| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9APE8
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
| GO:0006766 | vitamin metabolic process | 3 | 11 |
| GO:0006767 | water-soluble vitamin metabolic process | 4 | 11 |
| GO:0006790 | sulfur compound metabolic process | 3 | 11 |
| GO:0006793 | phosphorus metabolic process | 3 | 11 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009058 | biosynthetic process | 2 | 11 |
| GO:0009110 | vitamin biosynthetic process | 4 | 11 |
| GO:0009229 | thiamine diphosphate biosynthetic process | 5 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016310 | phosphorylation | 5 | 10 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
| GO:0019637 | organophosphate metabolic process | 3 | 11 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
| GO:0042357 | thiamine diphosphate metabolic process | 4 | 11 |
| GO:0042364 | water-soluble vitamin biosynthetic process | 5 | 11 |
| GO:0042723 | thiamine-containing compound metabolic process | 4 | 11 |
| GO:0042724 | thiamine-containing compound biosynthetic process | 5 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044249 | cellular biosynthetic process | 3 | 11 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
| GO:0044272 | sulfur compound biosynthetic process | 4 | 11 |
| GO:0044281 | small molecule metabolic process | 2 | 11 |
| GO:0044283 | small molecule biosynthetic process | 3 | 11 |
| GO:0046483 | heterocycle metabolic process | 3 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0072527 | pyrimidine-containing compound metabolic process | 4 | 11 |
| GO:0072528 | pyrimidine-containing compound biosynthetic process | 5 | 11 |
| GO:0090407 | organophosphate biosynthetic process | 4 | 11 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 11 |
| GO:1901576 | organic substance biosynthetic process | 3 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 11 |
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0004788 | thiamine diphosphokinase activity | 5 | 11 |
| GO:0005488 | binding | 1 | 11 |
| GO:0005524 | ATP binding | 5 | 11 |
| GO:0016301 | kinase activity | 4 | 10 |
| GO:0016740 | transferase activity | 2 | 11 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
| GO:0016778 | diphosphotransferase activity | 4 | 11 |
| GO:0017076 | purine nucleotide binding | 4 | 11 |
| GO:0019842 | vitamin binding | 3 | 11 |
| GO:0030554 | adenyl nucleotide binding | 5 | 11 |
| GO:0030975 | thiamine binding | 3 | 11 |
| GO:0032553 | ribonucleotide binding | 3 | 11 |
| GO:0032555 | purine ribonucleotide binding | 4 | 11 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
| GO:0036094 | small molecule binding | 2 | 11 |
| GO:0043167 | ion binding | 2 | 11 |
| GO:0043168 | anion binding | 3 | 11 |
| GO:0043169 | cation binding | 3 | 11 |
| GO:0043178 | alcohol binding | 3 | 11 |
| GO:0097159 | organic cyclic compound binding | 2 | 11 |
| GO:0097367 | carbohydrate derivative binding | 2 | 11 |
| GO:1901265 | nucleoside phosphate binding | 3 | 11 |
| GO:1901363 | heterocyclic compound binding | 2 | 11 |
| GO:1901681 | sulfur compound binding | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.568 |
| CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.300 |
| CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.454 |
| CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.731 |
| CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.555 |
| CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.597 |
| CLV_PCSK_FUR_1 | 219 | 223 | PF00082 | 0.559 |
| CLV_PCSK_FUR_1 | 328 | 332 | PF00082 | 0.421 |
| CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.487 |
| CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.720 |
| CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.618 |
| CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.471 |
| CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.546 |
| CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.487 |
| CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.618 |
| CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.593 |
| CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.509 |
| CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.362 |
| CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.390 |
| DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.503 |
| DEG_SPOP_SBC_1 | 232 | 236 | PF00917 | 0.446 |
| DOC_CYCLIN_RxL_1 | 327 | 337 | PF00134 | 0.504 |
| DOC_MAPK_MEF2A_6 | 354 | 361 | PF00069 | 0.530 |
| DOC_PP1_RVXF_1 | 197 | 204 | PF00149 | 0.606 |
| DOC_PP1_RVXF_1 | 466 | 472 | PF00149 | 0.586 |
| DOC_PP2B_LxvP_1 | 527 | 530 | PF13499 | 0.572 |
| DOC_PP2B_PxIxI_1 | 356 | 362 | PF00149 | 0.442 |
| DOC_PP4_FxxP_1 | 408 | 411 | PF00568 | 0.323 |
| DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.524 |
| DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.536 |
| DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.404 |
| DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.784 |
| DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.612 |
| DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.644 |
| DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.561 |
| DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.437 |
| DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.593 |
| DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.417 |
| LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.530 |
| LIG_Actin_WH2_2 | 481 | 496 | PF00022 | 0.377 |
| LIG_APCC_ABBAyCdc20_2 | 199 | 205 | PF00400 | 0.658 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.726 |
| LIG_BIR_III_2 | 181 | 185 | PF00653 | 0.696 |
| LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.462 |
| LIG_BRCT_BRCA1_2 | 250 | 256 | PF00533 | 0.452 |
| LIG_EVH1_2 | 521 | 525 | PF00568 | 0.417 |
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.702 |
| LIG_FHA_1 | 233 | 239 | PF00498 | 0.651 |
| LIG_FHA_1 | 253 | 259 | PF00498 | 0.497 |
| LIG_FHA_1 | 31 | 37 | PF00498 | 0.699 |
| LIG_FHA_1 | 351 | 357 | PF00498 | 0.461 |
| LIG_FHA_1 | 404 | 410 | PF00498 | 0.366 |
| LIG_FHA_1 | 441 | 447 | PF00498 | 0.544 |
| LIG_FHA_1 | 480 | 486 | PF00498 | 0.518 |
| LIG_FHA_1 | 524 | 530 | PF00498 | 0.554 |
| LIG_FHA_2 | 234 | 240 | PF00498 | 0.696 |
| LIG_FHA_2 | 57 | 63 | PF00498 | 0.491 |
| LIG_LIR_Apic_2 | 406 | 411 | PF02991 | 0.311 |
| LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 122 | 128 | PF02991 | 0.340 |
| LIG_LIR_Gen_1 | 239 | 247 | PF02991 | 0.567 |
| LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.390 |
| LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.330 |
| LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.572 |
| LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.491 |
| LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.531 |
| LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.572 |
| LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.280 |
| LIG_PTAP_UEV_1 | 337 | 342 | PF05743 | 0.493 |
| LIG_SH2_CRK | 113 | 117 | PF00017 | 0.507 |
| LIG_SH2_CRK | 382 | 386 | PF00017 | 0.508 |
| LIG_SH2_CRK | 394 | 398 | PF00017 | 0.442 |
| LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.511 |
| LIG_SH2_PTP2 | 124 | 127 | PF00017 | 0.337 |
| LIG_SH2_STAP1 | 382 | 386 | PF00017 | 0.511 |
| LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.360 |
| LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.425 |
| LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.484 |
| LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.188 |
| LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.586 |
| LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.412 |
| LIG_SH3_3 | 234 | 240 | PF00018 | 0.705 |
| LIG_SH3_3 | 24 | 30 | PF00018 | 0.313 |
| LIG_SH3_3 | 335 | 341 | PF00018 | 0.619 |
| LIG_SH3_3 | 478 | 484 | PF00018 | 0.591 |
| LIG_SH3_3 | 496 | 502 | PF00018 | 0.482 |
| LIG_SH3_3 | 511 | 517 | PF00018 | 0.650 |
| LIG_SUMO_SIM_par_1 | 482 | 489 | PF11976 | 0.502 |
| LIG_SUMO_SIM_par_1 | 49 | 55 | PF11976 | 0.417 |
| LIG_TRFH_1 | 241 | 245 | PF08558 | 0.486 |
| LIG_TRFH_1 | 408 | 412 | PF08558 | 0.348 |
| LIG_TYR_ITAM | 110 | 127 | PF00017 | 0.280 |
| LIG_TYR_ITIM | 380 | 385 | PF00017 | 0.520 |
| LIG_UBA3_1 | 388 | 393 | PF00899 | 0.519 |
| MOD_CK1_1 | 132 | 138 | PF00069 | 0.568 |
| MOD_CK1_1 | 140 | 146 | PF00069 | 0.600 |
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.539 |
| MOD_CK1_1 | 299 | 305 | PF00069 | 0.395 |
| MOD_CK2_1 | 233 | 239 | PF00069 | 0.711 |
| MOD_CK2_1 | 310 | 316 | PF00069 | 0.504 |
| MOD_CK2_1 | 79 | 85 | PF00069 | 0.494 |
| MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.701 |
| MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.604 |
| MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.344 |
| MOD_GlcNHglycan | 229 | 233 | PF01048 | 0.673 |
| MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.694 |
| MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.621 |
| MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.321 |
| MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.691 |
| MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.502 |
| MOD_GSK3_1 | 123 | 130 | PF00069 | 0.608 |
| MOD_GSK3_1 | 133 | 140 | PF00069 | 0.555 |
| MOD_GSK3_1 | 154 | 161 | PF00069 | 0.553 |
| MOD_GSK3_1 | 228 | 235 | PF00069 | 0.705 |
| MOD_GSK3_1 | 248 | 255 | PF00069 | 0.591 |
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.606 |
| MOD_GSK3_1 | 30 | 37 | PF00069 | 0.749 |
| MOD_GSK3_1 | 332 | 339 | PF00069 | 0.559 |
| MOD_GSK3_1 | 410 | 417 | PF00069 | 0.602 |
| MOD_GSK3_1 | 473 | 480 | PF00069 | 0.532 |
| MOD_GSK3_1 | 52 | 59 | PF00069 | 0.476 |
| MOD_NEK2_1 | 142 | 147 | PF00069 | 0.574 |
| MOD_NEK2_1 | 158 | 163 | PF00069 | 0.351 |
| MOD_NEK2_1 | 228 | 233 | PF00069 | 0.679 |
| MOD_NEK2_1 | 332 | 337 | PF00069 | 0.589 |
| MOD_NEK2_1 | 350 | 355 | PF00069 | 0.374 |
| MOD_NEK2_1 | 421 | 426 | PF00069 | 0.469 |
| MOD_NEK2_2 | 277 | 282 | PF00069 | 0.457 |
| MOD_PIKK_1 | 403 | 409 | PF00454 | 0.365 |
| MOD_PIKK_1 | 459 | 465 | PF00454 | 0.586 |
| MOD_PIKK_1 | 9 | 15 | PF00454 | 0.726 |
| MOD_PKA_2 | 421 | 427 | PF00069 | 0.645 |
| MOD_PKB_1 | 220 | 228 | PF00069 | 0.589 |
| MOD_Plk_1 | 295 | 301 | PF00069 | 0.616 |
| MOD_Plk_4 | 520 | 526 | PF00069 | 0.454 |
| MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.605 |
| MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.632 |
| MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.575 |
| MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.447 |
| MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.593 |
| MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.412 |
| TRG_DiLeu_BaEn_1 | 239 | 244 | PF01217 | 0.515 |
| TRG_DiLeu_BaEn_1 | 442 | 447 | PF01217 | 0.475 |
| TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.533 |
| TRG_DiLeu_BaLyEn_6 | 328 | 333 | PF01217 | 0.397 |
| TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.410 |
| TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.414 |
| TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.510 |
| TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.451 |
| TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.412 |
| TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.514 |
| TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.481 |
| TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.590 |
| TRG_NES_CRM1_1 | 279 | 293 | PF08389 | 0.543 |
| TRG_Pf-PMV_PEXEL_1 | 200 | 205 | PF00026 | 0.474 |
| TRG_Pf-PMV_PEXEL_1 | 330 | 334 | PF00026 | 0.485 |
| TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.439 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PFZ8 | Leptomonas seymouri | 44% | 100% |
| A0A1X0NMY7 | Trypanosomatidae | 30% | 100% |
| A0A3Q8IBS6 | Leishmania donovani | 86% | 99% |
| A0A422N0R9 | Trypanosoma rangeli | 27% | 100% |
| A4H7A7 | Leishmania braziliensis | 70% | 100% |
| A4HVQ2 | Leishmania infantum | 87% | 100% |
| D0A6I9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
| Q4QG30 | Leishmania major | 85% | 100% |
| V5ARR9 | Trypanosoma cruzi | 27% | 100% |