blastp_kegg |
lcl|pper:PRUPE_ppa001035mg
|
1 |
394 |
+ |
394 |
Gaps:83 |
42.93 |
927 |
73.12 |
3e-123 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103341595
|
1 |
394 |
+ |
394 |
Gaps:83 |
41.48 |
962 |
72.93 |
4e-123 |
uncharacterized LOC103341595
|
blastp_kegg |
lcl|pop:POPTR_0010s12280g
|
1 |
394 |
+ |
394 |
Gaps:83 |
44.03 |
888 |
74.17 |
5e-123 |
POPTRDRAFT_726887 ATP-dependent DNA helicase family protein
|
blastp_kegg |
lcl|mtr:MTR_1g031120
|
7 |
291 |
+ |
285 |
Gaps:24 |
67.36 |
432 |
66.32 |
4e-122 |
ATP-dependent DNA helicase recG
|
blastp_kegg |
lcl|mtr:MTR_3g079900
|
7 |
291 |
+ |
285 |
Gaps:24 |
68.96 |
422 |
66.32 |
7e-122 |
ATP-dependent DNA helicase recG
|
blastp_kegg |
lcl|cic:CICLE_v10017747mg
|
1 |
394 |
+ |
394 |
Gaps:81 |
42.45 |
874 |
75.74 |
2e-121 |
hypothetical protein
|
blastp_kegg |
lcl|pvu:PHAVU_003G032900g
|
10 |
394 |
+ |
385 |
Gaps:81 |
64.64 |
560 |
74.03 |
1e-120 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102606824
|
1 |
394 |
+ |
394 |
Gaps:81 |
38.53 |
963 |
75.74 |
2e-120 |
uncharacterized LOC102606824
|
blastp_kegg |
lcl|mdm:103402596
|
1 |
394 |
+ |
394 |
Gaps:83 |
38.84 |
999 |
73.20 |
4e-120 |
uncharacterized LOC103402596
|
blastp_kegg |
lcl|pxb:103948642
|
1 |
394 |
+ |
394 |
Gaps:83 |
41.95 |
925 |
72.68 |
1e-119 |
uncharacterized LOC103948642
|
blastp_pdb |
1gm5_A
|
21 |
394 |
+ |
374 |
Gaps:78 |
44.62 |
780 |
38.51 |
1e-32 |
mol:protein length:780 RECG
|
blastp_pdb |
2eyq_B
|
20 |
268 |
+ |
249 |
Gaps:80 |
18.85 |
1151 |
34.10 |
3e-17 |
mol:protein length:1151 Transcription-repair coupling factor
|
blastp_pdb |
2eyq_A
|
20 |
268 |
+ |
249 |
Gaps:80 |
18.85 |
1151 |
34.10 |
3e-17 |
mol:protein length:1151 Transcription-repair coupling factor
|
blastp_uniprot_sprot |
sp|Q55681|RECG_SYNY3
|
10 |
394 |
+ |
385 |
Gaps:78 |
41.16 |
831 |
44.74 |
1e-44 |
ATP-dependent DNA helicase RecG OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O34942|RECG_BACSU
|
18 |
394 |
+ |
377 |
Gaps:85 |
49.41 |
682 |
37.39 |
2e-36 |
ATP-dependent DNA helicase RecG OS Bacillus subtilis (strain 168) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q54900|RECG_STRPN
|
11 |
294 |
+ |
284 |
Gaps:67 |
37.41 |
671 |
39.04 |
3e-36 |
ATP-dependent DNA helicase RecG OS Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) GN recG PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q5HGK6|RECG_STAAC
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
36.90 |
7e-35 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain COL) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O50581|RECG_STAA8
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
36.90 |
7e-35 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain NCTC 8325) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q8NX11|RECG_STAAW
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
37.20 |
1e-34 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain MW2) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6G9Y6|RECG_STAAS
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
37.20 |
1e-34 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain MSSA476) GN recG PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P64325|RECG_STAAN
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
37.20 |
1e-34 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain N315) GN recG PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P64324|RECG_STAAM
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
37.20 |
1e-34 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain Mu50 / ATCC 700699) GN recG PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6GHK8|RECG_STAAR
|
19 |
394 |
+ |
376 |
Gaps:73 |
48.98 |
686 |
37.20 |
1e-34 |
ATP-dependent DNA helicase RecG OS Staphylococcus aureus (strain MRSA252) GN recG PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|161975
|
10 |
394 |
+ |
385 |
Gaps:79 |
54.76 |
630 |
46.38 |
2e-75 |
TIGR00643 recG ATP-dependent DNA helicase RecG.
|
rpsblast_cdd |
gnl|CDD|182836
|
10 |
394 |
+ |
385 |
Gaps:83 |
52.42 |
681 |
42.58 |
4e-68 |
PRK10917 PRK10917 ATP-dependent DNA helicase RecG Provisional.
|
rpsblast_cdd |
gnl|CDD|31393
|
10 |
394 |
+ |
385 |
Gaps:79 |
53.91 |
677 |
40.82 |
8e-60 |
COG1200 RecG RecG-like helicase [DNA replication recombination and repair / Transcription].
|
rpsblast_cdd |
gnl|CDD|161938
|
19 |
268 |
+ |
250 |
Gaps:80 |
23.54 |
926 |
36.24 |
7e-30 |
TIGR00580 mfd transcription-repair coupling factor (mfd). All proteins in this family for which functions are known are DNA-dependent ATPases that function in the process of transcription-coupled DNA repair in which the repair of the transcribed strand of actively transcribed genes is repaired at a higher rate than the repair of non-transcribed regions of the genome and than the non-transcribed strand of the same gene. This family is based on the phylogenomic analysis of JA Eisen (1999 Ph.D. Thesis Stanford University). This family is closely related to the RecG and UvrB families.
|
rpsblast_cdd |
gnl|CDD|31390
|
19 |
268 |
+ |
250 |
Gaps:84 |
19.14 |
1139 |
34.86 |
2e-29 |
COG1197 Mfd Transcription-repair coupling factor (superfamily II helicase) [DNA replication recombination and repair / Transcription].
|
rpsblast_cdd |
gnl|CDD|182649
|
20 |
268 |
+ |
249 |
Gaps:100 |
18.92 |
1147 |
36.41 |
1e-17 |
PRK10689 PRK10689 transcription-repair coupling factor Provisional.
|
rpsblast_cdd |
gnl|CDD|201125
|
156 |
224 |
+ |
69 |
Gaps:1 |
87.18 |
78 |
27.94 |
7e-10 |
pfam00271 Helicase_C Helicase conserved C-terminal domain. The Prosite family is restricted to DEAD/H helicases whereas this domain family is found in a wide variety of helicases and helicase related proteins. It may be that this is not an autonomously folding unit but an integral part of the helicase.
|