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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0005732 | sno(s)RNA-containing ribonucleoprotein complex | 3 | 10 |
GO:0030684 | preribosome | 3 | 2 |
GO:0032040 | small-subunit processome | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0034457 | Mpp10 complex | 3 | 10 |
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:0140513 | nuclear protein-containing complex | 2 | 10 |
GO:1990904 | ribonucleoprotein complex | 2 | 10 |
Related structures:
AlphaFold database: E9ADS7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006364 | rRNA processing | 8 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0016072 | rRNA metabolic process | 7 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.629 |
CLV_PCSK_FUR_1 | 236 | 240 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.288 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.485 |
CLV_PCSK_PC7_1 | 634 | 640 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.155 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.401 |
DEG_APCC_DBOX_1 | 434 | 442 | PF00400 | 0.444 |
DEG_APCC_DBOX_1 | 53 | 61 | PF00400 | 0.487 |
DEG_MDM2_SWIB_1 | 418 | 425 | PF02201 | 0.485 |
DOC_ANK_TNKS_1 | 265 | 272 | PF00023 | 0.252 |
DOC_MAPK_gen_1 | 432 | 441 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 505 | 513 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.642 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.252 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.406 |
DOC_USP7_UBL2_3 | 186 | 190 | PF12436 | 0.423 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.204 |
DOC_USP7_UBL2_3 | 411 | 415 | PF12436 | 0.485 |
DOC_USP7_UBL2_3 | 642 | 646 | PF12436 | 0.384 |
DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 416 | 425 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 615 | 624 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 536 | 551 | PF00022 | 0.321 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.615 |
LIG_BIR_III_4 | 322 | 326 | PF00653 | 0.369 |
LIG_BRCT_BRCA1_1 | 617 | 621 | PF00533 | 0.416 |
LIG_Clathr_ClatBox_1 | 438 | 442 | PF01394 | 0.444 |
LIG_deltaCOP1_diTrp_1 | 205 | 212 | PF00928 | 0.348 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.369 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.359 |
LIG_FHA_1 | 624 | 630 | PF00498 | 0.429 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.384 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.345 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.344 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.369 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.444 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.633 |
LIG_LIR_Gen_1 | 420 | 430 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 618 | 629 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 420 | 425 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 618 | 624 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.372 |
LIG_PCNA_yPIPBox_3 | 177 | 191 | PF02747 | 0.406 |
LIG_Pex14_1 | 208 | 212 | PF04695 | 0.344 |
LIG_Pex14_2 | 418 | 422 | PF04695 | 0.401 |
LIG_PTB_Apo_2 | 440 | 447 | PF02174 | 0.485 |
LIG_PTB_Apo_2 | 563 | 570 | PF02174 | 0.344 |
LIG_PTB_Phospho_1 | 563 | 569 | PF10480 | 0.401 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.561 |
LIG_SH2_SRC | 477 | 480 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 328 | 331 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.401 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.725 |
LIG_SH3_3 | 529 | 535 | PF00018 | 0.429 |
LIG_SH3_4 | 572 | 579 | PF00018 | 0.401 |
LIG_SUMO_SIM_par_1 | 436 | 442 | PF11976 | 0.403 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.444 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.408 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.346 |
LIG_UBA3_1 | 510 | 516 | PF00899 | 0.344 |
MOD_CDC14_SPxK_1 | 10 | 13 | PF00782 | 0.779 |
MOD_CDK_SPK_2 | 567 | 572 | PF00069 | 0.344 |
MOD_CDK_SPK_2 | 627 | 632 | PF00069 | 0.444 |
MOD_CDK_SPxK_1 | 7 | 13 | PF00069 | 0.786 |
MOD_CDK_SPxxK_3 | 627 | 634 | PF00069 | 0.444 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.640 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.345 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.689 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.571 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.373 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.466 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.291 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.432 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.415 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.344 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.369 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.436 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.501 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.660 |
MOD_Cter_Amidation | 147 | 150 | PF01082 | 0.372 |
MOD_Cter_Amidation | 644 | 647 | PF01082 | 0.444 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.400 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.394 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.210 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.741 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.544 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.740 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.382 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.370 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.695 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.598 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.339 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.330 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.501 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.429 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.693 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.593 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.584 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.505 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.344 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.485 |
MOD_PKA_1 | 190 | 196 | PF00069 | 0.291 |
MOD_PKA_1 | 481 | 487 | PF00069 | 0.384 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.444 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.291 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.610 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.601 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.631 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.326 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.583 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.385 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.450 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.399 |
MOD_Plk_2-3 | 391 | 397 | PF00069 | 0.485 |
MOD_Plk_2-3 | 538 | 544 | PF00069 | 0.344 |
MOD_Plk_2-3 | 623 | 629 | PF00069 | 0.429 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.369 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.429 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.344 |
MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.344 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.444 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.588 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.749 |
MOD_SUMO_for_1 | 462 | 465 | PF00179 | 0.369 |
MOD_SUMO_for_1 | 535 | 538 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 648 | 654 | PF00179 | 0.354 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 279 | 285 | PF01217 | 0.331 |
TRG_DiLeu_BaEn_4 | 311 | 317 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.401 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 258 | 261 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 662 | 665 | PF00400 | 0.589 |
TRG_NLS_Bipartite_1 | 646 | 668 | PF00514 | 0.663 |
TRG_NLS_MonoCore_2 | 662 | 667 | PF00514 | 0.676 |
TRG_NLS_MonoExtC_3 | 189 | 194 | PF00514 | 0.459 |
TRG_NLS_MonoExtN_4 | 190 | 195 | PF00514 | 0.389 |
TRG_NLS_MonoExtN_4 | 663 | 668 | PF00514 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 285 | 290 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q4 | Leptomonas seymouri | 70% | 99% |
A0A0S4JKJ8 | Bodo saltans | 46% | 100% |
A0A3S7X283 | Leishmania donovani | 93% | 100% |
A0A422NRR1 | Trypanosoma rangeli | 48% | 100% |
A4HH82 | Leishmania braziliensis | 82% | 99% |
A4I4C8 | Leishmania infantum | 93% | 100% |
C9ZL36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AM03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |