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 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WUG8
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.798 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.541 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.840 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 616 | 620 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 776 | 778 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.314 |
CLV_PCSK_FUR_1 | 148 | 152 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.636 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.662 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.740 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.788 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.817 |
DOC_CKS1_1 | 593 | 598 | PF01111 | 0.721 |
DOC_MAPK_DCC_7 | 436 | 446 | PF00069 | 0.840 |
DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.637 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.726 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.688 |
DOC_PP2B_LxvP_1 | 737 | 740 | PF13499 | 0.794 |
DOC_PP4_MxPP_1 | 425 | 428 | PF00568 | 0.730 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.833 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.579 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.723 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 346 | 352 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.753 |
LIG_14-3-3_CanoR_1 | 482 | 489 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 615 | 623 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 646 | 652 | PF00244 | 0.741 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.627 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.649 |
LIG_BIR_III_4 | 129 | 133 | PF00653 | 0.688 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.730 |
LIG_EVH1_1 | 429 | 433 | PF00568 | 0.727 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.492 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.600 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.704 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.638 |
LIG_FHA_1 | 696 | 702 | PF00498 | 0.676 |
LIG_FHA_1 | 762 | 768 | PF00498 | 0.581 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.546 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.567 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.837 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.676 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.714 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.723 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.575 |
LIG_LIR_Apic_2 | 51 | 56 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 691 | 700 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 691 | 695 | PF02991 | 0.617 |
LIG_Pex14_2 | 79 | 83 | PF04695 | 0.543 |
LIG_SH2_CRK | 648 | 652 | PF00017 | 0.529 |
LIG_SH2_CRK | 710 | 714 | PF00017 | 0.627 |
LIG_SH2_GRB2like | 516 | 519 | PF00017 | 0.611 |
LIG_SH2_NCK_1 | 648 | 652 | PF00017 | 0.529 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.514 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.527 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.603 |
LIG_SH2_STAT3 | 800 | 803 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 648 | 651 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 712 | 715 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.514 |
LIG_SH3_2 | 430 | 435 | PF14604 | 0.724 |
LIG_SH3_2 | 466 | 471 | PF14604 | 0.746 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.704 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.748 |
LIG_SUMO_SIM_par_1 | 442 | 447 | PF11976 | 0.847 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.557 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.590 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.704 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.724 |
LIG_TRAF2_1 | 447 | 450 | PF00917 | 0.835 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.546 |
LIG_TYR_ITIM | 708 | 713 | PF00017 | 0.528 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.634 |
LIG_WRC_WIRS_1 | 418 | 423 | PF05994 | 0.618 |
LIG_WW_2 | 427 | 430 | PF00397 | 0.794 |
MOD_CDK_SPxxK_3 | 699 | 706 | PF00069 | 0.641 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.640 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.721 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.797 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.411 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.762 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.799 |
MOD_CK1_1 | 761 | 767 | PF00069 | 0.517 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.520 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.558 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.822 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.840 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.758 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.683 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.716 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.585 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.411 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.411 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.609 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.596 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.702 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.653 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.774 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.736 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.725 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.763 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.636 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.758 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.620 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.725 |
MOD_GlcNHglycan | 727 | 730 | PF01048 | 0.700 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.618 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.581 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.692 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.766 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.712 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.598 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.453 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.727 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.694 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.525 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.675 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.627 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.436 |
MOD_N-GLC_1 | 542 | 547 | PF02516 | 0.703 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.544 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.604 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.731 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.684 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.693 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.604 |
MOD_PIKK_1 | 630 | 636 | PF00454 | 0.800 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.703 |
MOD_PIKK_1 | 749 | 755 | PF00454 | 0.462 |
MOD_PK_1 | 442 | 448 | PF00069 | 0.805 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.564 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.603 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.829 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.614 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.683 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.614 |
MOD_PKB_1 | 756 | 764 | PF00069 | 0.593 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.773 |
MOD_Plk_1 | 792 | 798 | PF00069 | 0.598 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.690 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.411 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.640 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.411 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.811 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.630 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.813 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.727 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.717 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.465 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.367 |
MOD_SUMO_for_1 | 112 | 115 | PF00179 | 0.481 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.554 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.724 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.615 |
MOD_SUMO_rev_2 | 390 | 398 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 65 | 73 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 648 | 651 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.628 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 569 | 571 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 756 | 759 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 775 | 777 | PF00400 | 0.408 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.600 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 293 | 298 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 749 | 753 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 777 | 781 | PF00026 | 0.682 |
TRG_Pf-PMV_PEXEL_1 | 794 | 798 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKC2 | Leptomonas seymouri | 54% | 100% |
A4H921 | Leishmania braziliensis | 82% | 100% |
A4HXF3 | Leishmania infantum | 100% | 100% |
E9AR48 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QEB5 | Leishmania major | 92% | 100% |