| 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 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
| GO:0005783 | endoplasmic reticulum | 5 | 1 |
| GO:0012505 | endomembrane system | 2 | 1 |
| 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: A4H937
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006629 | lipid metabolic process | 3 | 1 |
| GO:0006644 | phospholipid metabolic process | 4 | 1 |
| GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
| GO:0006793 | phosphorus metabolic process | 3 | 1 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0019637 | organophosphate metabolic process | 3 | 1 |
| GO:0036149 | phosphatidylinositol acyl-chain remodeling | 7 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044255 | cellular lipid metabolic process | 3 | 1 |
| GO:0046486 | glycerolipid metabolic process | 4 | 1 |
| GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016746 | acyltransferase activity | 3 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.532 |
| CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.309 |
| CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.377 |
| CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.418 |
| CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.431 |
| CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.151 |
| CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.272 |
| CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.339 |
| CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.411 |
| CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.421 |
| CLV_PCSK_PC7_1 | 383 | 389 | PF00082 | 0.318 |
| CLV_PCSK_PC7_1 | 463 | 469 | PF00082 | 0.390 |
| CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.209 |
| CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.254 |
| CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.304 |
| CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.266 |
| CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.534 |
| CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.395 |
| DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.311 |
| DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.263 |
| DEG_MDM2_SWIB_1 | 415 | 423 | PF02201 | 0.313 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.633 |
| DOC_CDC14_PxL_1 | 164 | 172 | PF14671 | 0.463 |
| DOC_CDC14_PxL_1 | 404 | 412 | PF14671 | 0.192 |
| DOC_CKS1_1 | 399 | 404 | PF01111 | 0.164 |
| DOC_CYCLIN_RxL_1 | 106 | 114 | PF00134 | 0.575 |
| DOC_CYCLIN_RxL_1 | 332 | 343 | PF00134 | 0.508 |
| DOC_CYCLIN_yCln2_LP_2 | 347 | 353 | PF00134 | 0.428 |
| DOC_MAPK_gen_1 | 293 | 299 | PF00069 | 0.549 |
| DOC_MAPK_gen_1 | 387 | 395 | PF00069 | 0.496 |
| DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.446 |
| DOC_MAPK_MEF2A_6 | 417 | 425 | PF00069 | 0.151 |
| DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.420 |
| DOC_PP1_RVXF_1 | 193 | 200 | PF00149 | 0.511 |
| DOC_PP2B_LxvP_1 | 117 | 120 | PF13499 | 0.549 |
| DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.164 |
| DOC_PP2B_PxIxI_1 | 206 | 212 | PF00149 | 0.446 |
| DOC_USP7_UBL2_3 | 161 | 165 | PF12436 | 0.475 |
| DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.511 |
| DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.511 |
| DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.288 |
| LIG_14-3-3_CanoR_1 | 150 | 160 | PF00244 | 0.552 |
| LIG_14-3-3_CanoR_1 | 78 | 84 | PF00244 | 0.495 |
| LIG_APCC_ABBA_1 | 209 | 214 | PF00400 | 0.425 |
| LIG_CaM_IQ_9 | 455 | 471 | PF13499 | 0.578 |
| LIG_deltaCOP1_diTrp_1 | 138 | 146 | PF00928 | 0.409 |
| LIG_eIF4E_1 | 25 | 31 | PF01652 | 0.164 |
| LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.379 |
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.307 |
| LIG_FHA_1 | 147 | 153 | PF00498 | 0.435 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.438 |
| LIG_FHA_1 | 245 | 251 | PF00498 | 0.418 |
| LIG_FHA_1 | 320 | 326 | PF00498 | 0.484 |
| LIG_FHA_2 | 80 | 86 | PF00498 | 0.532 |
| LIG_IRF3_LxIS_1 | 420 | 426 | PF10401 | 0.164 |
| LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.495 |
| LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.409 |
| LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.398 |
| LIG_LIR_Gen_1 | 444 | 455 | PF02991 | 0.552 |
| LIG_LIR_LC3C_4 | 12 | 17 | PF02991 | 0.164 |
| LIG_LIR_Nem_3 | 108 | 113 | PF02991 | 0.517 |
| LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.441 |
| LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.429 |
| LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.289 |
| LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.524 |
| LIG_MAD2 | 115 | 123 | PF02301 | 0.514 |
| LIG_Pex14_1 | 139 | 143 | PF04695 | 0.433 |
| LIG_Pex14_1 | 385 | 389 | PF04695 | 0.517 |
| LIG_Pex14_2 | 177 | 181 | PF04695 | 0.402 |
| LIG_Pex14_2 | 414 | 418 | PF04695 | 0.356 |
| LIG_Pex14_2 | 432 | 436 | PF04695 | 0.335 |
| LIG_REV1ctd_RIR_1 | 412 | 421 | PF16727 | 0.415 |
| LIG_SH2_CRK | 141 | 145 | PF00017 | 0.430 |
| LIG_SH2_CRK | 390 | 394 | PF00017 | 0.563 |
| LIG_SH2_CRK | 56 | 60 | PF00017 | 0.196 |
| LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.472 |
| LIG_SH2_STAP1 | 141 | 145 | PF00017 | 0.463 |
| LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.511 |
| LIG_SH2_STAP1 | 25 | 29 | PF00017 | 0.164 |
| LIG_SH2_STAP1 | 272 | 276 | PF00017 | 0.483 |
| LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.504 |
| LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.493 |
| LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.532 |
| LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.520 |
| LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.369 |
| LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.420 |
| LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.483 |
| LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.370 |
| LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.387 |
| LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.291 |
| LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.559 |
| LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.371 |
| LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.471 |
| LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.447 |
| LIG_SH3_2 | 120 | 125 | PF14604 | 0.506 |
| LIG_SH3_3 | 113 | 119 | PF00018 | 0.469 |
| LIG_SH3_3 | 207 | 213 | PF00018 | 0.351 |
| LIG_SH3_3 | 238 | 244 | PF00018 | 0.389 |
| LIG_SH3_3 | 378 | 384 | PF00018 | 0.574 |
| LIG_SH3_3 | 396 | 402 | PF00018 | 0.345 |
| LIG_SH3_3 | 447 | 453 | PF00018 | 0.611 |
| LIG_SUMO_SIM_anti_2 | 205 | 212 | PF11976 | 0.446 |
| LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.368 |
| LIG_SUMO_SIM_anti_2 | 26 | 33 | PF11976 | 0.237 |
| LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.387 |
| LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.596 |
| LIG_TRFH_1 | 404 | 408 | PF08558 | 0.275 |
| LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.191 |
| LIG_TYR_ITIM | 79 | 84 | PF00017 | 0.452 |
| LIG_UBA3_1 | 152 | 161 | PF00899 | 0.541 |
| LIG_UBA3_1 | 252 | 261 | PF00899 | 0.364 |
| LIG_UBA3_1 | 29 | 37 | PF00899 | 0.233 |
| LIG_UBA3_1 | 48 | 53 | PF00899 | 0.174 |
| LIG_WRC_WIRS_1 | 140 | 145 | PF05994 | 0.463 |
| LIG_WW_1 | 408 | 411 | PF00397 | 0.164 |
| MOD_CK2_1 | 20 | 26 | PF00069 | 0.322 |
| MOD_Cter_Amidation | 465 | 468 | PF01082 | 0.277 |
| MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.259 |
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.485 |
| MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.345 |
| MOD_GSK3_1 | 1 | 8 | PF00069 | 0.599 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.332 |
| MOD_GSK3_1 | 266 | 273 | PF00069 | 0.412 |
| MOD_GSK3_1 | 79 | 86 | PF00069 | 0.480 |
| MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.168 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.556 |
| MOD_NEK2_1 | 146 | 151 | PF00069 | 0.524 |
| MOD_NEK2_1 | 20 | 25 | PF00069 | 0.265 |
| MOD_NEK2_1 | 298 | 303 | PF00069 | 0.556 |
| MOD_NEK2_1 | 340 | 345 | PF00069 | 0.483 |
| MOD_NEK2_1 | 40 | 45 | PF00069 | 0.280 |
| MOD_NEK2_1 | 423 | 428 | PF00069 | 0.212 |
| MOD_NEK2_1 | 430 | 435 | PF00069 | 0.177 |
| MOD_NEK2_1 | 74 | 79 | PF00069 | 0.329 |
| MOD_NEK2_2 | 96 | 101 | PF00069 | 0.616 |
| MOD_PIKK_1 | 118 | 124 | PF00454 | 0.579 |
| MOD_PIKK_1 | 223 | 229 | PF00454 | 0.496 |
| MOD_PKA_1 | 314 | 320 | PF00069 | 0.437 |
| MOD_PKA_2 | 244 | 250 | PF00069 | 0.433 |
| MOD_Plk_1 | 266 | 272 | PF00069 | 0.403 |
| MOD_Plk_1 | 282 | 288 | PF00069 | 0.600 |
| MOD_Plk_1 | 453 | 459 | PF00069 | 0.636 |
| MOD_Plk_4 | 1 | 7 | PF00069 | 0.488 |
| MOD_Plk_4 | 139 | 145 | PF00069 | 0.502 |
| MOD_Plk_4 | 24 | 30 | PF00069 | 0.278 |
| MOD_Plk_4 | 282 | 288 | PF00069 | 0.473 |
| MOD_Plk_4 | 442 | 448 | PF00069 | 0.517 |
| MOD_Plk_4 | 453 | 459 | PF00069 | 0.561 |
| MOD_Plk_4 | 79 | 85 | PF00069 | 0.460 |
| MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.511 |
| MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.511 |
| MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.288 |
| TRG_AP2beta_CARGO_1 | 175 | 184 | PF09066 | 0.446 |
| TRG_DiLeu_BaEn_1 | 26 | 31 | PF01217 | 0.164 |
| TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.528 |
| TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.515 |
| TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.351 |
| TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.510 |
| TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.511 |
| TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.420 |
| TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.562 |
| TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.262 |
| TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.571 |
| TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.197 |
| TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.459 |
| TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.409 |
| TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.519 |
| TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.637 |
| TRG_ER_diLys_1 | 474 | 477 | PF00400 | 0.676 |
| TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.299 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IKC7 | Leptomonas seymouri | 57% | 100% |
| A0A0S4J7G6 | Bodo saltans | 35% | 100% |
| A0A1X0NU94 | Trypanosomatidae | 40% | 100% |
| A0A3Q8IE09 | Leishmania donovani | 77% | 100% |
| A0A422NH08 | Trypanosoma rangeli | 43% | 100% |
| A4HXG9 | Leishmania infantum | 77% | 100% |
| C9ZP55 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
| E9AR64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
| Q4QE99 | Leishmania major | 75% | 100% |
| Q5F3X0 | Gallus gallus | 28% | 100% |
| V5BF39 | Trypanosoma cruzi | 41% | 100% |