blastp_kegg |
lcl|mdm:103413515
|
204 |
660 |
+ |
457 |
Gaps:6 |
23.51 |
1952 |
71.68 |
0.0 |
callose synthase 1-like
|
blastp_kegg |
lcl|cic:CICLE_v10030476mg
|
267 |
659 |
+ |
393 |
Gaps:1 |
20.18 |
1952 |
79.70 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cit:102624514
|
267 |
659 |
+ |
393 |
Gaps:1 |
20.18 |
1952 |
79.70 |
0.0 |
callose synthase 2-like
|
blastp_kegg |
lcl|pxb:103954919
|
204 |
660 |
+ |
457 |
Gaps:6 |
23.51 |
1952 |
71.02 |
0.0 |
callose synthase 1
|
blastp_kegg |
lcl|pxb:103945817
|
217 |
660 |
+ |
444 |
Gaps:8 |
22.44 |
1952 |
73.74 |
0.0 |
callose synthase 1-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa000074mg
|
217 |
646 |
+ |
430 |
Gaps:8 |
21.71 |
1953 |
75.47 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|ath:AT2G31960
|
267 |
646 |
+ |
380 |
Gaps:1 |
19.54 |
1950 |
79.53 |
0.0 |
GSL03 glucan synthase-like 3
|
blastp_kegg |
lcl|brp:103867676
|
267 |
646 |
+ |
380 |
Gaps:1 |
19.50 |
1954 |
79.79 |
0.0 |
callose synthase 2
|
blastp_kegg |
lcl|eus:EUTSA_v10016125mg
|
267 |
646 |
+ |
380 |
Gaps:1 |
19.54 |
1950 |
79.53 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_040369
|
267 |
646 |
+ |
380 |
Gaps:2 |
76.55 |
499 |
76.18 |
0.0 |
Glucan synthase-like 12 isoform 1
|
blastp_uniprot_sprot |
sp|Q9SL03|CALS2_ARATH
|
267 |
646 |
+ |
380 |
Gaps:1 |
19.54 |
1950 |
79.53 |
0.0 |
Callose synthase 2 OS Arabidopsis thaliana GN CALS2 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q9AUE0|CALS1_ARATH
|
267 |
647 |
+ |
381 |
Gaps:1 |
19.59 |
1950 |
78.27 |
0.0 |
Callose synthase 1 OS Arabidopsis thaliana GN CALS1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9LXT9|CALS3_ARATH
|
267 |
636 |
+ |
370 |
Gaps:2 |
19.03 |
1955 |
77.69 |
0.0 |
Callose synthase 3 OS Arabidopsis thaliana GN CALS3 PE 2 SV 3
|
blastp_uniprot_sprot |
sp|Q3B724|CALS5_ARATH
|
206 |
633 |
+ |
428 |
Gaps:13 |
22.72 |
1923 |
53.32 |
3e-137 |
Callose synthase 5 OS Arabidopsis thaliana GN CALS5 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LTG5|CALS4_ARATH
|
291 |
646 |
+ |
356 |
Gaps:10 |
19.03 |
1871 |
57.87 |
7e-115 |
Callose synthase 4 OS Arabidopsis thaliana GN CALS4 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9LUD7|CALS8_ARATH
|
285 |
634 |
+ |
350 |
Gaps:17 |
17.16 |
1976 |
54.57 |
9e-104 |
Putative callose synthase 8 OS Arabidopsis thaliana GN CALS8 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|F4HW04|DPOE1_ARATH
|
709 |
901 |
+ |
193 |
Gaps:1 |
8.98 |
2161 |
81.96 |
5e-94 |
DNA polymerase epsilon catalytic subunit A OS Arabidopsis thaliana GN POL2A PE 1 SV 1
|
blastp_uniprot_sprot |
sp|F4IFN6|DPOE2_ARATH
|
709 |
901 |
+ |
193 |
none |
9.03 |
2138 |
78.76 |
2e-89 |
DNA polymerase epsilon catalytic subunit B OS Arabidopsis thaliana GN POL2B PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9FNB0|CHLH_ARATH
|
902 |
1113 |
+ |
212 |
Gaps:8 |
15.21 |
1381 |
78.10 |
1e-86 |
Magnesium-chelatase subunit ChlH chloroplastic OS Arabidopsis thaliana GN CHLH PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9LYS6|CALS6_ARATH
|
267 |
638 |
+ |
372 |
Gaps:21 |
19.63 |
1921 |
44.83 |
4e-85 |
Putative callose synthase 6 OS Arabidopsis thaliana GN CALS6 PE 3 SV 2
|
rpsblast_cdd |
gnl|CDD|178618
|
956 |
1113 |
+ |
158 |
Gaps:1 |
13.03 |
1220 |
75.47 |
2e-81 |
PLN03069 PLN03069 magnesiumprotoporphyrin-IX chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|206456
|
511 |
627 |
+ |
117 |
Gaps:6 |
100.00 |
113 |
54.87 |
5e-55 |
pfam14288 FKS1_dom1 1 3-beta-glucan synthase subunit FKS1 domain-1. The FKS1_dom1 domain is likely to be the 'Class I' region just N-terminal to the first set of transmembrane helices that is involved in 1 3-beta-glucan synthesis itself. This family is found on proteins with family Glucan_synthase pfam02364.
