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: 5 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0005685 | U1 snRNP | 5 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071004 | U2-type prespliceosome | 5 | 1 |
GO:0071010 | prespliceosome | 4 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4H8P0
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 | 1 |
GO:0003723 | RNA 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 | 301 | 305 | PF00656 | 0.692 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.778 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.399 |
DEG_SPOP_SBC_1 | 365 | 369 | PF00917 | 0.815 |
DOC_ANK_TNKS_1 | 299 | 306 | PF00023 | 0.553 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.538 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.547 |
DOC_CYCLIN_RxL_1 | 426 | 438 | PF00134 | 0.667 |
DOC_CYCLIN_RxL_1 | 75 | 84 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.632 |
DOC_CYCLIN_yCln2_LP_2 | 511 | 517 | PF00134 | 0.233 |
DOC_CYCLIN_yCln2_LP_2 | 579 | 585 | PF00134 | 0.485 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.398 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.805 |
DOC_PP2B_LxvP_1 | 37 | 40 | PF13499 | 0.341 |
DOC_PP2B_LxvP_1 | 511 | 514 | PF13499 | 0.233 |
DOC_PP2B_LxvP_1 | 579 | 582 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.801 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.802 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 545 | 553 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 565 | 570 | PF00244 | 0.763 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.504 |
LIG_BIR_III_4 | 415 | 419 | PF00653 | 0.550 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.547 |
LIG_EVH1_2 | 332 | 336 | PF00568 | 0.525 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.221 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.597 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.786 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.813 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.670 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.580 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.420 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.498 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.759 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.498 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.454 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.414 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.518 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.526 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.478 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.485 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.485 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.424 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.562 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.787 |
LIG_LIR_Apic_2 | 422 | 427 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 486 | 492 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 567 | 572 | PF02991 | 0.718 |
LIG_LIR_Apic_2 | 603 | 609 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 397 | 401 | PF02991 | 0.601 |
LIG_Pex14_1 | 398 | 402 | PF04695 | 0.486 |
LIG_SH2_GRB2like | 528 | 531 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 559 | 562 | PF00017 | 0.702 |
LIG_SH2_GRB2like | 596 | 599 | PF00017 | 0.369 |
LIG_SH2_NCK_1 | 402 | 406 | PF00017 | 0.405 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.444 |
LIG_SH2_SRC | 528 | 531 | PF00017 | 0.401 |
LIG_SH2_SRC | 596 | 599 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.418 |
LIG_SH3_2 | 427 | 432 | PF14604 | 0.683 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.728 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.699 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.761 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.719 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.766 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.584 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.679 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.746 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.494 |
LIG_WW_2 | 262 | 265 | PF00397 | 0.528 |
MOD_CDK_SPK_2 | 346 | 351 | PF00069 | 0.556 |
MOD_CDK_SPxxK_3 | 285 | 292 | PF00069 | 0.552 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.708 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.674 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.662 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.749 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.790 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.808 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.772 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.491 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.753 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.471 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.477 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.439 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.752 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.748 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.485 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.485 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.424 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.534 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.462 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.703 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.479 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.650 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.588 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.751 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.814 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.752 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.718 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.798 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.536 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.569 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.679 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.630 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.699 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.674 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.635 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.674 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.643 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.761 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.563 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.713 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.466 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.280 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.767 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.418 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.390 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.697 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.707 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.735 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.362 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.374 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.496 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.604 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.672 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.768 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.535 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.618 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.735 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.590 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.593 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.608 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.453 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.547 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.520 |
MOD_PKA_1 | 238 | 244 | PF00069 | 0.494 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.776 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.576 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.546 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.755 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.640 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.713 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.750 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.424 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.666 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.505 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.730 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.776 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.741 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.478 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.534 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.548 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.695 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.680 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.711 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.523 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.463 |
MOD_SUMO_rev_2 | 18 | 25 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 221 | 231 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 34 | 39 | PF01217 | 0.333 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 78 | 83 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ37 | Leptomonas seymouri | 50% | 100% |
A0A3Q8IJ47 | Leishmania donovani | 72% | 95% |
A0A3R7LE31 | Trypanosoma rangeli | 35% | 94% |
A4HX11 | Leishmania infantum | 73% | 95% |
C9ZVZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 99% |
E9AQS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 94% |
Q4QEQ3 | Leishmania major | 72% | 97% |
V5BML0 | Trypanosoma cruzi | 34% | 100% |