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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4Q0L7
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.764 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.623 |
DEG_APCC_DBOX_1 | 45 | 53 | PF00400 | 0.624 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.782 |
DOC_AGCK_PIF_2 | 359 | 364 | PF00069 | 0.517 |
DOC_CKS1_1 | 206 | 211 | PF01111 | 0.729 |
DOC_CYCLIN_RxL_1 | 43 | 51 | PF00134 | 0.647 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 530 | 539 | PF00134 | 0.564 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 603 | 611 | PF00069 | 0.534 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.808 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.494 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.479 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.679 |
LIG_deltaCOP1_diTrp_1 | 588 | 596 | PF00928 | 0.573 |
LIG_eIF4E_1 | 156 | 162 | PF01652 | 0.610 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.523 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.768 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.432 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.547 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.612 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.631 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.707 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.746 |
LIG_Integrin_isoDGR_2 | 3 | 5 | PF01839 | 0.810 |
LIG_LIR_Gen_1 | 595 | 601 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 595 | 599 | PF02991 | 0.522 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.534 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.526 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.727 |
LIG_Rb_pABgroove_1 | 150 | 158 | PF01858 | 0.584 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.600 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.575 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.639 |
LIG_SH3_2 | 206 | 211 | PF14604 | 0.789 |
LIG_SH3_2 | 276 | 281 | PF14604 | 0.501 |
LIG_SH3_2 | 419 | 424 | PF14604 | 0.718 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.771 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.712 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.487 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.787 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.766 |
LIG_SUMO_SIM_anti_2 | 30 | 36 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 149 | 158 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.711 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.552 |
LIG_TYR_ITIM | 438 | 443 | PF00017 | 0.659 |
LIG_UBA3_1 | 539 | 547 | PF00899 | 0.560 |
LIG_UBA3_1 | 607 | 613 | PF00899 | 0.514 |
LIG_WRPW_2 | 340 | 343 | PF00400 | 0.476 |
MOD_CDC14_SPxK_1 | 254 | 257 | PF00782 | 0.726 |
MOD_CDK_SPxK_1 | 205 | 211 | PF00069 | 0.674 |
MOD_CDK_SPxK_1 | 251 | 257 | PF00069 | 0.737 |
MOD_CDK_SPxxK_3 | 183 | 190 | PF00069 | 0.717 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.680 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.593 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.573 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.719 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.691 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.776 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.715 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.614 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.639 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.685 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.472 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.439 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.733 |
MOD_Cter_Amidation | 262 | 265 | PF01082 | 0.533 |
MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.732 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.754 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.805 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.672 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.697 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.756 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.655 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.666 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.367 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.432 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.655 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.637 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.588 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.579 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.783 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.670 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.652 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.696 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.657 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.787 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.669 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.668 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.691 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.584 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.580 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.607 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.693 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.591 |
MOD_PKA_1 | 281 | 287 | PF00069 | 0.589 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.717 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.637 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.790 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.656 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.682 |
MOD_PKB_1 | 88 | 96 | PF00069 | 0.660 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.430 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.627 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.729 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.550 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.668 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.530 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.644 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.421 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.729 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.705 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.653 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.641 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.729 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.669 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.693 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.600 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.722 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.730 |
MOD_SUMO_for_1 | 585 | 588 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 433 | 438 | PF00179 | 0.696 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.804 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.654 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMT0 | Leptomonas seymouri | 56% | 98% |
A0A0S4JTW8 | Bodo saltans | 35% | 100% |
A0A1X0P060 | Trypanosomatidae | 33% | 100% |
A0A3R7LYT2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7XBW1 | Leishmania donovani | 93% | 100% |
A4HQ59 | Leishmania braziliensis | 77% | 100% |
A4IDV8 | Leishmania infantum | 93% | 100% |
D0A458 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ATX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BQB1 | Trypanosoma cruzi | 34% | 100% |