| 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: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:0005789 | endoplasmic reticulum membrane | 4 | 5 |
| GO:0031090 | organelle membrane | 3 | 5 |
Related structures:
AlphaFold database: A4HNI6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006486 | protein glycosylation | 4 | 5 |
| GO:0006487 | protein N-linked glycosylation | 5 | 1 |
| GO:0006490 | oligosaccharide-lipid intermediate biosynthetic process | 4 | 1 |
| GO:0006629 | lipid metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
| GO:0008152 | metabolic process | 1 | 5 |
| GO:0009058 | biosynthetic process | 2 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0019538 | protein metabolic process | 3 | 5 |
| GO:0036211 | protein modification process | 4 | 5 |
| GO:0043170 | macromolecule metabolic process | 3 | 5 |
| GO:0043412 | macromolecule modification | 4 | 5 |
| GO:0043413 | macromolecule glycosylation | 3 | 5 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 5 |
| GO:0044255 | cellular lipid metabolic process | 3 | 1 |
| GO:0070085 | glycosylation | 2 | 5 |
| GO:0071704 | organic substance metabolic process | 2 | 5 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
| GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
| GO:1901576 | organic substance biosynthetic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000026 | alpha-1,2-mannosyltransferase activity | 6 | 12 |
| GO:0000030 | mannosyltransferase activity | 5 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004376 | glycolipid mannosyltransferase activity | 6 | 12 |
| GO:0004377 | GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity | 7 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016757 | glycosyltransferase activity | 3 | 12 |
| GO:0016758 | hexosyltransferase activity | 4 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.334 |
| CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.337 |
| CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.228 |
| CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.352 |
| CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.277 |
| CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.297 |
| CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.469 |
| CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.277 |
| CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.338 |
| CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.308 |
| CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.382 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.425 |
| DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.258 |
| DOC_MAPK_FxFP_2 | 159 | 162 | PF00069 | 0.326 |
| DOC_MAPK_gen_1 | 286 | 295 | PF00069 | 0.261 |
| DOC_MAPK_gen_1 | 304 | 314 | PF00069 | 0.394 |
| DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.337 |
| DOC_PP1_RVXF_1 | 41 | 47 | PF00149 | 0.243 |
| DOC_PP1_RVXF_1 | 429 | 436 | PF00149 | 0.315 |
| DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.387 |
| DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.360 |
| DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.326 |
| DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.488 |
| DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.277 |
| DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.280 |
| DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.302 |
| LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.357 |
| LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.324 |
| LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.414 |
| LIG_14-3-3_CanoR_1 | 278 | 283 | PF00244 | 0.396 |
| LIG_BIR_III_2 | 119 | 123 | PF00653 | 0.315 |
| LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.388 |
| LIG_eIF4E_1 | 121 | 127 | PF01652 | 0.243 |
| LIG_eIF4E_1 | 161 | 167 | PF01652 | 0.258 |
| LIG_eIF4E_1 | 216 | 222 | PF01652 | 0.337 |
| LIG_FHA_1 | 111 | 117 | PF00498 | 0.252 |
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.225 |
| LIG_FHA_1 | 146 | 152 | PF00498 | 0.264 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.280 |
| LIG_FHA_1 | 195 | 201 | PF00498 | 0.246 |
| LIG_FHA_1 | 451 | 457 | PF00498 | 0.445 |
| LIG_FHA_1 | 9 | 15 | PF00498 | 0.404 |
| LIG_FHA_2 | 364 | 370 | PF00498 | 0.188 |
| LIG_FHA_2 | 408 | 414 | PF00498 | 0.278 |
| LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.268 |
| LIG_LIR_Gen_1 | 351 | 362 | PF02991 | 0.163 |
| LIG_LIR_Gen_1 | 403 | 414 | PF02991 | 0.387 |
| LIG_LIR_Gen_1 | 453 | 463 | PF02991 | 0.360 |
| LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.295 |
| LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.268 |
| LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.401 |
| LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.392 |
| LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.237 |
| LIG_LIR_Nem_3 | 403 | 409 | PF02991 | 0.339 |
| LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.337 |
| LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.444 |
| LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.173 |
| LIG_LYPXL_S_1 | 160 | 164 | PF13949 | 0.216 |
| LIG_LYPXL_yS_3 | 121 | 124 | PF13949 | 0.277 |
| LIG_LYPXL_yS_3 | 161 | 164 | PF13949 | 0.243 |
| LIG_LYPXL_yS_3 | 178 | 181 | PF13949 | 0.243 |
| LIG_NRBOX | 123 | 129 | PF00104 | 0.326 |
| LIG_PCNA_yPIPBox_3 | 340 | 354 | PF02747 | 0.163 |
| LIG_PDZ_Class_2 | 461 | 466 | PF00595 | 0.426 |
| LIG_Pex14_2 | 451 | 455 | PF04695 | 0.306 |
| LIG_SH2_CRK | 107 | 111 | PF00017 | 0.371 |
| LIG_SH2_GRB2like | 68 | 71 | PF00017 | 0.163 |
| LIG_SH2_SRC | 462 | 465 | PF00017 | 0.370 |
| LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.277 |
| LIG_SH2_STAP1 | 414 | 418 | PF00017 | 0.277 |
| LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.272 |
| LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.243 |
| LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.315 |
| LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.178 |
| LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.273 |
| LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.370 |
| LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.254 |
| LIG_SH3_3 | 152 | 158 | PF00018 | 0.243 |
| LIG_SH3_3 | 300 | 306 | PF00018 | 0.280 |
| LIG_SUMO_SIM_anti_2 | 11 | 16 | PF11976 | 0.416 |
| LIG_SUMO_SIM_anti_2 | 3 | 9 | PF11976 | 0.421 |
| LIG_SUMO_SIM_anti_2 | 395 | 401 | PF11976 | 0.315 |
| LIG_SUMO_SIM_par_1 | 124 | 130 | PF11976 | 0.291 |
| LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.302 |
| LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.258 |
| LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.331 |
| LIG_SUMO_SIM_par_1 | 86 | 93 | PF11976 | 0.315 |
| LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.279 |
| LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.258 |
| LIG_Vh1_VBS_1 | 207 | 225 | PF01044 | 0.315 |
| LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.401 |
| LIG_WRC_WIRS_1 | 443 | 448 | PF05994 | 0.409 |
| MOD_CK1_1 | 183 | 189 | PF00069 | 0.329 |
| MOD_CK1_1 | 237 | 243 | PF00069 | 0.243 |
| MOD_CK1_1 | 79 | 85 | PF00069 | 0.315 |
| MOD_CK1_1 | 93 | 99 | PF00069 | 0.297 |
| MOD_CK2_1 | 407 | 413 | PF00069 | 0.259 |
| MOD_CK2_1 | 75 | 81 | PF00069 | 0.388 |
| MOD_CK2_1 | 86 | 92 | PF00069 | 0.365 |
| MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.329 |
| MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.308 |
| MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.243 |
| MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.269 |
| MOD_GSK3_1 | 110 | 117 | PF00069 | 0.337 |
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.291 |
| MOD_GSK3_1 | 188 | 195 | PF00069 | 0.247 |
| MOD_GSK3_1 | 348 | 355 | PF00069 | 0.256 |
| MOD_GSK3_1 | 442 | 449 | PF00069 | 0.479 |
| MOD_GSK3_1 | 75 | 82 | PF00069 | 0.384 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.392 |
| MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.326 |
| MOD_NEK2_1 | 127 | 132 | PF00069 | 0.373 |
| MOD_NEK2_1 | 232 | 237 | PF00069 | 0.229 |
| MOD_NEK2_1 | 446 | 451 | PF00069 | 0.441 |
| MOD_NEK2_1 | 8 | 13 | PF00069 | 0.346 |
| MOD_NEK2_1 | 90 | 95 | PF00069 | 0.199 |
| MOD_NEK2_2 | 363 | 368 | PF00069 | 0.315 |
| MOD_PIKK_1 | 183 | 189 | PF00454 | 0.337 |
| MOD_PIKK_1 | 237 | 243 | PF00454 | 0.323 |
| MOD_PIKK_1 | 90 | 96 | PF00454 | 0.233 |
| MOD_PK_1 | 278 | 284 | PF00069 | 0.315 |
| MOD_PKA_1 | 437 | 443 | PF00069 | 0.410 |
| MOD_PKA_2 | 122 | 128 | PF00069 | 0.329 |
| MOD_PKA_2 | 24 | 30 | PF00069 | 0.337 |
| MOD_PKA_2 | 437 | 443 | PF00069 | 0.315 |
| MOD_PKA_2 | 76 | 82 | PF00069 | 0.336 |
| MOD_Plk_1 | 235 | 241 | PF00069 | 0.326 |
| MOD_Plk_4 | 122 | 128 | PF00069 | 0.258 |
| MOD_Plk_4 | 168 | 174 | PF00069 | 0.248 |
| MOD_Plk_4 | 243 | 249 | PF00069 | 0.414 |
| MOD_Plk_4 | 86 | 92 | PF00069 | 0.390 |
| MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.280 |
| MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.302 |
| MOD_SUMO_rev_2 | 321 | 326 | PF00179 | 0.280 |
| TRG_DiLeu_BaEn_1 | 217 | 222 | PF01217 | 0.233 |
| TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.243 |
| TRG_DiLeu_BaLyEn_6 | 203 | 208 | PF01217 | 0.272 |
| TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.416 |
| TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.243 |
| TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.249 |
| TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.243 |
| TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.271 |
| TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.282 |
| TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.258 |
| TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.256 |
| TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.404 |
| TRG_NLS_MonoExtN_4 | 17 | 23 | PF00514 | 0.344 |
| TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.302 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P6F7 | Leptomonas seymouri | 66% | 100% |
| A0A0S4INF7 | Bodo saltans | 23% | 92% |
| A0A0S4JLQ0 | Bodo saltans | 42% | 99% |
| A0A1X0P5V7 | Trypanosomatidae | 50% | 98% |
| A0A3R7K7Z3 | Trypanosoma rangeli | 49% | 98% |
| A0A3S7XA76 | Leishmania donovani | 87% | 100% |
| A4IC43 | Leishmania infantum | 87% | 100% |
| C9ZYD9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
| E9AFZ8 | Leishmania major | 87% | 100% |
| E9B751 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
| O74878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 99% |
| P53954 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 85% |
| P53993 | Caenorhabditis elegans | 32% | 99% |
| Q08B22 | Xenopus laevis | 37% | 96% |
| Q2TAA5 | Homo sapiens | 37% | 95% |
| Q3TZM9 | Mus musculus | 37% | 95% |
| Q54DM9 | Dictyostelium discoideum | 34% | 92% |
| Q59S72 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 77% |
| Q5R7Z6 | Pongo abelii | 37% | 95% |
| Q6BVB2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 30% | 76% |
| Q6C9T3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 33% | 73% |
| Q6CLD6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 82% |
| Q6FWD1 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 33% | 92% |
| Q6P312 | Xenopus tropicalis | 36% | 96% |
| Q75B12 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 30% | 80% |
| Q7ZW24 | Danio rerio | 37% | 93% |
| Q8X092 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 32% | 84% |
| Q9XEE9 | Arabidopsis thaliana | 38% | 100% |
| V5BPD4 | Trypanosoma cruzi | 50% | 98% |