_A
|
212 |
392 |
+ |
181 |
Gaps:27 |
28.24 |
602 |
32.94 |
6e-13 |
mol:protein length:602 DNA REPAIR HELICASE RAD3 RELATED PROTEIN
|
blastp_pdb |
4a15_A
|
212 |
392 |
+ |
181 |
Gaps:27 |
27.42 |
620 |
32.94 |
7e-13 |
mol:protein length:620 ATP-DEPENDENT DNA HELICASE TA0057
|
blastp_uniprot_sprot |
sp|A8MPP1|D11L8_HUMAN
|
14 |
910 |
+ |
897 |
Gaps:132 |
98.02 |
907 |
36.11 |
2e-162 |
Putative ATP-dependent RNA helicase DDX11-like protein 8 OS Homo sapiens GN DDX11L8 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6AXC6|DDX11_MOUSE
|
24 |
910 |
+ |
887 |
Gaps:134 |
96.70 |
880 |
37.60 |
3e-156 |
Probable ATP-dependent RNA helicase DDX11 OS Mus musculus GN Ddx11 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q92771|DDX12_HUMAN
|
27 |
909 |
+ |
883 |
Gaps:142 |
92.53 |
950 |
36.29 |
5e-154 |
Putative ATP-dependent RNA helicase DDX12 OS Homo sapiens GN DDX12P PE 5 SV 3
|
blastp_uniprot_sprot |
sp|A1D8E4|CHL1_NEOFI
|
18 |
892 |
+ |
875 |
Gaps:129 |
95.93 |
861 |
36.56 |
3e-151 |
ATP-dependent RNA helicase chl1 OS Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN chl1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q96FC9|DDX11_HUMAN
|
14 |
843 |
+ |
830 |
Gaps:116 |
87.22 |
970 |
35.70 |
4e-145 |
Probable ATP-dependent RNA helicase DDX11 OS Homo sapiens GN DDX11 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|A2QY22|CHL1_ASPNC
|
18 |
909 |
+ |
892 |
Gaps:179 |
98.28 |
874 |
36.79 |
9e-144 |
ATP-dependent RNA helicase chl1 OS Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN chl1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O14147|CHL1_SCHPO
|
6 |
913 |
+ |
908 |
Gaps:161 |
99.17 |
844 |
36.80 |
2e-140 |
ATP-dependent RNA helicase chl1 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN chl1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A3LN13|CHL1_PICST
|
18 |
909 |
+ |
892 |
Gaps:126 |
97.25 |
835 |
35.71 |
2e-139 |
ATP-dependent RNA helicase CHL1 OS Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN CHL1 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q1E5T3|CHL1_COCIM
|
18 |
909 |
+ |
892 |
Gaps:139 |
97.44 |
861 |
34.80 |
7e-135 |
ATP-dependent RNA helicase CHL1 OS Coccidioides immitis (strain RS) GN CHL1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|A5DNW6|CHL1_PICGU
|
18 |
909 |
+ |
892 |
Gaps:127 |
97.58 |
825 |
35.78 |
1e-133 |
ATP-dependent RNA helicase CHL1 OS Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN CHL1 PE 3 SV 2
|
rpsblast_cdd |
gnl|CDD|161953
|
208 |
895 |
+ |
688 |
Gaps:113 |
91.21 |
705 |
32.04 |
1e-111 |
TIGR00604 rad3 DNA repair helicase (rad3). All proteins in this family for which funcitons are known are DNA-DNA helicases that funciton in the initiation of transcription and nucleotide excision repair as part of the TFIIH complex. This family is based on the phylogenomic analysis of JA Eisen (1999 Ph.D. Thesis Stanford University).
|
rpsblast_cdd |
gnl|CDD|191597
|
219 |
407 |
+ |
189 |
Gaps:21 |
100.00 |
168 |
50.60 |
1e-49 |
pfam06733 DEAD_2 DEAD_2. This represents a conserved region within a number of RAD3-like DNA-binding helicases that are seemingly ubiquitous - members include proteins of eukaryotic bacterial and archaeal origin. RAD3 is involved in nucleotide excision repair and forms part of the transcription factor TFIIH in yeast.
|
rpsblast_cdd |
gnl|CDD|31392
|
18 |
911 |
+ |
894 |
Gaps:120 |
98.17 |
654 |
21.50 |
3e-41 |
COG1199 DinG Rad3-related DNA helicases [Transcription / DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|128764
|
17 |
421 |
+ |
405 |
Gaps:37 |
95.16 |
289 |
37.45 |
1e-39 |
smart00488 DEXDc2 DEAD-like helicases superfamily.
|
rpsblast_cdd |
gnl|CDD|205487
|
664 |
889 |
+ |
226 |
Gaps:62 |
99.39 |
165 |
31.71 |
8e-35 |
pfam13307 Helicase_C_2 Helicase C-terminal domain. This domain is the second of two tandem AAA domains found in a wide variety of helicase enzymes.
|
rpsblast_cdd |
gnl|CDD|128767
|
687 |
868 |
+ |
182 |
Gaps:46 |
95.77 |
142 |
41.91 |
3e-31 |
smart00491 HELICc2 helicase superfamily c-terminal domain.
|
rpsblast_kog |
gnl|CDD|36348
|
5 |
914 |
+ |
910 |
Gaps:109 |
99.51 |
821 |
46.02 |
0.0 |
KOG1133 KOG1133 KOG1133 Helicase of the DEAD superfamily [Replication recombination and repair].
|
rpsblast_kog |
gnl|CDD|36347
|
17 |
917 |
+ |
901 |
Gaps:122 |
80.85 |
945 |
31.41 |
1e-77 |
KOG1132 KOG1132 KOG1132 Helicase of the DEAD superfamily [Replication recombination and repair].
|