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: A0A3S7XBW1
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_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.581 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.527 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.723 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.608 |
DEG_APCC_DBOX_1 | 45 | 53 | PF00400 | 0.571 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.739 |
DOC_AGCK_PIF_2 | 359 | 364 | PF00069 | 0.474 |
DOC_CYCLIN_RxL_1 | 43 | 51 | PF00134 | 0.610 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 531 | 540 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 29 | 35 | PF00134 | 0.626 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 604 | 612 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.517 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 232 | 236 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 307 | 311 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 447 | 451 | PF12436 | 0.347 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 298 | 306 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 595 | 601 | PF00244 | 0.433 |
LIG_APCC_ABBA_1 | 153 | 158 | PF00400 | 0.413 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 528 | 532 | PF00533 | 0.645 |
LIG_deltaCOP1_diTrp_1 | 589 | 597 | PF00928 | 0.535 |
LIG_eIF4E_1 | 156 | 162 | PF01652 | 0.462 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.459 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.724 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.369 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.543 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.588 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.679 |
LIG_FHA_2 | 74 | 80 | PF00498 | 0.752 |
LIG_Integrin_isoDGR_2 | 3 | 5 | PF01839 | 0.667 |
LIG_LIR_Gen_1 | 596 | 602 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 572 | 576 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 596 | 600 | PF02991 | 0.472 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.411 |
LIG_Pex14_2 | 218 | 222 | PF04695 | 0.692 |
LIG_Rb_pABgroove_1 | 150 | 158 | PF01858 | 0.542 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.556 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.587 |
LIG_SH3_2 | 206 | 211 | PF14604 | 0.637 |
LIG_SH3_2 | 419 | 424 | PF14604 | 0.602 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.617 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.735 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.442 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.683 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.755 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.717 |
LIG_SUMO_SIM_par_1 | 149 | 158 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 372 | 378 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.485 |
LIG_TYR_ITIM | 438 | 443 | PF00017 | 0.615 |
LIG_UBA3_1 | 540 | 548 | PF00899 | 0.417 |
LIG_UBA3_1 | 608 | 614 | PF00899 | 0.458 |
LIG_WRPW_2 | 340 | 343 | PF00400 | 0.431 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.679 |
MOD_CDC14_SPxK_1 | 254 | 257 | PF00782 | 0.668 |
MOD_CDC14_SPxK_1 | 425 | 428 | PF00782 | 0.516 |
MOD_CDK_SPxK_1 | 18 | 24 | PF00069 | 0.693 |
MOD_CDK_SPxK_1 | 251 | 257 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 422 | 428 | PF00069 | 0.521 |
MOD_CDK_SPxxK_3 | 18 | 25 | PF00069 | 0.691 |
MOD_CDK_SPxxK_3 | 183 | 190 | PF00069 | 0.676 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.517 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.676 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.648 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.733 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.613 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.603 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.636 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.407 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.332 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.351 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.685 |
MOD_Cter_Amidation | 3 | 6 | PF01082 | 0.620 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.712 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.803 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.642 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.654 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.705 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.593 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.608 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.318 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.450 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.641 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.665 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.583 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.547 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.722 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.614 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.597 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.768 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.622 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.648 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.655 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.543 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.520 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.493 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.570 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.754 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.569 |
MOD_PK_1 | 281 | 287 | PF00069 | 0.473 |
MOD_PKA_1 | 281 | 287 | PF00069 | 0.522 |
MOD_PKA_1 | 5 | 11 | PF00069 | 0.616 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.588 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.657 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.595 |
MOD_PKB_1 | 88 | 96 | PF00069 | 0.609 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.398 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.493 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.634 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.358 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.679 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.679 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.688 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.646 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.680 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.652 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.767 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.536 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.684 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 586 | 589 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 229 | 239 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 433 | 438 | PF00179 | 0.645 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.627 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 413 | 415 | PF00400 | 0.723 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.788 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMT0 | Leptomonas seymouri | 56% | 99% |
A0A0S4JTW8 | Bodo saltans | 32% | 100% |
A0A1X0P060 | Trypanosomatidae | 35% | 100% |
A0A3R7LYT2 | Trypanosoma rangeli | 32% | 100% |
A4HQ59 | Leishmania braziliensis | 76% | 99% |
A4IDV8 | Leishmania infantum | 100% | 100% |
D0A458 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ATX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4Q0L7 | Leishmania major | 93% | 100% |
V5BQB1 | Trypanosoma cruzi | 34% | 100% |