| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 4 |
| Forrest at al. (procyclic) | no | yes: 4 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 3 |
| 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: 12 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005730 | nucleolus | 5 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HI66
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006606 | protein import into nucleus | 5 | 12 |
| GO:0006810 | transport | 3 | 12 |
| GO:0006886 | intracellular protein transport | 4 | 12 |
| GO:0006913 | nucleocytoplasmic transport | 5 | 12 |
| GO:0008104 | protein localization | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0015031 | protein transport | 4 | 12 |
| GO:0033036 | macromolecule localization | 2 | 12 |
| GO:0033365 | protein localization to organelle | 5 | 12 |
| GO:0034504 | protein localization to nucleus | 6 | 12 |
| GO:0045184 | establishment of protein localization | 3 | 12 |
| GO:0046907 | intracellular transport | 3 | 12 |
| GO:0051169 | nuclear transport | 4 | 12 |
| GO:0051170 | import into nucleus | 6 | 12 |
| GO:0051179 | localization | 1 | 12 |
| GO:0051234 | establishment of localization | 2 | 12 |
| GO:0051641 | cellular localization | 2 | 12 |
| GO:0051649 | establishment of localization in cell | 3 | 12 |
| GO:0070727 | cellular macromolecule localization | 3 | 12 |
| GO:0071702 | organic substance transport | 4 | 12 |
| GO:0071705 | nitrogen compound transport | 4 | 12 |
| GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
| GO:0006607 | NLS-bearing protein import into nucleus | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0061608 | nuclear import signal receptor activity | 3 | 12 |
| GO:0140104 | molecular carrier activity | 1 | 12 |
| GO:0140142 | nucleocytoplasmic carrier activity | 2 | 12 |
| GO:0005048 | signal sequence binding | 4 | 1 |
| GO:0005488 | binding | 1 | 1 |
| GO:0008139 | nuclear localization sequence binding | 5 | 1 |
| GO:0033218 | amide binding | 2 | 1 |
| GO:0042277 | peptide binding | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.357 |
| CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.568 |
| CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.334 |
| CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.568 |
| CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.307 |
| CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.322 |
| CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.320 |
| CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.341 |
| CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.402 |
| CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.644 |
| CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.445 |
| CLV_Separin_Metazoa | 346 | 350 | PF03568 | 0.448 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.628 |
| DEG_SPOP_SBC_1 | 122 | 126 | PF00917 | 0.448 |
| DOC_CDC14_PxL_1 | 423 | 431 | PF14671 | 0.483 |
| DOC_CDC14_PxL_1 | 82 | 90 | PF14671 | 0.540 |
| DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.583 |
| DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.322 |
| DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.443 |
| DOC_MAPK_MEF2A_6 | 491 | 500 | PF00069 | 0.569 |
| DOC_MAPK_RevD_3 | 385 | 399 | PF00069 | 0.341 |
| DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.400 |
| DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.448 |
| DOC_PP2B_PxIxI_1 | 315 | 321 | PF00149 | 0.448 |
| DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.336 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.322 |
| DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.657 |
| DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.765 |
| DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.366 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.579 |
| LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.397 |
| LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.341 |
| LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.602 |
