blastp_kegg |
lcl|pmum:103336719
|
1 |
320 |
+ |
320 |
Gaps:1 |
45.18 |
706 |
83.39 |
0.0 |
mediator of RNA polymerase II transcription subunit 34
|
blastp_kegg |
lcl|vvi:100256266
|
1 |
320 |
+ |
320 |
none |
45.01 |
711 |
83.12 |
0.0 |
ATP-dependent DNA helicase Q-like 2-like
|
blastp_kegg |
lcl|fve:101300545
|
13 |
320 |
+ |
308 |
Gaps:1 |
43.36 |
708 |
84.69 |
0.0 |
mediator of RNA polymerase II transcription subunit 34-like
|
blastp_kegg |
lcl|cam:101503147
|
13 |
319 |
+ |
307 |
Gaps:1 |
43.75 |
704 |
83.77 |
0.0 |
mediator of RNA polymerase II transcription subunit 34-like
|
blastp_kegg |
lcl|pxb:103935168
|
13 |
320 |
+ |
308 |
Gaps:1 |
43.55 |
705 |
83.71 |
0.0 |
mediator of RNA polymerase II transcription subunit 34
|
blastp_kegg |
lcl|pda:103718974
|
13 |
319 |
+ |
307 |
none |
78.92 |
389 |
81.76 |
0.0 |
mediator of RNA polymerase II transcription subunit 34-like
|
blastp_kegg |
lcl|pvu:PHAVU_002G126800g
|
1 |
320 |
+ |
320 |
Gaps:1 |
45.44 |
702 |
80.25 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cic:CICLE_v10001056mg
|
13 |
320 |
+ |
308 |
Gaps:3 |
66.45 |
468 |
82.32 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102630216
|
13 |
320 |
+ |
308 |
Gaps:3 |
43.50 |
715 |
82.32 |
0.0 |
mediator of RNA polymerase II transcription subunit 34-like
|
blastp_kegg |
lcl|sly:101268017
|
1 |
320 |
+ |
320 |
none |
45.20 |
708 |
78.75 |
0.0 |
mediator of RNA polymerase II transcription subunit 34-like
|
blastp_pdb |
2wwy_B
|
61 |
321 |
+ |
261 |
Gaps:1 |
43.99 |
591 |
53.46 |
1e-91 |
mol:protein length:591 ATP-DEPENDENT DNA HELICASE Q1
|
blastp_pdb |
2wwy_A
|
61 |
321 |
+ |
261 |
Gaps:1 |
43.99 |
591 |
53.46 |
1e-91 |
mol:protein length:591 ATP-DEPENDENT DNA HELICASE Q1
|
blastp_pdb |
2v1x_B
|
61 |
321 |
+ |
261 |
Gaps:1 |
43.99 |
591 |
53.46 |
1e-91 |
mol:protein length:591 ATP-DEPENDENT DNA HELICASE Q1
|
blastp_pdb |
2v1x_A
|
61 |
321 |
+ |
261 |
Gaps:1 |
43.99 |
591 |
53.46 |
1e-91 |
mol:protein length:591 ATP-DEPENDENT DNA HELICASE Q1
|
blastp_pdb |
1oyy_A
|
64 |
317 |
+ |
254 |
Gaps:13 |
46.08 |
523 |
43.98 |
2e-58 |
mol:protein length:523 ATP-dependent DNA helicase
|
blastp_pdb |
1oyw_A
|
64 |
317 |
+ |
254 |
Gaps:13 |
46.08 |
523 |
43.98 |
2e-58 |
mol:protein length:523 ATP-dependent DNA helicase
|
blastp_uniprot_sprot |
sp|Q9FT73|MED34_ARATH
|
14 |
320 |
+ |
307 |
Gaps:1 |
43.69 |
705 |
79.55 |
0.0 |
Mediator of RNA polymerase II transcription subunit 34 OS Arabidopsis thaliana GN MED34 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6AYJ1|RECQ1_RAT
|
14 |
321 |
+ |
308 |
Gaps:11 |
49.76 |
621 |
48.54 |
1e-93 |
ATP-dependent DNA helicase Q1 OS Rattus norvegicus GN Recql PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P46063|RECQ1_HUMAN
|
14 |
321 |
+ |
308 |
Gaps:3 |
47.61 |
649 |
48.54 |
1e-91 |
