| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I4S6
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
| GO:0006396 | RNA processing | 6 | 8 |
| GO:0006399 | tRNA metabolic process | 7 | 8 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
| GO:0008033 | tRNA processing | 8 | 8 |
| GO:0008152 | metabolic process | 1 | 8 |
| GO:0009987 | cellular process | 1 | 8 |
| GO:0016070 | RNA metabolic process | 5 | 8 |
| GO:0034470 | ncRNA processing | 7 | 8 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
| GO:0034660 | ncRNA metabolic process | 6 | 8 |
| GO:0043170 | macromolecule metabolic process | 3 | 8 |
| GO:0044237 | cellular metabolic process | 2 | 8 |
| GO:0044238 | primary metabolic process | 2 | 8 |
| GO:0046483 | heterocycle metabolic process | 3 | 8 |
| GO:0071704 | organic substance metabolic process | 2 | 8 |
| GO:0090304 | nucleic acid metabolic process | 4 | 8 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 8 |
| GO:0016432 | tRNA-uridine aminocarboxypropyltransferase activity | 4 | 8 |
| GO:0016740 | transferase activity | 2 | 8 |
| GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 8 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 8 |
| GO:0140101 | catalytic activity, acting on a tRNA | 4 | 8 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.543 |
| CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.357 |
| CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.340 |
| CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.338 |
| CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.241 |
| CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.508 |
| CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.292 |
| CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.391 |
| CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.422 |
| CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.433 |
| CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.576 |
| CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.506 |
| CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.539 |
| CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.504 |
| CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.605 |
| CLV_PCSK_FUR_1 | 576 | 580 | PF00082 | 0.586 |
| CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.329 |
| CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.262 |
| CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.401 |
| CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.237 |
| CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.275 |
| CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.351 |
| CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.266 |
| CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.400 |
| CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.466 |
| CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.610 |
| CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.576 |
| CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.506 |
| CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.539 |
| CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.498 |
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.606 |
| CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.387 |
| CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.236 |
| CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.351 |
| CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.266 |
| CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.606 |
| CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.428 |
| CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.409 |
| CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.398 |
| CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.395 |
| CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.400 |
| CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.478 |
| CLV_Separin_Metazoa | 224 | 228 | PF03568 | 0.292 |
| CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.471 |
| DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.378 |
| DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.536 |
| DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.236 |
| DOC_ANK_TNKS_1 | 311 | 318 | PF00023 | 0.291 |
| DOC_CKS1_1 | 46 | 51 | PF01111 | 0.454 |
| DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.351 |
| DOC_MAPK_DCC_7 | 132 | 141 | PF00069 | 0.442 |
| DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.437 |
| DOC_MAPK_gen_1 | 168 | 174 | PF00069 | 0.289 |
| DOC_MAPK_gen_1 | 31 | 37 | PF00069 | 0.376 |
| DOC_MAPK_gen_1 | 374 | 382 | PF00069 | 0.369 |
| DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.510 |
| DOC_MAPK_MEF2A_6 | 132 | 141 | PF00069 | 0.500 |
