Orthologous to animal ER-localized signal peptide peptidases, including minor histocompatibility antigen H13.. Localization: ER (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ADU8
Term | Name | Level | Count |
---|---|---|---|
GO:0006465 | signal peptide processing | 5 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016485 | protein processing | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033619 | membrane protein proteolysis | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004190 | aspartic-type endopeptidase activity | 5 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0042500 | aspartic endopeptidase activity, intramembrane cleaving | 6 | 2 |
GO:0070001 | aspartic-type peptidase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.259 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.270 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.305 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.470 |
DOC_CDC14_PxL_1 | 223 | 231 | PF14671 | 0.268 |
DOC_CYCLIN_yClb1_LxF_4 | 145 | 150 | PF00134 | 0.281 |
DOC_MAPK_gen_1 | 160 | 166 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 188 | 194 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 3 | 10 | PF00069 | 0.611 |
DOC_MAPK_MEF2A_6 | 38 | 47 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 145 | 151 | PF00149 | 0.257 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.346 |
DOC_PP4_FxxP_1 | 224 | 227 | PF00568 | 0.287 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.629 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.495 |
DOC_USP7_UBL2_3 | 62 | 66 | PF12436 | 0.597 |
LIG_AP2alpha_1 | 123 | 127 | PF02296 | 0.287 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.378 |
LIG_deltaCOP1_diTrp_1 | 125 | 130 | PF00928 | 0.268 |
LIG_EH1_1 | 192 | 200 | PF00400 | 0.495 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.481 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.453 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.231 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.417 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.272 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.395 |
LIG_LIR_Gen_1 | 112 | 123 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 232 | 239 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 28 | 37 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 232 | 236 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.175 |
LIG_MLH1_MIPbox_1 | 190 | 194 | PF16413 | 0.504 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.439 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.287 |
LIG_Pex14_2 | 224 | 228 | PF04695 | 0.310 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.347 |
LIG_SH2_GRB2like | 40 | 43 | PF00017 | 0.292 |
LIG_SH2_PTP2 | 30 | 33 | PF00017 | 0.268 |
LIG_SH2_PTP2 | 64 | 67 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.503 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.690 |
LIG_SUMO_SIM_anti_2 | 112 | 120 | PF11976 | 0.441 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.119 |
LIG_SUMO_SIM_anti_2 | 202 | 208 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 132 | 141 | PF11976 | 0.239 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.506 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.649 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.657 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.484 |
LIG_WRC_WIRS_1 | 44 | 49 | PF05994 | 0.333 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.304 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.590 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.516 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.344 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.597 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.602 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.395 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.387 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.413 |
MOD_GlcNHglycan | 292 | 296 | PF01048 | 0.492 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.302 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.268 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.427 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.539 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.728 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.143 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.361 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.146 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.359 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.368 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.469 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.287 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.252 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.273 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.196 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.318 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.378 |
MOD_PKA_1 | 188 | 194 | PF00069 | 0.440 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.465 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.618 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.444 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.253 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.196 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.296 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.434 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.287 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.247 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.519 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.559 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.277 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.460 |
MOD_SUMO_rev_2 | 292 | 301 | PF00179 | 0.673 |
MOD_SUMO_rev_2 | 302 | 309 | PF00179 | 0.649 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.268 |
TRG_ER_diLys_1 | 304 | 309 | PF00400 | 0.672 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Y2 | Leptomonas seymouri | 66% | 91% |
A0A0S4JJ36 | Bodo saltans | 46% | 82% |
A0A1X0P170 | Trypanosomatidae | 58% | 87% |
A0A3Q8IDL5 | Leishmania donovani | 93% | 100% |
A0A3R7NBZ0 | Trypanosoma rangeli | 58% | 100% |
A4HHA2 | Leishmania braziliensis | 85% | 100% |
A4I4E8 | Leishmania infantum | 93% | 100% |
B9FJ61 | Oryza sativa subsp. japonica | 39% | 90% |
C9ZLJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 88% |
E9ALY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
O81062 | Arabidopsis thaliana | 36% | 90% |
P49049 | Caenorhabditis elegans | 40% | 66% |
Q6ZGL9 | Oryza sativa subsp. japonica | 39% | 90% |
Q8TCT6 | Homo sapiens | 30% | 80% |
Q8TCT9 | Homo sapiens | 31% | 82% |
Q9CUS9 | Mus musculus | 30% | 80% |
Q9D8V0 | Mus musculus | 33% | 82% |
Q9UTA3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |