blastp_kegg |
lcl|cic:CICLE_v10012027mg
|
12 |
383 |
+ |
372 |
Gaps:15 |
98.35 |
363 |
84.87 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102629303
|
12 |
383 |
+ |
372 |
Gaps:15 |
98.35 |
363 |
85.15 |
0.0 |
origin recognition complex subunit 2-like
|
blastp_kegg |
lcl|vvi:100253929
|
12 |
383 |
+ |
372 |
Gaps:16 |
98.34 |
362 |
82.58 |
0.0 |
origin recognition complex subunit 2-like
|
blastp_kegg |
lcl|tcc:TCM_021969
|
12 |
382 |
+ |
371 |
Gaps:16 |
98.34 |
361 |
83.94 |
0.0 |
Origin recognition complex second largest subunit 2
|
blastp_kegg |
lcl|pop:POPTR_0003s09350g
|
1 |
383 |
+ |
383 |
Gaps:20 |
100.00 |
363 |
82.09 |
0.0 |
Origin recognition complex subunit 2 family protein
|
blastp_kegg |
lcl|rcu:RCOM_1248790
|
5 |
383 |
+ |
379 |
Gaps:19 |
99.17 |
363 |
82.22 |
0.0 |
plant origin recognition complex subunit putative
|
blastp_kegg |
lcl|mdm:103441127
|
1 |
383 |
+ |
383 |
Gaps:21 |
100.00 |
362 |
79.83 |
0.0 |
origin recognition complex subunit 2
|
blastp_kegg |
lcl|csv:101204992
|
6 |
382 |
+ |
377 |
Gaps:18 |
99.72 |
360 |
78.83 |
0.0 |
origin recognition complex subunit 2-like
|
blastp_kegg |
lcl|cmo:103487905
|
6 |
382 |
+ |
377 |
Gaps:18 |
99.72 |
360 |
79.11 |
0.0 |
origin recognition complex subunit 2
|
blastp_kegg |
lcl|pmum:103320319
|
1 |
383 |
+ |
383 |
Gaps:23 |
100.00 |
360 |
79.44 |
0.0 |
origin recognition complex subunit 2
|
blastp_uniprot_sprot |
sp|Q38899|ORC2_ARATH
|
16 |
383 |
+ |
368 |
Gaps:16 |
96.97 |
363 |
74.15 |
0.0 |
Origin recognition complex subunit 2 OS Arabidopsis thaliana GN ORC2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q13416|ORC2_HUMAN
|
45 |
378 |
+ |
334 |
Gaps:30 |
52.69 |
577 |
38.49 |
2e-62 |
Origin recognition complex subunit 2 OS Homo sapiens GN ORC2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q75PQ8|ORC2_RAT
|
45 |
378 |
+ |
334 |
Gaps:30 |
52.78 |
576 |
36.84 |
5e-58 |
Origin recognition complex subunit 2 OS Rattus norvegicus GN Orc2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A6QNM3|ORC2_BOVIN
|
10 |
378 |
+ |
369 |
Gaps:40 |
58.75 |
577 |
36.87 |
7e-58 |
Origin recognition complex subunit 2 OS Bos taurus GN ORC2 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q60862|ORC2_MOUSE
|
45 |
378 |
+ |
334 |
Gaps:30 |
52.78 |
576 |
35.53 |
5e-55 |
Origin recognition complex subunit 2 OS Mus musculus GN Orc2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q91628|ORC2_XENLA
|
45 |
378 |
+ |
334 |
Gaps:30 |
54.48 |
558 |
35.86 |
3e-53 |
Origin recognition complex subunit 2 OS Xenopus laevis GN orc2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q24168|ORC2_DROME
|
60 |
380 |
+ |
321 |
Gaps:30 |
47.09 |
618 |
35.40 |
9e-48 |
Origin recognition complex subunit 2 OS Drosophila melanogaster GN Orc2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q09142|ORC2_SCHPO
|
9 |
381 |
+ |
373 |
Gaps:48 |
67.85 |
535 |
30.85 |
2e-35 |
Origin recognition complex subunit 2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN orc2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q55CU7|ORC2_DICDI
|
10 |
381 |
+ |
372 |
Gaps:60 |
98.72 |
391 |
29.53 |
9e-35 |
Origin recognition complex subunit 2 OS Dictyostelium discoideum GN orcB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P32833|ORC2_YEAST
|
73 |
381 |
+ |
309 |
Gaps:54 |
51.45 |
620 |
29.15 |
7e-32 |
Origin recognition complex subunit 2 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN ORC2 PE 1 SV 2
|
rpsblast_cdd |
gnl|CDD|202882
|
35 |
374 |
+ |
340 |
Gaps:30 |
100.00 |
318 |
41.19 |
4e-86 |
pfam04084 ORC2 Origin recognition complex subunit 2. All DNA replication initiation is driven by a single conserved eukaryotic initiator complex termed he origin recognition complex (ORC). The ORC is a six protein complex. The function of ORC is reviewed in.
|
rpsblast_cdd |
gnl|CDD|35134
|
33 |
378 |
+ |
346 |
Gaps:36 |
60.93 |
535 |
27.61 |
1e-36 |
COG5575 ORC2 Origin recognition complex subunit 2 [DNA replication recombination and repair].
|
rpsblast_kog |
gnl|CDD|38139
|
2 |
383 |
+ |
382 |
Gaps:34 |
68.73 |
518 |
41.57 |
2e-96 |
KOG2928 KOG2928 KOG2928 Origin recognition complex subunit 2 [Replication recombination and repair].
|