|
blastp_kegg |
lcl|vvi:100256388
|
5 |
1220 |
+ |
1216 |
Gaps:140 |
46.27 |
2667 |
57.13 |
0.0 |
uncharacterized LOC100256388
|
|
blastp_kegg |
lcl|tcc:TCM_043328
|
1 |
1272 |
+ |
1272 |
Gaps:247 |
81.14 |
1596 |
54.44 |
0.0 |
Kow domain-containing transcription factor 1 putative
|
|
blastp_kegg |
lcl|rcu:RCOM_1010880
|
5 |
908 |
+ |
904 |
Gaps:75 |
55.66 |
1547 |
60.86 |
0.0 |
suppressor of ty putative
|
|
blastp_kegg |
lcl|cit:102627386
|
5 |
908 |
+ |
904 |
Gaps:106 |
50.20 |
1741 |
62.36 |
0.0 |
uncharacterized LOC102627386
|
|
blastp_kegg |
lcl|cic:CICLE_v10030480mg
|
5 |
908 |
+ |
904 |
Gaps:106 |
48.37 |
1807 |
62.36 |
0.0 |
hypothetical protein
|
|
blastp_kegg |
lcl|pper:PRUPE_ppa000178mg
|
1 |
1252 |
+ |
1252 |
Gaps:208 |
75.59 |
1516 |
53.75 |
0.0 |
hypothetical protein
|
|
blastp_kegg |
lcl|fve:101311630
|
5 |
691 |
+ |
687 |
Gaps:35 |
95.11 |
696 |
64.95 |
0.0 |
transcription elongation factor SPT5-like
|
|
blastp_kegg |
lcl|pvu:PHAVU_007G024600g
|
8 |
735 |
+ |
728 |
Gaps:48 |
56.19 |
1228 |
63.19 |
0.0 |
hypothetical protein
|
|
blastp_kegg |
lcl|gmx:100787703
|
15 |
619 |
+ |
605 |
Gaps:14 |
41.80 |
1457 |
65.35 |
0.0 |
uncharacterized LOC100787703
|
|
blastp_kegg |
lcl|ath:AT5G04290
|
22 |
910 |
+ |
889 |
Gaps:106 |
63.56 |
1493 |
48.58 |
0.0 |
KTF1 kow domain-containing transcription factor 1
|
|
blastp_pdb |
3h7h_B
|
76 |
165 |
+ |
90 |
Gaps:4 |
86.79 |
106 |
39.13 |
8e-12 |
mol:protein length:106 Transcription elongation factor SPT5
|
|
blastp_pdb |
2exu_A
|
81 |
169 |
+ |
89 |
Gaps:2 |
45.50 |
200 |
38.46 |
3e-08 |
mol:protein length:200 Transcription initiation protein SPT4/SPT5
|
|
blastp_uniprot_sprot |
sp|O80770|SPT52_ARATH
|
28 |
591 |
+ |
564 |
Gaps:57 |
57.03 |
989 |
37.06 |
9e-63 |
Putative transcription elongation factor SPT5 homolog 2 OS Arabidopsis thaliana GN At2g34210 PE 3 SV 2
|
|
blastp_uniprot_sprot |
sp|Q9STN3|SPT51_ARATH
|
28 |
617 |
+ |
590 |
Gaps:43 |
58.79 |
1041 |
36.60 |
2e-61 |
Putative transcription elongation factor SPT5 homolog 1 OS Arabidopsis thaliana GN At4g08350 PE 1 SV 2
|
|
blastp_uniprot_sprot |
sp|O13936|SPT5_SCHPO
|
31 |
621 |
+ |
591 |
Gaps:51 |
54.04 |
990 |
31.96 |
6e-37 |
Transcription elongation factor spt5 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN spt5 PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q4PIC4|SPT5_USTMA
|
5 |
480 |
+ |
476 |
Gaps:37 |
42.19 |
1057 |
32.29 |
2e-32 |
Transcription elongation factor SPT5 OS Ustilago maydis (strain 521 / FGSC 9021) GN SPT5 PE 3 SV 1
|
|
blastp_uniprot_sprot |
sp|Q21338|SPT5H_CAEEL
|
31 |
311 |
+ |
281 |
Gaps:17 |
22.85 |
1208 |
33.70 |
7e-32 |
Transcription elongation factor SPT5 OS Caenorhabditis elegans GN spt-5 PE 3 SV 3
|
|
blastp_uniprot_sprot |
sp|Q6FRZ5|SPT5_CANGA
|
31 |
448 |
+ |
418 |
Gaps:63 |
38.12 |
1010 |
30.91 |
2e-30 |
Transcription elongation factor SPT5 OS Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN SPT5 PE 3 SV 1
|
|
blastp_uniprot_sprot |
sp|Q6CC84|SPT5_YARLI
|
68 |
457 |
+ |
390 |
Gaps:112 |
47.96 |
980 |
27.45 |
6e-28 |
Transcription elongation factor SPT5 OS Yarrowia lipolytica (strain CLIB 122 / E 150) GN SPT5 PE 3 SV 1
|
|
blastp_uniprot_sprot |
sp|Q9DDT5|SPT5H_DANRE
|
68 |
617 |
+ |
550 |
Gaps:81 |
49.54 |
1084 |
29.98 |
5e-27 |
Transcription elongation factor SPT5 OS Danio rerio GN supt5h PE 1 SV 1
|
|
blastp_uniprot_sprot |
sp|Q5ZI08|SPT5H_CHICK
|
68 |
617 |
+ |
550 |
Gaps:71 |
49.40 |
1079 |
31.33 |
8e-27 |
Transcription elongation factor SPT5 OS Gallus gallus GN SUPT5H PE 2 SV 1
|
|
blastp_uniprot_sprot |