ATP-dependent DNA helicase Q1 OS Homo sapiens GN RECQL PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q5RF63|RECQ1_PONAB
|
14 |
321 |
+ |
308 |
Gaps:3 |
47.61 |
649 |
48.54 |
3e-91 |
ATP-dependent DNA helicase Q1 OS Pongo abelii GN RECQL PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9Z129|RECQ1_MOUSE
|
14 |
321 |
+ |
308 |
Gaps:7 |
47.69 |
648 |
47.57 |
5e-91 |
ATP-dependent DNA helicase Q1 OS Mus musculus GN Recql PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9TXJ8|RECQ1_CAEEL
|
7 |
320 |
+ |
314 |
Gaps:3 |
49.92 |
631 |
43.49 |
6e-80 |
Putative ATP-dependent DNA helicase Q1 OS Caenorhabditis elegans GN K02F3.12 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|A8WK63|RECQ1_CAEBR
|
7 |
320 |
+ |
314 |
Gaps:3 |
50.97 |
618 |
43.49 |
1e-79 |
Putative ATP-dependent DNA helicase Q1 OS Caenorhabditis briggsae GN CBG24191 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8L840|RQL4A_ARATH
|
46 |
319 |
+ |
274 |
Gaps:5 |
22.81 |
1188 |
47.60 |
2e-75 |
ATP-dependent DNA helicase Q-like 4A OS Arabidopsis thaliana GN RECQL4A PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FT70|RQL4B_ARATH
|
46 |
332 |
+ |
287 |
Gaps:5 |
24.70 |
1150 |
45.77 |
2e-73 |
ATP-dependent DNA helicase Q-like 4B OS Arabidopsis thaliana GN RECQL4B PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9VGI8|BLM_DROME
|
75 |
319 |
+ |
245 |
Gaps:3 |
16.27 |
1487 |
50.83 |
2e-71 |
Bloom syndrome protein homolog OS Drosophila melanogaster GN Blm PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|129701
|
73 |
319 |
+ |
247 |
Gaps:9 |
50.64 |
470 |
53.36 |
5e-87 |
TIGR00614 recQ_fam ATP-dependent DNA helicase RecQ family. All proteins in this family for which functions are known are 3'-5' DNA-DNA helicases. These proteins are used for recombination recombinational repair and possibly maintenance of chromosome stability. This family is based on the phylogenomic analysis of JA Eisen (1999 Ph.D. Thesis Stanford University).
|
rpsblast_cdd |
gnl|CDD|178682
|
46 |
319 |
+ |
274 |
Gaps:5 |
22.68 |
1195 |
47.60 |
3e-76 |
PLN03137 PLN03137 ATP-dependent DNA helicase Q4-like Provisional.
|
rpsblast_cdd |
gnl|CDD|130456
|
74 |
319 |
+ |
246 |
Gaps:13 |
39.42 |
591 |
45.92 |
3e-72 |
TIGR01389 recQ ATP-dependent DNA helicase RecQ. The ATP-dependent DNA helicase RecQ of E. coli is about 600 residues long. This model represents bacterial proteins with a high degree of similarity in domain architecture and in primary sequence to E. coli RecQ. The model excludes eukaryotic and archaeal proteins with RecQ-like regions as well as more distantly related bacterial helicases related to RecQ.
|
rpsblast_cdd |
gnl|CDD|30860
|
73 |
320 |
+ |
248 |
Gaps:11 |
40.17 |
590 |
47.26 |
4e-72 |
COG0514 RecQ Superfamily II DNA helicase [DNA replication recombination and repair].
|