| LIG_Actin_WH2_2 | 216 | 234 | PF00022 | 0.400 |
| LIG_APCC_ABBAyCdc20_2 | 31 | 37 | PF00400 | 0.613 |
| LIG_deltaCOP1_diTrp_1 | 400 | 410 | PF00928 | 0.448 |
| LIG_EH1_1 | 371 | 379 | PF00400 | 0.448 |
| LIG_eIF4E_1 | 372 | 378 | PF01652 | 0.448 |
| LIG_FHA_1 | 103 | 109 | PF00498 | 0.382 |
| LIG_FHA_1 | 161 | 167 | PF00498 | 0.345 |
| LIG_FHA_1 | 233 | 239 | PF00498 | 0.341 |
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.411 |
| LIG_FHA_1 | 440 | 446 | PF00498 | 0.352 |
| LIG_FHA_2 | 257 | 263 | PF00498 | 0.448 |
| LIG_FHA_2 | 485 | 491 | PF00498 | 0.582 |
| LIG_FHA_2 | 504 | 510 | PF00498 | 0.399 |
| LIG_FHA_2 | 95 | 101 | PF00498 | 0.482 |
| LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.448 |
| LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.468 |
| LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.428 |
| LIG_LYPXL_yS_3 | 141 | 144 | PF13949 | 0.400 |
| LIG_MAD2 | 110 | 118 | PF02301 | 0.498 |
| LIG_MAD2 | 301 | 309 | PF02301 | 0.448 |
| LIG_MYND_3 | 247 | 251 | PF01753 | 0.508 |
| LIG_NRBOX | 131 | 137 | PF00104 | 0.400 |
| LIG_NRBOX | 259 | 265 | PF00104 | 0.322 |
| LIG_PDZ_Class_2 | 534 | 539 | PF00595 | 0.618 |
| LIG_Pex14_1 | 277 | 281 | PF04695 | 0.307 |
| LIG_Pex14_2 | 146 | 150 | PF04695 | 0.307 |
| LIG_PTB_Apo_2 | 404 | 411 | PF02174 | 0.448 |
| LIG_SH2_CRK | 120 | 124 | PF00017 | 0.449 |
| LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.448 |
| LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.322 |
| LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.352 |
| LIG_SH3_1 | 243 | 249 | PF00018 | 0.391 |
| LIG_SH3_3 | 243 | 249 | PF00018 | 0.391 |
| LIG_SH3_3 | 310 | 316 | PF00018 | 0.408 |
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.448 |
| LIG_SH3_3 | 422 | 428 | PF00018 | 0.367 |
| LIG_SH3_3 | 59 | 65 | PF00018 | 0.573 |
| LIG_SUMO_SIM_anti_2 | 259 | 269 | PF11976 | 0.448 |
| LIG_SUMO_SIM_par_1 | 110 | 115 | PF11976 | 0.386 |
| LIG_SUMO_SIM_par_1 | 219 | 225 | PF11976 | 0.448 |
| LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.413 |
| LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.350 |
| LIG_UBA3_1 | 107 | 116 | PF00899 | 0.467 |
| LIG_UBA3_1 | 217 | 224 | PF00899 | 0.392 |
| LIG_WRC_WIRS_1 | 501 | 506 | PF05994 | 0.569 |
| MOD_CK1_1 | 160 | 166 | PF00069 | 0.362 |
| MOD_CK1_1 | 280 | 286 | PF00069 | 0.307 |
| MOD_CK1_1 | 307 | 313 | PF00069 | 0.369 |
| MOD_CK1_1 | 503 | 509 | PF00069 | 0.567 |
| MOD_CK2_1 | 219 | 225 | PF00069 | 0.448 |
| MOD_CK2_1 | 388 | 394 | PF00069 | 0.448 |
| MOD_CK2_1 | 504 | 510 | PF00069 | 0.511 |
| MOD_CK2_1 | 60 | 66 | PF00069 | 0.650 |
| MOD_CK2_1 | 94 | 100 | PF00069 | 0.431 |
| MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.413 |
| MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.448 |
| MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.509 |
| MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.351 |
| MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.445 |
| MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.609 |
| MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.536 |
| MOD_GSK3_1 | 156 | 163 | PF00069 | 0.328 |
| MOD_GSK3_1 | 232 | 239 | PF00069 | 0.341 |
| MOD_GSK3_1 | 304 | 311 | PF00069 | 0.339 |
| MOD_GSK3_1 | 325 | 332 | PF00069 | 0.379 |
| MOD_GSK3_1 | 406 | 413 | PF00069 | 0.495 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.490 |
| MOD_GSK3_1 | 72 | 79 | PF00069 | 0.554 |
| MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.448 |
| MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.341 |
| MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.392 |
| MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.341 |
| MOD_N-GLC_2 | 240 | 242 | PF02516 | 0.341 |
| MOD_N-GLC_2 | 381 | 383 | PF02516 | 0.437 |
| MOD_N-GLC_2 | 90 | 92 | PF02516 | 0.522 |
| MOD_NEK2_1 | 102 | 107 | PF00069 | 0.435 |
| MOD_NEK2_1 | 377 | 382 | PF00069 | 0.392 |
| MOD_NEK2_1 | 410 | 415 | PF00069 | 0.521 |
| MOD_PIKK_1 | 329 | 335 | PF00454 | 0.308 |
