| 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 |
Related structures:
AlphaFold database: E9AY93
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009451 | RNA modification | 5 | 1 |
| GO:0009892 | negative regulation of metabolic process | 4 | 1 |
| GO:0009893 | positive regulation of metabolic process | 4 | 1 |
| GO:0009894 | regulation of catabolic process | 4 | 1 |
| GO:0009895 | negative regulation of catabolic process | 5 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0010468 | regulation of gene expression | 5 | 1 |
| GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
| GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
| GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
| GO:0010628 | positive regulation of gene expression | 6 | 1 |
| GO:0016070 | RNA metabolic process | 5 | 1 |
| GO:0016553 | base conversion or substitution editing | 6 | 1 |
| GO:0016554 | cytidine to uridine editing | 7 | 1 |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
| GO:0019222 | regulation of metabolic process | 3 | 1 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
| GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
| GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
| GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0043487 | regulation of RNA stability | 3 | 1 |
| GO:0043488 | regulation of mRNA stability | 4 | 1 |
| GO:0043489 | RNA stabilization | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
| GO:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0048255 | mRNA stabilization | 5 | 1 |
| GO:0048518 | positive regulation of biological process | 3 | 1 |
| GO:0048519 | negative regulation of biological process | 3 | 1 |
| GO:0048523 | negative regulation of cellular process | 4 | 1 |
| GO:0050789 | regulation of biological process | 2 | 1 |
| GO:0050794 | regulation of cellular process | 3 | 1 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
| GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
| GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
| GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
| GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
| GO:0065007 | biological regulation | 1 | 1 |
| GO:0065008 | regulation of biological quality | 2 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0080090 | regulation of primary metabolic process | 4 | 1 |
| GO:0090304 | nucleic acid metabolic process | 4 | 1 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
| GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
| GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
| GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
| GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 1 |
| GO:0003723 | RNA binding | 4 | 1 |
| GO:0005488 | binding | 1 | 1 |
| GO:0097159 | organic cyclic compound binding | 2 | 1 |
| GO:1901363 | heterocyclic compound binding | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.339 |
| CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.331 |
| CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.483 |
| CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.413 |
| CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.376 |
| CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.364 |
| CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.641 |
| CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.553 |
| CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.339 |
| CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.331 |
| CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.484 |
| CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.371 |
| CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.360 |
| CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.463 |
| CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.616 |
| CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.553 |
| CLV_PCSK_PC1ET2_1 | 489 | 491 | PF00082 | 0.463 |
| CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.518 |
| CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.372 |
| CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.289 |
| CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.614 |
| CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.394 |
| CLV_Separin_Metazoa | 219 | 223 | PF03568 | 0.344 |
| DEG_APCC_DBOX_1 | 294 | 302 | PF00400 | 0.327 |
| DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.382 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.580 |
| DEG_SCF_FBW7_1 | 22 | 27 | PF00400 | 0.596 |
| DEG_SCF_FBW7_1 | 30 | 37 | PF00400 | 0.552 |
| DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.689 |
| DOC_CKS1_1 | 31 | 36 | PF01111 | 0.539 |
| DOC_CYCLIN_RxL_1 | 254 | 265 | PF00134 | 0.481 |
| DOC_MAPK_gen_1 | 361 | 368 | PF00069 | 0.369 |
| DOC_MAPK_HePTP_8 | 464 | 476 | PF00069 | 0.411 |
| DOC_MAPK_MEF2A_6 | 361 | 370 | PF00069 | 0.348 |
| DOC_MAPK_MEF2A_6 | 467 | 476 | PF00069 | 0.506 |
| DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.533 |
| DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.342 |
| DOC_PP4_MxPP_1 | 329 | 332 | PF00568 | 0.440 |
| DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.676 |
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.470 |
| DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.755 |
| DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.374 |
| DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.690 |
| DOC_USP7_UBL2_3 | 522 | 526 | PF12436 | 0.504 |
| DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.434 |
| DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.720 |
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.736 |
| DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.391 |
| DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.344 |
| DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.697 |
| DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.572 |
| LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.716 |
| LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.339 |
| LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.343 |
| LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.460 |
| LIG_14-3-3_CanoR_1 | 361 | 366 | PF00244 | 0.381 |
| LIG_14-3-3_CanoR_1 | 377 | 384 | PF00244 | 0.342 |
| LIG_14-3-3_CanoR_1 | 492 | 497 | PF00244 | 0.546 |
| LIG_14-3-3_CanoR_1 | 61 | 71 | PF00244 | 0.643 |
| LIG_Actin_RPEL_3 | 216 | 235 | PF02755 | 0.344 |
| LIG_Clathr_ClatBox_1 | 365 | 369 | PF01394 | 0.429 |
| LIG_DLG_GKlike_1 | 361 | 368 | PF00625 | 0.351 |
| LIG_FHA_1 | 108 | 114 | PF00498 | 0.455 |
| LIG_FHA_1 | 162 | 168 | PF00498 | 0.401 |
| LIG_FHA_1 | 17 | 23 | PF00498 | 0.560 |
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.373 |
| LIG_FHA_1 | 237 | 243 | PF00498 | 0.345 |
| LIG_FHA_1 | 288 | 294 | PF00498 | 0.412 |
| LIG_FHA_1 | 34 | 40 | PF00498 | 0.652 |
| LIG_FHA_1 | 340 | 346 | PF00498 | 0.386 |
| LIG_FHA_1 | 436 | 442 | PF00498 | 0.411 |
| LIG_FHA_1 | 464 | 470 | PF00498 | 0.473 |
| LIG_FHA_2 | 140 | 146 | PF00498 | 0.631 |
| LIG_FHA_2 | 161 | 167 | PF00498 | 0.514 |
| LIG_FHA_2 | 323 | 329 | PF00498 | 0.340 |
| LIG_FHA_2 | 347 | 353 | PF00498 | 0.354 |
| LIG_FHA_2 | 378 | 384 | PF00498 | 0.484 |
| LIG_LIR_Apic_2 | 202 | 206 | PF02991 | 0.441 |
| LIG_LIR_Apic_2 | 311 | 315 | PF02991 | 0.349 |
| LIG_LIR_Gen_1 | 398 | 405 | PF02991 | 0.431 |
| LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.411 |
| LIG_NRBOX | 501 | 507 | PF00104 | 0.346 |
| LIG_NRBOX | 516 | 522 | PF00104 | 0.338 |
| LIG_SH2_CRK | 209 | 213 | PF00017 | 0.464 |
| LIG_SH2_CRK | 400 | 404 | PF00017 | 0.390 |
| LIG_SH2_CRK | 57 | 61 | PF00017 | 0.705 |
| LIG_SH2_NCK_1 | 25 | 29 | PF00017 | 0.471 |
| LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.388 |
| LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.410 |
| LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.321 |
| LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.322 |
| LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.391 |
| LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.329 |
| LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.333 |
| LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.348 |
| LIG_SH3_3 | 225 | 231 | PF00018 | 0.466 |
| LIG_SH3_3 | 28 | 34 | PF00018 | 0.508 |
| LIG_SUMO_SIM_anti_2 | 163 | 171 | PF11976 | 0.506 |
| LIG_SUMO_SIM_anti_2 | 217 | 222 | PF11976 | 0.366 |
| LIG_SUMO_SIM_par_1 | 214 | 219 | PF11976 | 0.359 |
| LIG_SUMO_SIM_par_1 | 391 | 398 | PF11976 | 0.411 |
| LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.499 |
| LIG_TYR_ITSM | 396 | 403 | PF00017 | 0.438 |
| MOD_CK1_1 | 20 | 26 | PF00069 | 0.727 |
| MOD_CK1_1 | 346 | 352 | PF00069 | 0.510 |
| MOD_CK1_1 | 37 | 43 | PF00069 | 0.671 |
| MOD_CK1_1 | 395 | 401 | PF00069 | 0.489 |
