| 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: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q1G1
| 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:0016567 | protein ubiquitination | 7 | 2 |
| GO:0019538 | protein metabolic process | 3 | 2 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
| GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
| GO:0036211 | protein modification process | 4 | 2 |
| GO:0043170 | macromolecule metabolic process | 3 | 2 |
| GO:0043412 | macromolecule modification | 4 | 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:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
| GO:0071704 | organic substance metabolic process | 2 | 2 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
| GO:1901575 | organic substance catabolic process | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 2 |
| GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
| GO:0016740 | transferase activity | 2 | 2 |
| GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
| GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
| GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.666 |
| CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.612 |
| CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.687 |
| CLV_C14_Caspase3-7 | 26 | 30 | PF00656 | 0.522 |
| CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.715 |
| CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.633 |
| CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.622 |
| CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.507 |
| CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.549 |
| CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.532 |
| CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.404 |
| CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.523 |
| CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.454 |
| CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.654 |
| CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.699 |
| CLV_PCSK_SKI1_1 | 615 | 619 | PF00082 | 0.701 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.606 |
| DEG_SCF_TRCP1_1 | 411 | 417 | PF00400 | 0.680 |
| DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.795 |
| DEG_SPOP_SBC_1 | 669 | 673 | PF00917 | 0.684 |
| DOC_CYCLIN_RxL_1 | 287 | 296 | PF00134 | 0.461 |
| DOC_MAPK_gen_1 | 194 | 202 | PF00069 | 0.685 |
| DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.746 |
| DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.566 |
| DOC_PP1_RVXF_1 | 288 | 294 | PF00149 | 0.469 |
| DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.543 |
| DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.680 |
| DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.663 |
| DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.702 |
| DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.441 |
| DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.698 |
| DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.738 |
| DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.607 |
| DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.567 |
| DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.601 |
| DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.618 |
| DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.744 |
| DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.680 |
| DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.606 |
| DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.781 |
| DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.711 |
| DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.596 |
| DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.544 |
| DOC_USP7_UBL2_3 | 611 | 615 | PF12436 | 0.686 |
| DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.725 |
| DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.674 |
| DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.612 |
| DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.665 |
| DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.762 |
| DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.688 |
| DOC_WW_Pin1_4 | 678 | 683 | PF00397 | 0.828 |
| LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.554 |
| LIG_14-3-3_CanoR_1 | 597 | 606 | PF00244 | 0.717 |
| LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.644 |
| LIG_BIR_III_2 | 36 | 40 | PF00653 | 0.524 |
