blastp_kegg |
lcl|pmum:103326371
|
31 |
569 |
+ |
539 |
Gaps:14 |
93.94 |
578 |
76.24 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial
|
blastp_kegg |
lcl|pper:PRUPE_ppa003402mg
|
31 |
569 |
+ |
539 |
Gaps:14 |
94.11 |
577 |
76.24 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103954011
|
2 |
570 |
+ |
569 |
Gaps:18 |
99.48 |
580 |
73.31 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial-like
|
blastp_kegg |
lcl|pxb:103964049
|
2 |
569 |
+ |
568 |
Gaps:34 |
99.65 |
578 |
73.09 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial-like
|
blastp_kegg |
lcl|mdm:103452438
|
35 |
569 |
+ |
535 |
Gaps:11 |
92.39 |
578 |
76.97 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial
|
blastp_kegg |
lcl|cam:101503230
|
52 |
577 |
+ |
526 |
Gaps:16 |
89.41 |
595 |
75.56 |
0.0 |
uncharacterized LOC101503230
|
blastp_kegg |
lcl|csv:101217981
|
3 |
573 |
+ |
571 |
Gaps:17 |
100.00 |
566 |
70.85 |
0.0 |
uncharacterized LOC101217981
|
blastp_kegg |
lcl|vvi:100244919
|
4 |
568 |
+ |
565 |
Gaps:20 |
97.77 |
584 |
71.10 |
0.0 |
uncharacterized LOC100244919
|
blastp_kegg |
lcl|cmo:103491566
|
3 |
573 |
+ |
571 |
Gaps:17 |
100.00 |
566 |
70.32 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial
|
blastp_kegg |
lcl|gmx:100787200
|
3 |
581 |
+ |
579 |
Gaps:24 |
99.83 |
592 |
70.05 |
0.0 |
NO-associated protein 1 chloroplastic/mitochondrial-like
|
blastp_pdb |
3h2y_A
|
128 |
525 |
+ |
398 |
Gaps:42 |
97.28 |
368 |
32.96 |
4e-42 |
mol:protein length:368 GTPase family protein
|
blastp_pdb |
3ec1_B
|
128 |
525 |
+ |
398 |
Gaps:45 |
97.29 |
369 |
33.43 |
3e-40 |
mol:protein length:369 YqeH GTPase
|
blastp_pdb |
3ec1_A
|
128 |
525 |
+ |
398 |
Gaps:45 |
97.29 |
369 |
33.43 |
3e-40 |
mol:protein length:369 YqeH GTPase
|
blastp_uniprot_sprot |
sp|P54453|YQEH_BACSU
|
128 |
525 |
+ |
398 |
Gaps:65 |
97.54 |
366 |
36.13 |
3e-42 |
Uncharacterized protein YqeH OS Bacillus subtilis (strain 168) GN yqeH PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q6YPG5|NOS_ORYSJ
|
72 |
500 |
+ |
429 |
Gaps:79 |
70.20 |
547 |
27.86 |
6e-25 |
Putative nitric oxide synthase OS Oryza sativa subsp. japonica GN Os02g0104700 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q66GP9|NOA1_ARATH
|
149 |
500 |
+ |
352 |
Gaps:46 |
63.10 |
561 |
27.12 |
1e-24 |
NO-associated protein 1 chloroplastic/mitochondrial OS Arabidopsis thaliana GN NOA1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9JJG9|NOA1_MOUSE
|
363 |
527 |
+ |
165 |
Gaps:5 |
24.24 |
693 |
29.76 |
9e-12 |
Nitric oxide-associated protein 1 OS Mus musculus GN Noa1 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q32LB9|NOA1_BOVIN
|
363 |
527 |
+ |
165 |
Gaps:6 |
24.35 |
694 |
30.18 |
2e-11 |
Nitric oxide-associated protein 1 OS Bos taurus GN NOA1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8NC60|NOA1_HUMAN
|
278 |
561 |
+ |
284 |
Gaps:22 |
54.73 |
698 |
27.49 |
6e-10 |
Nitric oxide-associated protein 1 OS Homo sapiens GN NOA1 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|C4QZZ7|GEP3_PICPG
|
70 |
397 |
+ |
328 |
Gaps:62 |
51.74 |
576 |
27.85 |
2e-08 |
Genetic interactor of prohibitins 3 mitochondrial OS Komagataella pastoris (strain GS115 / ATCC 20864) GN GEP3 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q09700|YA29_SCHPO
|
153 |
422 |
+ |
270 |
Gaps:66 |
51.32 |
491 |
28.57 |
3e-06 |
Uncharacterized protein C2F7.09c OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN SPAC2F7.09c PE 4 SV 1
|
rpsblast_cdd |
gnl|CDD|184332
|
76 |
525 |
+ |
450 |
Gaps:85 |
100.00 |
365 |
38.90 |
9e-59 |
PRK13796 PRK13796 GTPase YqeH Provisional.