| MOD_CK1_1 | 460 | 466 | PF00069 | 0.384 |
| MOD_CK1_1 | 65 | 71 | PF00069 | 0.658 |
| MOD_CK1_1 | 96 | 102 | PF00069 | 0.610 |
| MOD_CK2_1 | 160 | 166 | PF00069 | 0.507 |
| MOD_CK2_1 | 346 | 352 | PF00069 | 0.367 |
| MOD_CK2_1 | 377 | 383 | PF00069 | 0.490 |
| MOD_Cter_Amidation | 487 | 490 | PF01082 | 0.476 |
| MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.658 |
| MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.446 |
| MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.461 |
| MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.631 |
| MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.677 |
| MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.584 |
| MOD_GSK3_1 | 104 | 111 | PF00069 | 0.511 |
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.374 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.669 |
| MOD_GSK3_1 | 236 | 243 | PF00069 | 0.353 |
| MOD_GSK3_1 | 30 | 37 | PF00069 | 0.627 |
| MOD_GSK3_1 | 339 | 346 | PF00069 | 0.517 |
| MOD_GSK3_1 | 38 | 45 | PF00069 | 0.610 |
| MOD_GSK3_1 | 388 | 395 | PF00069 | 0.470 |
| MOD_GSK3_1 | 87 | 94 | PF00069 | 0.710 |
| MOD_LATS_1 | 15 | 21 | PF00433 | 0.736 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.656 |
| MOD_NEK2_1 | 18 | 23 | PF00069 | 0.478 |
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.336 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.310 |
| MOD_NEK2_1 | 255 | 260 | PF00069 | 0.275 |
| MOD_NEK2_1 | 279 | 284 | PF00069 | 0.403 |
| MOD_NEK2_1 | 38 | 43 | PF00069 | 0.698 |
| MOD_NEK2_1 | 388 | 393 | PF00069 | 0.454 |
| MOD_NEK2_2 | 194 | 199 | PF00069 | 0.342 |
| MOD_NEK2_2 | 392 | 397 | PF00069 | 0.314 |
| MOD_PIKK_1 | 354 | 360 | PF00454 | 0.384 |
| MOD_PKA_1 | 222 | 228 | PF00069 | 0.490 |
| MOD_PKA_1 | 361 | 367 | PF00069 | 0.401 |
| MOD_PKA_2 | 16 | 22 | PF00069 | 0.627 |
| MOD_PKA_2 | 188 | 194 | PF00069 | 0.334 |
| MOD_PKA_2 | 222 | 228 | PF00069 | 0.490 |
| MOD_PKA_2 | 339 | 345 | PF00069 | 0.386 |
| MOD_PKA_2 | 401 | 407 | PF00069 | 0.559 |
| MOD_PKB_1 | 490 | 498 | PF00069 | 0.399 |
| MOD_Plk_1 | 255 | 261 | PF00069 | 0.414 |
| MOD_Plk_1 | 432 | 438 | PF00069 | 0.494 |
| MOD_Plk_4 | 208 | 214 | PF00069 | 0.453 |
| MOD_Plk_4 | 255 | 261 | PF00069 | 0.414 |
| MOD_Plk_4 | 313 | 319 | PF00069 | 0.332 |
| MOD_Plk_4 | 34 | 40 | PF00069 | 0.658 |
| MOD_Plk_4 | 460 | 466 | PF00069 | 0.390 |
| MOD_Plk_4 | 516 | 522 | PF00069 | 0.481 |
| MOD_Plk_4 | 87 | 93 | PF00069 | 0.690 |
| MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.430 |
| MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.724 |
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.738 |
| MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.392 |
| MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.340 |
| MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.697 |
| MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.571 |
| MOD_SUMO_rev_2 | 153 | 162 | PF00179 | 0.368 |
| TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.378 |
| TRG_DiLeu_BaEn_1 | 256 | 261 | PF01217 | 0.505 |
| TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.492 |
| TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.419 |
| TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.385 |
| TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.381 |
| TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.340 |
| TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.337 |
| TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.386 |
| TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.375 |
| TRG_ER_diArg_1 | 490 | 493 | PF00400 | 0.440 |
| TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.582 |
| TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.637 |
| TRG_NES_CRM1_1 | 358 | 372 | PF08389 | 0.403 |
| TRG_NLS_MonoExtC_3 | 488 | 493 | PF00514 | 0.464 |
| TRG_Pf-PMV_PEXEL_1 | 214 | 219 | PF00026 | 0.343 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IGU4 | Leptomonas seymouri | 78% | 94% |
| A0A0S4JSB1 | Bodo saltans | 58% | 100% |
| A0A1X0NS86 | Trypanosomatidae | 67% | 99% |
| A0A3Q8IDM7 | Leishmania donovani | 96% | 99% |
| A0A422N6M4 | Trypanosoma rangeli | 64% | 100% |
| A4HEW9 | Leishmania braziliensis | 89% | 100% |
| A4I243 | Leishmania infantum | 95% | 99% |
| C9ZRW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 99% |
| Q4Q980 | Leishmania major | 93% | 100% |
| V5B995 | Trypanosoma cruzi | 65% | 100% |