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: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 |
Related structures:
AlphaFold database: Q4Q3Z2
Term | Name | Level | Count |
---|---|---|---|
GO:0000966 | RNA 5'-end processing | 7 | 2 |
GO:0001682 | tRNA 5'-leader removal | 9 | 2 |
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 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0004519 | endonuclease activity | 5 | 8 |
GO:0004521 | RNA endonuclease activity | 5 | 8 |
GO:0004526 | ribonuclease P activity | 6 | 8 |
GO:0004540 | RNA nuclease activity | 4 | 8 |
GO:0004549 | tRNA-specific ribonuclease activity | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 8 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 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 | 36 | 40 | PF00656 | 0.760 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.450 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.340 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 149 | 155 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.494 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.335 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.491 |
DEG_SCF_TRCP1_1 | 39 | 45 | PF00400 | 0.506 |
DOC_CDC14_PxL_1 | 247 | 255 | PF14671 | 0.536 |
DOC_CKS1_1 | 572 | 577 | PF01111 | 0.733 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 231 | 239 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 324 | 332 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 523 | 532 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 212 | 221 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 233 | 241 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 401 | 409 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 151 | 158 | PF00149 | 0.399 |
DOC_PP1_RVXF_1 | 527 | 533 | PF00149 | 0.300 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.471 |
DOC_PP2B_LxvP_1 | 547 | 550 | PF13499 | 0.358 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.459 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.280 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 135 | 140 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 55 | 63 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.415 |
LIG_Actin_WH2_2 | 121 | 139 | PF00022 | 0.280 |
LIG_APCC_ABBA_1 | 349 | 354 | PF00400 | 0.429 |
LIG_APCC_ABBA_1 | 686 | 691 | PF00400 | 0.481 |
LIG_APCC_ABBAyCdc20_2 | 348 | 354 | PF00400 | 0.423 |
LIG_APCC_ABBAyCdc20_2 | 540 | 546 | PF00400 | 0.349 |
LIG_BIR_III_2 | 484 | 488 | PF00653 | 0.314 |
LIG_Clathr_ClatBox_1 | 329 | 333 | PF01394 | 0.452 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.455 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.415 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.604 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.351 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.442 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.399 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.526 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.748 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.506 |
LIG_HP1_1 | 217 | 221 | PF01393 | 0.335 |
LIG_HP1_1 | 428 | 432 | PF01393 | 0.358 |
LIG_LIR_Apic_2 | 542 | 548 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 599 | 604 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.281 |
LIG_Pex14_1 | 601 | 605 | PF04695 | 0.471 |
LIG_SH2_CRK | 460 | 464 | PF00017 | 0.280 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.128 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 551 | 555 | PF00017 | 0.280 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.280 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.358 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.300 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 427 | 434 | PF11976 | 0.273 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.321 |
LIG_UBA3_1 | 310 | 315 | PF00899 | 0.432 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.288 |
MOD_CDC14_SPxK_1 | 496 | 499 | PF00782 | 0.450 |
MOD_CDK_SPK_2 | 514 | 519 | PF00069 | 0.280 |
MOD_CDK_SPxK_1 | 493 | 499 | PF00069 | 0.450 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.463 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.677 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.520 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.301 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.742 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.271 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.443 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.147 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.712 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.453 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.286 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.615 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.714 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.758 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.488 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.736 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.727 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.705 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.669 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.472 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.753 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.549 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.700 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.335 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.609 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.674 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.573 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.585 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.683 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.475 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.605 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.709 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.359 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.322 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.662 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.702 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.764 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.389 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.343 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.307 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.301 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.582 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.615 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.480 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.398 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.555 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.392 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.302 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.280 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.271 |
MOD_PK_1 | 135 | 141 | PF00069 | 0.279 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.398 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.581 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.370 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.411 |
MOD_PKB_1 | 135 | 143 | PF00069 | 0.300 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.737 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.314 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.249 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.390 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.473 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.333 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.417 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.725 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.641 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.335 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.303 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.332 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.280 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.280 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.757 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 308 | 317 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 434 | 442 | PF00179 | 0.325 |
MOD_SUMO_rev_2 | 617 | 627 | PF00179 | 0.714 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.406 |
TRG_DiLeu_BaEn_1 | 313 | 318 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 511 | 516 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.176 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 527 | 530 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.389 |
TRG_NES_CRM1_1 | 468 | 481 | PF08389 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 312 | 316 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 567 | 572 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM55 | Leptomonas seymouri | 54% | 92% |
A0A1X0P3X4 | Trypanosomatidae | 46% | 100% |
A0A3Q8IHV9 | Leishmania donovani | 92% | 100% |
A0A422MWI6 | Trypanosoma rangeli | 47% | 100% |
A4HLQ7 | Leishmania braziliensis | 80% | 98% |
A4I957 | Leishmania infantum | 92% | 100% |
D0A6B5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B432 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
F4JKB6 | Arabidopsis thaliana | 22% | 100% |
Q680B9 | Arabidopsis thaliana | 21% | 100% |
V5BPA7 | Trypanosoma cruzi | 47% | 100% |