blastp_kegg |
lcl|tcc:TCM_036825
|
3 |
202 |
+ |
200 |
Gaps:47 |
82.70 |
185 |
69.28 |
5e-65 |
STS14 protein putative
|
blastp_kegg |
lcl|pop:POPTR_0018s03600g
|
7 |
202 |
+ |
196 |
Gaps:47 |
64.50 |
231 |
71.81 |
2e-63 |
POPTRDRAFT_261668 hypothetical protein
|
blastp_kegg |
lcl|rcu:RCOM_0107330
|
80 |
202 |
+ |
123 |
none |
71.93 |
171 |
75.61 |
3e-62 |
STS14 protein precursor putative
|
blastp_kegg |
lcl|pmum:103325397
|
11 |
202 |
+ |
192 |
Gaps:47 |
84.30 |
172 |
69.66 |
3e-58 |
pathogenesis-related protein PRMS-like
|
blastp_kegg |
lcl|pper:PRUPE_ppa016600mg
|
11 |
202 |
+ |
192 |
Gaps:47 |
98.64 |
147 |
68.97 |
1e-57 |
hypothetical protein
|
blastp_kegg |
lcl|fve:101293281
|
15 |
202 |
+ |
188 |
Gaps:47 |
80.11 |
176 |
68.09 |
1e-56 |
pathogenesis-related protein PR-1-like
|
blastp_kegg |
lcl|atr:s00019p00199860
|
4 |
202 |
+ |
199 |
Gaps:47 |
83.52 |
182 |
61.18 |
6e-56 |
AMTR_s00019p00199860 hypothetical protein
|
blastp_kegg |
lcl|mdm:103446143
|
12 |
202 |
+ |
191 |
Gaps:47 |
61.54 |
234 |
67.36 |
1e-55 |
pathogenesis-related protein PR-1-like
|
blastp_kegg |
lcl|sly:101264239
|
12 |
202 |
+ |
191 |
Gaps:47 |
79.56 |
181 |
64.58 |
3e-54 |
pathogenesis-related protein PR-1-like
|
blastp_kegg |
lcl|sot:102594592
|
8 |
202 |
+ |
195 |
Gaps:47 |
70.81 |
209 |
63.51 |
4e-54 |
pathogenesis-related protein PR-1-like
|
blastp_pdb |
1cfe_A
|
80 |
202 |
+ |
123 |
Gaps:3 |
88.89 |
135 |
45.00 |
1e-27 |
mol:protein length:135 PATHOGENESIS-RELATED PROTEIN P14A
|
blastp_pdb |
2vzn_B
|
82 |
198 |
+ |
117 |
Gaps:14 |
60.09 |
218 |
25.95 |
8e-06 |
mol:protein length:218 VENOM ALLERGEN 3
|
blastp_pdb |
2vzn_A
|
82 |
198 |
+ |
117 |
Gaps:14 |
60.09 |
218 |
25.95 |
8e-06 |
mol:protein length:218 VENOM ALLERGEN 3
|
blastp_uniprot_sprot |
sp|Q00008|PRMS_MAIZE
|
80 |
202 |
+ |
123 |
Gaps:2 |
74.85 |
167 |
49.60 |
1e-37 |
Pathogenesis-related protein PRMS OS Zea mays GN PRMS PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q40374|PR1_MEDTR
|
77 |
202 |
+ |
126 |
Gaps:1 |
73.41 |
173 |
48.82 |
5e-37 |
Pathogenesis-related protein PR-1 OS Medicago truncatula GN PR-1 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P09042|PR1C_TOBAC
|
80 |
202 |
+ |
123 |
none |
73.21 |
168 |
46.34 |
4e-36 |
Pathogenesis-related protein 1C OS Nicotiana tabacum PE 2 SV 3
|
blastp_uniprot_sprot |
sp|P35792|PR12_HORVU
|
80 |
202 |
+ |
123 |
Gaps:2 |
76.22 |
164 |
46.40 |
3e-35 |
Pathogenesis-related protein PRB1-2 OS Hordeum vulgare PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P07053|PR1B_TOBAC
|
80 |
202 |
+ |
123 |
none |
73.21 |
168 |
45.53 |
9e-35 |
Pathogenesis-related protein 1B OS Nicotiana tabacum PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q05968|PR1_HORVU
|
80 |
202 |
+ |
123 |
Gaps:2 |
76.22 |
164 |
46.40 |
9e-35 |
Pathogenesis-related protein 1 OS Hordeum vulgare PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P35793|PR13_HORVU
|
88 |
202 |
+ |
115 |
Gaps:2 |
71.34 |
164 |
47.86 |
4e-33 |
Pathogenesis-related protein PRB1-3 OS Hordeum vulgare PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P08299|PR1A_TOBAC
|
80 |
202 |
+ |
123 |
none |
73.21 |
168 |
43.90 |
8e-33 |
Pathogenesis-related protein 1A OS Nicotiana tabacum PE 1 SV 1
|
blastp_uniprot_sprot |
sp|Q41359|PR1_SAMNI
|
80 |
202 |
+ |
123 |
Gaps:1 |
74.25 |
167 |
44.35 |
3e-31 |
Pathogenesis-related protein PR-1 type OS Sambucus nigra PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P33154|PR1_ARATH
|
80 |
202 |
+ |
123 |
Gaps:3 |
74.53 |
161 |
45.00 |
3e-31 |
Pathogenesis-related protein 1 OS Arabidopsis thaliana GN At2g14610 PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|88560
|
80 |
202 |
+ |
123 |
Gaps:1 |
91.18 |
136 |
51.61 |
8e-45 |
cd05381 SCP_PR-1_like SCP_PR-1_like: SCP-like extracellular protein domain PR-1 like subfamily. The wider family of SCP containing proteins includes plant pathogenesis-related protein 1 (PR-1) which accumulates after infections with pathogens and may act as an anti-fungal agent or be involved in cell wall loosening. It also includes CRISPs mammalian cysteine-rich secretory proteins and allergen 5 from vespid venom. It has been proposed that SCP domains may function as endopeptidases..
