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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 9 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9ACY1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0016485 | protein processing | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0051604 | protein maturation | 4 | 11 |
GO:0071586 | CAAX-box protein processing | 6 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004222 | metalloendopeptidase activity | 5 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008237 | metallopeptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 173 | 179 | PF00089 | 0.289 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.340 |
CLV_PCSK_FUR_1 | 29 | 33 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.181 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.361 |
DEG_APCC_DBOX_1 | 135 | 143 | PF00400 | 0.363 |
DEG_APCC_KENBOX_2 | 389 | 393 | PF00400 | 0.467 |
DOC_CDC14_PxL_1 | 82 | 90 | PF14671 | 0.201 |
DOC_CYCLIN_RxL_1 | 149 | 160 | PF00134 | 0.457 |
DOC_CYCLIN_RxL_1 | 377 | 389 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 69 | 77 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 121 | 127 | PF00134 | 0.324 |
DOC_CYCLIN_yCln2_LP_2 | 161 | 167 | PF00134 | 0.378 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 321 | 329 | PF00069 | 0.163 |
DOC_MAPK_gen_1 | 382 | 388 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 10 | 18 | PF00069 | 0.266 |
DOC_MAPK_MEF2A_6 | 153 | 161 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 274 | 283 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 292 | 300 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.234 |
DOC_MAPK_RevD_3 | 16 | 32 | PF00069 | 0.266 |
DOC_PP1_RVXF_1 | 166 | 173 | PF00149 | 0.266 |
DOC_PP1_RVXF_1 | 313 | 320 | PF00149 | 0.289 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.310 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.324 |
DOC_PP2B_PxIxI_1 | 278 | 284 | PF00149 | 0.379 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.282 |
DOC_SPAK_OSR1_1 | 370 | 374 | PF12202 | 0.506 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.287 |
DOC_USP7_UBL2_3 | 149 | 153 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 245 | 253 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.310 |
LIG_Actin_WH2_2 | 144 | 160 | PF00022 | 0.458 |
LIG_Actin_WH2_2 | 220 | 238 | PF00022 | 0.467 |
LIG_APCC_ABBA_1 | 338 | 343 | PF00400 | 0.393 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.359 |
LIG_Clathr_ClatBox_1 | 316 | 320 | PF01394 | 0.310 |
LIG_EH1_1 | 186 | 194 | PF00400 | 0.179 |
LIG_eIF4E_1 | 221 | 227 | PF01652 | 0.426 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.538 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.438 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.424 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.573 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.467 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.477 |
LIG_GBD_Chelix_1 | 300 | 308 | PF00786 | 0.266 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 126 | 133 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 399 | 410 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.469 |
LIG_LIR_LC3C_4 | 190 | 195 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.211 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 350 | 355 | PF02991 | 0.251 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.445 |
LIG_PCNA_yPIPBox_3 | 166 | 180 | PF02747 | 0.310 |
LIG_Pex14_2 | 177 | 181 | PF04695 | 0.211 |
LIG_Pex14_2 | 341 | 345 | PF04695 | 0.278 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.411 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 128 | 131 | PF00017 | 0.457 |
LIG_SH2_GRB2like | 297 | 300 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 407 | 411 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 297 | 300 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 163 | 166 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.378 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.282 |
LIG_SUMO_SIM_anti_2 | 115 | 122 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 190 | 195 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 384 | 389 | PF11976 | 0.426 |
LIG_TRAF2_1 | 48 | 51 | PF00917 | 0.477 |
LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.411 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.201 |
LIG_UBA3_1 | 161 | 168 | PF00899 | 0.266 |
LIG_UBA3_1 | 269 | 274 | PF00899 | 0.482 |
LIG_UBA3_1 | 385 | 390 | PF00899 | 0.446 |
LIG_WRC_WIRS_1 | 349 | 354 | PF05994 | 0.266 |
MOD_CDK_SPxxK_3 | 215 | 222 | PF00069 | 0.482 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.414 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.473 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.271 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.314 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.363 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.465 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.451 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.257 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.453 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.459 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.262 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.226 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.315 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.249 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.442 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.337 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.446 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.443 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.411 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.324 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.424 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.426 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.325 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.410 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.455 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.448 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.294 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.195 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.431 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.279 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.410 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.347 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.462 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.408 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.224 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.489 |
TRG_ER_diLys_1 | 424 | 427 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 230 | 242 | PF08389 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC87 | Leptomonas seymouri | 60% | 100% |
A0A0S4J5R2 | Bodo saltans | 46% | 100% |
A0A1X0P508 | Trypanosomatidae | 46% | 100% |
A0A3S7X0A9 | Leishmania donovani | 96% | 100% |
A4HFC3 | Leishmania braziliensis | 77% | 100% |
A4I2K0 | Leishmania infantum | 96% | 100% |
C9ZYC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AYQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O75844 | Homo sapiens | 33% | 90% |
P40769 | Bacillus subtilis (strain 168) | 25% | 100% |
P47154 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 94% |
Q10071 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 90% |
Q3Y6B8 | Taenia solium | 32% | 90% |
Q54FH7 | Dictyostelium discoideum | 35% | 100% |
Q6EPN8 | Oryza sativa subsp. japonica | 38% | 100% |
Q80W54 | Mus musculus | 33% | 90% |
Q8RX88 | Arabidopsis thaliana | 39% | 100% |
Q9XVE5 | Caenorhabditis elegans | 32% | 97% |
V5DQF4 | Trypanosoma cruzi | 46% | 100% |