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 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HQ59
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0043130 | ubiquitin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.621 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.494 |
DEG_APCC_DBOX_1 | 45 | 53 | PF00400 | 0.611 |
DEG_APCC_DBOX_1 | 56 | 64 | PF00400 | 0.692 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.468 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.682 |
DOC_AGCK_PIF_2 | 359 | 364 | PF00069 | 0.517 |
DOC_ANK_TNKS_1 | 64 | 71 | PF00023 | 0.527 |
DOC_CKS1_1 | 206 | 211 | PF01111 | 0.720 |
DOC_CYCLIN_RxL_1 | 43 | 51 | PF00134 | 0.641 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 525 | 534 | PF00134 | 0.571 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 597 | 604 | PF00069 | 0.477 |
DOC_MAPK_HePTP_8 | 594 | 606 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 597 | 606 | PF00069 | 0.527 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.456 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.812 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.701 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 92 | 102 | PF00244 | 0.542 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.478 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.661 |
LIG_BRCT_BRCA1_1 | 522 | 526 | PF00533 | 0.679 |
LIG_deltaCOP1_diTrp_1 | 583 | 591 | PF00928 | 0.549 |
LIG_eIF4E_1 | 156 | 162 | PF01652 | 0.609 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.507 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.785 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.731 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.443 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.589 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.417 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.582 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.625 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.710 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.732 |
LIG_Integrin_isoDGR_2 | 3 | 5 | PF01839 | 0.804 |
LIG_LIR_Gen_1 | 573 | 580 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 590 | 596 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 590 | 594 | PF02991 | 0.504 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.731 |
LIG_Rb_pABgroove_1 | 150 | 158 | PF01858 | 0.581 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.597 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.638 |
LIG_SH2_SRC | 441 | 444 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.382 |
LIG_SH3_2 | 206 | 211 | PF14604 | 0.780 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.777 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.763 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.740 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.476 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.714 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 289 | 294 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 149 | 158 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 286 | 291 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.476 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.407 |
LIG_TYR_ITIM | 439 | 444 | PF00017 | 0.667 |
LIG_UBA3_1 | 534 | 542 | PF00899 | 0.560 |
LIG_UBA3_1 | 602 | 608 | PF00899 | 0.497 |
LIG_WRPW_2 | 340 | 343 | PF00400 | 0.476 |
MOD_CDK_SPK_2 | 272 | 277 | PF00069 | 0.537 |
MOD_CDK_SPxK_1 | 205 | 211 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 251 | 257 | PF00069 | 0.768 |
MOD_CDK_SPxxK_3 | 58 | 65 | PF00069 | 0.509 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.686 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.625 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.692 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.428 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.599 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.679 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.427 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.479 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.717 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.742 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.703 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.774 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.663 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.531 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.536 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.648 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.369 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.380 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.687 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.604 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.566 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.759 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.678 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.685 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.650 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.651 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.661 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.487 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.580 |
MOD_NEK2_2 | 521 | 526 | PF00069 | 0.588 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.773 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.472 |
MOD_PIKK_1 | 503 | 509 | PF00454 | 0.566 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.495 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.455 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.671 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.497 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.634 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.809 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.651 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.485 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.655 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.423 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.634 |
MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.713 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.538 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.478 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.645 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.406 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.744 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.639 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.631 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.759 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.675 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.707 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.703 |
MOD_SUMO_for_1 | 580 | 583 | PF00179 | 0.609 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMT0 | Leptomonas seymouri | 53% | 97% |
A0A0S4JTW8 | Bodo saltans | 35% | 100% |
A0A1X0P060 | Trypanosomatidae | 35% | 100% |
A0A3R7LYT2 | Trypanosoma rangeli | 33% | 100% |
A0A3S7XBW1 | Leishmania donovani | 76% | 99% |
A4IDV8 | Leishmania infantum | 76% | 99% |
D0A458 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ATX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q0L7 | Leishmania major | 77% | 100% |
V5BQB1 | Trypanosoma cruzi | 32% | 100% |