|
rpsblast_cdd |
gnl|CDD|88563
|
83 |
198 |
+ |
116 |
Gaps:6 |
86.82 |
129 |
36.61 |
2e-18 |
cd05384 SCP_PRY1_like SCP_PRY1_like: SCP-like extracellular protein domain PRY1-like sub-family restricted to fungi. The wider family of SCP containing proteins includes plant pathogenesis-related protein 1 (PR-1) CRISPs mammalian cysteine-rich secretory proteins and allergen 5 from vespid venom. It has been proposed that SCP domains may function as endopeptidases. PRY1 is a yeast protein that is up-regulated in core ESCRT mutants. This PRY1-like group also contains fruiting body proteins SC7/14 from Schizophyllum commune..
|
rpsblast_cdd |
gnl|CDD|197569
|
85 |
192 |
+ |
108 |
Gaps:14 |
79.17 |
144 |
35.09 |
7e-18 |
smart00198 SCP SCP / Tpx-1 / Ag5 / PR-1 / Sc7 family of extracellular domains. Human glioma pathogenesis-related protein GliPR and the plant pathogenesis-related protein represent functional links between plant defense systems and human immune system. This family has no known function.
|
rpsblast_cdd |
gnl|CDD|88561
|
21 |
196 |
+ |
176 |
Gaps:48 |
98.48 |
132 |
32.31 |
3e-16 |
cd05382 SCP_GAPR-1_like SCP_GAPR-1_like: SCP-like extracellular protein domain golgi-associated plant pathogenesis related protein (GAPR)-like sub-family. The wider family of SCP containing proteins includes plant pathogenesis-related protein 1 (PR-1) CRISPs mammalian cysteine-rich secretory proteins which combine SCP with a C-terminal cysteine rich domain and allergen 5 from vespid venom. It has been proposed that SCP domains may function as endopeptidases. The human GAPR-1 protein has been reported to dimerize and such a dimer may form an active site containing a catalytic triad. GAPR-1 and GLIPR-2 appear to be synonyms..
|
rpsblast_cdd |
gnl|CDD|88557
|
83 |
191 |
+ |
109 |
Gaps:11 |
86.89 |
122 |
32.08 |
1e-14 |
cd00168 SCP SCP: SCP-like extracellular protein domain found in eukaryotes and prokaryotes. This family includes plant pathogenesis-related protein 1 (PR-1) which accumulates after infections with pathogens and may act as an anti-fungal agent or be involved in cell wall loosening. This family also includes CRISPs mammalian cysteine-rich secretory proteins which combine SCP with a C-terminal cysteine rich domain and allergen 5 from vespid venom. Roles for CRISP in response to pathogens fertilization and sperm maturation have been proposed. One member Tex31 from the venom duct of Conus textile has been shown to possess proteolytic activity sensitive to serine protease inhibitors. The human GAPR-1 protein has been reported to dimerize and such a dimer may form an active site containing a catalytic triad. SCP has also been proposed to be a Ca++ chelating serine protease. The Ca++-chelating function would fit with various signaling processes that members of this family such as the CRISPs are involved in and is supported by sequence and structural evidence of a conserved pocket containing two histidines and a glutamate. It also may explain how helothermine a toxic peptide secreted by the beaded lizard blocks Ca++ transporting ryanodine receptors. Little is known about the biological roles of the bacterial and archaeal SCP domains..
|
rpsblast_cdd |
gnl|CDD|88559
|
84 |
191 |
+ |
108 |
Gaps:8 |
80.56 |
144 |
27.59 |
1e-13 |
cd05380 SCP_euk SCP_euk: SCP-like extracellular protein domain as found mainly in eukaryotes. This family includes plant pathogenesis-related protein 1 (PR-1) CRISPs mammalian cysteine-rich secretory proteins and allergen 5 from vespid venom. It has been proposed that SCP domains may function as endopeptidases..
|
rpsblast_cdd |
gnl|CDD|88565
|
87 |
190 |
+ |
104 |
Gaps:7 |
81.62 |
136 |
34.23 |
7e-13 |
cd05559 SCP_HrTT-1 SCP_HrTT-1: SCP-like extracellular protein domain in HrTT-1 a tail-tip epidermis marker in ascidians. The wider family of SCP containing proteins includes plant pathogenesis-related protein 1 (PR-1) CRISPs mammalian cysteine-rich secretory proteins and allergen 5 from vespid venom. It has been proposed that SCP domains may function as endopeptidases..
|