sp|Q4WP96|SPT5_ASPFU
|
32 |
312 |
+ |
281 |
Gaps:44 |
26.75 |
1058 |
31.80 |
9e-27 |
Transcription elongation factor spt5 OS Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN spt5 PE 3 SV 1
|
|
rpsblast_cdd |
gnl|CDD|193577
|
82 |
166 |
+ |
85 |
none |
98.84 |
86 |
43.53 |
1e-29 |
cd09888 NGN_Euk Eukaryotic N-Utilization Substance G (NusG) N-terminal (NGN) domain including plant KTF1 (KOW domain-containing Transcription Factor 1). The N-Utilization Substance G (NusG) protein and its eukaryotic homolog Spt5 are involved in transcription elongation and termination. NusG contains an NGN domain at its N-terminus and Kyrpides Ouzounis and Woese (KOW) repeats at its C-terminus. Spt5 forms an Spt4-Spt5 complex that is an essential RNA polymerase II elongation factor. NusG was originally discovered as an N-dependent antitermination enhancing activity in Escherichia coli and has a variety of functions such as its involvement in RNA polymerase elongation and Rho-termination in bacteria. Orthologs of the NusG gene exist in all bacteria but their functions and requirements are different. Spt5-like is homologous to the Spt5 proteins present in all eukaryotes which is unique as it encodes a protein with an additional long carboxy-terminal extension that contains WG/GW motifs. Spt5-like or KTF1 (KOW domain-containing Transcription Factor 1) is a RNA-directed DNA methylation (RdDM) pathway effector in plants.
|
|
rpsblast_cdd |
gnl|CDD|202630
|
82 |
165 |
+ |
84 |
Gaps:1 |
98.81 |
84 |
42.17 |
1e-22 |
pfam03439 Spt5-NGN Early transcription elongation factor of RNA pol II NGN section. Spt5p and prokaryotic NusG are shown to contain a novel 'NGN' domain. The combined NGN and KOW motif regions of Spt5 form the binding domain with Spt4. Spt5 complexes with Spt4 as a 1:1 heterodimer snf this Spt5-Spt4 complex regulates early transcription elongation by RNA polymerase II and has an imputed role in pre-mRNA processing via its physical association with mRNA capping enzymes. The Schizosaccharomyces pombe core Spt5-Spt4 complex is a heterodimer bearing a trypsin-resistant Spt4-binding domain within the Spt5 subunit.
|
|
rpsblast_cdd |
gnl|CDD|185479
|
1242 |
1347 |
+ |
106 |
Gaps:9 |
19.45 |
293 |
91.23 |
1e-10 |
PTZ00146 PTZ00146 fibrillarin Provisional.
|
|
rpsblast_cdd |
gnl|CDD|181467
|
82 |
209 |
+ |
128 |
Gaps:5 |
80.39 |
153 |
28.46 |
4e-10 |
PRK08559 nusG transcription antitermination protein NusG Validated.
|
|
rpsblast_cdd |
gnl|CDD|129499
|
85 |
209 |
+ |
125 |
Gaps:5 |
82.76 |
145 |
24.17 |
4e-09 |
TIGR00405 L26e_arch ribosomal protein L24p/L26e archaeal. This protein contains a KOW domain shared by bacterial NusG and the L24p/L26e family of ribosomal proteins. Although called archaeal NusG in several publications it is the only close homolog of eukaryotic L26e in archaeal genomes shares an operon with L11 in many genomes and has been sequenced from purified ribosomes. It is here designated as a ribosomal protein for these reasons.
|
|
rpsblast_cdd |
gnl|CDD|34765
|
330 |
752 |
+ |
423 |
Gaps:50 |
64.74 |
607 |
20.87 |
4e-07 |
COG5164 SPT5 Transcription elongation factor [Transcription].
|
|
rpsblast_kog |
gnl|CDD|37210
|
6 |
931 |
+ |
926 |
Gaps:224 |
88.57 |
1024 |
37.16 |
9e-85 |
KOG1999 KOG1999 KOG1999 RNA polymerase II transcription elongation factor DSIF/SUPT5H/SPT5 [Transcription].
|
|
rpsblast_kog |
gnl|CDD|36139
|
1183 |
1349 |
+ |
167 |
Gaps:42 |
9.59 |
1282 |
59.35 |
1e-12 |
KOG0921 KOG0921 KOG0921 Dosage compensation complex subunit MLE [Transcription].
|