blastp_kegg |
lcl|tcc:TCM_004979
|
1 |
288 |
+ |
288 |
Gaps:32 |
85.05 |
301 |
80.08 |
4e-146 |
Expansin A17 ALPHA 1.13 EXPA17 putative
|
blastp_kegg |
lcl|tcc:TCM_046987
|
1 |
288 |
+ |
288 |
Gaps:32 |
100.00 |
256 |
80.08 |
8e-146 |
Expansin A17 ALPHA 1.13 EXPA17
|
blastp_kegg |
lcl|vvi:100248670
|
1 |
288 |
+ |
288 |
Gaps:32 |
100.00 |
256 |
78.91 |
6e-145 |
putative expansin-A17-like
|
blastp_kegg |
lcl|pop:POPTR_0002s18550g
|
12 |
288 |
+ |
277 |
Gaps:33 |
96.06 |
254 |
84.43 |
2e-144 |
POPTRDRAFT_411151 hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_1342060
|
1 |
288 |
+ |
288 |
Gaps:33 |
100.00 |
255 |
80.39 |
4e-144 |
Alpha-expansin 8 precursor putative
|
blastp_kegg |
lcl|rcu:RCOM_1342080
|
6 |
288 |
+ |
283 |
Gaps:33 |
98.04 |
255 |
80.80 |
2e-143 |
Alpha-expansin 1 precursor putative
|
blastp_kegg |
lcl|cam:101509282
|
1 |
288 |
+ |
288 |
Gaps:33 |
90.43 |
282 |
78.43 |
9e-143 |
putative expansin-A17-like
|
blastp_kegg |
lcl|gmx:100813434
|
1 |
288 |
+ |
288 |
Gaps:34 |
100.00 |
254 |
79.53 |
6e-142 |
putative expansin-A17-like
|
blastp_kegg |
lcl|gmx:100783801
|
1 |
288 |
+ |
288 |
Gaps:34 |
100.00 |
254 |
79.53 |
8e-142 |
putative expansin-A17-like
|
blastp_kegg |
lcl|pvu:PHAVU_007G207600g
|
1 |
288 |
+ |
288 |
Gaps:34 |
100.00 |
254 |
80.31 |
2e-141 |
hypothetical protein
|
blastp_pdb |
2hcz_X
|
74 |
288 |
+ |
215 |
Gaps:34 |
86.12 |
245 |
35.55 |
5e-26 |
mol:protein length:245 Beta-expansin 1a
|
blastp_pdb |
1n10_B
|
71 |
285 |
+ |
215 |
Gaps:34 |
87.55 |
241 |
32.23 |
1e-18 |
mol:protein length:241 Pollen allergen Phl p 1
|
blastp_pdb |
1n10_A
|
71 |
285 |
+ |
215 |
Gaps:34 |
87.55 |
241 |
32.23 |
1e-18 |
mol:protein length:241 Pollen allergen Phl p 1
|
blastp_uniprot_sprot |
sp|Q9ZSI1|EXP17_ARATH
|
1 |
288 |
+ |
288 |
Gaps:33 |
100.00 |
255 |
74.51 |
2e-132 |
Putative expansin-A17 OS Arabidopsis thaliana GN EXPA17 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9XHX0|EXPA8_ORYSJ
|
26 |
288 |
+ |
263 |
Gaps:34 |
91.24 |
251 |
68.12 |
5e-107 |
Expansin-A8 OS Oryza sativa subsp. japonica GN EXPA8 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q4PR39|EXP29_ORYSJ
|
7 |
288 |
+ |
282 |
Gaps:34 |
95.06 |
263 |
58.40 |
3e-105 |
Expansin-A29 OS Oryza sativa subsp. japonica GN EXPA29 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q4PR44|EXP22_ORYSJ
|
29 |
288 |
+ |
260 |
Gaps:32 |
81.43 |
280 |
63.16 |
3e-104 |
Expansin-A22 OS Oryza sativa subsp. japonica GN EXPA22 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q7XWU8|EXPA1_ORYSJ
|
8 |
288 |
+ |
281 |
Gaps:38 |
96.93 |
261 |
62.45 |
1e-103 |
Expansin-A1 OS Oryza sativa subsp. japonica GN EXPA1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q4PR42|EXP24_ORYSJ
|
29 |
288 |
+ |
260 |
