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. | yes | 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 | 2 |
GO:0005684 | U2-type spliceosomal complex | 4 | 2 |
GO:0005685 | U1 snRNP | 5 | 2 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0071004 | U2-type prespliceosome | 5 | 2 |
GO:0071010 | prespliceosome | 4 | 2 |
GO:0097525 | spliceosomal snRNP complex | 4 | 2 |
GO:0120114 | Sm-like protein family complex | 2 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QEQ3
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 | 2 |
GO:0003723 | RNA 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 | 549 | 553 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 635 | 637 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.551 |
DEG_Kelch_Keap1_1 | 154 | 159 | PF01344 | 0.576 |
DEG_SPOP_SBC_1 | 333 | 337 | PF00917 | 0.770 |
DEG_SPOP_SBC_1 | 355 | 359 | PF00917 | 0.844 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.670 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.540 |
DOC_CKS1_1 | 479 | 484 | PF01111 | 0.586 |
DOC_CKS1_1 | 590 | 595 | PF01111 | 0.696 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.628 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.671 |
DOC_CYCLIN_RxL_1 | 415 | 427 | PF00134 | 0.691 |
DOC_CYCLIN_RxL_1 | 75 | 84 | PF00134 | 0.578 |
DOC_CYCLIN_yCln2_LP_2 | 37 | 43 | PF00134 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 607 | 613 | PF00134 | 0.459 |
DOC_MAPK_DCC_7 | 299 | 309 | PF00069 | 0.647 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 51 | 58 | PF00149 | 0.531 |
DOC_PP1_RVXF_1 | 76 | 83 | PF00149 | 0.554 |
DOC_PP2B_LxvP_1 | 271 | 274 | PF13499 | 0.784 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.459 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.769 |
DOC_PP4_MxPP_1 | 352 | 355 | PF00568 | 0.699 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.594 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.853 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 410 | 414 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 458 | 462 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 511 | 517 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 574 | 579 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.638 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.402 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.699 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.800 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.851 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.610 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.424 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.641 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.529 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.440 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.753 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.527 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.563 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.653 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.615 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.694 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.587 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.459 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.459 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.579 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.683 |
LIG_GBD_Chelix_1 | 29 | 37 | PF00786 | 0.460 |
LIG_LIR_Apic_2 | 270 | 275 | PF02991 | 0.773 |
LIG_LIR_Apic_2 | 411 | 416 | PF02991 | 0.544 |
LIG_LIR_Apic_2 | 469 | 475 | PF02991 | 0.369 |
LIG_LIR_Apic_2 | 524 | 530 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 576 | 581 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 631 | 637 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 386 | 394 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.592 |
LIG_Pex14_1 | 387 | 391 | PF04695 | 0.454 |
LIG_SH2_GRB2like | 517 | 520 | PF00017 | 0.401 |
LIG_SH2_GRB2like | 568 | 571 | PF00017 | 0.453 |
LIG_SH2_GRB2like | 624 | 627 | PF00017 | 0.366 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.453 |
LIG_SH2_SRC | 517 | 520 | PF00017 | 0.401 |
LIG_SH2_SRC | 624 | 627 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 624 | 627 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.557 |
LIG_SH3_2 | 416 | 421 | PF14604 | 0.648 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.734 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.699 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.777 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.749 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.644 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.753 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.853 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.766 |
LIG_SH3_3 | 602 | 608 | PF00018 | 0.579 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.645 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.580 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.575 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.713 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.798 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.685 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.517 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.691 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.756 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.782 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.560 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.602 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.710 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.548 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.753 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.724 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.507 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.459 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.609 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.582 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.739 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.736 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.640 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.594 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.706 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.736 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.780 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.778 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.684 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.819 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.871 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.726 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.714 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.675 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.634 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.700 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.668 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.763 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.592 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.790 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.528 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.610 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.507 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.242 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.781 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.389 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.602 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.453 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.371 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.666 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.719 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.754 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.671 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.660 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.663 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.726 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.550 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.595 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.533 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.693 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.673 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.575 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.649 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.607 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.410 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.459 |
MOD_PKB_1 | 79 | 87 | PF00069 | 0.569 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.663 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.619 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.706 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.820 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.740 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.670 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.533 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.680 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.663 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.742 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.632 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.748 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.643 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.857 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.579 |
MOD_SUMO_rev_2 | 222 | 232 | PF00179 | 0.621 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 78 | 83 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ37 | Leptomonas seymouri | 49% | 100% |
A0A3Q8IJ47 | Leishmania donovani | 93% | 99% |
A0A3R7LE31 | Trypanosoma rangeli | 33% | 98% |
A4H8P0 | Leishmania braziliensis | 72% | 100% |
A4HX11 | Leishmania infantum | 93% | 99% |
C9ZVZ1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AQS4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 98% |
V5BML0 | Trypanosoma cruzi | 36% | 100% |