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: 5 |
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:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005739 | mitochondrion | 5 | 1 |
Related structures:
AlphaFold database: A4HLQ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000966 | RNA 5'-end processing | 7 | 1 |
GO:0001682 | tRNA 5'-leader removal | 9 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006399 | tRNA metabolic process | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008033 | tRNA processing | 8 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:0099116 | tRNA 5'-end processing | 8 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 8 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004521 | RNA endonuclease activity | 5 | 7 |
GO:0004526 | ribonuclease P activity | 6 | 7 |
GO:0004540 | RNA nuclease activity | 4 | 7 |
GO:0004549 | tRNA-specific ribonuclease activity | 5 | 7 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 7 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 7 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.301 |
CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.288 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 571 | 573 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.462 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.408 |
DEG_SCF_FBW7_2 | 636 | 643 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.401 |
DOC_CYCLIN_RxL_1 | 186 | 198 | PF00134 | 0.179 |
DOC_MAPK_gen_1 | 324 | 332 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.343 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.368 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.395 |
DOC_PP1_RVXF_1 | 188 | 195 | PF00149 | 0.179 |
DOC_PP1_RVXF_1 | 527 | 533 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.413 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.462 |
DOC_PP2B_LxvP_1 | 618 | 621 | PF13499 | 0.482 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 135 | 143 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 233 | 241 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 55 | 63 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.274 |
LIG_APCC_ABBA_1 | 349 | 354 | PF00400 | 0.422 |
LIG_APCC_ABBA_1 | 697 | 702 | PF00400 | 0.408 |
LIG_APCC_ABBAyCdc20_2 | 540 | 546 | PF00400 | 0.452 |
LIG_eIF4E_1 | 175 | 181 | PF01652 | 0.179 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.450 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.531 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.332 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.432 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.451 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.519 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.316 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.395 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.522 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.646 |
LIG_FHA_2 | 696 | 702 | PF00498 | 0.425 |
LIG_HP1_1 | 428 | 432 | PF01393 | 0.386 |
LIG_LIR_Apic_2 | 542 | 548 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 559 | 564 | PF02991 | 0.659 |
LIG_LIR_Apic_2 | 599 | 604 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 27 | 35 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.427 |
LIG_Pex14_1 | 601 | 605 | PF04695 | 0.524 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.333 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.358 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.493 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.191 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.389 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.487 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.353 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.293 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.591 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.478 |
LIG_TRAF2_1 | 678 | 681 | PF00917 | 0.746 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.356 |
MOD_CDK_SPK_2 | 514 | 519 | PF00069 | 0.398 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.695 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.532 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.584 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.689 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.565 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.465 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.451 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.577 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.571 |
MOD_CK2_1 | 695 | 701 | PF00069 | 0.409 |
MOD_Cter_Amidation | 8 | 11 | PF01082 | 0.307 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.366 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.769 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.528 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.726 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.466 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.701 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.701 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.569 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.563 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.560 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.620 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.704 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.711 |
MOD_GlcNHglycan | 643 | 648 | PF01048 | 0.555 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.379 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.716 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.687 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.634 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.422 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.620 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.755 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.514 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.653 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.347 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.438 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.512 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.528 |
MOD_NEK2_2 | 16 | 21 | PF00069 | 0.240 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.274 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.460 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.350 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.331 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.490 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.513 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.501 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.331 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.274 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.473 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.317 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.501 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.403 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.688 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.386 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.528 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.393 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.749 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.624 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.515 |
MOD_SUMO_rev_2 | 434 | 442 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 619 | 627 | PF00179 | 0.715 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.296 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.323 |
TRG_NES_CRM1_1 | 468 | 481 | PF08389 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 312 | 316 | PF00026 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM55 | Leptomonas seymouri | 53% | 94% |
A0A1X0P3X4 | Trypanosomatidae | 43% | 100% |
A0A3Q8IHV9 | Leishmania donovani | 81% | 100% |
A0A422MWI6 | Trypanosoma rangeli | 45% | 100% |
A4HNH1 | Leishmania braziliensis | 30% | 100% |
A4I957 | Leishmania infantum | 81% | 100% |
D0A6B5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B432 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
F4JKB6 | Arabidopsis thaliana | 22% | 100% |
Q4Q3Z2 | Leishmania major | 80% | 98% |
Q680B9 | Arabidopsis thaliana | 23% | 100% |
V5BPA7 | Trypanosoma cruzi | 45% | 100% |