blastp_kegg |
lcl|pper:PRUPE_ppa023076mg
|
1 |
346 |
+ |
346 |
Gaps:15 |
70.95 |
475 |
73.89 |
3e-160 |
hypothetical protein
|
blastp_kegg |
lcl|pmum:103325023
|
1 |
346 |
+ |
346 |
Gaps:15 |
70.95 |
475 |
73.89 |
1e-158 |
C-terminal processing peptidase chloroplastic
|
blastp_kegg |
lcl|cit:102631414
|
43 |
346 |
+ |
304 |
Gaps:5 |
64.48 |
473 |
74.75 |
1e-155 |
C-terminal processing peptidase chloroplastic-like
|
blastp_kegg |
lcl|mdm:103427871
|
23 |
346 |
+ |
324 |
Gaps:19 |
66.88 |
471 |
75.24 |
8e-154 |
C-terminal processing peptidase chloroplastic-like
|
blastp_kegg |
lcl|vvi:100250320
|
47 |
346 |
+ |
300 |
Gaps:1 |
65.15 |
462 |
73.75 |
9e-153 |
carboxyl-terminal-processing protease-like
|
blastp_kegg |
lcl|tcc:TCM_029558
|
3 |
346 |
+ |
344 |
Gaps:24 |
70.44 |
477 |
68.45 |
2e-149 |
Peptidase S41 family protein isoform 1
|
blastp_kegg |
lcl|rcu:RCOM_0634390
|
43 |
346 |
+ |
304 |
Gaps:1 |
61.71 |
491 |
74.26 |
2e-148 |
Carboxyl-terminal-processing protease precursor putative (EC:3.4.21.102)
|
blastp_kegg |
lcl|cic:CICLE_v10018134mg
|
43 |
346 |
+ |
304 |
Gaps:30 |
66.27 |
498 |
68.48 |
2e-147 |
hypothetical protein
|
blastp_kegg |
lcl|gmx:100804192
|
57 |
346 |
+ |
290 |
Gaps:17 |
62.22 |
442 |
74.55 |
4e-145 |
C-terminal processing peptidase chloroplastic-like
|
blastp_kegg |
lcl|cam:101506541
|
34 |
346 |
+ |
313 |
Gaps:15 |
68.55 |
461 |
68.04 |
1e-144 |
carboxyl-terminal-processing protease-like
|
blastp_pdb |
1fc6_A
|
120 |
344 |
+ |
225 |
Gaps:22 |
60.05 |
388 |
34.76 |
4e-28 |
mol:protein length:388 PHOTOSYSTEM II D1 PROTEASE
|
blastp_pdb |
1fcf_A
|
120 |
344 |
+ |
225 |
Gaps:22 |
60.05 |
388 |
34.33 |
2e-27 |
mol:protein length:388 PHOTOSYSTEM II D1 PROTEASE
|
blastp_pdb |
1fc9_A
|
120 |
344 |
+ |
225 |
Gaps:22 |
60.05 |
388 |
34.33 |
2e-27 |
mol:protein length:388 PHOTOSYSTEM II D1 PROTEASE
|
blastp_pdb |
1fc7_A
|
120 |
344 |
+ |
225 |
Gaps:22 |
60.05 |
388 |
34.33 |
2e-27 |
mol:protein length:388 PHOTOSYSTEM II D1 PROTEASE
|
blastp_uniprot_sprot |
sp|Q55669|CTPA_SYNY3
|
120 |
346 |
+ |
227 |
Gaps:10 |
52.22 |
427 |
34.53 |
2e-36 |
Carboxyl-terminal-processing protease OS Synechocystis sp. (strain PCC 6803 / Kazusa) GN ctpA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P42784|CTPA_SYNP2
|
120 |
346 |
+ |
227 |
Gaps:11 |
53.62 |
414 |
33.78 |
7e-34 |
Carboxyl-terminal-processing protease OS Synechococcus sp. (strain ATCC 27264 / PCC 7002 / PR-6) GN ctpA PE 3 SV 2
|
blastp_uniprot_sprot |
sp|O04073|CTPA_ACUOB
|
120 |
344 |
+ |
225 |
Gaps:22 |
50.22 |
464 |
34.33 |
4e-27 |
C-terminal processing peptidase chloroplastic OS Acutodesmus obliquus GN ctpA PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O34666|CTPA_BACSU
|
164 |
346 |
+ |
183 |
Gaps:18 |
37.55 |
466 |
32.00 |
1e-14 |
Carboxy-terminal processing protease CtpA OS Bacillus subtilis (strain 168) GN ctpA PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q8CSK8|CTPAL_STAES
|
164 |
347 |
+ |
184 |
Gaps:16 |
35.44 |
491 |
29.89 |
1e-12 |
Probable CtpA-like serine protease OS Staphylococcus epidermidis (strain ATCC 12228) GN SE_1113 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5HPB7|CTPAL_STAEQ
|
164 |
347 |
+ |
184 |
Gaps:16 |
35.44 |
491 |
29.89 |
2e-12 |
Probable CtpA-like serine protease OS Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN SERP0996 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q44879|CTPA_BARBK
|
153 |
345 |
+ |
193 |
Gaps:20 |
43.55 |
434 |
31.22 |
5e-12 |
Carboxy-terminal-processing protease OS Bartonella bacilliformis (strain ATCC 35685 / KC583) GN ctpA PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q2YXZ9|CTPAL_STAAB
