blastp_kegg |
lcl|vvi:100259549
|
11 |
269 |
+ |
259 |
Gaps:3 |
80.12 |
327 |
80.15 |
2e-148 |
syntaxin-43-like
|
blastp_kegg |
lcl|vvi:100248594
|
2 |
269 |
+ |
268 |
Gaps:11 |
87.74 |
318 |
76.34 |
2e-147 |
syntaxin-41-like
|
blastp_kegg |
lcl|cic:CICLE_v10001826mg
|
11 |
269 |
+ |
259 |
Gaps:3 |
80.37 |
326 |
79.39 |
3e-147 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_004740
|
17 |
269 |
+ |
253 |
Gaps:3 |
79.50 |
322 |
80.08 |
5e-146 |
Syntaxin of plants 41 isoform 2
|
blastp_kegg |
lcl|cit:102612546
|
11 |
269 |
+ |
259 |
Gaps:3 |
80.37 |
326 |
79.01 |
6e-146 |
syntaxin-43-like
|
blastp_kegg |
lcl|atr:s00057p00109670
|
11 |
269 |
+ |
259 |
Gaps:3 |
82.65 |
317 |
77.48 |
1e-144 |
AMTR_s00057p00109670 hypothetical protein
|
blastp_kegg |
lcl|gmx:100803629
|
15 |
269 |
+ |
255 |
Gaps:4 |
79.94 |
324 |
78.76 |
4e-143 |
syntaxin-43-like
|
blastp_kegg |
lcl|pvu:PHAVU_001G210900g
|
15 |
269 |
+ |
255 |
Gaps:4 |
80.94 |
320 |
79.54 |
2e-142 |
hypothetical protein
|
blastp_kegg |
lcl|gmx:100797056
|
15 |
269 |
+ |
255 |
Gaps:4 |
80.94 |
320 |
77.99 |
3e-141 |
syntaxin-43-like
|
blastp_kegg |
lcl|tcc:TCM_026730
|
11 |
269 |
+ |
259 |
Gaps:4 |
79.46 |
331 |
77.19 |
2e-140 |
Syntaxin of plants 43 isoform 1
|
blastp_pdb |
3ipd_F
|
177 |
267 |
+ |
91 |
Gaps:3 |
80.73 |
109 |
30.68 |
8e-07 |
mol:protein length:109 Syntaxin-1A
|
blastp_pdb |
3ipd_B
|
177 |
267 |
+ |
91 |
Gaps:3 |
80.73 |
109 |
30.68 |
8e-07 |
mol:protein length:109 Syntaxin-1A
|
blastp_pdb |
3hd7_F
|
177 |
267 |
+ |
91 |
Gaps:3 |
80.73 |
109 |
30.68 |
8e-07 |
mol:protein length:109 Syntaxin-1A
|
blastp_pdb |
3hd7_B
|
177 |
267 |
+ |
91 |
Gaps:3 |
80.73 |
109 |
30.68 |
8e-07 |
mol:protein length:109 Syntaxin-1A
|
blastp_pdb |
2nps_B
|
179 |
242 |
+ |
64 |
none |
90.14 |
71 |
37.50 |
1e-06 |
mol:protein length:71 Syntaxin 13
|
blastp_uniprot_sprot |
sp|Q9SUJ1|SYP43_ARATH
|
11 |
269 |
+ |
259 |
Gaps:5 |
78.55 |
331 |
73.85 |
2e-132 |
Syntaxin-43 OS Arabidopsis thaliana GN SYP43 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O65359|SYP41_ARATH
|
11 |
269 |
+ |
259 |
Gaps:6 |
80.43 |
322 |
73.36 |
4e-130 |
Syntaxin-41 OS Arabidopsis thaliana GN SYP41 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q9SWH4|SYP42_ARATH
|
11 |
269 |
+ |
259 |
Gaps:4 |
81.42 |
323 |
68.82 |
3e-127 |
Syntaxin-42 OS Arabidopsis thaliana GN SYP42 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O14662|STX16_HUMAN
|
23 |
241 |
+ |
219 |
Gaps:11 |
68.92 |
325 |
38.84 |
1e-42 |
Syntaxin-16 OS Homo sapiens GN STX16 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q8BVI5|STX16_MOUSE
|
23 |
242 |
+ |
220 |
Gaps:14 |
69.33 |
326 |
38.94 |
6e-42 |
Syntaxin-16 OS Mus musculus GN Stx16 PE 1 SV 3
|
blastp_uniprot_sprot |
sp|Q9P6P1|TLG2_SCHPO
|
22 |
265 |
+ |
244 |
Gaps:27 |
81.40 |
301 |
35.92 |
3e-32 |
t-SNARE affecting a late Golgi compartment protein 2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN tlg2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q08144|TLG2_YEAST
|
6 |
264 |
+ |
259 |
Gaps:40 |
70.28 |
397 |
29.03 |
2e-21 |
T-SNARE affecting a late Golgi compartment protein 2 OS Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN TLG2 PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q5RBW6|STX12_PONAB
|
141 |
253 |
+ |
113 |
Gaps:7 |
38.41 |
276 |
36.79 |
6e-09 |
Syntaxin-12 OS Pongo abelii GN STX12 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|O94651|PEP12_SCHPO
|
141 |
262 |
+ |
122 |
Gaps:6 |
44.11 |
263 |
32.76 |
2e-08 |
Syntaxin pep12 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN pep12 PE 1 SV 2
|
blastp_uniprot_sprot |
sp|Q54JY7|STX7A_DICDI
|
177 |
264 |
+ |
88 |
Gaps:2 |
25.28 |
356 |
32.22 |
6e-08 |
Syntaxin-7A OS Dictyostelium discoideum GN syn7A PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|34907
|
20 |
265 |
+ |
246 |
Gaps:4 |
88.34 |
283 |
24.80 |
9e-25 |
COG5325 COG5325 t-SNARE complex subunit syntaxin [Intracellular trafficking and secretion].
|
rpsblast_cdd |
gnl|CDD|203323
|
179 |
240 |
+ |
62 |
none |
100.00 |
62 |
35.48 |
1e-09 |
pfam05739 SNARE SNARE domain. Most if not all vesicular membrane fusion events in eukaryotic cells are believed to be mediated by a conserved fusion machinery the SNARE [soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptors] machinery. The SNARE domain is thought to act as a protein-protein interaction module in the assembly of a SNARE protein complex.
|
rpsblast_cdd |
gnl|CDD|128779
|
24 |
130 |
+ |
107 |
Gaps:7 |
95.73 |
117 |
29.46 |
7e-09 |
smart00503 SynN Syntaxin N-terminal domain. Three-helix domain that (in Sso1p) slows the rate of its reaction with the SNAP-25 homologue Sec9p.
|
rpsblast_kog |
gnl|CDD|36027
|
21 |
267 |
+ |
247 |
Gaps:8 |
82.30 |
305 |
47.01 |
1e-66 |
KOG0809 KOG0809 KOG0809 SNARE protein TLG2/Syntaxin 16 [Intracellular trafficking secretion and vesicular transport].
|
rpsblast_kog |
gnl|CDD|36029
|
30 |
268 |
+ |
239 |
Gaps:16 |
91.08 |
269 |
22.04 |
8e-14 |
KOG0811 KOG0811 KOG0811 SNARE protein PEP12/VAM3/Syntaxin 7/Syntaxin 17 [Intracellular trafficking secretion and vesicular transport].
|