blastp_kegg |
lcl|gmx:100813920
|
1 |
193 |
+ |
193 |
Gaps:23 |
58.86 |
367 |
69.44 |
3e-102 |
meiotic recombination protein SPO11-1-like
|
blastp_kegg |
lcl|pop:POPTR_0001s37540g
|
1 |
189 |
+ |
189 |
Gaps:23 |
58.08 |
365 |
72.17 |
6e-102 |
POPTRDRAFT_550198 DNA topoisomerase VIA family protein
|
blastp_kegg |
lcl|fve:101293370
|
1 |
195 |
+ |
195 |
Gaps:23 |
59.73 |
365 |
67.89 |
3e-100 |
meiotic recombination protein SPO11-1-like
|
blastp_kegg |
lcl|pmum:103342724
|
1 |
195 |
+ |
195 |
Gaps:23 |
59.73 |
365 |
68.81 |
4e-99 |
meiotic recombination protein SPO11-1
|
blastp_kegg |
lcl|vvi:100256655
|
1 |
190 |
+ |
190 |
Gaps:23 |
59.00 |
361 |
70.89 |
9e-99 |
meiotic recombination protein SPO11-1-like
|
blastp_kegg |
lcl|pxb:103941907
|
1 |
195 |
+ |
195 |
Gaps:24 |
59.84 |
366 |
68.04 |
3e-97 |
meiotic recombination protein SPO11-1-like
|
blastp_kegg |
lcl|pxb:103965437
|
1 |
195 |
+ |
195 |
Gaps:24 |
59.84 |
366 |
68.04 |
3e-97 |
meiotic recombination protein SPO11-1-like
|
blastp_kegg |
lcl|mdm:103448311
|
1 |
195 |
+ |
195 |
Gaps:23 |
59.73 |
365 |
68.35 |
4e-97 |
meiotic recombination protein SPO11-1
|
blastp_kegg |
lcl|pper:PRUPE_ppa006320mg
|
1 |
195 |
+ |
195 |
Gaps:23 |
52.28 |
417 |
68.35 |
6e-97 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_030659
|
1 |
182 |
+ |
182 |
Gaps:23 |
42.36 |
484 |
71.71 |
1e-96 |
Spo11/DNA topoisomerase VI
|
blastp_pdb |
2zbk_G
|
1 |
195 |
+ |
195 |
Gaps:44 |
57.84 |
389 |
31.56 |
6e-21 |
mol:protein length:389 Type II DNA topoisomerase VI subunit A
|
blastp_pdb |
2zbk_E
|
1 |
195 |
+ |
195 |
Gaps:44 |
57.84 |
389 |
31.56 |
6e-21 |
mol:protein length:389 Type II DNA topoisomerase VI subunit A
|
blastp_pdb |
2zbk_C
|
1 |
195 |
+ |
195 |
Gaps:44 |
57.84 |
389 |
31.56 |
6e-21 |
mol:protein length:389 Type II DNA topoisomerase VI subunit A
|
blastp_pdb |
2zbk_A
|
1 |
195 |
+ |
195 |
Gaps:44 |
57.84 |
389 |
31.56 |
6e-21 |
mol:protein length:389 Type II DNA topoisomerase VI subunit A
|
blastp_pdb |
1d3y_B
|
8 |
190 |
+ |
183 |
Gaps:28 |
67.44 |
301 |
29.06 |
2e-17 |
mol:protein length:301 DNA TOPOISOMERASE VI A SUBUNIT
|
blastp_pdb |
1d3y_A
|
8 |
190 |
+ |
183 |
Gaps:28 |
67.44 |
301 |
29.06 |
2e-17 |
mol:protein length:301 DNA TOPOISOMERASE VI A SUBUNIT
|
blastp_pdb |
2q2e_A
|
22 |
190 |
+ |
169 |
Gaps:28 |
50.68 |
369 |
22.46 |
9e-08 |
mol:protein length:369 Type II DNA topoisomerase VI subunit A
|
blastp_uniprot_sprot |
sp|Q9M4A2|SPO11_ARATH
|
1 |
193 |
+ |
193 |
Gaps:23 |
59.67 |
362 |
64.35 |
2e-93 |
Meiotic recombination protein SPO11-1 OS Arabidopsis thaliana GN SPO11-1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LZ03|TOP6A_ARATH
|
1 |
190 |
+ |
190 |
Gaps:24 |
49.65 |
427 |
36.79 |
1e-36 |
DNA topoisomerase 6 subunit A OS Arabidopsis thaliana GN TOP6A PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9Y5K1|SPO11_HUMAN
|
2 |
192 |
+ |
191 |
Gaps:27 |
54.04 |
396 |
35.05 |
1e-35 |
Meiotic recombination protein SPO11 OS Homo sapiens GN SPO11 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9WTK8|SPO11_MOUSE
|
2 |
192 |
+ |
191 |
Gaps:27 |
54.04 |
396 |
33.18 |
4e-35 |
Meiotic recombination protein SPO11 OS Mus musculus GN Spo11 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|A2XFC1|TOP6A_ORYSI
|
1 |
190 |
+ |
190 |
Gaps:24 |
47.96 |
442 |
35.38 |
2e-33 |
DNA topoisomerase 6 subunit A OS Oryza sativa subsp. indica GN TOP6A PE 2 SV 2
|
blastp_uniprot_sprot |
sp|A2BLE8|TOP6A_HYPBU
|
1 |
192 |
+ |
192 |
Gaps:48 |
57.36 |
387 |
31.53 |
1e-20 |
Type 2 DNA topoisomerase 6 subunit A OS Hyperthermus butylicus (strain DSM 5456 / JCM 9403) GN top6A PE 3 SV 1
|
blastp_uniprot_sprot |
sp|O05208|TOP6A_SULSH
|
1 |
195 |
+ |
195 |
Gaps:44 |
57.84 |
389 |
31.56 |
2e-20 |
Type 2 DNA topoisomerase 6 subunit A OS Sulfolobus shibatae GN top6A PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9YE67|TOP6A_AERPE
|
1 |
192 |
+ |
192 |
Gaps:47 |
57.33 |
389 |
29.60 |
4e-19 |
Type 2 DNA topoisomerase 6 subunit A OS Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) GN top6A PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q971T1|TOP6A_SULTO
|
34 |
195 |
+ |
162 |
Gaps:35 |
49.87 |
387 |
30.57 |
3e-18 |
Type 2 DNA topoisomerase 6 subunit A OS Sulfolobus tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) GN top6A PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9M4A1|SPO12_ARATH
|
39 |
195 |
+ |
157 |
Gaps:25 |
45.43 |
383 |
32.76 |
7e-17 |
Meiotic recombination protein SPO11-2 OS Arabidopsis thaliana GN SPO11-2 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|173774
|
40 |
179 |
+ |
140 |
Gaps:26 |
100.00 |
160 |
41.88 |
3e-38 |
cd00223 TOPRIM_TopoIIB_SPO TOPRIM_TopoIIB_SPO: topoisomerase-primase (TOPRIM) nucleotidyl transferase/hydrolase domain of the type found in the type IIB family of DNA topoisomerases and Spo11. This subgroup contains proteins similar to Sulfolobus shibatae topoisomerase VI (TopoVI) and Saccharomyces cerevisiae meiotic recombination factor: Spo11. Type II DNA topoisomerases catalyze the ATP-dependent transport of one DNA duplex through another in the process generating transient double strand breaks via covalent attachments to both DNA strands at the 5' positions. TopoVI enzymes are heterotetramers found in archaea and plants. Spo11 plays a role in generating the double strand breaks that initiate homologous recombination during meiosis. S. shibatae TopoVI relaxes both positive and negative supercoils and in addition has a strong decatenase activity. The TOPRIM domain has two conserved motifs one of which centers at a conserved glutamate and the other one at two conserved aspartates (DxD. For topoisomerases the conserved glutamate is believed to act as a general base in strand joining and as a general acid in strand cleavage. The DXD motif may co-ordinate Mg2+ a cofactor required for full catalytic function.
|
rpsblast_cdd |
gnl|CDD|179833
|
1 |
192 |
+ |
192 |
Gaps:32 |
57.77 |
367 |
30.66 |
2e-33 |
PRK04342 PRK04342 DNA topoisomerase VI subunit A Provisional.
|
rpsblast_cdd |
gnl|CDD|31883
|
1 |
189 |
+ |
189 |
Gaps:28 |
58.71 |
356 |
31.58 |
7e-27 |
COG1697 COG1697 DNA topoisomerase VI subunit A [DNA replication recombination and repair].
|