|
164 |
347 |
+ |
184 |
Gaps:16 |
35.08 |
496 |
29.31 |
4e-11 |
Probable CtpA-like serine protease OS Staphylococcus aureus (strain bovine RF122 / ET3-1) GN SAB1275c PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6GGY8|CTPAL_STAAR
|
164 |
347 |
+ |
184 |
Gaps:16 |
35.08 |
496 |
29.31 |
4e-11 |
Probable CtpA-like serine protease OS Staphylococcus aureus (strain MRSA252) GN SAR1432 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5HG01|CTPAL_STAAC
|
164 |
347 |
+ |
184 |
Gaps:16 |
35.08 |
496 |
29.31 |
4e-11 |
Probable CtpA-like serine protease OS Staphylococcus aureus (strain COL) GN SACOL1455 PE 3 SV 1
|
rpsblast_cdd |
gnl|CDD|177681
|
120 |
344 |
+ |
225 |
Gaps:15 |
58.61 |
389 |
35.53 |
7e-38 |
PLN00049 PLN00049 carboxyl-terminal processing protease Provisional.
|
rpsblast_cdd |
gnl|CDD|161775
|
163 |
346 |
+ |
184 |
Gaps:10 |
53.89 |
334 |
32.78 |
8e-29 |
TIGR00225 prc C-terminal peptidase (prc). A C-terminal peptidase with different substrates in different species including processing of D1 protein of the photosystem II reaction center in higher plants and cleavage of a peptide of 11 residues from the precursor form of penicillin-binding protein in E.coli E.coli and H influenza have the most distal branch of the tree and their proteins have an N-terminal 200 amino acids that show no homology to other proteins in the database.
|
rpsblast_cdd |
gnl|CDD|31136
|
110 |
347 |
+ |
238 |
Gaps:10 |
59.11 |
406 |
26.25 |
4e-28 |
COG0793 Prc Periplasmic protease [Cell envelope biogenesis outer membrane].
|
rpsblast_cdd |
gnl|CDD|188415
|
152 |
344 |
+ |
193 |
Gaps:15 |
19.12 |
973 |
28.49 |
2e-14 |
TIGR03900 prc_long_Delta putative carboxyl-terminal-processing protease deltaproteobacterial. This model describes a multidomain protein of about 1070 residues restricted to the order Myxococcales in the Deltaproteobacteria. Members contain a PDZ domain (pfam00595) an S41 family peptidase domain (pfam03572) and an SH3 domain (pfam06347). A core region of this family including PDZ and S41 regions is described by TIGR00225 C-terminal processing peptidase which recognizes the Prc protease. The species distribution of this family approximates that of largely Deltaproteobacterial C-terminal putative protein-sorting domain TIGR03901 analogous to LPXTG and PEP-CTERM but the co-occurrence may reflect shared restriction to the Myxococcales rather than a substrate/target relationship.
|
rpsblast_cdd |
gnl|CDD|29045
|
192 |
281 |
+ |
90 |
Gaps:6 |
98.82 |
85 |
33.33 |
1e-12 |
cd00988 PDZ_CTP_protease PDZ domain of C-terminal processing- tail-specific- and tricorn proteases which function in posttranslational protein processing maturation and disassembly or degradation in Bacteria Archaea and plant chloroplasts. May be responsible for substrate recognition and/or binding as most PDZ domains bind C-terminal polypeptides and binding to internal (non-C-terminal) polypeptides and even to lipids has been demonstrated. In this subfamily of protease-associated PDZ domains a C-terminal beta-strand forms the peptide-binding groove base a circular permutation with respect to PDZ domains found in Eumetazoan signaling proteins..
|
rpsblast_cdd |
gnl|CDD|197587
|
194 |
269 |
+ |
76 |
Gaps:3 |
85.88 |
85 |
36.99 |
4e-10 |
smart00228 PDZ Domain present in PSD-95 Dlg and ZO-1/2. Also called DHR (Dlg homologous region) or GLGF (relatively well conserved tetrapeptide in these domains). Some PDZs have been shown to bind C-terminal polypeptides others appear to bind internal (non-C-terminal) polypeptides. Different PDZs possess different binding specificities.
|