|
rpsblast_cdd |
gnl|CDD|132636
|
78 |
525 |
+ |
448 |
Gaps:88 |
100.00 |
360 |
36.39 |
4e-58 |
TIGR03597 GTPase_YqeH ribosome biogenesis GTPase YqeH. This family describes YqeH a member of a larger family of GTPases involved in ribosome biogenesis. Like YqlF it shows a cyclical permutation relative to GTPases EngA (in which the GTPase domain is duplicated) Era and others. Members of this protein family are found in a relatively small number of bacterial species including Bacillus subtilis but not Escherichia coli.
|
rpsblast_cdd |
gnl|CDD|206748
|
153 |
369 |
+ |
217 |
Gaps:32 |
100.00 |
191 |
42.41 |
4e-53 |
cd01855 YqeH Circularly permuted YqeH GTPase. YqeH is an essential GTP-binding protein. Depletion of YqeH induces an excess initiation of DNA replication suggesting that it negatively controls initiation of chromosome replication. The YqeH subfamily is common in eukaryotes and sporadically present in bacteria with probable acquisition by plants from chloroplasts. Proteins of the YqeH family contain all sequence motifs typical of the vast class of P-loop-containing GTPases but show a circular permutation with a G4-G1-G3 pattern of motifs as opposed to the regular G1-G3-G4 pattern seen in most GTPases.
|
rpsblast_cdd |
gnl|CDD|31355
|
153 |
525 |
+ |
373 |
Gaps:80 |
99.69 |
322 |
26.48 |
8e-21 |
COG1161 COG1161 Predicted GTPases [General function prediction only].
|
rpsblast_cdd |
gnl|CDD|206746
|
196 |
369 |
+ |
174 |
Gaps:39 |
99.32 |
146 |
31.72 |
6e-08 |
cd01849 YlqF_related_GTPase Circularly permuted YlqF-related GTPases. These proteins are found in bacteria eukaryotes and archaea. They all exhibit a circular permutation of the GTPase signature motifs so that the order of the conserved G box motifs is G4-G5-G1-G2-G3 with G4 and G5 being permuted from the C-terminal region of proteins in the Ras superfamily to the N-terminus of YlqF-related GTPases.
|
rpsblast_cdd |
gnl|CDD|202050
|
310 |
389 |
+ |
80 |
Gaps:8 |
61.54 |
117 |
33.33 |
6e-08 |
pfam01926 MMR_HSR1 50S ribosome-binding GTPase. The full-length GTPase protein is required for the complete activity of the protein of interacting with the 50S ribosome and binding of both adenine and guanine nucleotides with a preference for guanine nucleotide.
|
rpsblast_cdd |
gnl|CDD|206646
|
310 |
383 |
+ |
74 |
Gaps:15 |
44.10 |
161 |
38.03 |
7e-08 |
cd00880 Era_like E. coli Ras-like protein (Era)-like GTPase. The Era (E. coli Ras-like protein)-like family includes several distinct subfamilies (TrmE/ThdF FeoB YihA (EngB) Era and EngA/YfgK) that generally show sequence conservation in the region between the Walker A and B motifs (G1 and G3 box motifs) to the exclusion of other GTPases. TrmE is ubiquitous in bacteria and is a widespread mitochondrial protein in eukaryotes but is absent from archaea. The yeast member of TrmE family MSS1 is involved in mitochondrial translation bacterial members are often present in translation-related operons. FeoB represents an unusual adaptation of GTPases for high-affinity iron (II) transport. YihA (EngB) family of GTPases is typified by the E. coli YihA which is an essential protein involved in cell division control. Era is characterized by a distinct derivative of the KH domain (the pseudo-KH domain) which is located C-terminal to the GTPase domain. EngA and its orthologs are composed of two GTPase domains and since the sequences of the two domains are more similar to each other than to other GTPases it is likely that an ancient gene duplication rather than a fusion of evolutionarily distinct GTPases gave rise to this family.
|
rpsblast_cdd |
gnl|CDD|206749
|
235 |
370 |
+ |
136 |
Gaps:41 |
74.27 |
171 |
33.86 |
1e-07 |
cd01856 YlqF Circularly permuted YlqF GTPase. Proteins of the YlqF family contain all sequence motifs typical of the vast class of P-loop-containing GTPases but show a circular permutation with a G4-G1-G3 pattern of motifs as opposed to the regular G1-G3-G4 pattern seen in most GTPases. The YlqF subfamily is represented in all eukaryotes as well as a phylogenetically diverse array of bacteria (including gram-positive bacteria proteobacteria Synechocystis Borrelia and Thermotoga).
|
rpsblast_cdd |
gnl|CDD|206752
|
196 |
368 |
+ |
173 |
Gaps:36 |
91.08 |
157 |
36.36 |
5e-07 |
cd01859 MJ1464 An uncharacterized circularly permuted subfamily of the Ras GTPases. This family represents archaeal GTPase typified by the protein MJ1464 from Methanococcus jannaschii. The members of this family show a circular permutation of the GTPase signature motifs so that C-terminal strands 5 6 and 7 (strands 6 contain the NKxD motif) are relocated to the N terminus.
|