| MOD_PK_1 | 110 | 116 | PF00069 | 0.413 |
| MOD_PKA_1 | 356 | 362 | PF00069 | 0.322 |
| MOD_Plk_1 | 160 | 166 | PF00069 | 0.370 |
| MOD_Plk_1 | 187 | 193 | PF00069 | 0.452 |
| MOD_Plk_1 | 232 | 238 | PF00069 | 0.341 |
| MOD_Plk_1 | 329 | 335 | PF00069 | 0.448 |
| MOD_Plk_1 | 406 | 412 | PF00069 | 0.341 |
| MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.535 |
| MOD_Plk_4 | 102 | 108 | PF00069 | 0.251 |
| MOD_Plk_4 | 160 | 166 | PF00069 | 0.389 |
| MOD_Plk_4 | 256 | 262 | PF00069 | 0.376 |
| MOD_Plk_4 | 500 | 506 | PF00069 | 0.495 |
| MOD_Plk_4 | 84 | 90 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.366 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.573 |
| MOD_SUMO_for_1 | 397 | 400 | PF00179 | 0.224 |
| MOD_SUMO_rev_2 | 431 | 441 | PF00179 | 0.385 |
| MOD_SUMO_rev_2 | 456 | 461 | PF00179 | 0.460 |
| TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.447 |
| TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.437 |
| TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.583 |
| TRG_NES_CRM1_1 | 373 | 388 | PF08389 | 0.448 |
| TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.448 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PFK7 | Leptomonas seymouri | 87% | 100% |
| A0A0S4KNG1 | Bodo saltans | 50% | 100% |
| A0A1X0P216 | Trypanosomatidae | 57% | 100% |
| A0A3R7LEH1 | Trypanosoma rangeli | 54% | 100% |
| A0A3S7X3A8 | Leishmania donovani | 95% | 100% |
| A2VE08 | Bos taurus | 40% | 100% |
| A4I5E3 | Leishmania infantum | 95% | 100% |
| A9QM74 | Homo sapiens | 41% | 100% |
| B6HJ92 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) | 40% | 98% |
| C0LLJ0 | Mus musculus | 38% | 100% |
| C1JZ66 | Bos taurus | 41% | 100% |
| C6K7I2 | Sus scrofa | 40% | 100% |
| C9ZQT2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
| E9B0P1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
| F4JL11 | Arabidopsis thaliana | 41% | 100% |
| F4KF65 | Arabidopsis thaliana | 28% | 100% |
| G5EB89 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 39% | 97% |
| O00505 | Homo sapiens | 39% | 100% |
| O00629 | Homo sapiens | 41% | 100% |
| O04294 | Arabidopsis thaliana | 41% | 100% |
| O14063 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 37% | 99% |
| O15131 | Homo sapiens | 42% | 100% |
| O22478 | Solanum lycopersicum | 39% | 100% |
| O35343 | Mus musculus | 42% | 100% |
| O35344 | Mus musculus | 39% | 100% |
| O35345 | Mus musculus | 42% | 100% |
| O60684 | Homo sapiens | 42% | 100% |
| O80480 | Arabidopsis thaliana | 40% | 100% |
| O94374 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
| P52170 | Xenopus laevis | 39% | 100% |
| P52171 | Xenopus laevis | 38% | 100% |
| P52292 | Homo sapiens | 45% | 100% |
| P52293 | Mus musculus | 45% | 100% |
| P52294 | Homo sapiens | 40% | 100% |
| P52295 | Drosophila melanogaster | 35% | 100% |
| P83953 | Rattus norvegicus | 40% | 100% |
| P91276 | Caenorhabditis elegans | 33% | 100% |
| Q02821 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 40% | 99% |
| Q0V7M0 | Bos taurus | 42% | 100% |
| Q19969 | Caenorhabditis elegans | 40% | 100% |
| Q4Q7J1 | Leishmania major | 94% | 100% |
| Q4WVW4 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 23% | 93% |
| Q503E9 | Danio rerio | 41% | 100% |
| Q557F4 | Dictyostelium discoideum | 32% | 98% |
| Q56R16 | Rattus norvegicus | 42% | 100% |
| Q5R909 | Pongo abelii | 40% | 100% |
| Q5RBV0 | Pongo abelii | 42% | 100% |
| Q5ZML1 | Gallus gallus | 40% | 100% |
| Q60960 | Mus musculus | 40% | 100% |
| Q71VM4 | Oryza sativa subsp. japonica | 41% | 100% |
| Q76P29 | Dictyostelium discoideum | 42% | 100% |
| Q96321 | Arabidopsis thaliana | 41% | 100% |
| Q9FJ09 | Arabidopsis thaliana | 41% | 100% |
| Q9FJ92 | Arabidopsis thaliana | 37% | 100% |
| Q9FWY7 | Arabidopsis thaliana | 41% | 100% |
| Q9FYP9 | Oryza sativa subsp. japonica | 28% | 100% |
| Q9M9X7 | Arabidopsis thaliana | 41% | 100% |
| Q9SLX0 | Oryza sativa subsp. japonica | 44% | 100% |
| V5B924 | Trypanosoma cruzi | 54% | 100% |