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:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5G8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006378 | mRNA polyadenylation | 7 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009894 | regulation of catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0031124 | mRNA 3'-end processing | 8 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031329 | regulation of cellular catabolic process | 5 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043487 | regulation of RNA stability | 3 | 2 |
GO:0043488 | regulation of mRNA stability | 4 | 2 |
GO:0043631 | RNA polyadenylation | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 2 |
GO:0043022 | ribosome binding | 4 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 346 | 350 | PF00656 | 0.760 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.613 |
DEG_APCC_DBOX_1 | 106 | 114 | PF00400 | 0.634 |
DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.563 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.598 |
DOC_ANK_TNKS_1 | 321 | 328 | PF00023 | 0.600 |
DOC_CYCLIN_RxL_1 | 221 | 231 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 322 | 330 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 391 | 401 | PF00069 | 0.533 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.830 |
DOC_USP7_UBL2_3 | 304 | 308 | PF12436 | 0.325 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.809 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 167 | 172 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 240 | 245 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 322 | 330 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 382 | 392 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 540 | 548 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 569 | 574 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 634 | 644 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.685 |
LIG_14-3-3_CterR_2 | 681 | 684 | PF00244 | 0.622 |
LIG_APCC_ABBA_1 | 646 | 651 | PF00400 | 0.436 |
LIG_BIR_III_2 | 79 | 83 | PF00653 | 0.708 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.682 |
LIG_deltaCOP1_diTrp_1 | 120 | 130 | PF00928 | 0.499 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.564 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.665 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.451 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.414 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.470 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.397 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.429 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.480 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.773 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.420 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.522 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.812 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.472 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.578 |
LIG_LIR_Gen_1 | 177 | 188 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 2 | 9 | PF02991 | 0.589 |
LIG_LIR_Gen_1 | 239 | 250 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 407 | 415 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 514 | 524 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 578 | 586 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 407 | 411 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.351 |
LIG_NRBOX | 505 | 511 | PF00104 | 0.489 |
LIG_PTB_Apo_2 | 414 | 421 | PF02174 | 0.443 |
LIG_PTB_Phospho_1 | 414 | 420 | PF10480 | 0.442 |
LIG_RPA_C_Fungi | 317 | 329 | PF08784 | 0.561 |
LIG_SH2_CRK | 408 | 412 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 420 | 423 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 579 | 583 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 599 | 603 | PF00017 | 0.210 |
LIG_SH2_STAP1 | 614 | 618 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.569 |
LIG_SH2_STAT3 | 588 | 591 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.488 |
LIG_SH3_2 | 95 | 100 | PF14604 | 0.592 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.639 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.598 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.701 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.607 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 562 | 567 | PF11976 | 0.529 |
LIG_SUMO_SIM_anti_2 | 615 | 620 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 615 | 620 | PF11976 | 0.537 |
LIG_TRAF2_2 | 192 | 197 | PF00917 | 0.663 |
LIG_TYR_ITIM | 406 | 411 | PF00017 | 0.541 |
LIG_UBA3_1 | 298 | 304 | PF00899 | 0.545 |
LIG_UBA3_1 | 395 | 403 | PF00899 | 0.608 |
LIG_UBA3_1 | 506 | 513 | PF00899 | 0.460 |
LIG_WRC_WIRS_1 | 659 | 664 | PF05994 | 0.554 |
LIG_WW_3 | 190 | 194 | PF00397 | 0.652 |
MOD_CDC14_SPxK_1 | 72 | 75 | PF00782 | 0.577 |
MOD_CDK_SPxK_1 | 69 | 75 | PF00069 | 0.575 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.580 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.617 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.608 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.471 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.729 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.608 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.580 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.790 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.623 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.638 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.608 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.644 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.508 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.671 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.527 |
MOD_CMANNOS | 570 | 573 | PF00535 | 0.575 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.445 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.713 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.463 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.724 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.695 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.799 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.680 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.672 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.501 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.675 |
MOD_GlcNHglycan | 633 | 637 | PF01048 | 0.554 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.764 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.753 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.657 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.638 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.444 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.662 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.671 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.802 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.628 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.549 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.519 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.409 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.581 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.773 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.634 |
MOD_N-GLC_1 | 654 | 659 | PF02516 | 0.362 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.406 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.449 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.503 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.573 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.608 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.607 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.491 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.532 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.733 |
MOD_PK_1 | 167 | 173 | PF00069 | 0.500 |
MOD_PK_1 | 240 | 246 | PF00069 | 0.560 |
MOD_PKA_1 | 268 | 274 | PF00069 | 0.531 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.614 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.675 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.360 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.516 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.512 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.756 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.544 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.651 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.535 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.686 |
MOD_PKB_1 | 674 | 682 | PF00069 | 0.585 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.484 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.497 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.498 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.570 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.559 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.676 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.727 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.692 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.804 |
TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_2 | 175 | 181 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 579 | 582 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.202 |
TRG_ENDOCYTIC_2 | 614 | 617 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 649 | 652 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.775 |
TRG_NES_CRM1_1 | 390 | 404 | PF08389 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 227 | 231 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 300 | 305 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGR3 | Leptomonas seymouri | 48% | 91% |
A0A1X0NVZ4 | Trypanosomatidae | 33% | 100% |
A0A3Q8IG45 | Leishmania donovani | 88% | 100% |
A0A3R7NTQ6 | Trypanosoma rangeli | 32% | 100% |
A4HKA1 | Leishmania braziliensis | 68% | 90% |
A4I7T1 | Leishmania infantum | 88% | 100% |
D0A9Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B2N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
V5BQR4 | Trypanosoma cruzi | 29% | 100% |