|
blastp_kegg |
lcl|rcu:RCOM_1504920
|
3 |
196 |
+ |
194 |
Gaps:39 |
56.36 |
385 |
69.59 |
1e-95 |
ribosomal pseudouridine synthase putative (EC:3.2.1.17)
|
|
blastp_kegg |
lcl|cam:101510279
|
1 |
191 |
+ |
191 |
Gaps:41 |
55.79 |
380 |
70.28 |
5e-95 |
RNA pseudourine synthase 7-like
|
|
blastp_kegg |
lcl|cmo:103502297
|
2 |
193 |
+ |
192 |
Gaps:37 |
55.36 |
392 |
68.20 |
8e-95 |
RNA pseudouridine synthase 7
|
|
blastp_kegg |
lcl|mtr:MTR_3g098940
|
1 |
191 |
+ |
191 |
Gaps:41 |
55.79 |
380 |
69.81 |
2e-93 |
RNA pseudourine synthase
|
|
blastp_kegg |
lcl|vvi:100255954
|
3 |
191 |
+ |
189 |
Gaps:41 |
54.40 |
386 |
70.95 |
3e-93 |
RNA pseudourine synthase 7-like
|
|
blastp_kegg |
lcl|pvu:PHAVU_009G162600g
|
3 |
191 |
+ |
189 |
Gaps:41 |
55.41 |
379 |
70.00 |
4e-93 |
hypothetical protein
|
|
blastp_kegg |
lcl|gmx:100811500
|
3 |
191 |
+ |
189 |
Gaps:40 |
55.38 |
381 |
70.14 |
8e-93 |
RNA pseudourine synthase 7-like
|
|
blastp_kegg |
lcl|pop:POPTR_0015s11340g
|
3 |
196 |
+ |
194 |
Gaps:36 |
56.70 |
388 |
65.91 |
2e-92 |
POPTRDRAFT_776329 hypothetical protein
|
|
blastp_kegg |
lcl|csv:101221837
|
2 |
193 |
+ |
192 |
Gaps:35 |
55.73 |
393 |
66.21 |
5e-92 |
RNA pseudourine synthase 7-like
|
|
blastp_kegg |
lcl|fve:101293481
|
20 |
193 |
+ |
174 |
Gaps:31 |
53.52 |
383 |
67.32 |
3e-91 |
RNA pseudourine synthase 7-like
|
|
blastp_uniprot_sprot |
sp|Q0E0Y3|PUS7_ORYSJ
|
24 |
191 |
+ |
168 |
Gaps:31 |
50.64 |
393 |
63.82 |
2e-84 |
RNA pseudouridine synthase 7 OS Oryza sativa subsp. japonica GN Os02g0512300 PE 2 SV 2
|
|
blastp_uniprot_sprot |
sp|Q9LU60|PUS7_ARATH
|
3 |
191 |
+ |
189 |
Gaps:41 |
58.23 |
395 |
58.70 |
2e-79 |
RNA pseudouridine synthase 7 OS Arabidopsis thaliana GN At5g51140 PE 2 SV 1
|
|
blastp_uniprot_sprot |
sp|Q8IZ73|RUSD2_HUMAN
|
38 |
191 |
+ |
154 |
Gaps:32 |
34.13 |
545 |
33.33 |
1e-28 |
RNA pseudouridylate synthase domain-containing protein 2 OS Homo sapiens GN RPUSD2 PE 1 SV 2
|
|
blastp_uniprot_sprot |
sp|Q149F1|RUSD2_MOUSE
|
38 |
191 |
+ |
154 |
Gaps:32 |
33.63 |
553 |
33.33 |
1e-28 |
RNA pseudouridylate synthase domain-containing protein 2 OS Mus musculus GN Rpusd2 PE 2 SV 2
|
|
blastp_uniprot_sprot |
sp|O16686|YK27_CAEEL
|
43 |
193 |
+ |
151 |
Gaps:11 |
37.50 |
432 |
37.65 |
7e-28 |
Uncharacterized protein K07E8.7 OS Caenorhabditis elegans GN K07E8.7 PE 3 SV 1
|
|
blastp_uniprot_sprot |
sp|Q12069|PUS9_YEAST
|
60 |
191 |
+ |
132 |
Gaps:4 |
29.44 |
462 |
37.50 |
8e-27 |
tRNA pseudouridine(32) synthase mitochondrial OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN PUS9 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q09709|YA32_SCHPO
|
31 |
193 |
+ |
163 |
Gaps:32 |
49.49 |
394 |
29.74 |
9e-25 |
Uncharacterized protein C18B11.02c OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN SPAC18B11.02c PE 3 SV 1
|
|
blastp_uniprot_sprot |
sp|Q12362|RIB2_YEAST
|
64 |
188 |
+ |
125 |
Gaps:4 |
21.83 |
591 |
37.98 |
1e-22 |
Bifunctional protein RIB2 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN RIB2 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|P53294|PUS6_YEAST
|
41 |
191 |
+ |
151 |
Gaps:50 |
49.75 |
404 |
28.86 |
1e-17 |
tRNA pseudouridine(31) synthase OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN PUS6 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|P72970|Y1592_SYNY3
|
61 |
185 |
+ |
125 |
Gaps:6 |
44.33 |
291 |
28.68 |
5e-09 |
Uncharacterized RNA pseudouridine synthase slr1592 OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN slr1592 PE 3 SV 1
|
|
rpsblast_cdd |
gnl|CDD|211331
|
86 |
191 |
+ |
106 |
Gaps:5 |
52.11 |
213 |
44.14 |
8e-37 |