| DOC_MAPK_MEF2A_6 | 374 | 381 | PF00069 | 0.236 |
| DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.292 |
| DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.351 |
| DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.530 |
| DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.549 |
| DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.615 |
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.550 |
| DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.500 |
| DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.357 |
| DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.355 |
| DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.469 |
| DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.476 |
| DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.357 |
| DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.451 |
| DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.453 |
| LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.371 |
| LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.306 |
| LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.302 |
| LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.494 |
| LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.357 |
| LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.647 |
| LIG_14-3-3_CanoR_1 | 540 | 546 | PF00244 | 0.476 |
| LIG_14-3-3_CanoR_1 | 548 | 558 | PF00244 | 0.437 |
| LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.437 |
| LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.515 |
| LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.351 |
| LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.292 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.469 |
| LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.351 |
| LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.344 |
| LIG_FHA_1 | 136 | 142 | PF00498 | 0.466 |
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.340 |
| LIG_FHA_1 | 363 | 369 | PF00498 | 0.274 |
| LIG_FHA_1 | 395 | 401 | PF00498 | 0.357 |
| LIG_FHA_1 | 540 | 546 | PF00498 | 0.463 |
| LIG_FHA_2 | 110 | 116 | PF00498 | 0.562 |
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.313 |
| LIG_FHA_2 | 454 | 460 | PF00498 | 0.357 |
| LIG_FHA_2 | 478 | 484 | PF00498 | 0.543 |
| LIG_FHA_2 | 55 | 61 | PF00498 | 0.501 |
| LIG_FHA_2 | 550 | 556 | PF00498 | 0.505 |
| LIG_HP1_1 | 401 | 405 | PF01393 | 0.351 |
| LIG_IBAR_NPY_1 | 28 | 30 | PF08397 | 0.432 |
| LIG_LIR_Apic_2 | 573 | 577 | PF02991 | 0.547 |
| LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.386 |
| LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.398 |
| LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.377 |
| LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.324 |
| LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.294 |
| LIG_PTB_Apo_2 | 472 | 479 | PF02174 | 0.395 |
| LIG_PTB_Apo_2 | 524 | 531 | PF02174 | 0.460 |
| LIG_PTB_Phospho_1 | 524 | 530 | PF10480 | 0.469 |
| LIG_SH2_CRK | 46 | 50 | PF00017 | 0.475 |
| LIG_SH2_CRK | 528 | 532 | PF00017 | 0.373 |
| LIG_SH2_GRB2like | 473 | 476 | PF00017 | 0.398 |
| LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.467 |
| LIG_SH2_SRC | 473 | 476 | PF00017 | 0.436 |
| LIG_SH2_STAP1 | 411 | 415 | PF00017 | 0.351 |
| LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.351 |
| LIG_SH2_STAT3 | 254 | 257 | PF00017 | 0.357 |
| LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.377 |
| LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.361 |
| LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.474 |
| LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.353 |
| LIG_SH3_3 | 339 | 345 | PF00018 | 0.440 |
| LIG_SH3_3 | 357 | 363 | PF00018 | 0.269 |
| LIG_SH3_3 | 566 | 572 | PF00018 | 0.582 |
| LIG_SH3_3 | 585 | 591 | PF00018 | 0.626 |
| LIG_SUMO_SIM_par_1 | 364 | 369 | PF11976 | 0.402 |
| LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.326 |
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.457 |
| LIG_TRAF2_1 | 319 | 322 | PF00917 | 0.312 |
| LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.511 |
| LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.396 |
| LIG_UBA3_1 | 414 | 420 | PF00899 | 0.309 |
| LIG_WW_3 | 53 | 57 | PF00397 | 0.476 |
| MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.437 |
| MOD_CK1_1 | 109 | 115 | PF00069 | 0.573 |
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.710 |
| MOD_CK1_1 | 18 | 24 | PF00069 | 0.447 |
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.399 |
| MOD_CK1_1 | 549 | 555 | PF00069 | 0.636 |
| MOD_CK1_1 | 563 | 569 | PF00069 | 0.395 |
| MOD_CK1_1 | 6 | 12 | PF00069 | 0.662 |
| MOD_CK2_1 | 139 | 145 | PF00069 | 0.437 |
| MOD_CK2_1 | 305 | 311 | PF00069 | 0.273 |
| MOD_CK2_1 | 316 | 322 | PF00069 | 0.274 |
