blastp_kegg |
lcl|vvi:100241865
|
5 |
225 |
+ |
221 |
Gaps:4 |
51.25 |
439 |
81.33 |
8e-132 |
DNA polymerase delta small subunit-like
|
blastp_kegg |
lcl|pmum:103339416
|
5 |
225 |
+ |
221 |
Gaps:4 |
51.02 |
441 |
80.44 |
1e-129 |
DNA polymerase delta small subunit
|
blastp_kegg |
lcl|tcc:TCM_024908
|
5 |
225 |
+ |
221 |
Gaps:4 |
50.90 |
442 |
79.11 |
3e-129 |
DNA polymerase delta small subunit isoform 1
|
blastp_kegg |
lcl|pper:PRUPE_ppa005894mg
|
5 |
225 |
+ |
221 |
Gaps:4 |
51.37 |
438 |
80.00 |
6e-129 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103958951
|
5 |
225 |
+ |
221 |
Gaps:4 |
50.90 |
442 |
79.11 |
5e-127 |
DNA polymerase delta small subunit
|
blastp_kegg |
lcl|mdm:103421761
|
5 |
225 |
+ |
221 |
Gaps:4 |
58.29 |
386 |
78.22 |
1e-126 |
DNA polymerase delta small subunit-like
|
blastp_kegg |
lcl|mdm:103411519
|
5 |
225 |
+ |
221 |
Gaps:4 |
55.42 |
406 |
78.22 |
9e-126 |
DNA polymerase delta small subunit-like
|
blastp_kegg |
lcl|mdm:103454327
|
5 |
225 |
+ |
221 |
Gaps:4 |
74.50 |
302 |
77.33 |
1e-125 |
DNA polymerase delta small subunit
|
blastp_kegg |
lcl|mdm:103429235
|
5 |
225 |
+ |
221 |
Gaps:4 |
50.90 |
442 |
78.22 |
2e-125 |
DNA polymerase delta small subunit-like
|
blastp_kegg |
lcl|cmo:103486765
|
5 |
224 |
+ |
220 |
Gaps:4 |
50.91 |
440 |
77.23 |
8e-125 |
DNA polymerase delta small subunit
|
blastp_pdb |
3e0j_G
|
23 |
219 |
+ |
197 |
none |
41.39 |
476 |
48.22 |
6e-64 |
mol:protein length:476 DNA polymerase subunit delta-2
|
blastp_pdb |
3e0j_E
|
23 |
219 |
+ |
197 |
none |
41.39 |
476 |
48.22 |
6e-64 |
mol:protein length:476 DNA polymerase subunit delta-2
|
blastp_pdb |
3e0j_C
|
23 |
219 |
+ |
197 |
none |
41.39 |
476 |
48.22 |
6e-64 |
mol:protein length:476 DNA polymerase subunit delta-2
|
blastp_pdb |
3e0j_A
|
23 |
219 |
+ |
197 |
none |
41.39 |
476 |
48.22 |
6e-64 |
mol:protein length:476 DNA polymerase subunit delta-2
|
blastp_uniprot_sprot |
sp|O48520|DPOD2_ARATH
|
5 |
224 |
+ |
220 |
Gaps:4 |
50.91 |
440 |
75.89 |
5e-121 |
DNA polymerase delta small subunit OS Arabidopsis thaliana GN POLD2 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9LRE5|DPOD2_ORYSJ
|
6 |
225 |
+ |
220 |
Gaps:4 |
52.21 |
429 |
68.75 |
4e-113 |
DNA polymerase delta small subunit OS Oryza sativa subsp. japonica GN POLD2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O93610|DPOD2_XENLA
|
23 |
219 |
+ |
197 |
none |
42.55 |
463 |
48.73 |
2e-64 |
DNA polymerase delta subunit 2 OS Xenopus laevis GN pold2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O35654|DPOD2_MOUSE
|
23 |
220 |
+ |
198 |
none |
42.22 |
469 |
47.98 |
3e-64 |
DNA polymerase delta subunit 2 OS Mus musculus GN Pold2 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|P49005|DPOD2_HUMAN
|
23 |
219 |
+ |
197 |
none |
42.00 |
469 |
48.22 |
2e-63 |
DNA polymerase delta subunit 2 OS Homo sapiens GN POLD2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6AXY4|DPOD2_RAT
|
23 |
220 |
+ |
198 |
none |
42.22 |
469 |
47.98 |
2e-63 |
DNA polymerase delta subunit 2 OS Rattus norvegicus GN Pold2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P49004|DPOD2_BOVIN
|
23 |
219 |
+ |
197 |
none |
42.00 |
469 |
48.22 |
3e-63 |
DNA polymerase delta subunit 2 OS Bos taurus GN POLD2 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9W088|DPOD2_DROME
|
41 |
222 |
+ |
182 |
none |
42.23 |
431 |
43.96 |
4e-55 |
DNA polymerase delta small subunit OS Drosophila melanogaster GN CG12018 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P87324|DPOD2_SCHPO
|
42 |
219 |
+ |
178 |
Gaps:3 |
38.74 |
462 |
40.22 |
6e-39 |
DNA polymerase subunit delta-2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN cdc1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|P46957|DPOD2_YEAST
|
30 |
219 |
+ |
190 |
Gaps:31 |
44.97 |
487 |
34.70 |
1e-37 |
DNA polymerase delta small subunit OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN POL31 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|163630
|
28 |
219 |
+ |
192 |
none |
74.71 |
257 |
58.33 |
5e-89 |
cd07387 MPP_PolD2_C PolD2 (DNA polymerase delta subunit 2) C-terminal domain. PolD2 (DNA polymerase delta subunit 2) is an auxiliary subunit of the eukaryotic DNA polymerase delta (PolD) complex thought to play a regulatory role and to serve as a scaffold for PolD assembly by interacting simultaneously with all of the other three subunits. PolD2 is catalytically inactive and lacks the active site residues required for phosphoesterase activity in other members of this superfamily. PolD2 is also involved in the recruitment of several proteins regulating DNA metabolism including p21 PDIP1 PDIP38 PDIP46 and WRN. Human PolD consists of four subunits: p125 (PolD1) p50 (PolD2) p66(PolD3) and p12(PolD4). PolD is one of three major replicases in eukaryotes. PolD also plays an essential role in translesion DNA synthesis homologous recombination and DNA repair. Within the PolD complex PolD2 tightly associates with PolD3. PolD2 belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse but share a conserved domain with an active site consisting of two metal ions (usually manganese iron or zinc) coordinated with octahedral geometry by a cage of histidine aspartate and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases Dbr1-like RNA lariat debranching enzymes YfcE-like phosphodiesterases purple acid phosphatases (PAPs) YbbF-like UDP-2 3-diacylglucosamine hydrolases and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.
|
rpsblast_cdd |
gnl|CDD|202861
|
23 |
177 |
+ |
155 |
Gaps:6 |
85.19 |
189 |
36.02 |
1e-37 |
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_cdd |
gnl|CDD|31502
|
41 |
222 |
+ |
182 |
Gaps:13 |
37.63 |
481 |
30.39 |
2e-26 |
COG1311 HYS2 Archaeal DNA polymerase II small subunit/DNA polymerase delta subunit B [DNA replication recombination and repair].
|
rpsblast_kog |
gnl|CDD|37943
|
30 |
219 |
+ |
190 |
Gaps:2 |
43.68 |
435 |
55.26 |
7e-73 |
KOG2732 KOG2732 KOG2732 DNA polymerase delta regulatory subunit 55 [Replication recombination and repair].
|