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: 1, no: 9 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 2 |
GO:0016604 | nuclear body | 2 | 2 |
GO:0016607 | nuclear speck | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: E9AP35
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 5 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 5 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 5 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006396 | RNA processing | 6 | 5 |
GO:0006397 | mRNA processing | 7 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0008380 | RNA splicing | 7 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0016071 | mRNA metabolic process | 6 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 390 | 394 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.571 |
DEG_APCC_DBOX_1 | 515 | 523 | PF00400 | 0.536 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.431 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.755 |
DEG_ODPH_VHL_1 | 297 | 308 | PF01847 | 0.613 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.603 |
DOC_CYCLIN_yCln2_LP_2 | 491 | 497 | PF00134 | 0.552 |
DOC_MAPK_MEF2A_6 | 38 | 46 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.507 |
DOC_PP2B_LxvP_1 | 267 | 270 | PF13499 | 0.664 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.520 |
DOC_PP4_MxPP_1 | 225 | 228 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.501 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.659 |
DOC_USP7_UBL2_3 | 96 | 100 | PF12436 | 0.568 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 258 | 267 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 463 | 469 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 545 | 551 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 617 | 625 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 76 | 80 | PF00244 | 0.476 |
LIG_Actin_RPEL_3 | 31 | 50 | PF02755 | 0.592 |
LIG_BIR_III_4 | 14 | 18 | PF00653 | 0.785 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 506 | 510 | PF00533 | 0.548 |
LIG_CSL_BTD_1 | 330 | 333 | PF09270 | 0.489 |
LIG_CtBP_PxDLS_1 | 228 | 232 | PF00389 | 0.672 |
LIG_EH1_1 | 453 | 461 | PF00400 | 0.502 |
LIG_eIF4E_1 | 454 | 460 | PF01652 | 0.480 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.548 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.556 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.510 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.668 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.746 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.497 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.561 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.516 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.463 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.554 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.470 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.397 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.405 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.453 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.278 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.562 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.537 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.539 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.594 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.445 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 165 | 174 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 242 | 253 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 292 | 302 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 147 | 151 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.500 |
LIG_NRBOX | 169 | 175 | PF00104 | 0.417 |
LIG_PCNA_yPIPBox_3 | 453 | 463 | PF02747 | 0.445 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.609 |
LIG_REV1ctd_RIR_1 | 148 | 156 | PF16727 | 0.430 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.484 |
LIG_SH2_GRB2like | 214 | 217 | PF00017 | 0.687 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 447 | 451 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 609 | 613 | PF00017 | 0.652 |
LIG_SH2_STAT3 | 596 | 599 | PF00017 | 0.769 |
LIG_SH2_STAT3 | 609 | 612 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.722 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.568 |
LIG_SH3_2 | 580 | 585 | PF14604 | 0.644 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.736 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.570 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.664 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.722 |
LIG_SUMO_SIM_par_1 | 227 | 232 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 26 | 33 | PF11976 | 0.646 |
LIG_SUMO_SIM_par_1 | 382 | 390 | PF11976 | 0.256 |
LIG_SUMO_SIM_par_1 | 423 | 428 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 635 | 644 | PF11976 | 0.522 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.546 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.673 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.529 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.564 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.495 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.493 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.242 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.580 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.633 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.594 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.545 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.547 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.566 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.603 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.538 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.559 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.509 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.664 |
MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.579 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.615 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.559 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.537 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.570 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.467 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.449 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.700 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.639 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.728 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.539 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.463 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.499 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.521 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.628 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.595 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.599 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.559 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.351 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.537 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.482 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.428 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.282 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.585 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.459 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.596 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.481 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.547 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.509 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.439 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.612 |
MOD_N-GLC_2 | 216 | 218 | PF02516 | 0.701 |
MOD_N-GLC_2 | 222 | 224 | PF02516 | 0.631 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.435 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.448 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.404 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.501 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.621 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.559 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.561 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.376 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.596 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.546 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.520 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.433 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.400 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.440 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.680 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.611 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.547 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.428 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.547 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.558 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.489 |
MOD_PIKK_1 | 595 | 601 | PF00454 | 0.739 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.633 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.596 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.546 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.480 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.567 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.579 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.594 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.599 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.554 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.437 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.480 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.484 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.513 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.539 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.393 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.650 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.656 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.455 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.341 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.611 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.596 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2V3 | Leptomonas seymouri | 70% | 97% |
A0A1X0NHC6 | Trypanosomatidae | 41% | 98% |
A0A3R7RLK0 | Trypanosoma rangeli | 43% | 98% |
A0A3S7WS82 | Leishmania donovani | 95% | 100% |
A4H709 | Leishmania braziliensis | 89% | 100% |
A4HVD7 | Leishmania infantum | 95% | 100% |
C9ZTR0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 87% |
Q4QGF3 | Leishmania major | 93% | 100% |
V5BXX9 | Trypanosoma cruzi | 42% | 98% |