blastp_kegg |
lcl|vvi:100244162
|
1 |
944 |
+ |
944 |
Gaps:17 |
97.75 |
977 |
81.15 |
0.0 |
eukaryotic translation initiation factor 3 subunit A-like
|
blastp_kegg |
lcl|gmx:100803796
|
1 |
948 |
+ |
948 |
Gaps:16 |
97.91 |
958 |
79.96 |
0.0 |
eukaryotic translation initiation factor 3 subunit A-like
|
blastp_kegg |
lcl|gmx:100782598
|
1 |
948 |
+ |
948 |
Gaps:17 |
97.91 |
957 |
80.04 |
0.0 |
eukaryotic translation initiation factor 3 subunit A-like
|
blastp_kegg |
lcl|pvu:PHAVU_001G169900g
|
1 |
948 |
+ |
948 |
Gaps:13 |
98.01 |
954 |
80.11 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103343795
|
1 |
975 |
+ |
975 |
Gaps:18 |
100.00 |
957 |
79.31 |
0.0 |
eukaryotic translation initiation factor 3 subunit A
|
blastp_kegg |
lcl|tcc:TCM_026722
|
1 |
972 |
+ |
972 |
Gaps:24 |
100.00 |
980 |
75.61 |
0.0 |
Eukaryotic translation initiation factor 3 subunit A
|
blastp_kegg |
lcl|rcu:RCOM_1434190
|
1 |
967 |
+ |
967 |
Gaps:42 |
99.90 |
994 |
74.42 |
0.0 |
Eukaryotic translation initiation factor 3 subunit putative
|
blastp_kegg |
lcl|mdm:103450881
|
1 |
971 |
+ |
971 |
Gaps:28 |
100.00 |
951 |
78.34 |
0.0 |
eukaryotic translation initiation factor 3 subunit A-like
|
blastp_kegg |
lcl|mtr:MTR_7g099920
|
1 |
940 |
+ |
940 |
Gaps:17 |
97.08 |
959 |
77.98 |
0.0 |
Eukaryotic translation initiation factor 3 subunit A
|
blastp_kegg |
lcl|csv:101230443
|
1 |
950 |
+ |
950 |
Gaps:11 |
98.25 |
970 |
76.81 |
0.0 |
eukaryotic translation initiation factor 3 subunit A-like
|
blastp_uniprot_sprot |
sp|Q40554|EIF3A_TOBAC
|
1 |
967 |
+ |
967 |
Gaps:16 |
99.90 |
958 |
74.19 |
0.0 |
Eukaryotic translation initiation factor 3 subunit A OS Nicotiana tabacum GN TIF3A1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q9LD55|EIF3A_ARATH
|
1 |
967 |
+ |
967 |
Gaps:18 |
99.39 |
987 |
70.34 |
0.0 |
Eukaryotic translation initiation factor 3 subunit A OS Arabidopsis thaliana GN TIF3A1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9XHR2|EIF3A_MAIZE
|
1 |
969 |
+ |
969 |
Gaps:54 |
98.44 |
962 |
66.95 |
0.0 |
Eukaryotic translation initiation factor 3 subunit A OS Zea mays GN TIF3A1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q6PCR7|EIF3A_DANRE
|
4 |
811 |
+ |
808 |
Gaps:53 |
64.48 |
1267 |
38.56 |
1e-157 |
Eukaryotic translation initiation factor 3 subunit A OS Danio rerio GN eif3a PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A4II09|EIF3A_XENTR
|
4 |
843 |
+ |
840 |
Gaps:64 |
61.39 |
1391 |
38.06 |
2e-157 |
Eukaryotic translation initiation factor 3 subunit A OS Xenopus tropicalis GN eif3a PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q1DXU0|EIF3A_COCIM
|
6 |
911 |
+ |
906 |
Gaps:153 |
94.36 |
1029 |
36.05 |
5e-156 |
Eukaryotic translation initiation factor 3 subunit A OS Coccidioides immitis (strain RS) GN TIF32 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|P23116|EIF3A_MOUSE
|
4 |
792 |
+ |
789 |
Gaps:58 |
59.15 |
1344 |
38.87 |
1e-155 |
Eukaryotic translation initiation factor 3 subunit A OS Mus musculus GN Eif3a PE 1 SV 5
|
blastp_uniprot_sprot |
sp|Q1JU68|EIF3A_RAT
|
4 |
792 |
+ |
789 |
Gaps:58 |
58.71 |
1354 |
38.87 |
2e-155 |
Eukaryotic translation initiation factor 3 subunit A OS Rattus norvegicus GN Eif3a PE 2 SV 2
|
blastp_uniprot_sprot |
sp|A2VD00|EIF3A_XENLA
|
4 |
843 |
+ |
840 |
Gaps:66 |
59.97 |
1424 |
37.59 |
1e-154 |
Eukaryotic translation initiation factor 3 subunit A OS Xenopus laevis GN eif3a PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q14152|EIF3A_HUMAN
|
4 |
778 |
+ |
775 |
Gaps:56 |
56.51 |
1382 |
38.80 |
3e-153 |
Eukaryotic translation initiation factor 3 subunit A OS Homo sapiens GN EIF3A PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|173412
|
543 |
871 |
+ |
329 |
Gaps:283 |
34.02 |
2084 |
63.47 |
1e-13 |
PTZ00121 PTZ00121 MAEBL Provisional.
|
rpsblast_cdd |
gnl|CDD|162740
|
553 |
882 |
+ |
330 |
Gaps:129 |
54.30 |
1164 |
37.97 |
1e-10 |
TIGR02169 SMC_prok_A chromosome segregation protein SMC primarily archaeal type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria archaea and eukaryotes. It is found in a single copy and is homodimeric in prokaryotes but six paralogs (excluded from this family) are found in eukarotes where SMC proteins are heterodimeric. This family represents the SMC protein of archaea and a few bacteria (Aquifex Synechocystis etc) the SMC of other bacteria is described by TIGR02168. The N- and C-terminal domains of this protein are well conserved but the central hinge region is skewed in composition and highly divergent.
|
rpsblast_cdd |
gnl|CDD|202246
|
553 |
864 |
+ |
312 |
Gaps:46 |
52.58 |
1162 |
23.24 |
2e-09 |
pfam02463 SMC_N RecF/RecN/SMC N terminal domain. This domain is found at the N terminus of SMC proteins. The SMC (structural maintenance of chromosomes) superfamily proteins have ATP-binding domains at the N- and C-termini and two extended coiled-coil domains separated by a hinge in the middle. The eukaryotic SMC proteins form two kind of heterodimers: the SMC1/SMC3 and the SMC2/SMC4 types. These heterodimers constitute an essential part of higher order complexes which are involved in chromatin and DNA dynamics. This family also includes the RecF and RecN proteins that are involved in DNA metabolism and recombination.
|
rpsblast_cdd |
gnl|CDD|162739
|
562 |
858 |
+ |
297 |
Gaps:66 |
48.26 |
1179 |
21.62 |
4e-09 |
TIGR02168 SMC_prok_B chromosome segregation protein SMC common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria archaea and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle.
|
rpsblast_cdd |
gnl|CDD|206039
|
582 |
850 |
+ |
269 |
Gaps:6 |
75.36 |
349 |
21.29 |
6e-09 |
pfam13868 Trichoplein Tumour suppressor Mitostatin. Trichoplein or mitostatin was first defined as a meiosis-specific nuclear structural protein. It has since been linked with mitochondrial movement. It is associated with the mitochondrial outer membrane and over-expression leads to reduction in mitochondrial motility whereas lack of it enhances mitochondrial movement. The activity appears to be mediated through binding the mitochondria to the actin intermediate filaments (IFs).
|
rpsblast_cdd |
gnl|CDD|31389
|
540 |
858 |
+ |
319 |
Gaps:47 |
56.32 |
1163 |
28.40 |
3e-08 |
COG1196 Smc Chromosome segregation ATPases [Cell division and chromosome partitioning].
|
rpsblast_cdd |
gnl|CDD|179675
|
559 |
848 |
+ |
290 |
Gaps:18 |
35.00 |
880 |
22.08 |
1e-07 |
PRK03918 PRK03918 chromosome segregation protein Provisional.
|
rpsblast_cdd |
gnl|CDD|30768
|
567 |
856 |
+ |
290 |
Gaps:5 |
32.49 |
908 |
20.00 |
1e-06 |
COG0419 SbcC ATPase involved in DNA repair [DNA replication recombination and repair].
|
rpsblast_kog |
gnl|CDD|37283
|
4 |
948 |
+ |
945 |
Gaps:61 |
96.96 |
988 |
43.74 |
0.0 |
KOG2072 KOG2072 KOG2072 Translation initiation factor 3 subunit a (eIF-3a) [Translation ribosomal structure and biogenesis].
|
rpsblast_kog |
gnl|CDD|35383
|
509 |
861 |
+ |
353 |
Gaps:178 |
43.16 |
1930 |
41.30 |
2e-09 |
KOG0161 KOG0161 KOG0161 Myosin class II heavy chain [Cytoskeleton].
|