| MOD_CK2_1 | 425 | 431 | PF00069 | 0.312 |
| MOD_CK2_1 | 477 | 483 | PF00069 | 0.487 |
| MOD_CK2_1 | 54 | 60 | PF00069 | 0.506 |
| MOD_CK2_1 | 549 | 555 | PF00069 | 0.505 |
| MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.559 |
| MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.553 |
| MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.635 |
| MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.399 |
| MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.570 |
| MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.646 |
| MOD_GlcNHglycan | 514 | 518 | PF01048 | 0.593 |
| MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.444 |
| MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.578 |
| MOD_GSK3_1 | 122 | 129 | PF00069 | 0.617 |
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.494 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.508 |
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.417 |
| MOD_GSK3_1 | 346 | 353 | PF00069 | 0.451 |
| MOD_GSK3_1 | 362 | 369 | PF00069 | 0.199 |
| MOD_GSK3_1 | 422 | 429 | PF00069 | 0.318 |
| MOD_GSK3_1 | 449 | 456 | PF00069 | 0.327 |
| MOD_GSK3_1 | 45 | 52 | PF00069 | 0.474 |
| MOD_GSK3_1 | 556 | 563 | PF00069 | 0.563 |
| MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.482 |
| MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.280 |
| MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.420 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.718 |
| MOD_NEK2_1 | 19 | 24 | PF00069 | 0.464 |
| MOD_NEK2_1 | 225 | 230 | PF00069 | 0.292 |
| MOD_NEK2_1 | 381 | 386 | PF00069 | 0.342 |
| MOD_NEK2_1 | 430 | 435 | PF00069 | 0.359 |
| MOD_NEK2_1 | 546 | 551 | PF00069 | 0.496 |
| MOD_NEK2_2 | 277 | 282 | PF00069 | 0.351 |
| MOD_PIKK_1 | 451 | 457 | PF00454 | 0.300 |
| MOD_PIKK_1 | 605 | 611 | PF00454 | 0.624 |
| MOD_PK_1 | 168 | 174 | PF00069 | 0.393 |
| MOD_PK_1 | 83 | 89 | PF00069 | 0.390 |
| MOD_PKA_1 | 168 | 174 | PF00069 | 0.388 |
| MOD_PKA_1 | 419 | 425 | PF00069 | 0.292 |
| MOD_PKA_1 | 83 | 89 | PF00069 | 0.390 |
| MOD_PKA_2 | 168 | 174 | PF00069 | 0.388 |
| MOD_PKA_2 | 201 | 207 | PF00069 | 0.435 |
| MOD_PKA_2 | 226 | 232 | PF00069 | 0.292 |
| MOD_PKA_2 | 23 | 29 | PF00069 | 0.515 |
| MOD_PKA_2 | 401 | 407 | PF00069 | 0.357 |
| MOD_PKA_2 | 422 | 428 | PF00069 | 0.272 |
| MOD_PKA_2 | 49 | 55 | PF00069 | 0.658 |
| MOD_PKA_2 | 539 | 545 | PF00069 | 0.374 |
| MOD_PKA_2 | 591 | 597 | PF00069 | 0.609 |
| MOD_PKA_2 | 83 | 89 | PF00069 | 0.489 |
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.482 |
| MOD_Plk_1 | 15 | 21 | PF00069 | 0.584 |
| MOD_Plk_1 | 214 | 220 | PF00069 | 0.351 |
| MOD_Plk_1 | 250 | 256 | PF00069 | 0.313 |
| MOD_Plk_1 | 382 | 388 | PF00069 | 0.351 |
| MOD_Plk_1 | 430 | 436 | PF00069 | 0.292 |
| MOD_Plk_4 | 135 | 141 | PF00069 | 0.431 |
| MOD_Plk_4 | 15 | 21 | PF00069 | 0.475 |
| MOD_Plk_4 | 162 | 168 | PF00069 | 0.511 |
| MOD_Plk_4 | 214 | 220 | PF00069 | 0.340 |
| MOD_Plk_4 | 250 | 256 | PF00069 | 0.384 |
| MOD_Plk_4 | 277 | 283 | PF00069 | 0.320 |
| MOD_Plk_4 | 410 | 416 | PF00069 | 0.383 |
| MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.357 |
| MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.447 |
| MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.455 |
| MOD_SUMO_for_1 | 596 | 599 | PF00179 | 0.520 |
| MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.422 |
| TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.351 |
| TRG_DiLeu_BaEn_2 | 147 | 153 | PF01217 | 0.405 |
| TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.404 |
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.423 |
| TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.303 |
| TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.389 |
| TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.390 |
| TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.351 |
| TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.473 |
| TRG_ER_diArg_1 | 518 | 521 | PF00400 | 0.539 |
| TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.513 |
| TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.523 |
| TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.478 |
| TRG_NLS_MonoExtC_3 | 418 | 423 | PF00514 | 0.351 |
| TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.502 |
| TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.510 |
| TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.501 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I6V5 | Leptomonas seymouri | 56% | 100% |
| A0A0S4JPN0 | Bodo saltans | 37% | 100% |
| A0A3Q8IHF3 | Leishmania donovani | 100% | 100% |
| A4HHL7 | Leishmania braziliensis | 75% | 100% |
| E9AE79 | Leishmania major | 91% | 100% |
| E9ALK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |