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: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
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:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
GO:0005840 | ribosome | 5 | 1 |
Related structures:
AlphaFold database: E9AVT0
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 633 | 635 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.421 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.679 |
DEG_SPOP_SBC_1 | 37 | 41 | PF00917 | 0.483 |
DEG_SPOP_SBC_1 | 417 | 421 | PF00917 | 0.611 |
DOC_CKS1_1 | 628 | 633 | PF01111 | 0.281 |
DOC_CYCLIN_yClb1_LxF_4 | 525 | 530 | PF00134 | 0.426 |
DOC_MAPK_DCC_7 | 367 | 376 | PF00069 | 0.433 |
DOC_MAPK_FxFP_2 | 637 | 640 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 253 | 260 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 367 | 374 | PF00069 | 0.470 |
DOC_MAPK_HePTP_8 | 364 | 376 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 207 | 215 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 283 | 290 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 658 | 665 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 525 | 531 | PF00149 | 0.423 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.718 |
DOC_PP4_FxxP_1 | 637 | 640 | PF00568 | 0.458 |
DOC_PP4_MxPP_1 | 479 | 482 | PF00568 | 0.456 |
DOC_SPAK_OSR1_1 | 283 | 287 | PF12202 | 0.377 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 347 | 351 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 404 | 408 | PF12436 | 0.553 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.288 |
LIG_14-3-3_CanoR_1 | 416 | 423 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 527 | 531 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 658 | 664 | PF00244 | 0.402 |
LIG_BIR_III_4 | 78 | 82 | PF00653 | 0.621 |
LIG_deltaCOP1_diTrp_1 | 122 | 126 | PF00928 | 0.424 |
LIG_EH1_1 | 184 | 192 | PF00400 | 0.426 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.416 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.537 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.318 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.487 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.493 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.506 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.437 |
LIG_FHA_1 | 679 | 685 | PF00498 | 0.558 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.392 |
LIG_FHA_2 | 552 | 558 | PF00498 | 0.448 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.509 |
LIG_GBD_Chelix_1 | 186 | 194 | PF00786 | 0.403 |
LIG_LIR_Apic_2 | 342 | 347 | PF02991 | 0.510 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.705 |
LIG_LIR_Gen_1 | 122 | 128 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 301 | 308 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 389 | 400 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 529 | 538 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 606 | 617 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 529 | 533 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.427 |
LIG_LYPXL_SIV_4 | 638 | 646 | PF13949 | 0.400 |
LIG_PDZ_Class_1 | 703 | 708 | PF00595 | 0.464 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.519 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.409 |
LIG_SH2_GRB2like | 165 | 168 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 609 | 613 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 208 | 211 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 561 | 564 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.416 |
LIG_SH3_2 | 44 | 49 | PF14604 | 0.532 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.473 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.466 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.686 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.659 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.482 |
LIG_SH3_4 | 404 | 411 | PF00018 | 0.558 |
LIG_SUMO_SIM_anti_2 | 287 | 292 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 529 | 535 | PF11976 | 0.447 |
LIG_SUMO_SIM_anti_2 | 551 | 560 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 459 | 464 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 495 | 502 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 661 | 667 | PF11976 | 0.422 |
LIG_TYR_ITSM | 299 | 306 | PF00017 | 0.490 |
LIG_TYR_ITSM | 605 | 612 | PF00017 | 0.399 |
MOD_CDK_SPxK_1 | 627 | 633 | PF00069 | 0.284 |
MOD_CDK_SPxxK_3 | 627 | 634 | PF00069 | 0.285 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.511 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.689 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.540 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.536 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.479 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.627 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.376 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.789 |
MOD_CK2_1 | 551 | 557 | PF00069 | 0.461 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.479 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.416 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.479 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.500 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.741 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.439 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.575 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.528 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.495 |
MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.369 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.465 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.497 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.521 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.467 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.499 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.444 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.546 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.632 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.700 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.459 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.419 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.241 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.723 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.584 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.661 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.496 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.494 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.290 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.429 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.569 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.478 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.436 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.503 |
MOD_NEK2_2 | 362 | 367 | PF00069 | 0.496 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.485 |
MOD_PIKK_1 | 308 | 314 | PF00454 | 0.555 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.776 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.634 |
MOD_PKA_2 | 492 | 498 | PF00069 | 0.423 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.415 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.386 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.482 |
MOD_Plk_1 | 556 | 562 | PF00069 | 0.497 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.464 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.440 |
MOD_Plk_2-3 | 83 | 89 | PF00069 | 0.568 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.442 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.467 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.471 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.576 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.397 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.400 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.430 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.279 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.440 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.450 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.496 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.284 |
MOD_SUMO_rev_2 | 145 | 152 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_2 | 121 | 127 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 41 | 46 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 679 | 684 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 272 | 274 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 682 | 687 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E7 | Leptomonas seymouri | 44% | 72% |
A0A3S7WX75 | Leishmania donovani | 93% | 100% |
A4HCB8 | Leishmania braziliensis | 74% | 96% |
A4HZX1 | Leishmania infantum | 93% | 100% |
Q4QBP9 | Leishmania major | 92% | 100% |
V5DMK2 | Trypanosoma cruzi | 27% | 100% |