Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 23 |
GO:0032991 | protein-containing complex | 1 | 23 |
GO:0043226 | organelle | 2 | 23 |
GO:0043228 | non-membrane-bounded organelle | 3 | 23 |
GO:0043229 | intracellular organelle | 3 | 23 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
GO:1990904 | ribonucleoprotein complex | 2 | 23 |
GO:0005730 | nucleolus | 5 | 6 |
GO:0097361 | CIA complex | 3 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:0000974 | Prp19 complex | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AKN1
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 4 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 4 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 4 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
GO:0006396 | RNA processing | 6 | 4 |
GO:0006397 | mRNA processing | 7 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0008380 | RNA splicing | 7 | 4 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 4 |
GO:0016071 | mRNA metabolic process | 6 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090304 | nucleic acid metabolic process | 4 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
GO:0006790 | sulfur compound metabolic process | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016226 | iron-sulfur cluster assembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0031163 | metallo-sulfur cluster assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0000027 | ribosomal large subunit assembly | 7 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.673 |
CLV_C14_Caspase3-7 | 524 | 528 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.363 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.357 |
DEG_APCC_DBOX_1 | 549 | 557 | PF00400 | 0.230 |
DEG_SCF_FBW7_1 | 275 | 282 | PF00400 | 0.391 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.545 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.399 |
DOC_CYCLIN_RxL_1 | 102 | 109 | PF00134 | 0.407 |
DOC_MAPK_gen_1 | 111 | 120 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.528 |
DOC_MAPK_gen_1 | 23 | 33 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 292 | 302 | PF00069 | 0.463 |
DOC_MAPK_HePTP_8 | 252 | 264 | PF00069 | 0.620 |
DOC_MAPK_HePTP_8 | 290 | 302 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 24 | 33 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.619 |
DOC_MAPK_MEF2A_6 | 293 | 302 | PF00069 | 0.522 |
DOC_PP1_RVXF_1 | 3 | 9 | PF00149 | 0.442 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.674 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.599 |
DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.389 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.472 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 445 | 455 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 512 | 517 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 593 | 598 | PF00244 | 0.455 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.411 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.583 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.495 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 519 | 523 | PF00533 | 0.491 |
LIG_Clathr_ClatBox_1 | 308 | 312 | PF01394 | 0.359 |
LIG_deltaCOP1_diTrp_1 | 622 | 628 | PF00928 | 0.482 |
LIG_eIF4E_1 | 303 | 309 | PF01652 | 0.433 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.621 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.590 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.609 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.628 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.635 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.496 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.527 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.536 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.499 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.524 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.446 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.509 |
LIG_Integrin_RGD_1 | 400 | 402 | PF01839 | 0.266 |
LIG_LIR_Gen_1 | 159 | 168 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 282 | 290 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 561 | 567 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 578 | 589 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 622 | 627 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 116 | 120 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.429 |
LIG_Pex14_1 | 563 | 567 | PF04695 | 0.482 |
LIG_Pex14_2 | 519 | 523 | PF04695 | 0.482 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 372 | 375 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 117 | 120 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 581 | 585 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.490 |
LIG_SH3_2 | 339 | 344 | PF14604 | 0.540 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.584 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 57 | 65 | PF11976 | 0.365 |
LIG_SUMO_SIM_par_1 | 514 | 520 | PF11976 | 0.434 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.449 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.546 |
LIG_TYR_ITIM | 115 | 120 | PF00017 | 0.608 |
LIG_UBA3_1 | 28 | 34 | PF00899 | 0.420 |
LIG_WRC_WIRS_1 | 144 | 149 | PF05994 | 0.499 |
LIG_WRC_WIRS_1 | 43 | 48 | PF05994 | 0.582 |
MOD_CDK_SPK_2 | 395 | 400 | PF00069 | 0.545 |
MOD_CDK_SPK_2 | 437 | 442 | PF00069 | 0.491 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.435 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.574 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.480 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.583 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.502 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.559 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.420 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.546 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.520 |
MOD_Cter_Amidation | 122 | 125 | PF01082 | 0.460 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.447 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.518 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.714 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.656 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.590 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.327 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.308 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.323 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.344 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.718 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.657 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.413 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.760 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.606 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.489 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.482 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.412 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.521 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.533 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.528 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.544 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.506 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.510 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.281 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.289 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.634 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.439 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.455 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.581 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.574 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.553 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.635 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.475 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.571 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.654 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.546 |
MOD_NEK2_2 | 493 | 498 | PF00069 | 0.482 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.570 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.542 |
MOD_PK_1 | 621 | 627 | PF00069 | 0.545 |
MOD_PKA_1 | 296 | 302 | PF00069 | 0.346 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.668 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.624 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.400 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.433 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.482 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.520 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.536 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.532 |
MOD_Plk_2-3 | 154 | 160 | PF00069 | 0.618 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.492 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.434 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.509 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.423 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.427 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.509 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.486 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.538 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.440 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.493 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.548 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.532 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 650 | 657 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 660 | 665 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 67 | 76 | PF00179 | 0.522 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_1 | 551 | 556 | PF01217 | 0.571 |
TRG_DiLeu_BaEn_3 | 158 | 164 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 330 | 335 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.592 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.598 |
TRG_NES_CRM1_1 | 27 | 39 | PF08389 | 0.457 |
TRG_NES_CRM1_1 | 315 | 328 | PF08389 | 0.416 |
TRG_NLS_MonoExtN_4 | 329 | 334 | PF00514 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 140 | 145 | PF00026 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHN2 | Leptomonas seymouri | 25% | 100% |
A0A0N1PBF5 | Leptomonas seymouri | 66% | 97% |
A0A0S4JTE0 | Bodo saltans | 42% | 89% |
A0A1X0NK47 | Trypanosomatidae | 48% | 96% |
A0A3Q8IGC4 | Leishmania donovani | 26% | 100% |
A0A3R7K7N9 | Trypanosoma rangeli | 48% | 97% |
A0A3S5H5M7 | Leishmania donovani | 86% | 100% |
A0A3S7XBP3 | Leishmania donovani | 27% | 100% |
A4H4H1 | Leishmania braziliensis | 67% | 99% |
A4HDT7 | Leishmania braziliensis | 26% | 100% |
A4HPZ9 | Leishmania braziliensis | 26% | 100% |
A4HSP6 | Leishmania infantum | 86% | 100% |
A4I135 | Leishmania infantum | 26% | 100% |
A4IDR0 | Leishmania infantum | 27% | 100% |
C9ZT89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 96% |
E9ATR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q0T1 | Leishmania major | 27% | 100% |
Q4QAA4 | Leishmania major | 26% | 100% |
Q4QJ76 | Leishmania major | 83% | 100% |
V5BDR9 | Trypanosoma cruzi | 49% | 98% |