blastp_kegg |
lcl|pmum:103340969
|
1 |
301 |
+ |
301 |
Gaps:12 |
88.86 |
341 |
74.26 |
4e-150 |
chloroplast processing peptidase
|
blastp_kegg |
lcl|pper:PRUPE_ppa008221mg
|
1 |
300 |
+ |
300 |
Gaps:11 |
88.53 |
340 |
75.08 |
1e-149 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103960693
|
1 |
301 |
+ |
301 |
Gaps:11 |
90.48 |
336 |
72.70 |
8e-142 |
chloroplast processing peptidase-like
|
blastp_kegg |
lcl|pxb:103946436
|
1 |
301 |
+ |
301 |
Gaps:19 |
90.48 |
336 |
72.70 |
3e-141 |
chloroplast processing peptidase-like
|
blastp_kegg |
lcl|mdm:103418020
|
1 |
301 |
+ |
301 |
Gaps:11 |
93.83 |
324 |
72.04 |
2e-139 |
chloroplast processing peptidase-like
|
blastp_kegg |
lcl|mdm:103448872
|
1 |
301 |
+ |
301 |
Gaps:11 |
93.83 |
324 |
72.04 |
2e-139 |
chloroplast processing peptidase-like
|
blastp_kegg |
lcl|pxb:103962974
|
1 |
301 |
+ |
301 |
Gaps:11 |
93.83 |
324 |
70.72 |
3e-139 |
chloroplast processing peptidase
|
blastp_kegg |
lcl|vvi:100252527
|
1 |
298 |
+ |
298 |
Gaps:15 |
93.11 |
334 |
69.45 |
4e-139 |
chloroplast processing peptidase-like
|
blastp_kegg |
lcl|mdm:103400495
|
1 |
301 |
+ |
301 |
Gaps:11 |
93.83 |
324 |
70.39 |
9e-139 |
chloroplast processing peptidase
|
blastp_kegg |
lcl|fve:101296317
|
1 |
301 |
+ |
301 |
Gaps:13 |
97.37 |
304 |
74.32 |
1e-138 |
chloroplast processing peptidase-like
|
blastp_uniprot_sprot |
sp|Q8H0W1|PLSP1_ARATH
|
1 |
294 |
+ |
294 |
Gaps:16 |
98.97 |
291 |
68.75 |
2e-121 |
Chloroplast processing peptidase OS Arabidopsis thaliana GN PLSP1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|O04348|TPP1_ARATH
|
87 |
284 |
+ |
198 |
Gaps:3 |
59.12 |
340 |
59.20 |
2e-79 |
Thylakoidal processing peptidase 1 chloroplastic OS Arabidopsis thaliana GN TPP1 PE 2 SV 2
|
blastp_uniprot_sprot |
sp|Q9M9Z2|TPP2_ARATH
|
101 |
284 |
+ |
184 |
none |
50.14 |
367 |
63.04 |
1e-76 |
Probable thylakoidal processing peptidase 2 chloroplastic OS Arabidopsis thaliana GN TPP2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q51876|LEP_PHOLA
|
119 |
281 |
+ |
163 |
none |
80.30 |
203 |
46.63 |
3e-49 |
Signal peptidase I OS Phormidium laminosum GN lepB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P72660|LEP1_SYNY3
|
132 |
279 |
+ |
148 |
none |
75.51 |
196 |
55.41 |
5e-49 |
Probable signal peptidase I-1 OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN lepB1 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P73157|LEP2_SYNY3
|
100 |
280 |
+ |
181 |
Gaps:6 |
80.28 |
218 |
44.57 |
7e-45 |
Probable signal peptidase I-2 OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN lepB2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q10789|LEP_MYCTU
|
121 |
279 |
+ |
159 |
Gaps:53 |
72.11 |
294 |
33.49 |
3e-21 |
Signal peptidase I OS Mycobacterium tuberculosis GN lepB PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O33021|LEP_MYCLE
|
121 |
282 |
+ |
162 |
Gaps:62 |
76.82 |
289 |
31.53 |
7e-20 |
Probable signal peptidase I OS Mycobacterium leprae (strain TN) GN lepB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P26844|LEP_PSEFL
|
118 |
276 |
+ |
159 |
Gaps:62 |
72.18 |
284 |
34.15 |
6e-17 |
Signal peptidase I OS Pseudomonas fluorescens GN lepB PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P28628|LEPS_BACSU
|
95 |
283 |
+ |
189 |
Gaps:33 |
97.83 |
184 |
32.78 |
7e-17 |
Signal peptidase I S OS Bacillus subtilis (strain 168) GN sipS PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|211726
|
118 |
278 |
+ |
161 |
Gaps:15 |
99.39 |
163 |
37.04 |
1e-39 |
TIGR02227 sigpep_I_bact signal peptidase I bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria as well as a microsomal (endoplasmic reticulum) protein in eukaryotes.
|
rpsblast_cdd |
gnl|CDD|119398
|
137 |
269 |
+ |
133 |
Gaps:49 |
98.82 |
85 |
50.00 |
2e-19 |
cd06530 S26_SPase_I The S26 Type I signal peptidase (SPase LepB leader peptidase B leader peptidase I EC 3.4.21.89) family members are essential membrane-bound serine proteases that function to cleave the amino-terminal signal peptide extension from proteins that are translocated across biological membranes. The bacterial signal peptidase I which is the most intensively studied has two N-terminal transmembrane segments inserted in the plasma membrane and a hydrophilic C-terminal catalytic region that is located in the periplasmic space. Although the bacterial signal peptidase I is monomeric signal peptidases of eukaryotic cells commonly function as oligomeric complexes containing two divergent copies of the catalytic monomer. These are the IMP1 and IMP2 signal peptidases of the mitochondrial inner membrane that remove leader peptides from nuclear- and mitochondrial-encoded proteins. Also two components of the endoplasmic reticulum signal peptidase in mammals (18-kDa and 21-kDa) belong to this family and they process many proteins that enter the ER for retention or for export to the Golgi apparatus secretory vesicles plasma membranes or vacuole. An atypical member of the S26 SPase type I family is the TraF peptidase which has the remarkable activity of producing a cyclic protein of the Pseudomonas pilin system. The type I signal peptidases are unique serine proteases that utilize a serine/lysine catalytic dyad mechanism in place of the classical serine/histidine/aspartic acid catalytic triad mechanism..
|
rpsblast_cdd |
gnl|CDD|182787
|
91 |
271 |
+ |
181 |
Gaps:30 |
45.68 |
324 |
43.24 |
1e-12 |
PRK10861 PRK10861 signal peptidase I Provisional.
|
rpsblast_cdd |
gnl|CDD|151062
|
172 |
271 |
+ |
100 |
Gaps:9 |
78.99 |
138 |
30.28 |
4e-11 |
pfam10502 Peptidase_S26 Signal peptidase peptidase S26. This is a family of membrane signal serine endopeptidases which function in the processing of newly-synthesised secreted proteins. Peptidase S26 removes the hydrophobic N-terminal signal peptides as proteins are translocated across membranes. The active site residues take the form of a catalytic dyad that is Ser Lys in subfamily S26A the Ser is the nucleophile in catalysis and the Lys is the general base.
|
rpsblast_cdd |
gnl|CDD|31025
|
121 |
275 |
+ |
155 |
Gaps:11 |
87.95 |
166 |
30.82 |
7e-11 |
COG0681 LepB Signal peptidase I [Intracellular trafficking and secretion].
|
rpsblast_cdd |
gnl|CDD|119396
|
140 |
269 |
+ |
130 |
Gaps:50 |
95.24 |
84 |
40.00 |
1e-10 |
cd06462 Peptidase_S24_S26 The S24 S26 LexA/signal peptidase superfamily contains LexA-related and type I signal peptidase families. The S24 LexA protein domains include: the lambda repressor CI/C2 family and related bacterial prophage repressor proteins LexA (EC 3.4.21.88) the repressor of genes in the cellular SOS response to DNA damage MucA and the related UmuD proteins which are lesion-bypass DNA polymerases induced in response to mitogenic DNA damage RulA a component of the rulAB locus that confers resistance to UV and RuvA which is a component of the RuvABC resolvasome that catalyzes the resolution of Holliday junctions that arise during genetic recombination and DNA repair. The S26 type I signal peptidase (SPase) family also includes mitochondrial inner membrane protease (IMP)-like members. SPases are essential membrane-bound proteases which function to cleave away the amino-terminal signal peptide from the translocated pre-protein thus playing a crucial role in the transport of proteins across membranes in all living organisms. All members in this superfamily are unique serine proteases that carry out catalysis using a serine/lysine dyad instead of the prototypical serine/histidine/aspartic acid triad found in most serine proteases..
|
rpsblast_cdd |
gnl|CDD|131818
|
171 |
269 |
+ |
99 |
Gaps:16 |
67.25 |
171 |
28.70 |
4e-07 |
TIGR02771 TraF_Ti conjugative transfer signal peptidase TraF. This protein is found in apparent operons encoding elements of conjugative transfer systems. This family is homologous to a broader family of signal (leader) peptidases such as lepB. This family is present in both Ti-type and I-type conjugative systems.
|
rpsblast_kog |
gnl|CDD|35392
|
99 |
294 |
+ |
196 |
Gaps:24 |
98.86 |
176 |
47.13 |
1e-43 |
KOG0171 KOG0171 KOG0171 Mitochondrial inner membrane protease subunit IMP1 [Posttranslational modification protein turnover chaperones].
|
rpsblast_kog |
gnl|CDD|36781
|
145 |
279 |
+ |
135 |
Gaps:35 |
65.52 |
174 |
39.47 |
4e-13 |
KOG1568 KOG1568 KOG1568 Mitochondrial inner membrane protease subunit IMP2 [Posttranslational modification protein turnover chaperones Intracellular trafficking secretion and vesicular transport].
|