| LIG_CaM_NSCaTE_8 | 506 | 513 | PF13499 | 0.509 |
| LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.493 |
| LIG_eIF4E_1 | 628 | 634 | PF01652 | 0.634 |
| LIG_FHA_1 | 251 | 257 | PF00498 | 0.366 |
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.582 |
| LIG_FHA_1 | 338 | 344 | PF00498 | 0.584 |
| LIG_FHA_1 | 40 | 46 | PF00498 | 0.694 |
| LIG_FHA_1 | 464 | 470 | PF00498 | 0.739 |
| LIG_FHA_1 | 519 | 525 | PF00498 | 0.674 |
| LIG_FHA_1 | 577 | 583 | PF00498 | 0.782 |
| LIG_FHA_1 | 628 | 634 | PF00498 | 0.634 |
| LIG_FHA_1 | 649 | 655 | PF00498 | 0.685 |
| LIG_FHA_1 | 696 | 702 | PF00498 | 0.797 |
| LIG_FHA_2 | 403 | 409 | PF00498 | 0.734 |
| LIG_FHA_2 | 446 | 452 | PF00498 | 0.550 |
| LIG_LIR_Apic_2 | 347 | 352 | PF02991 | 0.545 |
| LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.376 |
| LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.564 |
| LIG_LIR_Gen_1 | 715 | 720 | PF02991 | 0.623 |
| LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.399 |
| LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.789 |
| LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.376 |
| LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.562 |
| LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.536 |
| LIG_LIR_Nem_3 | 715 | 719 | PF02991 | 0.618 |
| LIG_SH2_CRK | 110 | 114 | PF00017 | 0.493 |
| LIG_SH2_CRK | 126 | 130 | PF00017 | 0.354 |
| LIG_SH2_CRK | 349 | 353 | PF00017 | 0.549 |
| LIG_SH2_CRK | 373 | 377 | PF00017 | 0.738 |
| LIG_SH2_CRK | 442 | 446 | PF00017 | 0.633 |
| LIG_SH2_CRK | 61 | 65 | PF00017 | 0.485 |
| LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.376 |
| LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.480 |
| LIG_SH2_PTP2 | 716 | 719 | PF00017 | 0.689 |
| LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.430 |
| LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.485 |
| LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.743 |
| LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.430 |
| LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.555 |
| LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.531 |
| LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.743 |
| LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.689 |
| LIG_SH3_3 | 150 | 156 | PF00018 | 0.592 |
| LIG_SH3_3 | 232 | 238 | PF00018 | 0.653 |
| LIG_SH3_3 | 332 | 338 | PF00018 | 0.499 |
| LIG_SH3_3 | 497 | 503 | PF00018 | 0.751 |
| LIG_SH3_3 | 551 | 557 | PF00018 | 0.731 |
| LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.509 |
| LIG_SUMO_SIM_par_1 | 252 | 257 | PF11976 | 0.376 |
| LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.507 |
| LIG_SUMO_SIM_par_1 | 351 | 356 | PF11976 | 0.548 |
| LIG_SUMO_SIM_par_1 | 661 | 666 | PF11976 | 0.686 |
| LIG_SUMO_SIM_par_1 | 67 | 75 | PF11976 | 0.499 |
| LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.424 |
| LIG_UBA3_1 | 45 | 53 | PF00899 | 0.540 |
| MOD_CK1_1 | 116 | 122 | PF00069 | 0.361 |
| MOD_CK1_1 | 133 | 139 | PF00069 | 0.565 |
| MOD_CK1_1 | 183 | 189 | PF00069 | 0.628 |
| MOD_CK1_1 | 208 | 214 | PF00069 | 0.660 |
| MOD_CK1_1 | 222 | 228 | PF00069 | 0.671 |
| MOD_CK1_1 | 23 | 29 | PF00069 | 0.444 |
| MOD_CK1_1 | 336 | 342 | PF00069 | 0.553 |
| MOD_CK1_1 | 382 | 388 | PF00069 | 0.577 |
| MOD_CK1_1 | 432 | 438 | PF00069 | 0.598 |
| MOD_CK1_1 | 576 | 582 | PF00069 | 0.716 |
| MOD_CK1_1 | 596 | 602 | PF00069 | 0.697 |
| MOD_CK1_1 | 692 | 698 | PF00069 | 0.697 |
| MOD_CK2_1 | 445 | 451 | PF00069 | 0.556 |
| MOD_CK2_1 | 86 | 92 | PF00069 | 0.505 |
| MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.385 |
| MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.614 |
| MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.640 |
| MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.746 |
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.478 |
| MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.760 |
| MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.698 |
| MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.436 |
| MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.720 |
| MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.675 |
| MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.739 |
| MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.751 |
| MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.718 |
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.628 |
| MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.524 |
| MOD_GSK3_1 | 109 | 116 | PF00069 | 0.304 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.517 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.581 |
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.731 |
| MOD_GSK3_1 | 204 | 211 | PF00069 | 0.658 |
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.637 |
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.353 |
| MOD_GSK3_1 | 329 | 336 | PF00069 | 0.559 |
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.553 |
| MOD_GSK3_1 | 379 | 386 | PF00069 | 0.603 |
| MOD_GSK3_1 | 445 | 452 | PF00069 | 0.489 |
| MOD_GSK3_1 | 506 | 513 | PF00069 | 0.685 |
| MOD_GSK3_1 | 536 | 543 | PF00069 | 0.714 |
| MOD_GSK3_1 | 572 | 579 | PF00069 | 0.644 |
| MOD_GSK3_1 | 589 | 596 | PF00069 | 0.667 |
| MOD_GSK3_1 | 623 | 630 | PF00069 | 0.650 |
| MOD_GSK3_1 | 689 | 696 | PF00069 | 0.700 |
| MOD_GSK3_1 | 82 | 89 | PF00069 | 0.598 |
| MOD_LATS_1 | 331 | 337 | PF00433 | 0.564 |
| MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.619 |
| MOD_N-GLC_1 | 703 | 708 | PF02516 | 0.695 |
| MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.376 |
| MOD_NEK2_1 | 20 | 25 | PF00069 | 0.543 |
| MOD_NEK2_1 | 254 | 259 | PF00069 | 0.376 |
| MOD_NEK2_1 | 274 | 279 | PF00069 | 0.303 |
| MOD_NEK2_1 | 281 | 286 | PF00069 | 0.430 |
| MOD_NEK2_1 | 329 | 334 | PF00069 | 0.569 |
| MOD_NEK2_1 | 429 | 434 | PF00069 | 0.707 |
| MOD_NEK2_1 | 449 | 454 | PF00069 | 0.406 |
| MOD_NEK2_1 | 510 | 515 | PF00069 | 0.520 |
| MOD_NEK2_1 | 604 | 609 | PF00069 | 0.668 |
| MOD_NEK2_1 | 654 | 659 | PF00069 | 0.637 |
| MOD_NEK2_1 | 72 | 77 | PF00069 | 0.478 |
| MOD_NEK2_2 | 189 | 194 | PF00069 | 0.706 |
| MOD_NEK2_2 | 372 | 377 | PF00069 | 0.695 |
| MOD_NEK2_2 | 506 | 511 | PF00069 | 0.639 |
| MOD_OFUCOSY | 571 | 578 | PF10250 | 0.550 |
| MOD_PIKK_1 | 254 | 260 | PF00454 | 0.385 |
| MOD_PKA_1 | 333 | 339 | PF00069 | 0.500 |
| MOD_PKA_2 | 333 | 339 | PF00069 | 0.562 |
| MOD_PKA_2 | 409 | 415 | PF00069 | 0.769 |
| MOD_PKA_2 | 596 | 602 | PF00069 | 0.775 |
| MOD_PKA_2 | 604 | 610 | PF00069 | 0.630 |
| MOD_PKA_2 | 620 | 626 | PF00069 | 0.501 |
| MOD_Plk_1 | 122 | 128 | PF00069 | 0.417 |
| MOD_Plk_1 | 383 | 389 | PF00069 | 0.612 |
| MOD_Plk_1 | 432 | 438 | PF00069 | 0.604 |
| MOD_Plk_4 | 113 | 119 | PF00069 | 0.345 |
| MOD_Plk_4 | 130 | 136 | PF00069 | 0.506 |
| MOD_Plk_4 | 250 | 256 | PF00069 | 0.362 |
| MOD_Plk_4 | 304 | 310 | PF00069 | 0.423 |
| MOD_Plk_4 | 383 | 389 | PF00069 | 0.590 |
| MOD_Plk_4 | 41 | 47 | PF00069 | 0.650 |
| MOD_Plk_4 | 506 | 512 | PF00069 | 0.575 |
| MOD_Plk_4 | 620 | 626 | PF00069 | 0.768 |
| MOD_Plk_4 | 628 | 634 | PF00069 | 0.585 |
| MOD_Plk_4 | 649 | 655 | PF00069 | 0.706 |
| MOD_Plk_4 | 696 | 702 | PF00069 | 0.722 |
| MOD_Plk_4 | 712 | 718 | PF00069 | 0.702 |
| MOD_Plk_4 | 86 | 92 | PF00069 | 0.496 |
| MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.723 |
| MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.676 |
| MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.618 |
| MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.664 |
| MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.763 |
| MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.688 |
| MOD_ProDKin_1 | 678 | 684 | PF00069 | 0.828 |
| MOD_SUMO_rev_2 | 347 | 352 | PF00179 | 0.545 |
| TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.671 |
| TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.493 |
| TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.354 |
| TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.657 |
| TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.467 |
| TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.560 |
| TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.435 |
| TRG_ENDOCYTIC_2 | 716 | 719 | PF00928 | 0.618 |
| TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.619 |
| TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.554 |
| TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.501 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PDB4 | Leptomonas seymouri | 44% | 100% |
| A0A3S7XAY5 | Leishmania donovani | 92% | 100% |
| A4HPC6 | Leishmania braziliensis | 72% | 100% |
| A4ICG6 | Leishmania infantum | 92% | 100% |
| E9AT37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
| V5BPT3 | Trypanosoma cruzi | 34% | 100% |