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: A0A3Q8IJ47
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_NRD_NRD_1 | 465 | 467 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.448 |
DEG_Kelch_Keap1_1 | 154 | 159 | PF01344 | 0.479 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.706 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.763 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.544 |
DOC_CKS1_1 | 597 | 602 | PF01111 | 0.594 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.532 |
DOC_CYCLIN_RxL_1 | 422 | 434 | PF00134 | 0.505 |
DOC_CYCLIN_RxL_1 | 75 | 84 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 614 | 620 | PF00134 | 0.341 |
DOC_MAPK_DCC_7 | 299 | 309 | PF00069 | 0.559 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 271 | 274 | PF13499 | 0.667 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.341 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.654 |
DOC_PP4_MxPP_1 | 359 | 362 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.708 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 465 | 469 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 518 | 524 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.581 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.346 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.562 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.754 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.791 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.487 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.579 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.366 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.489 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.379 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.489 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.526 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.576 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.559 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.520 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.341 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.341 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.365 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.615 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.658 |
LIG_LIR_Apic_2 | 418 | 423 | PF02991 | 0.457 |
LIG_LIR_Apic_2 | 476 | 482 | PF02991 | 0.303 |
LIG_LIR_Apic_2 | 531 | 537 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 583 | 588 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 638 | 644 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 393 | 401 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.518 |
LIG_Pex14_1 | 394 | 398 | PF04695 | 0.379 |
LIG_SH2_GRB2like | 524 | 527 | PF00017 | 0.335 |
LIG_SH2_GRB2like | 575 | 578 | PF00017 | 0.393 |
LIG_SH2_GRB2like | 631 | 634 | PF00017 | 0.300 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.393 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.335 |
LIG_SH2_SRC | 631 | 634 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.513 |
LIG_SH3_2 | 423 | 428 | PF14604 | 0.522 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.667 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.647 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.690 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.694 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.515 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.688 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.548 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.811 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.699 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.520 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.543 |
LIG_SH3_4 | 589 | 596 | PF00018 | 0.576 |
LIG_SH3_CIN85_PxpxPR_1 | 262 | 267 | PF14604 | 0.531 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.527 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.494 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.641 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.634 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.702 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.538 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.475 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.692 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.507 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.514 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.482 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.714 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.651 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.341 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.341 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.365 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.537 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.543 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.684 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.671 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.566 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.502 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.661 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.704 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.714 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.622 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.618 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.790 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.825 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.665 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.588 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.539 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.645 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.606 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.649 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.718 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.794 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.603 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.687 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.448 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.545 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.341 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.314 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.754 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.323 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.393 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.569 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.342 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.559 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.698 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.637 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.640 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.632 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.566 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.678 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.522 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.504 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.471 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.637 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.567 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.473 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.472 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.345 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.790 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.341 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.514 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.654 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.587 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.648 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.774 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.736 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.544 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.619 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.585 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.634 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.687 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.810 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 18 | 25 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 222 | 232 | PF00179 | 0.561 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 78 | 83 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ37 | Leptomonas seymouri | 50% | 100% |
A0A3R7LE31 | Trypanosoma rangeli | 34% | 99% |
A4H8P0 | Leishmania braziliensis | 72% | 93% |
A4HX11 | Leishmania infantum | 98% | 100% |
C9ZVZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QEQ3 | Leishmania major | 93% | 99% |
V5BML0 | Trypanosoma cruzi | 36% | 100% |