blastp_kegg |
lcl|vvi:100241331
|
81 |
794 |
+ |
714 |
Gaps:15 |
42.59 |
1660 |
83.73 |
0.0 |
transcription elongation factor SPT6-like
|
blastp_kegg |
lcl|pmum:103342255
|
80 |
794 |
+ |
715 |
Gaps:12 |
43.42 |
1633 |
84.77 |
0.0 |
transcription elongation factor SPT6
|
blastp_kegg |
lcl|pper:PRUPE_ppa000164mg
|
80 |
794 |
+ |
715 |
Gaps:12 |
45.65 |
1553 |
84.20 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|cmo:103485847
|
78 |
794 |
+ |
717 |
Gaps:12 |
43.90 |
1615 |
80.96 |
0.0 |
transcription elongation factor SPT6
|
blastp_kegg |
lcl|pxb:103966217
|
80 |
794 |
+ |
715 |
Gaps:13 |
42.98 |
1652 |
80.70 |
0.0 |
transcription elongation factor SPT6
|
blastp_kegg |
lcl|csv:101219281
|
60 |
794 |
+ |
735 |
Gaps:14 |
44.45 |
1631 |
79.45 |
0.0 |
transcription elongation factor SPT6-like
|
blastp_kegg |
lcl|mdm:103426069
|
80 |
794 |
+ |
715 |
Gaps:13 |
42.59 |
1667 |
80.42 |
0.0 |
transcription elongation factor SPT6
|
blastp_kegg |
lcl|tcc:TCM_044643
|
81 |
794 |
+ |
714 |
Gaps:14 |
43.66 |
1617 |
81.44 |
0.0 |
Global transcription factor group B1 isoform 1
|
blastp_kegg |
lcl|cit:102621404
|
1 |
794 |
+ |
794 |
Gaps:37 |
50.71 |
1623 |
76.67 |
0.0 |
transcription elongation factor SPT6-like
|
blastp_kegg |
lcl|pvu:PHAVU_001G117200g
|
50 |
794 |
+ |
745 |
Gaps:39 |
45.86 |
1679 |
75.84 |
0.0 |
hypothetical protein
|
blastp_pdb |
3psf_A
|
227 |
721 |
+ |
495 |
Gaps:69 |
45.05 |
1030 |
22.20 |
4e-08 |
mol:protein length:1030 Transcription elongation factor SPT6
|
blastp_uniprot_sprot |
sp|Q09915|SPT6_SCHPO
|
28 |
792 |
+ |
765 |
Gaps:133 |
54.80 |
1365 |
28.88 |
5e-42 |
Transcription elongation factor spt6 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN spt6 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q9W420|SPT6H_DROME
|
120 |
794 |
+ |
675 |
Gaps:158 |
40.03 |
1831 |
26.47 |
1e-39 |
Transcription elongation factor SPT6 OS Drosophila melanogaster GN Spt6 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q93148|SPT6H_CAEBR
|
227 |
795 |
+ |
569 |
Gaps:96 |
38.07 |
1521 |
26.42 |
1e-38 |
Suppressor of Ty 6 homolog OS Caenorhabditis briggsae GN emb-5 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q2U561|SPT6_ASPOR
|
85 |
788 |
+ |
704 |
Gaps:107 |
47.47 |
1422 |
28.74 |
1e-35 |
Transcription elongation factor spt6 OS Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN spt6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q4WWH6|SPT6_ASPFU
|
135 |
720 |
+ |
586 |
Gaps:98 |
41.27 |
1420 |
30.38 |
2e-34 |
Transcription elongation factor spt6 OS Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN spt6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q4PI89|SPT6_USTMA
|
190 |
794 |
+ |
605 |
Gaps:113 |
38.89 |
1723 |
23.58 |
4e-34 |
Transcription elongation factor SPT6 OS Ustilago maydis (strain 521 / FGSC 9021) GN SPT6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5B7Q7|SPT6_EMENI
|
83 |
788 |
+ |
706 |
Gaps:83 |
47.49 |
1417 |
27.64 |
4e-33 |
Transcription elongation factor spt6 OS Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN spt6 PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q8NIV6|SPT6_NEUCR
|
179 |
792 |
+ |
614 |
Gaps:75 |
42.01 |
1402 |
25.30 |
8e-31 |
Transcription elongation factor spt-6 OS Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN spt-6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P0CR73|SPT6_CRYNB
|
190 |
790 |
+ |
601 |
Gaps:69 |
39.84 |
1506 |
26.00 |
6e-29 |
Transcription elongation factor SPT6 OS Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN SPT6 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q4HYQ4|SPT6_GIBZE
|
195 |
792 |
+ |
598 |
Gaps:69 |
40.55 |
1408 |
25.92 |
5e-26 |
Transcription elongation factor SPT6 OS Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN SPT6 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|32366
|
305 |
700 |
+ |
396 |
Gaps:86 |
40.51 |
780 |
25.32 |
8e-14 |
COG2183 Tex Transcriptional accessory protein [Transcription].
|
rpsblast_cdd |
gnl|CDD|128971
|
710 |
794 |
+ |
85 |
Gaps:12 |
73.74 |
99 |
24.66 |
3e-09 |
smart00732 YqgFc Likely ribonuclease with RNase H fold. YqgF proteins are likely to function as an alternative to RuvC in most bacteria and could be the principal holliday junction resolvases in low-GC Gram-positive bacteria. In Spt6p orthologues the catalytic residues are substituted indicating that they lack enzymatic functions.
|
rpsblast_cdd |
gnl|CDD|34868
|
7 |
174 |
+ |
168 |
Gaps:37 |
3.07 |
4600 |
28.37 |
4e-07 |
COG5271 MDN1 AAA ATPase containing von Willebrand factor type A (vWA) domain [General function prediction only].
|
rpsblast_kog |
gnl|CDD|37067
|
102 |
794 |
+ |
693 |
Gaps:75 |
52.96 |
1299 |
32.70 |
1e-118 |
KOG1856 KOG1856 KOG1856 Transcription elongation factor SPT6 [RNA processing and modification].
|
rpsblast_kog |
gnl|CDD|37043
|
30 |
174 |
+ |
145 |
Gaps:35 |
7.26 |
1516 |
31.82 |
2e-07 |
KOG1832 KOG1832 KOG1832 HIV-1 Vpr-binding protein [Cell cycle control cell division chromosome partitioning].
|