|
rpsblast_cdd |
gnl|CDD|183556
|
964 |
1113 |
+ |
150 |
Gaps:4 |
11.60 |
1310 |
46.05 |
2e-46 |
PRK12493 PRK12493 magnesium chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|152400
|
978 |
1115 |
+ |
138 |
Gaps:12 |
86.59 |
164 |
36.62 |
3e-34 |
pfam11965 DUF3479 Domain of unknown function (DUF3479). This presumed domain is functionally uncharacterized. This domain is found in bacteria archaea and eukaryotes. This domain is about 160 amino acids in length. This domain is found associated with pfam02514.
|
rpsblast_cdd |
gnl|CDD|99822
|
821 |
894 |
+ |
74 |
none |
36.27 |
204 |
71.62 |
5e-34 |
cd05779 DNA_polB_epsilon_exo DEDDy 3'-5' exonuclease domain of eukaryotic DNA polymerase epsilon a family-B DNA polymerase. The 3'-5' exonuclease domain of eukaryotic DNA polymerase epsilon. DNA polymerase epsilon is a family-B DNA polymerase with a catalytic subunit that contains a DEDDy-type DnaQ-like 3'-5' exonuclease domain. It is one of the three DNA-dependent type B DNA polymerases (alpha and delta are the other two) that have been identified as essential for nuclear DNA replication in eukaryotes. DNA polymerase epsilon plays a role in elongating the leading strand during DNA replication. It is also involved in DNA repair. The catalytic subunit contains both polymerase and 3'-5' exonuclease activities. The N-terminal exonuclease domain contains three sequence motifs termed ExoI ExoII and ExoIII with a specific YX(3)D pattern at ExoIII. These motifs are clustered around the active site and are involved in metal binding and catalysis. DNA polymerase epsilon also carries a unique large C-terminal domain with an unknown function. Phylogenetic analyses indicate that it is orthologous to the archaeal DNA polymerase B3 rather than to the eukaryotic alpha delta or zeta polymerases. The exonuclease domain of family-B polymerases contains a beta hairpin structure that plays an important role in active site switching in the event of nucleotide misincorporation.
|
rpsblast_cdd |
gnl|CDD|188195
|
979 |
1141 |
+ |
163 |
Gaps:2 |
13.15 |
1224 |
28.57 |
3e-25 |
TIGR02025 BchH magnesium chelatase H subunit. This model represents the H subunit of the magnesium chelatase complex responsible for magnesium insertion into the protoporphyrin IX ring in the biosynthesis of both chlorophyll and bacteriochlorophyll. In chlorophyll-utilizing species this gene is known as ChlH while in bacteriochlorophyll-utilizing spoecies it is called BchH. Subunit H is the largest (~140kDa) of the three subunits (the others being BchD/ChlD and BchI/ChlI) and is known to bind protoporphyrin IX. Subunit H is homologous to the CobN subunit of cobaltochelatase and by anology with that enzyme subunit H is believed to also bind the magnesium ion which is inserted into the ring. In conjunction with the hydrolysis of ATP by subunits I and D a conformation change is believed to happen in subunit H causing the magnesium ion insertion into the distorted protoporphyrin ring.
|
rpsblast_cdd |
gnl|CDD|202537
|
778 |
898 |
+ |
121 |
Gaps:27 |
51.97 |
254 |
30.30 |
5e-20 |
pfam03104 DNA_pol_B_exo1 DNA polymerase family B exonuclease domain. This domain has 3' to 5' exonuclease activity and adopts a ribonuclease H type fold.
|
rpsblast_cdd |
gnl|CDD|30766
|
770 |
875 |
+ |
106 |
Gaps:2 |
13.64 |
792 |
33.33 |
8e-15 |
COG0417 PolB DNA polymerase elongation subunit (family B) [DNA replication recombination and repair].
|
rpsblast_cdd |
gnl|CDD|165506
|
66 |
288 |
+ |
223 |
Gaps:181 |
20.82 |
3151 |
41.31 |
2e-13 |
PHA03247 PHA03247 large tegument protein UL36 Provisional.
|
rpsblast_cdd |
gnl|CDD|177580
|
65 |
309 |
+ |
245 |
Gaps:105 |
28.40 |
1352 |
38.28 |
1e-10 |
PHA03307 PHA03307 transcriptional regulator ICP4 Provisional.
|