| 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: E9ALK6
| 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 | 0.580 | 
| CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.357 | 
| CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.374 | 
| CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.328 | 
| CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.508 | 
| CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.317 | 
| CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.411 | 
| CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.456 | 
| CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.550 | 
| CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.511 | 
| CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.541 | 
| CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.524 | 
| CLV_PCSK_FUR_1 | 576 | 580 | PF00082 | 0.625 | 
| CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.323 | 
| CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.412 | 
| CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.371 | 
| CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.399 | 
| CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.472 | 
| CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.594 | 
| CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.544 | 
| CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.765 | 
| CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.548 | 
| CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.517 | 
| CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.397 | 
| CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.351 | 
| CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.496 | 
| CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.561 | 
| CLV_PCSK_PC7_1 | 492 | 498 | PF00082 | 0.440 | 
| CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.405 | 
| CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.405 | 
| CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.400 | 
| CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.433 | 
| CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.453 | 
| CLV_Separin_Metazoa | 224 | 228 | PF03568 | 0.292 | 
| CLV_Separin_Metazoa | 97 | 101 | PF03568 | 0.470 | 
| DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.392 | 
| DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.520 | 
| DEG_COP1_1 | 566 | 574 | PF00400 | 0.415 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 | 
| DOC_CDC14_PxL_1 | 520 | 528 | PF14671 | 0.341 | 
| DOC_CKS1_1 | 46 | 51 | PF01111 | 0.461 | 
| DOC_CYCLIN_yCln2_LP_2 | 239 | 245 | PF00134 | 0.351 | 
| DOC_MAPK_DCC_7 | 132 | 141 | PF00069 | 0.428 | 
| DOC_MAPK_gen_1 | 168 | 174 | PF00069 | 0.305 | 
| DOC_MAPK_gen_1 | 31 | 37 | PF00069 | 0.388 | 
| DOC_MAPK_gen_1 | 375 | 382 | PF00069 | 0.349 | 
| DOC_MAPK_gen_1 | 83 | 89 | PF00069 | 0.516 | 
| DOC_MAPK_MEF2A_6 | 132 | 141 | PF00069 | 0.486 | 
| DOC_MAPK_MEF2A_6 | 398 | 407 | PF00069 | 0.292 | 
| DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.351 | 
| DOC_PP4_FxxP_1 | 574 | 577 | PF00568 | 0.591 | 
| DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.656 | 
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.623 | 
| DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.618 | 
| DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.478 | 
| DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.305 | 
| DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.277 | 
| 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 | 0.509 | 
| DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.473 | 
| DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.420 | 
| DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.357 | 
| DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.464 | 
| LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.321 | 
| LIG_14-3-3_CanoR_1 | 202 | 206 | PF00244 | 0.302 | 
| LIG_14-3-3_CanoR_1 | 402 | 406 | PF00244 | 0.435 | 
| LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.501 | 
| LIG_14-3-3_CanoR_1 | 56 | 64 | PF00244 | 0.438 | 
| LIG_14-3-3_CanoR_1 | 585 | 591 | PF00244 | 0.482 | 
| LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.461 | 
| LIG_Actin_WH2_2 | 458 | 474 | PF00022 | 0.351 | 
| LIG_APCC_ABBA_1 | 218 | 223 | PF00400 | 0.292 | 
| LIG_Clathr_ClatBox_1 | 379 | 383 | PF01394 | 0.351 | 
| LIG_deltaCOP1_diTrp_1 | 148 | 152 | PF00928 | 0.346 | 
| LIG_EVH1_1 | 359 | 363 | PF00568 | 0.247 | 
| LIG_FHA_1 | 136 | 142 | PF00498 | 0.488 | 
| LIG_FHA_1 | 215 | 221 | PF00498 | 0.292 | 
| LIG_FHA_1 | 395 | 401 | PF00498 | 0.357 | 
| LIG_FHA_2 | 110 | 116 | PF00498 | 0.683 | 
| LIG_FHA_2 | 118 | 124 | PF00498 | 0.728 | 
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.313 | 
| LIG_FHA_2 | 454 | 460 | PF00498 | 0.357 | 
| LIG_FHA_2 | 478 | 484 | PF00498 | 0.436 | 
| LIG_FHA_2 | 55 | 61 | PF00498 | 0.500 | 
| LIG_FHA_2 | 550 | 556 | PF00498 | 0.480 | 
| LIG_HP1_1 | 401 | 405 | PF01393 | 0.351 | 
| LIG_IBAR_NPY_1 | 28 | 30 | PF08397 | 0.430 | 
| LIG_LIR_Apic_2 | 573 | 577 | PF02991 | 0.584 | 
| LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.389 | 
| LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.365 | 
| LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.380 | 
| LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.324 | 
| LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.242 | 
| LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.303 | 
| LIG_PTB_Apo_2 | 472 | 479 | PF02174 | 0.397 | 
| LIG_PTB_Apo_2 | 524 | 531 | PF02174 | 0.454 | 
| LIG_PTB_Phospho_1 | 524 | 530 | PF10480 | 0.462 | 
| LIG_SH2_CRK | 46 | 50 | PF00017 | 0.509 | 
| LIG_SH2_CRK | 528 | 532 | PF00017 | 0.372 | 
| LIG_SH2_GRB2like | 473 | 476 | PF00017 | 0.399 | 
| LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.414 | 
| LIG_SH2_SRC | 473 | 476 | PF00017 | 0.438 | 
| 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 | 0.387 | 
| LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.357 | 
| LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.486 | 
| LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.399 | 
| LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.350 | 
| LIG_SH3_3 | 339 | 345 | PF00018 | 0.508 | 
| LIG_SH3_3 | 357 | 363 | PF00018 | 0.383 | 
| LIG_SH3_3 | 566 | 572 | PF00018 | 0.565 | 
| LIG_SUMO_SIM_par_1 | 378 | 385 | PF11976 | 0.326 | 
| LIG_SxIP_EBH_1 | 556 | 567 | PF03271 | 0.326 | 
| LIG_TRAF2_1 | 142 | 145 | PF00917 | 0.468 | 
| LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.307 | 
| LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.510 | 
| LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.387 | 
| LIG_UBA3_1 | 414 | 420 | PF00899 | 0.292 | 
| LIG_WW_3 | 53 | 57 | PF00397 | 0.471 | 
| MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.449 | 
| MOD_CK1_1 | 109 | 115 | PF00069 | 0.613 | 
| MOD_CK1_1 | 122 | 128 | PF00069 | 0.747 | 
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.351 | 
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.524 | 
| MOD_CK1_1 | 563 | 569 | PF00069 | 0.442 | 
| MOD_CK2_1 | 139 | 145 | PF00069 | 0.483 | 
| MOD_CK2_1 | 316 | 322 | PF00069 | 0.274 | 
| MOD_CK2_1 | 348 | 354 | PF00069 | 0.285 | 
| MOD_CK2_1 | 425 | 431 | PF00069 | 0.331 | 
| MOD_CK2_1 | 477 | 483 | PF00069 | 0.379 | 
| MOD_CK2_1 | 54 | 60 | PF00069 | 0.502 | 
| MOD_CK2_1 | 549 | 555 | PF00069 | 0.500 | 
| MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.586 | 
| MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.356 | 
| MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.263 | 
| MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.290 | 
| MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.502 | 
| MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.489 | 
| MOD_GlcNHglycan | 514 | 518 | PF01048 | 0.524 | 
| MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.459 | 
| MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.692 | 
| MOD_GSK3_1 | 135 | 142 | PF00069 | 0.371 | 
| MOD_GSK3_1 | 19 | 26 | PF00069 | 0.521 | 
| MOD_GSK3_1 | 2 | 9 | PF00069 | 0.516 | 
| MOD_GSK3_1 | 277 | 284 | PF00069 | 0.440 | 
| MOD_GSK3_1 | 346 | 353 | PF00069 | 0.464 | 
| MOD_GSK3_1 | 366 | 373 | PF00069 | 0.289 | 
| MOD_GSK3_1 | 422 | 429 | PF00069 | 0.313 | 
| MOD_GSK3_1 | 45 | 52 | PF00069 | 0.529 | 
| MOD_GSK3_1 | 451 | 458 | PF00069 | 0.376 | 
| MOD_GSK3_1 | 556 | 563 | PF00069 | 0.551 | 
| MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.413 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 | 
| MOD_NEK2_1 | 19 | 24 | PF00069 | 0.591 | 
| MOD_NEK2_1 | 225 | 230 | PF00069 | 0.292 | 
| MOD_NEK2_1 | 299 | 304 | PF00069 | 0.236 | 
| MOD_NEK2_1 | 381 | 386 | PF00069 | 0.339 | 
| MOD_NEK2_1 | 430 | 435 | PF00069 | 0.292 | 
| MOD_NEK2_1 | 565 | 570 | PF00069 | 0.495 | 
| MOD_NEK2_2 | 277 | 282 | PF00069 | 0.351 | 
| MOD_PIKK_1 | 299 | 305 | PF00454 | 0.335 | 
| MOD_PIKK_1 | 370 | 376 | PF00454 | 0.274 | 
| MOD_PIKK_1 | 451 | 457 | PF00454 | 0.300 | 
| MOD_PK_1 | 168 | 174 | PF00069 | 0.393 | 
| MOD_PKA_1 | 168 | 174 | PF00069 | 0.388 | 
| MOD_PKA_1 | 419 | 425 | PF00069 | 0.292 | 
| MOD_PKA_1 | 584 | 590 | PF00069 | 0.480 | 
| MOD_PKA_2 | 168 | 174 | PF00069 | 0.388 | 
| MOD_PKA_2 | 201 | 207 | PF00069 | 0.357 | 
| MOD_PKA_2 | 226 | 232 | PF00069 | 0.292 | 
| MOD_PKA_2 | 401 | 407 | PF00069 | 0.435 | 
| MOD_PKA_2 | 422 | 428 | PF00069 | 0.272 | 
| MOD_PKA_2 | 49 | 55 | PF00069 | 0.513 | 
| MOD_PKA_2 | 584 | 590 | PF00069 | 0.655 | 
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.592 | 
| MOD_Plk_1 | 214 | 220 | PF00069 | 0.399 | 
| MOD_Plk_1 | 250 | 256 | PF00069 | 0.313 | 
| MOD_Plk_1 | 382 | 388 | PF00069 | 0.361 | 
| MOD_Plk_1 | 430 | 436 | PF00069 | 0.292 | 
| MOD_Plk_4 | 135 | 141 | PF00069 | 0.419 | 
| MOD_Plk_4 | 214 | 220 | PF00069 | 0.292 | 
| MOD_Plk_4 | 250 | 256 | PF00069 | 0.313 | 
| MOD_Plk_4 | 277 | 283 | PF00069 | 0.351 | 
| MOD_Plk_4 | 410 | 416 | PF00069 | 0.351 | 
| MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.404 | 
| MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.357 | 
| MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.460 | 
| MOD_SUMO_rev_2 | 142 | 152 | PF00179 | 0.426 | 
| TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.351 | 
| TRG_DiLeu_BaEn_2 | 147 | 153 | PF01217 | 0.408 | 
| TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.415 | 
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.433 | 
| TRG_ENDOCYTIC_2 | 411 | 414 | PF00928 | 0.324 | 
| TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.386 | 
| TRG_ER_diArg_1 | 167 | 169 | PF00400 | 0.361 | 
| TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.351 | 
| TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.555 | 
| TRG_ER_diArg_1 | 519 | 522 | PF00400 | 0.519 | 
| TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.526 | 
| TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.495 | 
| TRG_NLS_MonoExtC_3 | 418 | 423 | PF00514 | 0.351 | 
| TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.451 | 
| TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.530 | 
| TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.502 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I6V5 | Leptomonas seymouri | 55% | 100% | 
| A0A0S4JPN0 | Bodo saltans | 37% | 100% | 
| A0A3Q8IHF3 | Leishmania donovani | 87% | 99% | 
| A4HHL7 | Leishmania braziliensis | 74% | 100% | 
| A4I4S6 | Leishmania infantum | 87% | 99% | 
| E9AE79 | Leishmania major | 86% | 100% |