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 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 3 |
GO:0005840 | ribosome | 5 | 2 |
Related structures:
AlphaFold database: A4HCB8
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 | 114 | 118 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.680 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.256 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 608 | 610 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.585 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.774 |
DOC_CYCLIN_yClb1_LxF_4 | 500 | 505 | PF00134 | 0.506 |
DOC_MAPK_DCC_7 | 352 | 361 | PF00069 | 0.554 |
DOC_MAPK_FxFP_2 | 612 | 615 | PF00069 | 0.568 |
DOC_MAPK_gen_1 | 103 | 113 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 352 | 359 | PF00069 | 0.510 |
DOC_MAPK_HePTP_8 | 349 | 361 | PF00069 | 0.629 |
DOC_MAPK_MEF2A_6 | 169 | 177 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 268 | 275 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 633 | 640 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 500 | 506 | PF00149 | 0.504 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.785 |
DOC_PP4_FxxP_1 | 612 | 615 | PF00568 | 0.568 |
DOC_PP4_MxPP_1 | 458 | 461 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.445 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 119 | 129 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.490 |
LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.343 |
LIG_EH1_1 | 169 | 177 | PF00400 | 0.547 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.514 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.527 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.513 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.541 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.505 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.513 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.575 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.688 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.459 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.661 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 171 | 179 | PF00786 | 0.495 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.582 |
LIG_LIR_Apic_2 | 47 | 53 | PF02991 | 0.784 |
LIG_LIR_Apic_2 | 647 | 653 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 286 | 293 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 504 | 513 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 581 | 592 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 533 | 539 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.494 |
LIG_LYPXL_L_2 | 613 | 622 | PF13949 | 0.295 |
LIG_PDZ_Class_1 | 678 | 683 | PF00595 | 0.577 |
LIG_PTB_Apo_2 | 662 | 669 | PF02174 | 0.424 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.493 |
LIG_SH2_CRK | 288 | 292 | PF00017 | 0.621 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.478 |
LIG_SH2_GRB2like | 150 | 153 | PF00017 | 0.565 |
LIG_SH2_NCK_1 | 109 | 113 | PF00017 | 0.343 |
LIG_SH2_NCK_1 | 584 | 588 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.521 |
LIG_SH2_PTP2 | 536 | 539 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.414 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.729 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.554 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.586 |
LIG_SUMO_SIM_anti_2 | 504 | 510 | PF11976 | 0.520 |
LIG_SUMO_SIM_anti_2 | 526 | 535 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 618 | 623 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 438 | 443 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 474 | 481 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 636 | 642 | PF11976 | 0.456 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.677 |
LIG_TYR_ITIM | 582 | 587 | PF00017 | 0.296 |
LIG_TYR_ITSM | 284 | 291 | PF00017 | 0.603 |
LIG_UBA3_1 | 1 | 7 | PF00899 | 0.527 |
LIG_UBA3_1 | 80 | 89 | PF00899 | 0.591 |
MOD_CDK_SPK_2 | 336 | 341 | PF00069 | 0.491 |
MOD_CDK_SPxxK_3 | 27 | 34 | PF00069 | 0.617 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.543 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.449 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.529 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.736 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.568 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.650 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.514 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.725 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.440 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.631 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.547 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.459 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.469 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.536 |
MOD_GlcNHglycan | 321 | 325 | PF01048 | 0.492 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.727 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.645 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.512 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.584 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.422 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.525 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.463 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.511 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.547 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.757 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.611 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.694 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.682 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.550 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.497 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.435 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.542 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.694 |
MOD_N-GLC_1 | 509 | 514 | PF02516 | 0.380 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.411 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.250 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.544 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.321 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.614 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.545 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.516 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.610 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.598 |
MOD_NEK2_2 | 204 | 209 | PF00069 | 0.505 |
MOD_PIKK_1 | 127 | 133 | PF00454 | 0.609 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.604 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.512 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.729 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.578 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.403 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.494 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.494 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.300 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.502 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.550 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.571 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.507 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.538 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.443 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.536 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.494 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.511 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.489 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.428 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.483 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.526 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.312 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.538 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.443 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.636 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.435 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.561 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.531 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 654 | 659 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 606 | 609 | PF00400 | 0.360 |
TRG_ER_FFAT_2 | 522 | 529 | PF00635 | 0.505 |
TRG_NLS_Bipartite_1 | 607 | 627 | PF00514 | 0.303 |
TRG_NLS_MonoExtN_4 | 606 | 611 | PF00514 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 657 | 662 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E7 | Leptomonas seymouri | 44% | 69% |
A0A3S7WX75 | Leishmania donovani | 74% | 97% |
A4HZX1 | Leishmania infantum | 74% | 97% |
C9ZSK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AVT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 96% |
Q4QBP9 | Leishmania major | 75% | 100% |
V5DMK2 | Trypanosoma cruzi | 27% | 100% |