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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0010494 | cytoplasmic stress granule | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0035770 | ribonucleoprotein granule | 3 | 2 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 2 |
GO:0043226 | organelle | 2 | 4 |
GO:0043228 | non-membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 4 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 4 |
GO:0005840 | ribosome | 5 | 2 |
Related structures:
AlphaFold database: Q4QBP9
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.406 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.409 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.351 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.358 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.741 |
DEG_SPOP_SBC_1 | 415 | 419 | PF00917 | 0.557 |
DOC_CYCLIN_yClb1_LxF_4 | 523 | 528 | PF00134 | 0.422 |
DOC_MAPK_DCC_7 | 365 | 374 | PF00069 | 0.462 |
DOC_MAPK_FxFP_2 | 635 | 638 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 117 | 125 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 251 | 258 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 365 | 372 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 469 | 477 | PF00069 | 0.362 |
DOC_MAPK_HePTP_8 | 362 | 374 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 182 | 190 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 205 | 213 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 281 | 288 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 365 | 374 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 656 | 663 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 523 | 529 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.289 |
DOC_PP4_FxxP_1 | 61 | 64 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 635 | 638 | PF00568 | 0.394 |
DOC_SPAK_OSR1_1 | 281 | 285 | PF12202 | 0.333 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 402 | 406 | PF12436 | 0.512 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 578 | 583 | PF00397 | 0.502 |
LIG_14-3-3_CanoR_1 | 525 | 529 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 656 | 662 | PF00244 | 0.405 |
LIG_BIR_III_4 | 76 | 80 | PF00653 | 0.561 |
LIG_deltaCOP1_diTrp_1 | 120 | 124 | PF00928 | 0.365 |
LIG_EH1_1 | 182 | 190 | PF00400 | 0.362 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.529 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.501 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.426 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.502 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.335 |
LIG_FHA_1 | 653 | 659 | PF00498 | 0.440 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.554 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.459 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.437 |
LIG_FHA_2 | 460 | 466 | PF00498 | 0.376 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.411 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.617 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.474 |
LIG_GBD_Chelix_1 | 184 | 192 | PF00786 | 0.404 |
LIG_LIR_Apic_2 | 340 | 345 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 58 | 64 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 120 | 126 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 204 | 214 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 299 | 306 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 387 | 398 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 527 | 536 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 604 | 615 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 204 | 209 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 556 | 562 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.450 |
LIG_LYPXL_SIV_4 | 636 | 644 | PF13949 | 0.400 |
LIG_PDZ_Class_1 | 701 | 706 | PF00595 | 0.402 |
LIG_RPA_C_Fungi | 248 | 260 | PF08784 | 0.313 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.586 |
LIG_SH2_CRK | 607 | 611 | PF00017 | 0.402 |
LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 607 | 611 | PF00017 | 0.402 |
LIG_SH2_PTP2 | 122 | 125 | PF00017 | 0.256 |
LIG_SH2_PTP2 | 206 | 209 | PF00017 | 0.356 |
LIG_SH2_PTP2 | 559 | 562 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.352 |
LIG_SH3_2 | 42 | 47 | PF14604 | 0.510 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.507 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.615 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.529 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.419 |
LIG_SH3_4 | 402 | 409 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 285 | 290 | PF11976 | 0.393 |
LIG_SUMO_SIM_anti_2 | 527 | 533 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 549 | 558 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 457 | 462 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 493 | 500 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 659 | 665 | PF11976 | 0.358 |
LIG_TYR_ITSM | 297 | 304 | PF00017 | 0.433 |
LIG_TYR_ITSM | 603 | 610 | PF00017 | 0.338 |
LIG_UBA3_1 | 97 | 101 | PF00899 | 0.444 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.393 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.567 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.755 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.512 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.470 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.473 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.572 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.379 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.358 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.608 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.378 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.621 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.403 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.329 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.431 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.542 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.659 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.493 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.414 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.481 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.454 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.332 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.604 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.433 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.487 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.503 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.434 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.436 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.462 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.685 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.458 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.408 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.598 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.359 |
MOD_N-GLC_1 | 518 | 523 | PF02516 | 0.518 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.690 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.479 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.592 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.511 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.436 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.579 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.459 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.360 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.365 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.341 |
MOD_NEK2_2 | 360 | 365 | PF00069 | 0.455 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.553 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.549 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.520 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.634 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.422 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.457 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.347 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.465 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.511 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.442 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.375 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.513 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.425 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.455 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.400 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.395 |
MOD_Plk_4 | 532 | 538 | PF00069 | 0.431 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.256 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.400 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.375 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.553 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.650 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.765 |
MOD_ProDKin_1 | 578 | 584 | PF00069 | 0.496 |
TRG_DiLeu_BaEn_2 | 119 | 125 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 677 | 682 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 559 | 562 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 265 | 268 | PF00400 | 0.314 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 575 | 578 | PF00400 | 0.556 |
TRG_ER_FFAT_2 | 545 | 552 | PF00635 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 680 | 685 | PF00026 | 0.364 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E7 | Leptomonas seymouri | 44% | 72% |
A0A3S7WX75 | Leishmania donovani | 95% | 100% |
A4HCB8 | Leishmania braziliensis | 75% | 100% |
A4HZX1 | Leishmania infantum | 95% | 100% |
C9ZSK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AVT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DMK2 | Trypanosoma cruzi | 26% | 100% |