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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000974 | Prp19 complex | 2 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QEB5
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 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:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 313 | 317 | PF00656 | 0.587 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 618 | 622 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.269 |
CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 760 | 764 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 772 | 776 | PF00082 | 0.554 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.537 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.625 |
DEG_APCC_DBOX_1 | 777 | 785 | PF00400 | 0.493 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.561 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.685 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.682 |
DOC_CKS1_1 | 595 | 600 | PF01111 | 0.605 |
DOC_MAPK_DCC_7 | 436 | 446 | PF00069 | 0.691 |
DOC_MAPK_gen_1 | 758 | 765 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 758 | 765 | PF00069 | 0.433 |
DOC_MAPK_NFAT4_5 | 758 | 766 | PF00069 | 0.433 |
DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.529 |
DOC_PP2B_LxvP_1 | 426 | 429 | PF13499 | 0.609 |
DOC_PP2B_LxvP_1 | 498 | 501 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 739 | 742 | PF13499 | 0.643 |
DOC_PP4_MxPP_1 | 425 | 428 | PF00568 | 0.625 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.593 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.473 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.727 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 701 | 706 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 572 | 577 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 602 | 608 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 617 | 625 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 648 | 654 | PF00244 | 0.637 |
LIG_Actin_WH2_2 | 749 | 766 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.549 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.539 |
LIG_BIR_III_4 | 129 | 133 | PF00653 | 0.573 |
LIG_BIR_III_4 | 316 | 320 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.607 |
LIG_EVH1_1 | 426 | 430 | PF00568 | 0.611 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.459 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.530 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.750 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.641 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.683 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.558 |
LIG_FHA_1 | 764 | 770 | PF00498 | 0.492 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.472 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.458 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.726 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.590 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.674 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.603 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.753 |
LIG_FHA_2 | 795 | 801 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 493 | 503 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 693 | 702 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 693 | 697 | PF02991 | 0.517 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.467 |
LIG_SH2_CRK | 712 | 716 | PF00017 | 0.527 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.401 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.539 |
LIG_SH2_STAT3 | 802 | 805 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 747 | 750 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.401 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.611 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.753 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.497 |
LIG_SUMO_SIM_par_1 | 442 | 447 | PF11976 | 0.690 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.450 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.497 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.592 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.723 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.469 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.488 |
LIG_WW_2 | 429 | 432 | PF00397 | 0.668 |
MOD_CDK_SPxxK_3 | 701 | 708 | PF00069 | 0.537 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.494 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.607 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.740 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.304 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.595 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.641 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.565 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.462 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.455 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.708 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.727 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.650 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.599 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.608 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.531 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.333 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.352 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.506 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.521 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.577 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.710 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.611 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.605 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.710 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.612 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.567 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.655 |
MOD_GlcNHglycan | 538 | 542 | PF01048 | 0.696 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.660 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.679 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.575 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.658 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.506 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.651 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.751 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.613 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.487 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.520 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.605 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.628 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.713 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.615 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.638 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.691 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.640 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.494 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.325 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.618 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.436 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.548 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.721 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.525 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.618 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.587 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.605 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.506 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.510 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.324 |
MOD_PIKK_1 | 549 | 555 | PF00454 | 0.532 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.682 |
MOD_PIKK_1 | 670 | 676 | PF00454 | 0.578 |
MOD_PK_1 | 442 | 448 | PF00069 | 0.664 |
MOD_PK_1 | 572 | 578 | PF00069 | 0.469 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.462 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.515 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.679 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.608 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.520 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.538 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.648 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.622 |
MOD_Plk_1 | 794 | 800 | PF00069 | 0.466 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.544 |
MOD_Plk_2-3 | 255 | 261 | PF00069 | 0.526 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.304 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.494 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.340 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.616 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.522 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.767 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.668 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.612 |
MOD_ProDKin_1 | 701 | 707 | PF00069 | 0.583 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.304 |
MOD_SUMO_for_1 | 112 | 115 | PF00179 | 0.373 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.451 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 390 | 398 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 65 | 73 | PF00179 | 0.304 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.304 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.304 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 758 | 761 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 777 | 779 | PF00400 | 0.487 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.510 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 779 | 783 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 796 | 800 | PF00026 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC2 | Leptomonas seymouri | 54% | 100% |
A0A3S7WUG8 | Leishmania donovani | 92% | 100% |
A4H921 | Leishmania braziliensis | 81% | 100% |
A4HXF3 | Leishmania infantum | 92% | 100% |
E9AR48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |