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 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HHA2
Term | Name | Level | Count |
---|---|---|---|
GO:0006465 | signal peptide processing | 5 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016485 | protein processing | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033619 | membrane protein proteolysis | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
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:0070001 | aspartic-type peptidase activity | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0042500 | aspartic endopeptidase activity, intramembrane cleaving | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.255 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.311 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.522 |
DEG_SPOP_SBC_1 | 253 | 257 | PF00917 | 0.525 |
DOC_CDC14_PxL_1 | 222 | 230 | PF14671 | 0.258 |
DOC_CYCLIN_yClb1_LxF_4 | 144 | 149 | PF00134 | 0.275 |
DOC_MAPK_gen_1 | 159 | 165 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 187 | 193 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 2 | 9 | PF00069 | 0.600 |
DOC_MAPK_MEF2A_6 | 37 | 46 | PF00069 | 0.280 |
DOC_PP1_RVXF_1 | 144 | 150 | PF00149 | 0.251 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.337 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.277 |
DOC_USP7_UBL2_3 | 183 | 187 | PF12436 | 0.490 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.591 |
LIG_AP2alpha_1 | 122 | 126 | PF02296 | 0.277 |
LIG_BRCT_BRCA1_1 | 282 | 286 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 103 | 110 | PF00928 | 0.175 |
LIG_deltaCOP1_diTrp_1 | 124 | 129 | PF00928 | 0.258 |
LIG_EH1_1 | 191 | 199 | PF00400 | 0.490 |
LIG_eIF4E_1 | 157 | 163 | PF01652 | 0.160 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.475 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.453 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.210 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.413 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.266 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.589 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.388 |
LIG_LIR_Gen_1 | 111 | 122 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 231 | 238 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 27 | 36 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 38 | 48 | PF02991 | 0.203 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.160 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.203 |
LIG_PCNA_yPIPBox_3 | 243 | 254 | PF02747 | 0.378 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.433 |
LIG_Pex14_2 | 122 | 126 | PF04695 | 0.277 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.310 |
LIG_Pex14_2 | 83 | 87 | PF04695 | 0.437 |
LIG_SH2_GRB2like | 39 | 42 | PF00017 | 0.233 |
LIG_SH2_PTP2 | 29 | 32 | PF00017 | 0.258 |
LIG_SH2_PTP2 | 63 | 66 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.258 |
LIG_SH2_STAP1 | 200 | 204 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.499 |
LIG_SUMO_SIM_anti_2 | 111 | 119 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 131 | 137 | PF11976 | 0.123 |
LIG_SUMO_SIM_anti_2 | 201 | 207 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 131 | 139 | PF11976 | 0.233 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.670 |
LIG_WRC_WIRS_1 | 229 | 234 | PF05994 | 0.315 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.323 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.280 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.334 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.605 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.388 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.343 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.277 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.279 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.424 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.143 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.352 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.229 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.365 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.277 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.462 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.216 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.266 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.266 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.190 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.308 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.343 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.615 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.433 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.248 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.191 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.258 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.277 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.368 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.250 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.462 |
MOD_SUMO_rev_2 | 290 | 299 | PF00179 | 0.635 |
TRG_DiLeu_BaEn_4 | 269 | 275 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.219 |
TRG_ER_diLys_1 | 303 | 306 | PF00400 | 0.618 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Y2 | Leptomonas seymouri | 64% | 90% |
A0A0S4JJ36 | Bodo saltans | 50% | 81% |
A0A1X0P170 | Trypanosomatidae | 59% | 86% |
A0A3Q8IDL5 | Leishmania donovani | 85% | 99% |
A0A3R7NBZ0 | Trypanosoma rangeli | 59% | 100% |
A4I4E8 | Leishmania infantum | 85% | 99% |
B9FJ61 | Oryza sativa subsp. japonica | 38% | 89% |
C9ZLJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 87% |
E9ADU8 | Leishmania major | 85% | 100% |
E9ALY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
O81062 | Arabidopsis thaliana | 35% | 89% |
Q6ZGL9 | Oryza sativa subsp. japonica | 40% | 89% |
Q8TCT6 | Homo sapiens | 27% | 80% |
Q8TCT9 | Homo sapiens | 31% | 81% |
Q93Z32 | Arabidopsis thaliana | 27% | 82% |
Q9CUS9 | Mus musculus | 27% | 80% |
Q9D8V0 | Mus musculus | 32% | 81% |
Q9UTA3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |