| 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:0005737 | cytoplasm | 2 | 12 | 
| GO:0110165 | cellular anatomical entity | 1 | 12 | 
| GO:0016020 | membrane | 2 | 1 | 
Related structures:
AlphaFold database: A4IBM5
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 | 
| GO:0006364 | rRNA processing | 8 | 12 | 
| GO:0006396 | RNA processing | 6 | 12 | 
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 | 
| GO:0008152 | metabolic process | 1 | 12 | 
| GO:0009987 | cellular process | 1 | 12 | 
| GO:0016070 | RNA metabolic process | 5 | 12 | 
| GO:0016072 | rRNA metabolic process | 7 | 12 | 
| GO:0032259 | methylation | 2 | 12 | 
| GO:0034470 | ncRNA processing | 7 | 12 | 
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 | 
| GO:0034660 | ncRNA metabolic process | 6 | 12 | 
| GO:0043170 | macromolecule metabolic process | 3 | 12 | 
| GO:0044237 | cellular metabolic process | 2 | 12 | 
| GO:0044238 | primary metabolic process | 2 | 12 | 
| GO:0046483 | heterocycle metabolic process | 3 | 12 | 
| GO:0071704 | organic substance metabolic process | 2 | 12 | 
| GO:0090304 | nucleic acid metabolic process | 4 | 12 | 
| GO:1901360 | organic cyclic compound metabolic process | 3 | 12 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 | 
| GO:0008168 | methyltransferase activity | 4 | 12 | 
| GO:0016740 | transferase activity | 2 | 12 | 
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.611 | 
| CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.256 | 
| CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.529 | 
| CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.501 | 
| CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.540 | 
| CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.497 | 
| CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.433 | 
| CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.390 | 
| CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.709 | 
| CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.645 | 
| CLV_PCSK_FUR_1 | 366 | 370 | PF00082 | 0.495 | 
| CLV_PCSK_FUR_1 | 430 | 434 | PF00082 | 0.503 | 
| CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.611 | 
| CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.384 | 
| CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.256 | 
| CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.490 | 
| CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.532 | 
| CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.540 | 
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.435 | 
| CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.351 | 
| CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.651 | 
| CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.384 | 
| CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.486 | 
| CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.492 | 
| CLV_PCSK_PC7_1 | 364 | 370 | PF00082 | 0.497 | 
| CLV_PCSK_PC7_1 | 421 | 427 | PF00082 | 0.539 | 
| CLV_PCSK_PC7_1 | 428 | 434 | PF00082 | 0.488 | 
| CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.277 | 
| CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.603 | 
| CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.488 | 
| CLV_Separin_Metazoa | 281 | 285 | PF03568 | 0.467 | 
| DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.562 | 
| DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.633 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.657 | 
| DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.717 | 
| DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.771 | 
| DOC_CYCLIN_RxL_1 | 124 | 132 | PF00134 | 0.475 | 
| DOC_MAPK_gen_1 | 284 | 290 | PF00069 | 0.499 | 
| DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.414 | 
| DOC_MAPK_gen_1 | 446 | 453 | PF00069 | 0.477 | 
| DOC_MAPK_MEF2A_6 | 337 | 345 | PF00069 | 0.399 | 
| DOC_MAPK_MEF2A_6 | 446 | 453 | PF00069 | 0.577 | 
| DOC_MAPK_NFAT4_5 | 338 | 346 | PF00069 | 0.408 | 
| DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.411 | 
| DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.536 | 
| DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.516 | 
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.737 | 
| DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.719 | 
| DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.754 | 
| DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.597 | 
| DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.545 | 
| DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.475 | 
| DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.687 | 
| DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.524 | 
| DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.608 | 
| LIG_14-3-3_CanoR_1 | 147 | 157 | PF00244 | 0.479 | 
| LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.628 | 
| LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.611 | 
| LIG_Actin_WH2_1 | 433 | 450 | PF00022 | 0.541 | 
| LIG_BIR_III_2 | 377 | 381 | PF00653 | 0.610 | 
| LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.487 | 
| LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.666 | 
| LIG_FHA_1 | 125 | 131 | PF00498 | 0.487 | 
| LIG_FHA_1 | 173 | 179 | PF00498 | 0.475 | 
| LIG_FHA_1 | 303 | 309 | PF00498 | 0.536 | 
| LIG_FHA_2 | 127 | 133 | PF00498 | 0.484 | 
| LIG_FHA_2 | 150 | 156 | PF00498 | 0.536 | 
| LIG_FHA_2 | 241 | 247 | PF00498 | 0.577 | 
| LIG_FHA_2 | 368 | 374 | PF00498 | 0.660 | 
| LIG_FHA_2 | 71 | 77 | PF00498 | 0.573 | 
| LIG_FHA_2 | 83 | 89 | PF00498 | 0.504 | 
| LIG_IRF3_LxIS_1 | 205 | 212 | PF10401 | 0.532 | 
| LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.536 | 
| LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.539 | 
| LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.655 | 
| LIG_MAD2 | 264 | 272 | PF02301 | 0.579 | 
| LIG_MLH1_MIPbox_1 | 247 | 251 | PF16413 | 0.487 | 
| LIG_NRBOX | 156 | 162 | PF00104 | 0.487 | 
| LIG_Pex14_2 | 275 | 279 | PF04695 | 0.562 | 
| LIG_Pex14_2 | 61 | 65 | PF04695 | 0.707 | 
| LIG_RPA_C_Fungi | 450 | 462 | PF08784 | 0.447 | 
| LIG_SH2_CRK | 67 | 71 | PF00017 | 0.651 | 
| LIG_SH2_STAT3 | 327 | 330 | PF00017 | 0.456 | 
| LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.328 | 
| LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.448 | 
| LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.542 | 
| LIG_SH3_3 | 131 | 137 | PF00018 | 0.448 | 
| LIG_SH3_3 | 16 | 22 | PF00018 | 0.662 | 
| LIG_SH3_3 | 92 | 98 | PF00018 | 0.317 | 
| LIG_SUMO_SIM_anti_2 | 129 | 135 | PF11976 | 0.343 | 
| LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.641 | 
| LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.565 | 
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.687 | 
| MOD_CK1_1 | 212 | 218 | PF00069 | 0.360 | 
| MOD_CK1_1 | 240 | 246 | PF00069 | 0.448 | 
| MOD_CK1_1 | 40 | 46 | PF00069 | 0.629 | 
| MOD_CK1_1 | 400 | 406 | PF00069 | 0.702 | 
| MOD_CK2_1 | 149 | 155 | PF00069 | 0.448 | 
| MOD_CK2_1 | 214 | 220 | PF00069 | 0.328 | 
| MOD_CK2_1 | 381 | 387 | PF00069 | 0.705 | 
| MOD_CK2_1 | 398 | 404 | PF00069 | 0.780 | 
| MOD_CK2_1 | 439 | 445 | PF00069 | 0.577 | 
| MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.328 | 
| MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.145 | 
| MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.342 | 
| MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.332 | 
| MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.267 | 
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.145 | 
| MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.145 | 
| MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.706 | 
| MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.800 | 
| MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.690 | 
| MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.648 | 
| MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.627 | 
| MOD_GSK3_1 | 168 | 175 | PF00069 | 0.448 | 
| MOD_GSK3_1 | 200 | 207 | PF00069 | 0.407 | 
| MOD_GSK3_1 | 209 | 216 | PF00069 | 0.260 | 
| MOD_GSK3_1 | 302 | 309 | PF00069 | 0.409 | 
| MOD_GSK3_1 | 381 | 388 | PF00069 | 0.759 | 
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.690 | 
| MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.343 | 
| MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.343 | 
| MOD_NEK2_1 | 15 | 20 | PF00069 | 0.608 | 
| MOD_NEK2_1 | 169 | 174 | PF00069 | 0.340 | 
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.395 | 
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.623 | 
| MOD_NEK2_1 | 209 | 214 | PF00069 | 0.362 | 
| MOD_NEK2_1 | 311 | 316 | PF00069 | 0.362 | 
| MOD_NEK2_1 | 367 | 372 | PF00069 | 0.587 | 
| MOD_NEK2_1 | 54 | 59 | PF00069 | 0.582 | 
| MOD_NEK2_1 | 61 | 66 | PF00069 | 0.540 | 
| MOD_PIKK_1 | 24 | 30 | PF00454 | 0.703 | 
| MOD_PKA_1 | 59 | 65 | PF00069 | 0.644 | 
| MOD_PKA_2 | 149 | 155 | PF00069 | 0.439 | 
| MOD_PKA_2 | 15 | 21 | PF00069 | 0.690 | 
| MOD_PKA_2 | 194 | 200 | PF00069 | 0.362 | 
| MOD_PKA_2 | 367 | 373 | PF00069 | 0.587 | 
| MOD_PKA_2 | 392 | 398 | PF00069 | 0.767 | 
| MOD_PKA_2 | 59 | 65 | PF00069 | 0.610 | 
| MOD_Plk_1 | 103 | 109 | PF00069 | 0.328 | 
| MOD_Plk_1 | 311 | 317 | PF00069 | 0.343 | 
| MOD_Plk_1 | 403 | 409 | PF00069 | 0.633 | 
| MOD_Plk_1 | 456 | 462 | PF00069 | 0.662 | 
| MOD_Plk_4 | 126 | 132 | PF00069 | 0.342 | 
| MOD_Plk_4 | 245 | 251 | PF00069 | 0.343 | 
| MOD_Plk_4 | 292 | 298 | PF00069 | 0.441 | 
| MOD_Plk_4 | 40 | 46 | PF00069 | 0.662 | 
| MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.328 | 
| MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.689 | 
| MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.396 | 
| MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.607 | 
| MOD_SUMO_for_1 | 410 | 413 | PF00179 | 0.613 | 
| TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.464 | 
| TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.343 | 
| TRG_DiLeu_BaLyEn_6 | 432 | 437 | PF01217 | 0.531 | 
| TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.647 | 
| TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.609 | 
| TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.328 | 
| TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.301 | 
| TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.490 | 
| TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.517 | 
| TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.490 | 
| TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.461 | 
| TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.325 | 
| TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.650 | 
| TRG_NLS_MonoCore_2 | 362 | 367 | PF00514 | 0.614 | 
| TRG_NLS_MonoExtC_3 | 417 | 423 | PF00514 | 0.615 | 
| TRG_NLS_MonoExtN_4 | 415 | 422 | PF00514 | 0.580 | 
| TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.631 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P4G3 | Leptomonas seymouri | 67% | 100% | 
| A0A0S4IXW1 | Bodo saltans | 43% | 100% | 
| A0A1X0P5K8 | Trypanosomatidae | 56% | 100% | 
| A0A3R7N6Y9 | Trypanosoma rangeli | 55% | 100% | 
| A0A3S7X9K0 | Leishmania donovani | 100% | 100% | 
| A4HN02 | Leishmania braziliensis | 84% | 100% | 
| C9ZZ09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% | 
| E9AFF9 | Leishmania major | 96% | 100% | 
| E9B6L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% | 
| V5BY28 | Trypanosoma cruzi | 57% | 100% |