| 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 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: E9B227
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 1 | 
| GO:0006518 | peptide metabolic process | 4 | 1 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 | 
| GO:0008152 | metabolic process | 1 | 1 | 
| GO:0009056 | catabolic process | 2 | 1 | 
| GO:0009987 | cellular process | 1 | 1 | 
| GO:0019538 | protein metabolic process | 3 | 1 | 
| GO:0043170 | macromolecule metabolic process | 3 | 1 | 
| GO:0043171 | peptide catabolic process | 4 | 1 | 
| GO:0043603 | amide metabolic process | 3 | 1 | 
| GO:0044237 | cellular metabolic process | 2 | 1 | 
| GO:0044238 | primary metabolic process | 2 | 1 | 
| GO:0044248 | cellular catabolic process | 3 | 1 | 
| GO:0071704 | organic substance metabolic process | 2 | 1 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 | 
| GO:1901565 | organonitrogen compound catabolic process | 4 | 1 | 
| GO:1901575 | organic substance catabolic process | 3 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 | 
| GO:0004177 | aminopeptidase activity | 5 | 10 | 
| GO:0005488 | binding | 1 | 11 | 
| GO:0008233 | peptidase activity | 3 | 11 | 
| GO:0008237 | metallopeptidase activity | 4 | 11 | 
| GO:0008238 | exopeptidase activity | 4 | 10 | 
| GO:0008270 | zinc ion binding | 6 | 11 | 
| GO:0016787 | hydrolase activity | 2 | 11 | 
| GO:0043167 | ion binding | 2 | 11 | 
| GO:0043169 | cation binding | 3 | 11 | 
| GO:0046872 | metal ion binding | 4 | 11 | 
| GO:0046914 | transition metal ion binding | 5 | 11 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 11 | 
| GO:0008235 | metalloexopeptidase activity | 5 | 1 | 
| GO:0033218 | amide binding | 2 | 1 | 
| GO:0042277 | peptide binding | 3 | 1 | 
| GO:0070006 | metalloaminopeptidase activity | 6 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.621 | 
| CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.558 | 
| CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.643 | 
| CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.419 | 
| CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.500 | 
| CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.447 | 
| CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.356 | 
| CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.466 | 
| CLV_PCSK_FUR_1 | 41 | 45 | PF00082 | 0.457 | 
| CLV_PCSK_FUR_1 | 77 | 81 | PF00082 | 0.516 | 
| CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.679 | 
| CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.500 | 
| CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.447 | 
| CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.341 | 
| CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.510 | 
| CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.728 | 
| CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.357 | 
| CLV_PCSK_PC7_1 | 367 | 373 | PF00082 | 0.496 | 
| CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.395 | 
| CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.314 | 
| CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.456 | 
| CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.514 | 
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.481 | 
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.519 | 
| DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.563 | 
| DEG_SPOP_SBC_1 | 517 | 521 | PF00917 | 0.400 | 
| DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.323 | 
| DOC_CKS1_1 | 602 | 607 | PF01111 | 0.397 | 
| DOC_CYCLIN_RxL_1 | 380 | 391 | PF00134 | 0.460 | 
| DOC_CYCLIN_yCln2_LP_2 | 477 | 483 | PF00134 | 0.259 | 
| DOC_MAPK_MEF2A_6 | 572 | 581 | PF00069 | 0.324 | 
| DOC_PP1_RVXF_1 | 187 | 194 | PF00149 | 0.359 | 
| DOC_PP1_RVXF_1 | 260 | 266 | PF00149 | 0.386 | 
| DOC_PP2B_LxvP_1 | 340 | 343 | PF13499 | 0.419 | 
| DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.259 | 
| DOC_PP2B_PxIxI_1 | 581 | 587 | PF00149 | 0.441 | 
| DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.433 | 
| DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.290 | 
| DOC_PP4_FxxP_1 | 399 | 402 | PF00568 | 0.290 | 
| DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.754 | 
| DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.579 | 
| DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.338 | 
| DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.314 | 
| DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.298 | 
| DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.653 | 
| DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.583 | 
| DOC_USP7_MATH_2 | 65 | 71 | PF00917 | 0.487 | 
| DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.605 | 
| DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.606 | 
| DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.493 | 
| DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.397 | 
| DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.569 | 
| DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.694 | 
| LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.346 | 
| LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.324 | 
| LIG_14-3-3_CanoR_1 | 375 | 384 | PF00244 | 0.438 | 
| LIG_14-3-3_CanoR_1 | 535 | 543 | PF00244 | 0.324 | 
| LIG_APCC_ABBA_1 | 199 | 204 | PF00400 | 0.482 | 
| LIG_APCC_Cbox_2 | 565 | 571 | PF00515 | 0.179 | 
| LIG_Clathr_ClatBox_1 | 190 | 194 | PF01394 | 0.468 | 
| LIG_deltaCOP1_diTrp_1 | 185 | 193 | PF00928 | 0.474 | 
| LIG_FHA_1 | 12 | 18 | PF00498 | 0.375 | 
| LIG_FHA_1 | 207 | 213 | PF00498 | 0.256 | 
| LIG_FHA_1 | 233 | 239 | PF00498 | 0.452 | 
| LIG_FHA_1 | 35 | 41 | PF00498 | 0.432 | 
| LIG_FHA_1 | 354 | 360 | PF00498 | 0.573 | 
| LIG_FHA_1 | 376 | 382 | PF00498 | 0.486 | 
| LIG_FHA_1 | 453 | 459 | PF00498 | 0.414 | 
| LIG_FHA_2 | 172 | 178 | PF00498 | 0.696 | 
| LIG_FHA_2 | 240 | 246 | PF00498 | 0.290 | 
| LIG_FHA_2 | 279 | 285 | PF00498 | 0.419 | 
| LIG_LIR_Gen_1 | 313 | 321 | PF02991 | 0.521 | 
| LIG_LIR_Gen_1 | 561 | 571 | PF02991 | 0.344 | 
| LIG_LIR_Gen_1 | 70 | 76 | PF02991 | 0.545 | 
| LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.335 | 
| LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.366 | 
| LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.331 | 
| LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.507 | 
| LIG_NRBOX | 410 | 416 | PF00104 | 0.383 | 
| LIG_PDZ_Class_1 | 616 | 621 | PF00595 | 0.502 | 
| LIG_Pex14_2 | 244 | 248 | PF04695 | 0.393 | 
| LIG_SH2_SRC | 438 | 441 | PF00017 | 0.324 | 
| LIG_SH2_SRC | 548 | 551 | PF00017 | 0.419 | 
| LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.532 | 
| LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.352 | 
| LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.324 | 
| LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.494 | 
| LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.279 | 
| LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.358 | 
| LIG_SH3_3 | 253 | 259 | PF00018 | 0.358 | 
| LIG_SH3_3 | 300 | 306 | PF00018 | 0.337 | 
| LIG_SH3_3 | 414 | 420 | PF00018 | 0.328 | 
| LIG_SH3_3 | 576 | 582 | PF00018 | 0.507 | 
| LIG_SUMO_SIM_anti_2 | 331 | 337 | PF11976 | 0.524 | 
| LIG_SUMO_SIM_anti_2 | 409 | 415 | PF11976 | 0.312 | 
| LIG_SUMO_SIM_par_1 | 104 | 110 | PF11976 | 0.383 | 
| LIG_SUMO_SIM_par_1 | 128 | 133 | PF11976 | 0.525 | 
| LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.535 | 
| LIG_WRC_WIRS_1 | 215 | 220 | PF05994 | 0.419 | 
| LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.430 | 
| MOD_CK1_1 | 141 | 147 | PF00069 | 0.684 | 
| MOD_CK1_1 | 175 | 181 | PF00069 | 0.621 | 
| MOD_CK1_1 | 20 | 26 | PF00069 | 0.545 | 
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.214 | 
| MOD_CK1_1 | 275 | 281 | PF00069 | 0.294 | 
| MOD_CK1_1 | 351 | 357 | PF00069 | 0.596 | 
| MOD_CK1_1 | 451 | 457 | PF00069 | 0.269 | 
| MOD_CK1_1 | 511 | 517 | PF00069 | 0.401 | 
| MOD_CK1_1 | 520 | 526 | PF00069 | 0.298 | 
| MOD_CK1_1 | 61 | 67 | PF00069 | 0.680 | 
| MOD_CK2_1 | 239 | 245 | PF00069 | 0.290 | 
| MOD_CK2_1 | 278 | 284 | PF00069 | 0.419 | 
| MOD_CK2_1 | 420 | 426 | PF00069 | 0.290 | 
| MOD_CK2_1 | 451 | 457 | PF00069 | 0.259 | 
| MOD_CK2_1 | 61 | 67 | PF00069 | 0.611 | 
| MOD_Cter_Amidation | 150 | 153 | PF01082 | 0.649 | 
| MOD_Cter_Amidation | 286 | 289 | PF01082 | 0.419 | 
