blastp_kegg |
lcl|rcu:RCOM_1081910
|
8 |
520 |
+ |
513 |
Gaps:14 |
84.54 |
621 |
75.05 |
0.0 |
alpha DNA polymerase putative
|
blastp_kegg |
lcl|vvi:100257984
|
8 |
520 |
+ |
513 |
Gaps:13 |
84.43 |
623 |
74.14 |
0.0 |
DNA polymerase alpha subunit B-like
|
blastp_kegg |
lcl|pop:POPTR_0010s06600g
|
8 |
520 |
+ |
513 |
Gaps:16 |
84.63 |
618 |
74.57 |
0.0 |
DNA polymerase alpha subunit B family protein
|
blastp_kegg |
lcl|pxb:103949897
|
8 |
520 |
+ |
513 |
Gaps:14 |
84.73 |
622 |
73.62 |
0.0 |
DNA polymerase alpha subunit B
|
blastp_kegg |
lcl|mdm:103452098
|
8 |
520 |
+ |
513 |
Gaps:13 |
84.70 |
621 |
74.52 |
0.0 |
DNA polymerase alpha subunit B
|
blastp_kegg |
lcl|tcc:TCM_010761
|
8 |
520 |
+ |
513 |
Gaps:13 |
84.70 |
621 |
72.43 |
0.0 |
DNA polymerase alpha 2
|
blastp_kegg |
lcl|mdm:103403125
|
8 |
520 |
+ |
513 |
Gaps:14 |
84.73 |
622 |
74.95 |
0.0 |
DNA polymerase alpha subunit B-like
|
blastp_kegg |
lcl|pmum:103321969
|
8 |
520 |
+ |
513 |
Gaps:17 |
84.70 |
621 |
77.76 |
0.0 |
DNA polymerase alpha subunit B
|
blastp_kegg |
lcl|fve:101297692
|
8 |
520 |
+ |
513 |
Gaps:17 |
84.52 |
620 |
74.81 |
0.0 |
DNA polymerase alpha subunit B-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa018609mg
|
8 |
520 |
+ |
513 |
Gaps:26 |
84.48 |
612 |
78.14 |
0.0 |
hypothetical protein
|
blastp_pdb |
3flo_G
|
118 |
504 |
+ |
387 |
Gaps:110 |
91.52 |
460 |
30.17 |
6e-41 |
mol:protein length:460 DNA polymerase alpha subunit B
|
blastp_pdb |
3flo_E
|
118 |
504 |
+ |
387 |
Gaps:110 |
91.52 |
460 |
30.17 |
6e-41 |
mol:protein length:460 DNA polymerase alpha subunit B
|
blastp_pdb |
3flo_C
|
118 |
504 |
+ |
387 |
Gaps:110 |
91.52 |
460 |
30.17 |
6e-41 |
mol:protein length:460 DNA polymerase alpha subunit B
|
blastp_pdb |
3flo_A
|
118 |
504 |
+ |
387 |
Gaps:110 |
91.52 |
460 |
30.17 |
6e-41 |
mol:protein length:460 DNA polymerase alpha subunit B
|
blastp_uniprot_sprot |
sp|Q14181|DPOA2_HUMAN
|
120 |
504 |
+ |
385 |
Gaps:49 |
61.20 |
598 |
36.89 |
1e-66 |
DNA polymerase alpha subunit B OS Homo sapiens GN POLA2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|P33611|DPOA2_MOUSE
|
156 |
504 |
+ |
349 |
Gaps:49 |
55.00 |
600 |
38.18 |
3e-65 |
DNA polymerase alpha subunit B OS Mus musculus GN Pola2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|O89043|DPOA2_RAT
|
113 |
515 |
+ |
403 |
Gaps:52 |
64.50 |
600 |
34.37 |
4e-63 |
DNA polymerase alpha subunit B OS Rattus norvegicus GN Pola2 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q58D13|DPOA2_BOVIN
|
113 |
469 |
+ |
357 |
Gaps:41 |
58.28 |
604 |
35.23 |
2e-59 |
DNA polymerase alpha subunit B OS Bos taurus GN POLA2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O74946|DPOA2_SCHPO
|
118 |
504 |
+ |
387 |
Gaps:60 |
67.07 |
574 |
35.84 |
3e-47 |
DNA polymerase alpha subunit B OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN pol12 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9VB62|DPOA2_DROME
|
119 |
504 |
+ |
386 |
Gaps:67 |
60.26 |
609 |
33.51 |
3e-43 |
DNA polymerase alpha subunit B OS Drosophila melanogaster GN DNApol-alpha73 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|P38121|DPOA2_YEAST
|
118 |
504 |
+ |
387 |
Gaps:110 |
59.72 |
705 |
30.17 |
3e-40 |
DNA polymerase alpha subunit B OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN POL12 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q21625|DPOA2_CAEEL
|
127 |
504 |
+ |
378 |
Gaps:66 |
64.03 |
581 |
27.69 |
4e-26 |
DNA polymerase alpha subunit B OS Caenorhabditis elegans GN div-1 PE 3 SV 3
|
blastp_uniprot_sprot |
sp|Q54S08|DPOA2_DICDI
|
89 |
504 |
+ |
416 |
Gaps:83 |
62.12 |
623 |
29.46 |
7e-21 |
DNA polymerase alpha subunit B OS Dictyostelium discoideum GN polA2 PE 3 SV 2
|
rpsblast_cdd |
gnl|CDD|34811
|
118 |
504 |
+ |
387 |
Gaps:65 |
67.13 |
581 |
30.77 |
3e-54 |
COG5214 POL12 DNA polymerase alpha-primase complex polymerase-associated subunit B [DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|202861
|
286 |
468 |
+ |
183 |
Gaps:28 |
100.00 |
189 |
29.63 |
4e-34 |
pfam04042 DNA_pol_E_B DNA polymerase alpha/epsilon subunit B. This family contains a number of DNA polymerase subunits. The B subunit of the DNA polymerase alpha plays an essential role at the initial stage of DNA replication in S. cerevisiae and is phosphorylated in a cell cycle-dependent manner. DNA polymerase epsilon is essential for cell viability and chromosomal DNA replication in budding yeast. In addition DNA polymerase epsilon may be involved in DNA repair and cell-cycle checkpoint control. The enzyme consists of at least four subunits in mammalian cells as well as in yeast. The largest subunit of DNA polymerase epsilon is responsible for polymerase epsilon is responsible for polymerase activity. In mouse the DNA polymerase epsilon subunit B is the second largest subunit of the DNA polymerase. A part of the N-terminal was found to be responsible for the interaction with SAP18. Experimental evidence suggests that this subunit may recruit histone deacetylase to the replication fork to modify the chromatin structure.
|
rpsblast_kog |
gnl|CDD|36838
|
9 |
506 |
+ |
498 |
Gaps:59 |
79.83 |
600 |
38.41 |
1e-114 |
KOG1625 KOG1625 KOG1625 DNA polymerase alpha-primase complex polymerase-associated subunit B [Replication recombination and repair].
|