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: E9AQS4
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 | 78 | 80 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.532 |
DEG_SPOP_SBC_1 | 350 | 354 | PF00917 | 0.763 |
DEG_SPOP_SBC_1 | 372 | 376 | PF00917 | 0.816 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.681 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.623 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.665 |
DOC_CYCLIN_RxL_1 | 432 | 444 | PF00134 | 0.658 |
DOC_CYCLIN_RxL_1 | 75 | 84 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.698 |
DOC_CYCLIN_yCln2_LP_2 | 617 | 623 | PF00134 | 0.485 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.515 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.543 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.809 |
DOC_PP2B_LxvP_1 | 303 | 306 | PF13499 | 0.754 |
DOC_PP2B_LxvP_1 | 617 | 620 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.799 |
DOC_PP4_MxPP_1 | 369 | 372 | PF00568 | 0.720 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.692 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 425 | 431 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 528 | 534 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 585 | 594 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.625 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.333 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.754 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.783 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.817 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.638 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.630 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.420 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.498 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.434 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.498 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.553 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.633 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.609 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.651 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.551 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.697 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.560 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.485 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.485 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.424 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.653 |
LIG_LIR_Apic_2 | 271 | 276 | PF02991 | 0.801 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.549 |
LIG_LIR_Apic_2 | 486 | 492 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 541 | 547 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.444 |
LIG_LIR_Apic_2 | 641 | 647 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 403 | 411 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.577 |
LIG_Pex14_1 | 404 | 408 | PF04695 | 0.458 |
LIG_SH2_GRB2like | 534 | 537 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 581 | 584 | PF00017 | 0.444 |
LIG_SH2_GRB2like | 634 | 637 | PF00017 | 0.369 |
LIG_SH2_SRC | 479 | 482 | PF00017 | 0.444 |
LIG_SH2_SRC | 534 | 537 | PF00017 | 0.401 |
LIG_SH2_SRC | 634 | 637 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.562 |
LIG_SH3_2 | 433 | 438 | PF14604 | 0.675 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.733 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.704 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.766 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.749 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.529 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.673 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.757 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.817 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.579 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.646 |
LIG_SH3_4 | 595 | 602 | PF00018 | 0.640 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.583 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.498 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.552 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.703 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.515 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.783 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.816 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.491 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.755 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.559 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.585 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.590 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.656 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.705 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.525 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.753 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.691 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.485 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.485 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.424 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.596 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.583 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.738 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.628 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.680 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.721 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.553 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.811 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.683 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.695 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.806 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.828 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.673 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.679 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.684 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.645 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.593 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.685 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.642 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.680 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.591 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.763 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.532 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.605 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.466 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.280 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.390 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.444 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.374 |
MOD_N-GLC_1 | 122 | 127 | PF02516 | 0.625 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.704 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.720 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.639 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.651 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.737 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.728 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.592 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.565 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.569 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.531 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.663 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.501 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.809 |
MOD_PKA_2 | 586 | 592 | PF00069 | 0.485 |
MOD_PKB_1 | 585 | 593 | PF00069 | 0.194 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.555 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.628 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.699 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.505 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.603 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.744 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.785 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.743 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.678 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.580 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.688 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.669 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.686 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.550 |
MOD_SUMO_rev_2 | 222 | 232 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 467 | 474 | PF00179 | 0.280 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 78 | 83 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ37 | Leptomonas seymouri | 49% | 100% |
A0A3Q8IJ47 | Leishmania donovani | 87% | 100% |
A0A3R7LE31 | Trypanosoma rangeli | 36% | 99% |
A4H8P0 | Leishmania braziliensis | 72% | 92% |
A4HX11 | Leishmania infantum | 88% | 100% |
C9ZVZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4QEQ3 | Leishmania major | 86% | 97% |
V5BML0 | Trypanosoma cruzi | 36% | 100% |