| MOD_Cter_Amidation | 440 | 443 | PF01082 | 0.399 | 
| MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.584 | 
| MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.649 | 
| MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.678 | 
| MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.623 | 
| MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.637 | 
| MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.484 | 
| MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.372 | 
| MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.654 | 
| MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.617 | 
| MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.290 | 
| MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.349 | 
| MOD_GlcNHglycan | 510 | 514 | PF01048 | 0.312 | 
| MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.734 | 
| MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.321 | 
| MOD_GlcNHglycan | 587 | 591 | PF01048 | 0.392 | 
| MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.519 | 
| MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.744 | 
| MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.570 | 
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.697 | 
| MOD_GSK3_1 | 17 | 24 | PF00069 | 0.524 | 
| MOD_GSK3_1 | 171 | 178 | PF00069 | 0.701 | 
| MOD_GSK3_1 | 227 | 234 | PF00069 | 0.399 | 
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.309 | 
| MOD_GSK3_1 | 353 | 360 | PF00069 | 0.589 | 
| MOD_GSK3_1 | 448 | 455 | PF00069 | 0.334 | 
| MOD_GSK3_1 | 50 | 57 | PF00069 | 0.725 | 
| MOD_GSK3_1 | 516 | 523 | PF00069 | 0.310 | 
| MOD_GSK3_1 | 530 | 537 | PF00069 | 0.386 | 
| MOD_GSK3_1 | 597 | 604 | PF00069 | 0.635 | 
| MOD_GSK3_1 | 63 | 70 | PF00069 | 0.626 | 
| MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.484 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.624 | 
| MOD_NEK2_1 | 17 | 22 | PF00069 | 0.422 | 
| MOD_NEK2_1 | 353 | 358 | PF00069 | 0.685 | 
| MOD_NEK2_1 | 543 | 548 | PF00069 | 0.480 | 
| MOD_NEK2_2 | 530 | 535 | PF00069 | 0.179 | 
| MOD_PIKK_1 | 206 | 212 | PF00454 | 0.324 | 
| MOD_PK_1 | 114 | 120 | PF00069 | 0.578 | 
| MOD_PK_1 | 128 | 134 | PF00069 | 0.520 | 
| MOD_PKA_1 | 153 | 159 | PF00069 | 0.630 | 
| MOD_PKA_2 | 20 | 26 | PF00069 | 0.489 | 
| MOD_PKA_2 | 385 | 391 | PF00069 | 0.496 | 
| MOD_PKA_2 | 441 | 447 | PF00069 | 0.218 | 
| MOD_PKA_2 | 47 | 53 | PF00069 | 0.605 | 
| MOD_PKA_2 | 534 | 540 | PF00069 | 0.414 | 
| MOD_Plk_1 | 1 | 7 | PF00069 | 0.332 | 
| MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.593 | 
| MOD_Plk_4 | 35 | 41 | PF00069 | 0.499 | 
| MOD_Plk_4 | 388 | 394 | PF00069 | 0.328 | 
| MOD_Plk_4 | 427 | 433 | PF00069 | 0.396 | 
| MOD_Plk_4 | 495 | 501 | PF00069 | 0.492 | 
| MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.600 | 
| MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.491 | 
| MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.397 | 
| MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.572 | 
| MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.696 | 
| MOD_SUMO_for_1 | 515 | 518 | PF00179 | 0.179 | 
| TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.344 | 
| TRG_DiLeu_BaEn_2 | 70 | 76 | PF01217 | 0.542 | 
| TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.393 | 
| TRG_DiLeu_LyEn_5 | 236 | 241 | PF01217 | 0.383 | 
| TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.538 | 
| TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.437 | 
| TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.514 | 
| TRG_Pf-PMV_PEXEL_1 | 104 | 109 | PF00026 | 0.326 | 
| TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.470 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1PC92 | Leptomonas seymouri | 58% | 100% | 
| A0A1X0NRQ5 | Trypanosomatidae | 38% | 100% | 
| A0A3S7X4Q1 | Leishmania donovani | 88% | 100% | 
| A0A422N3Z8 | Trypanosoma rangeli | 35% | 100% | 
| A4HJK9 | Leishmania braziliensis | 75% | 99% | 
| A4I709 | Leishmania infantum | 88% | 100% | 
| C9ZWP4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 96% | 
| Q4Q635 | Leishmania major | 88% | 100% | 
| V5AMB1 | Trypanosoma cruzi | 36% | 100% |