blastp_kegg |
lcl|aly:ARALYDRAFT_916071
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.02 |
767 |
74.73 |
0.0 |
DNA repair and transcription factor XPB1
|
blastp_kegg |
lcl|ath:AT5G41360
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.09 |
766 |
74.47 |
0.0 |
XPB2 DNA repair helicase XPB2
|
blastp_kegg |
lcl|eus:EUTSA_v10027651mg
|
3 |
347 |
+ |
345 |
Gaps:107 |
48.89 |
769 |
73.94 |
2e-178 |
hypothetical protein
|
blastp_kegg |
lcl|mus:103973317
|
3 |
347 |
+ |
345 |
Gaps:107 |
48.58 |
774 |
73.40 |
1e-176 |
DNA repair helicase XPB1-like
|
blastp_kegg |
lcl|crb:CARUB_v10004199mg
|
3 |
347 |
+ |
345 |
Gaps:107 |
48.96 |
768 |
73.94 |
3e-176 |
hypothetical protein
|
blastp_kegg |
lcl|pda:103706419
|
3 |
347 |
+ |
345 |
Gaps:107 |
48.89 |
769 |
73.40 |
3e-176 |
DNA repair helicase XPB1
|
blastp_kegg |
lcl|sita:101779540
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.15 |
765 |
73.14 |
7e-175 |
DNA repair helicase XPB1-like
|
blastp_kegg |
lcl|bdi:100822542
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.09 |
766 |
73.14 |
1e-174 |
DNA repair helicase XPB2-like
|
blastp_kegg |
lcl|ath:AT5G41370
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.02 |
767 |
75.53 |
8e-174 |
XPB1 DNA repair helicase XPB1
|
blastp_kegg |
lcl|brp:103864077
|
3 |
367 |
+ |
365 |
Gaps:107 |
51.63 |
767 |
72.22 |
1e-173 |
DNA repair helicase XPB1
|
blastp_pdb |
2fwr_D
|
3 |
336 |
+ |
334 |
Gaps:93 |
75.64 |
472 |
26.89 |
6e-13 |
mol:protein length:472 DNA repair protein RAD25
|
blastp_pdb |
2fwr_C
|
3 |
336 |
+ |
334 |
Gaps:93 |
75.64 |
472 |
26.89 |
6e-13 |
mol:protein length:472 DNA repair protein RAD25
|
blastp_pdb |
2fwr_B
|
3 |
336 |
+ |
334 |
Gaps:93 |
75.64 |
472 |
26.89 |
6e-13 |
mol:protein length:472 DNA repair protein RAD25
|
blastp_pdb |
2fwr_A
|
3 |
336 |
+ |
334 |
Gaps:93 |
75.64 |
472 |
26.89 |
6e-13 |
mol:protein length:472 DNA repair protein RAD25
|
blastp_pdb |
2fzl_A
|
208 |
331 |
+ |
124 |
Gaps:30 |
53.88 |
219 |
44.07 |
2e-10 |
mol:protein length:219 DNA repair protein RAD25 XPB
|
blastp_uniprot_sprot |
sp|Q9FUG4|XPB2_ARATH
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.09 |
766 |
74.47 |
0.0 |
DNA repair helicase XPB2 OS Arabidopsis thaliana GN XPB2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q38861|XPB1_ARATH
|
3 |
347 |
+ |
345 |
Gaps:107 |
49.02 |
767 |
75.53 |
3e-175 |
DNA repair helicase XPB1 OS Arabidopsis thaliana GN XPB1 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|O00835|ERCC3_DICDI
|
3 |
347 |
+ |
345 |
Gaps:115 |
46.00 |
800 |
55.43 |
1e-112 |
TFIIH basal transcription factor complex helicase repB subunit OS Dictyostelium discoideum GN repB PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5ZKK7|ERCC3_CHICK
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.57 |
788 |
51.50 |
3e-106 |
TFIIH basal transcription factor complex helicase XPB subunit OS Gallus gallus GN ERCC3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P19447|ERCC3_HUMAN
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.93 |
782 |
51.50 |
2e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Homo sapiens GN ERCC3 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q60HG1|ERCC3_MACFA
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.93 |
782 |
51.50 |
2e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Macaca fascicularis GN ERCC3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5RA62|ERCC3_PONAB
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.93 |
782 |
51.50 |
2e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Pongo abelii GN ERCC3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P49135|ERCC3_MOUSE
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.87 |
783 |
51.50 |
2e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Mus musculus GN Ercc3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q1RMT1|ERCC3_BOVIN
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.93 |
782 |
51.23 |
4e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Bos taurus GN ERCC3 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q4G005|ERCC3_RAT
|
3 |
347 |
+ |
345 |
Gaps:116 |
46.93 |
782 |
51.23 |
4e-105 |
TFIIH basal transcription factor complex helicase XPB subunit OS Rattus norvegicus GN Ercc3 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|161952
|
12 |
347 |
+ |
336 |
Gaps:115 |
49.04 |
732 |
59.89 |
1e-145 |
TIGR00603 rad25 DNA repair helicase rad25. All proteins in this family for which functions are known are DNA-DNA helicases used for the initiation of nucleotide excision repair and transacription 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|31261
|
10 |
349 |
+ |
340 |
Gaps:120 |
83.26 |
442 |
27.72 |
1e-37 |
COG1061 SSL2 DNA or RNA helicases of superfamily II [Transcription / DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|201125
|
250 |
308 |
+ |
59 |
Gaps:9 |
84.62 |
78 |
30.30 |
1e-08 |
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.
|
rpsblast_cdd |
gnl|CDD|28960
|
202 |
307 |
+ |
106 |
Gaps:15 |
89.31 |
131 |
26.50 |
3e-07 |
cd00079 HELICc Helicase superfamily c-terminal domain associated with DEXDc- DEAD- and DEAH-box proteins yeast initiation factor 4A Ski2p and Hepatitis C virus NS3 helicases this domain is found in a wide variety of helicases and helicase related proteins may not be an autonomously folding unit but an integral part of the helicase 4 helicase superfamilies at present according to the organization of their signature motifs all helicases share the ability to unwind nucleic acid duplexes with a distinct directional polarity they utilize the free energy from nucleoside triphosphate hydrolysis to fuel their translocation along DNA unwinding the duplex in the process.
|
rpsblast_cdd |
gnl|CDD|197757
|
250 |
308 |
+ |
59 |
Gaps:9 |
80.49 |
82 |
27.27 |
4e-07 |
smart00490 HELICc helicase superfamily c-terminal domain.
|