| 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: 6, no: 5 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:0005886 | plasma membrane | 3 | 7 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HAY2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0010960 | magnesium ion homeostasis | 8 | 12 |
| GO:0042592 | homeostatic process | 3 | 12 |
| GO:0048878 | chemical homeostasis | 4 | 12 |
| GO:0050801 | monoatomic ion homeostasis | 5 | 12 |
| GO:0055065 | obsolete metal ion homeostasis | 7 | 12 |
| GO:0055080 | monoatomic cation homeostasis | 6 | 12 |
| GO:0065007 | biological regulation | 1 | 12 |
| GO:0065008 | regulation of biological quality | 2 | 12 |
| GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 12 |
| GO:0098771 | inorganic ion homeostasis | 6 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.489 |
| CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.516 |
| CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.559 |
| CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.489 |
| CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.529 |
| CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.614 |
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.548 |
| CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.614 |
| CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.448 |
| CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.448 |
| CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.498 |
| DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.248 |
| DEG_COP1_1 | 531 | 539 | PF00400 | 0.345 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.607 |
| DOC_CKS1_1 | 258 | 263 | PF01111 | 0.259 |
| DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.466 |
| DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.454 |
| DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.335 |
| DOC_MAPK_MEF2A_6 | 297 | 305 | PF00069 | 0.249 |
| DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.338 |
| DOC_MAPK_MEF2A_6 | 512 | 519 | PF00069 | 0.375 |
| DOC_PP1_RVXF_1 | 219 | 226 | PF00149 | 0.248 |
| DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.723 |
| DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.353 |
| DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.459 |
| DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.262 |
| DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.576 |
| DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.403 |
| DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.499 |
| DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.376 |
| DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.428 |
| DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.643 |
| DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.334 |
| DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.255 |
| LIG_14-3-3_CanoR_1 | 573 | 581 | PF00244 | 0.546 |
| LIG_14-3-3_CanoR_1 | 584 | 588 | PF00244 | 0.467 |
| LIG_APCC_ABBA_1 | 486 | 491 | PF00400 | 0.391 |
| LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.342 |
| LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.303 |
| LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.392 |
| LIG_Clathr_ClatBox_1 | 375 | 379 | PF01394 | 0.287 |
| LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.447 |
| LIG_Clathr_ClatBox_1 | 86 | 90 | PF01394 | 0.534 |
| LIG_EH1_1 | 369 | 377 | PF00400 | 0.294 |
| LIG_eIF4E_1 | 370 | 376 | PF01652 | 0.292 |
| LIG_eIF4E_1 | 557 | 563 | PF01652 | 0.239 |
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.310 |
| LIG_FHA_1 | 276 | 282 | PF00498 | 0.283 |
| LIG_FHA_1 | 316 | 322 | PF00498 | 0.314 |
| LIG_FHA_1 | 336 | 342 | PF00498 | 0.162 |
| LIG_FHA_1 | 497 | 503 | PF00498 | 0.284 |
| LIG_FHA_1 | 525 | 531 | PF00498 | 0.363 |
| LIG_FHA_1 | 81 | 87 | PF00498 | 0.300 |
| LIG_FHA_1 | 89 | 95 | PF00498 | 0.442 |
| LIG_FHA_2 | 252 | 258 | PF00498 | 0.311 |
| LIG_FHA_2 | 375 | 381 | PF00498 | 0.283 |
| LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.330 |
| LIG_LIR_Gen_1 | 495 | 506 | PF02991 | 0.291 |
| LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.298 |
| LIG_LIR_Gen_1 | 555 | 563 | PF02991 | 0.349 |
| LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.348 |
| LIG_LIR_LC3C_4 | 499 | 502 | PF02991 | 0.360 |
| LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.335 |
| LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.352 |
| LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.287 |
| LIG_LIR_Nem_3 | 521 | 525 | PF02991 | 0.299 |
| LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.351 |
| LIG_PCNA_yPIPBox_3 | 116 | 127 | PF02747 | 0.448 |
| LIG_PDZ_Class_3 | 585 | 590 | PF00595 | 0.540 |
| LIG_Pex14_2 | 188 | 192 | PF04695 | 0.300 |
| LIG_Pex14_2 | 535 | 539 | PF04695 | 0.344 |
| LIG_Pex14_2 | 75 | 79 | PF04695 | 0.316 |
| LIG_SH2_SRC | 394 | 397 | PF00017 | 0.298 |
| LIG_SH2_STAP1 | 108 | 112 | PF00017 | 0.473 |
| LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.303 |
| LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.382 |
| LIG_SH3_3 | 192 | 198 | PF00018 | 0.348 |
| LIG_SH3_3 | 255 | 261 | PF00018 | 0.246 |
| LIG_SH3_3 | 466 | 472 | PF00018 | 0.342 |
| LIG_SUMO_SIM_anti_2 | 240 | 245 | PF11976 | 0.324 |
| LIG_SUMO_SIM_anti_2 | 318 | 324 | PF11976 | 0.309 |
| LIG_SUMO_SIM_anti_2 | 352 | 359 | PF11976 | 0.299 |
| LIG_SUMO_SIM_anti_2 | 64 | 70 | PF11976 | 0.280 |
| LIG_SUMO_SIM_anti_2 | 83 | 88 | PF11976 | 0.380 |
| LIG_SUMO_SIM_anti_2 | 93 | 100 | PF11976 | 0.448 |
| LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.258 |
| LIG_SUMO_SIM_par_1 | 498 | 503 | PF11976 | 0.294 |
| LIG_SUMO_SIM_par_1 | 513 | 518 | PF11976 | 0.371 |
| LIG_SUMO_SIM_par_1 | 64 | 70 | PF11976 | 0.336 |
| LIG_SUMO_SIM_par_1 | 90 | 95 | PF11976 | 0.448 |
| LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.195 |
| LIG_WRC_WIRS_1 | 536 | 541 | PF05994 | 0.321 |
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.415 |
| MOD_CK1_1 | 410 | 416 | PF00069 | 0.419 |
| MOD_CK1_1 | 421 | 427 | PF00069 | 0.410 |
| MOD_CK1_1 | 496 | 502 | PF00069 | 0.370 |
| MOD_CK1_1 | 569 | 575 | PF00069 | 0.488 |
| MOD_CK2_1 | 251 | 257 | PF00069 | 0.392 |
| MOD_CK2_1 | 441 | 447 | PF00069 | 0.373 |
| MOD_CK2_1 | 97 | 103 | PF00069 | 0.440 |
| MOD_Cter_Amidation | 9 | 12 | PF01082 | 0.485 |
| MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.253 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.287 |
| MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.577 |
| MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 451 | 456 | PF01048 | 0.631 |
| MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.684 |
| MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.625 |
| MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.358 |
| MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.248 |
| MOD_GSK3_1 | 148 | 155 | PF00069 | 0.300 |
| MOD_GSK3_1 | 335 | 342 | PF00069 | 0.304 |
| MOD_GSK3_1 | 417 | 424 | PF00069 | 0.405 |
| MOD_GSK3_1 | 492 | 499 | PF00069 | 0.305 |
| MOD_GSK3_1 | 520 | 527 | PF00069 | 0.386 |
| MOD_GSK3_1 | 53 | 60 | PF00069 | 0.459 |
| MOD_GSK3_1 | 568 | 575 | PF00069 | 0.471 |
| MOD_N-GLC_1 | 407 | 412 | PF02516 | 0.675 |
| MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.711 |
| MOD_NEK2_1 | 122 | 127 | PF00069 | 0.293 |
| MOD_NEK2_1 | 132 | 137 | PF00069 | 0.275 |
| MOD_NEK2_1 | 441 | 446 | PF00069 | 0.321 |
| MOD_NEK2_1 | 500 | 505 | PF00069 | 0.320 |
| MOD_NEK2_1 | 57 | 62 | PF00069 | 0.400 |
| MOD_NEK2_2 | 537 | 542 | PF00069 | 0.292 |
| MOD_PKA_2 | 572 | 578 | PF00069 | 0.562 |
| MOD_PKA_2 | 583 | 589 | PF00069 | 0.328 |
| MOD_Plk_1 | 104 | 110 | PF00069 | 0.452 |
| MOD_Plk_1 | 251 | 257 | PF00069 | 0.306 |
| MOD_Plk_1 | 275 | 281 | PF00069 | 0.259 |
| MOD_Plk_1 | 407 | 413 | PF00069 | 0.440 |
| MOD_Plk_1 | 451 | 457 | PF00069 | 0.380 |
| MOD_Plk_1 | 461 | 467 | PF00069 | 0.358 |
| MOD_Plk_1 | 53 | 59 | PF00069 | 0.371 |
| MOD_Plk_1 | 545 | 551 | PF00069 | 0.306 |
| MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.438 |
| MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.438 |
| MOD_Plk_4 | 122 | 128 | PF00069 | 0.300 |
| MOD_Plk_4 | 132 | 138 | PF00069 | 0.300 |
| MOD_Plk_4 | 148 | 154 | PF00069 | 0.300 |
| MOD_Plk_4 | 15 | 21 | PF00069 | 0.366 |
| MOD_Plk_4 | 197 | 203 | PF00069 | 0.287 |
| MOD_Plk_4 | 251 | 257 | PF00069 | 0.306 |
| MOD_Plk_4 | 462 | 468 | PF00069 | 0.373 |
| MOD_Plk_4 | 493 | 499 | PF00069 | 0.383 |
| MOD_Plk_4 | 545 | 551 | PF00069 | 0.303 |
| MOD_Plk_4 | 61 | 67 | PF00069 | 0.335 |
| MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.255 |
| MOD_SUMO_rev_2 | 216 | 223 | PF00179 | 0.248 |
| MOD_SUMO_rev_2 | 336 | 341 | PF00179 | 0.289 |
| MOD_SUMO_rev_2 | 367 | 375 | PF00179 | 0.310 |
| TRG_DiLeu_BaEn_1 | 219 | 224 | PF01217 | 0.248 |
| TRG_DiLeu_BaEn_1 | 277 | 282 | PF01217 | 0.259 |
| TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.283 |
| TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.324 |
| TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.334 |
| TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.351 |
| TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.419 |
| TRG_NES_CRM1_1 | 257 | 272 | PF08389 | 0.289 |
| TRG_Pf-PMV_PEXEL_1 | 116 | 121 | PF00026 | 0.248 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0B7P9G0 | Drosophila melanogaster | 33% | 71% |
| A0A0N1PDI6 | Leptomonas seymouri | 88% | 98% |
| A0A0S4JSF9 | Bodo saltans | 69% | 100% |
| A0A131MCZ8 | Caenorhabditis elegans | 30% | 74% |
| A0A1X0P6Q5 | Trypanosomatidae | 31% | 79% |
| A0A1X0PAL3 | Trypanosomatidae | 70% | 100% |
| A0A3Q8IC75 | Leishmania donovani | 25% | 100% |
| A0A3Q8IL77 | Leishmania donovani | 90% | 97% |
| A0A3Q8ITK0 | Leishmania donovani | 23% | 100% |
| A0A422NS01 | Trypanosoma rangeli | 70% | 100% |
| A0JPA0 | Xenopus tropicalis | 36% | 77% |
| A3QM97 | Caenorhabditis elegans | 31% | 73% |
| A4HIN7 | Leishmania braziliensis | 22% | 100% |
| A4HKU5 | Leishmania braziliensis | 23% | 100% |
| A4I5Y4 | Leishmania infantum | 25% | 100% |
| A4I8C4 | Leishmania infantum | 23% | 100% |
| A4IA41 | Leishmania infantum | 90% | 97% |
| C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
| D0A017 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 80% |
| E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
| E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
| E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 97% |
| P0C588 | Rattus norvegicus | 35% | 76% |
| Q12296 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 84% |
| Q32NY4 | Mus musculus | 29% | 83% |
| Q3TWN3 | Mus musculus | 35% | 67% |
| Q4Q2T0 | Leishmania major | 90% | 100% |
| Q4Q4X2 | Leishmania major | 21% | 100% |
| Q4Q6Y7 | Leishmania major | 24% | 100% |
| Q4QE29 | Leishmania major | 32% | 100% |
| Q5U2P1 | Rattus norvegicus | 35% | 67% |
| Q69ZF7 | Mus musculus | 36% | 77% |
| Q6P4Q7 | Homo sapiens | 36% | 76% |
| Q8NE01 | Homo sapiens | 28% | 83% |
| Q9GYL2 | Caenorhabditis elegans | 30% | 77% |
| Q9H8M5 | Homo sapiens | 35% | 67% |
| V5BKR5 | Trypanosoma cruzi | 71% | 100% |