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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3Q8IHV9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0000966 | RNA 5'-end processing | 7 | 1 |
GO:0001682 | tRNA 5'-leader removal | 9 | 1 |
GO:0099116 | tRNA 5'-end processing | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 9 |
GO:0004521 | RNA endonuclease activity | 5 | 9 |
GO:0004526 | ribonuclease P activity | 6 | 9 |
GO:0004540 | RNA nuclease activity | 4 | 9 |
GO:0004549 | tRNA-specific ribonuclease activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 9 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.455 |
CLV_C14_Caspase3-7 | 634 | 638 | PF00656 | 0.746 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.345 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.279 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.504 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.329 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.472 |
DEG_ODPH_VHL_1 | 675 | 688 | PF01847 | 0.359 |
DOC_CDC14_PxL_1 | 247 | 255 | PF14671 | 0.523 |
DOC_CKS1_1 | 572 | 577 | PF01111 | 0.791 |
DOC_MAPK_gen_1 | 231 | 239 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 324 | 332 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 424 | 432 | PF00069 | 0.238 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.279 |
DOC_MAPK_gen_1 | 533 | 543 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 424 | 432 | PF00069 | 0.234 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.404 |
DOC_PP1_RVXF_1 | 527 | 533 | PF00149 | 0.310 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.465 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.381 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.470 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 55 | 63 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 567 | 575 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.373 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.291 |
LIG_APCC_ABBA_1 | 349 | 354 | PF00400 | 0.434 |
LIG_APCC_ABBA_1 | 541 | 546 | PF00400 | 0.218 |
LIG_APCC_ABBA_1 | 686 | 691 | PF00400 | 0.471 |
LIG_APCC_ABBAyCdc20_2 | 348 | 354 | PF00400 | 0.429 |
LIG_APCC_ABBAyCdc20_2 | 540 | 546 | PF00400 | 0.357 |
LIG_BIR_III_2 | 637 | 641 | PF00653 | 0.551 |
LIG_Clathr_ClatBox_1 | 329 | 333 | PF01394 | 0.457 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.430 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.418 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.606 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.457 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.406 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.523 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.689 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.496 |
LIG_HP1_1 | 217 | 221 | PF01393 | 0.329 |
LIG_HP1_1 | 428 | 432 | PF01393 | 0.367 |
LIG_LIR_Apic_2 | 542 | 548 | PF02991 | 0.410 |
LIG_LIR_Apic_2 | 599 | 604 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 438 | 449 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 438 | 444 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.275 |
LIG_Pex14_1 | 601 | 605 | PF04695 | 0.461 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.291 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.291 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.291 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.542 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.367 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.310 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.656 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 427 | 434 | PF11976 | 0.268 |
LIG_TRAF2_1 | 666 | 669 | PF00917 | 0.771 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.315 |
LIG_UBA3_1 | 310 | 315 | PF00899 | 0.437 |
MOD_CDC14_SPxK_1 | 496 | 499 | PF00782 | 0.450 |
MOD_CDK_SPK_2 | 514 | 519 | PF00069 | 0.291 |
MOD_CDK_SPxK_1 | 493 | 499 | PF00069 | 0.450 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.585 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.558 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.750 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.697 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.426 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.298 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.675 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.791 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.478 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.371 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.349 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.730 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.650 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.440 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.752 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.572 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.508 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.355 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.595 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.646 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.567 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.596 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.706 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.469 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.591 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.403 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.340 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.702 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.598 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.734 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.347 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.330 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.346 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.694 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.766 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.761 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.544 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.497 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.618 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.555 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.447 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.692 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.413 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.312 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.275 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.621 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.311 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.393 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.558 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.387 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.586 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.393 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.328 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.773 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.317 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.398 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.458 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.335 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.391 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.699 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.463 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.454 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.290 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.330 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.364 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.309 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.793 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.642 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.653 |
MOD_SUMO_rev_2 | 308 | 317 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 434 | 442 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 637 | 647 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.367 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.140 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.293 |
TRG_NES_CRM1_1 | 468 | 481 | PF08389 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 312 | 316 | PF00026 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM55 | Leptomonas seymouri | 55% | 92% |
A0A0S4IT05 | Bodo saltans | 30% | 100% |
A0A1X0P3X4 | Trypanosomatidae | 45% | 100% |
A0A422MWI6 | Trypanosoma rangeli | 46% | 100% |
A4HLQ7 | Leishmania braziliensis | 81% | 100% |
A4I957 | Leishmania infantum | 100% | 100% |
D0A6B5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9B432 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4JKB6 | Arabidopsis thaliana | 23% | 100% |
Q4Q3Z2 | Leishmania major | 92% | 100% |
Q680B9 | Arabidopsis thaliana | 22% | 100% |
V5BPA7 | Trypanosoma cruzi | 46% | 100% |