cd02557 PseudoU_synth_ScRIB2 Pseudouridine synthases similar to Saccharomyces cerevisiae RIB2. Pseudouridine synthase Saccharomyces cerevisiae RIB2_like. This group is comprised of eukaryotic and bacterial proteins similar to Saccharomyces cerevisiae RIB2 S. cerevisiae Pus6p and human hRPUDSD2. S. cerevisiae RIB2 displays two distinct catalytic activities. The N-terminal domain of RIB2 is RNA:psi-synthase which makes psi32 on cytoplasmic tRNAs. Psi32 is highly phylogenetically conserved. The C-terminal domain of RIB2 has a DRAP deaminase activity which catalyses the formation of 5-amino-6-ribitylamino-2 4(1H 3H)-pyrimidinedione 5'-phosphate from 2 5-diamino-6-ribitylamino-4(3H)-pyrimidinone 5'-phosphate during riboflavin biosynthesis. S. cerevisiae Pus6p makes the psi31 of cytoplasmic and mitochondrial tRNAs.
|
|
rpsblast_cdd |
gnl|CDD|30910
|
60 |
193 |
+ |
134 |
Gaps:11 |
50.17 |
289 |
30.34 |
7e-17 |
COG0564 RluA Pseudouridylate synthases 23S RNA-specific [Translation ribosomal structure and biogenesis].
|
|
rpsblast_cdd |
gnl|CDD|161659
|
48 |
188 |
+ |
141 |
Gaps:19 |
49.50 |
299 |
27.03 |
1e-16 |
TIGR00005 rluA_subfam pseudouridine synthase RluA family. In E. coli RluD (SfhB) modifies uridine to pseudouridine at 23S RNA U1911 1915 and 1917 RluC modifies 955 2504 and 2580 and RluA modifies U746 and tRNA U32. An additional homolog from E. coli outside this family TruC modifies uracil-65 in transfer RNAs to pseudouridine.
|
|
rpsblast_cdd |
gnl|CDD|211346
|
115 |
193 |
+ |
79 |
Gaps:9 |
47.57 |
185 |
36.36 |
3e-12 |
cd02869 PseudoU_synth_RluCD_like Pseudouridine synthase RsuA/RluD family. This group is comprised of eukaryotic bacterial and archeal proteins similar to eight site specific Escherichia coli pseudouridine synthases: RsuA RluA RluB RluC RluD RluE RluF and TruA. Pseudouridine synthases catalyze the isomerization of specific uridines in a n RNA molecule to pseudouridines (5-ribosyluracil psi) requiring no cofactors. E. coli RluC for example makes psi955 2504 and 2580 in 23S RNA. Some psi sites such as psi1917 in 23S RNA made by RluD are universally conserved. Other psi sites occur in a more restricted fashion for example psi2819 in 21S mitochondrial ribosomal RNA made by S. cerevisiae Pus5p is only found in mitochondrial large subunit rRNAs from some other species and in gram negative bacteria. The E. coli counterpart of this psi residue is psi2580 in 23S rRNA. psi2604in 23S RNA made by RluF has only been detected in E.coli.
|
|
rpsblast_cdd |
gnl|CDD|201472
|
110 |
195 |
+ |
86 |
Gaps:6 |
61.74 |
149 |
31.52 |
2e-10 |
pfam00849 PseudoU_synth_2 RNA pseudouridylate synthase. Members of this family are involved in modifying bases in RNA molecules. They carry out the conversion of uracil bases to pseudouridine. This family includes RluD a pseudouridylate synthase that converts specific uracils to pseudouridine in 23S rRNA. RluA from E. coli converts bases in both rRNA and tRNA.
|
|
rpsblast_cdd |
gnl|CDD|211332
|
69 |
181 |
+ |
113 |
Gaps:11 |
47.97 |
246 |
26.27 |
1e-09 |
cd02558 PSRA_1 Pseudouridine synthase a subgroup of the RluA family. This group is comprised of bacterial proteins assigned to the RluA family of pseudouridine synthases. Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil psi). No cofactors are required. The RluA family is comprised of proteins related to Escherichia coli RluA.
|
|
rpsblast_kog |
gnl|CDD|37130
|
36 |
194 |
+ |
159 |
Gaps:32 |
51.48 |
371 |
37.70 |
7e-38 |
KOG1919 KOG1919 KOG1919 RNA pseudouridylate synthases [RNA processing and modification].
|