Gaps:32 |
82.01 |
278 |
62.28 |
4e-103 |
Expansin-A24 OS Oryza sativa subsp. japonica GN EXPA24 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q4PR43|EXP23_ORYSJ
|
29 |
288 |
+ |
260 |
Gaps:32 |
85.39 |
267 |
61.84 |
1e-102 |
Expansin-A23 OS Oryza sativa subsp. japonica GN EXPA23.1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q4PR52|EXP13_ORYSJ
|
27 |
288 |
+ |
262 |
Gaps:32 |
87.79 |
262 |
61.74 |
2e-102 |
Expansin-A13 OS Oryza sativa subsp. japonica GN EXPA13 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9LNU3|EXP11_ARATH
|
33 |
288 |
+ |
256 |
Gaps:33 |
88.49 |
252 |
65.47 |
4e-101 |
Expansin-A11 OS Arabidopsis thaliana GN EXPA11 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q38866|EXPA2_ARATH
|
9 |
282 |
+ |
274 |
Gaps:40 |
95.69 |
255 |
61.48 |
8e-101 |
Expansin-A2 OS Arabidopsis thaliana GN EXPA2 PE 2 SV 2
|
rpsblast_cdd |
gnl|CDD|177787
|
4 |
288 |
+ |
285 |
Gaps:36 |
97.27 |
256 |
64.26 |
2e-97 |
PLN00193 PLN00193 expansin-A Provisional.
|
rpsblast_cdd |
gnl|CDD|165628
|
26 |
283 |
+ |
258 |
Gaps:36 |
89.88 |
247 |
70.27 |
8e-83 |
PLN00050 PLN00050 expansin A Provisional.
|
rpsblast_cdd |
gnl|CDD|129070
|
96 |
184 |
+ |
89 |
Gaps:2 |
100.00 |
87 |
72.41 |
1e-40 |
smart00837 DPBB_1 Rare lipoprotein A (RlpA)-like double-psi beta-barrel. Rare lipoprotein A (RlpA) contains a conserved region that has the double-psi beta-barrel (DPBB) fold. The function of RlpA is not well understood but it has been shown to act as a prc mutant suppressor in Escherichia coli. The DPBB fold is often an enzymatic domain. The members of this family are quite diverse and if catalytic this family may contain several different functions. Another example of this domain is found in the N terminus of pollen allergen.
|
rpsblast_cdd |
gnl|CDD|201746
|
195 |
273 |
+ |
79 |
Gaps:3 |
100.00 |
82 |
54.88 |
3e-26 |
pfam01357 Pollen_allerg_1 Pollen allergen. This family contains allergens lol PI PII and PIII from Lolium perenne.
|
rpsblast_cdd |
gnl|CDD|202595
|
96 |
184 |
+ |
89 |
Gaps:14 |
100.00 |
77 |
50.65 |
2e-24 |
pfam03330 DPBB_1 Rare lipoprotein A (RlpA)-like double-psi beta-barrel. Rare lipoprotein A (RlpA) contains a conserved region that has the double-psi beta-barrel (DPBB) fold. The function of RlpA is not well understood but it has been shown to act as a prc mutant suppressor in Escherichia coli. The DPBB fold is often an enzymatic domain. The members of this family are quite diverse and if catalytic this family may contain several different functions. Another example of this domain is found in the N terminus of pollen allergen.
|
rpsblast_cdd |
gnl|CDD|178594
|
80 |
287 |
+ |
208 |
Gaps:34 |
81.78 |
247 |
30.20 |
2e-16 |
PLN03023 PLN03023 Expansin-like B1 Provisional.
|