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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AF29
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004843 | cysteine-type deubiquitinase activity | 5 | 7 |
GO:0008233 | peptidase activity | 3 | 7 |
GO:0008234 | cysteine-type peptidase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 7 |
GO:0101005 | deubiquitinase activity | 5 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1990380 | K48-linked deubiquitinase activity | 6 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.280 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 398 | 400 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.402 |
CLV_Separin_Metazoa | 466 | 470 | PF03568 | 0.389 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.627 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.513 |
DEG_SCF_TRCP1_1 | 513 | 518 | PF00400 | 0.397 |
DOC_ANK_TNKS_1 | 76 | 83 | PF00023 | 0.561 |
DOC_CDC14_PxL_1 | 9 | 17 | PF14671 | 0.675 |
DOC_MAPK_gen_1 | 480 | 489 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 516 | 523 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 537 | 544 | PF00149 | 0.389 |
DOC_PP1_RVXF_1 | 655 | 662 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 519 | 522 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.696 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.832 |
LIG_14-3-3_CanoR_1 | 255 | 260 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 526 | 530 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 578 | 586 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 672 | 678 | PF00244 | 0.524 |
LIG_Actin_WH2_2 | 2 | 18 | PF00022 | 0.640 |
LIG_Actin_WH2_2 | 454 | 471 | PF00022 | 0.436 |
LIG_BRCT_BRCA1_1 | 487 | 491 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 657 | 661 | PF00533 | 0.513 |
LIG_Clathr_ClatBox_1 | 67 | 71 | PF01394 | 0.423 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.492 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.353 |
LIG_FHA_1 | 618 | 624 | PF00498 | 0.411 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.515 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.581 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.702 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.389 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.411 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.376 |
LIG_FHA_2 | 643 | 649 | PF00498 | 0.411 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.504 |
LIG_GBD_Chelix_1 | 404 | 412 | PF00786 | 0.513 |
LIG_GBD_Chelix_1 | 486 | 494 | PF00786 | 0.474 |
LIG_LIR_Apic_2 | 475 | 481 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 452 | 461 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 488 | 499 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 609 | 617 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 192 | 196 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 609 | 614 | PF02991 | 0.513 |
LIG_NRBOX | 489 | 495 | PF00104 | 0.513 |
LIG_REV1ctd_RIR_1 | 540 | 548 | PF16727 | 0.513 |
LIG_SH2_GRB2like | 592 | 595 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 592 | 596 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 556 | 560 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.387 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.663 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.411 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.402 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 635 | 640 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 421 | 427 | PF11976 | 0.367 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.534 |
LIG_TRAF2_1 | 218 | 221 | PF00917 | 0.676 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.389 |
LIG_WRC_WIRS_1 | 486 | 491 | PF05994 | 0.513 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.763 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.738 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.608 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.626 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.490 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.373 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.721 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.770 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.344 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.411 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.377 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.457 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.517 |
MOD_CMANNOS | 603 | 606 | PF00535 | 0.513 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.765 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.807 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.822 |
MOD_GlcNHglycan | 308 | 313 | PF01048 | 0.630 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.360 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.351 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.409 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.418 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.413 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.411 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.550 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.733 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.775 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.729 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.813 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.602 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.420 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.424 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.422 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.515 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.411 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.220 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.442 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.411 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.499 |
MOD_N-GLC_1 | 632 | 637 | PF02516 | 0.397 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.800 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.702 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.818 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.509 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.528 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.507 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.389 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.411 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.499 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.420 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.410 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.411 |
MOD_PK_1 | 457 | 463 | PF00069 | 0.280 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.700 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.546 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.770 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.397 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.411 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.399 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.351 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.358 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.513 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.280 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.397 |
MOD_Plk_2-3 | 642 | 648 | PF00069 | 0.411 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.326 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.436 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.411 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.411 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.416 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.362 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.411 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.517 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.682 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.805 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 78 | 81 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.514 |
TRG_DiLeu_LyEn_5 | 100 | 105 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.613 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.558 |
TRG_NES_CRM1_1 | 84 | 96 | PF08389 | 0.515 |
TRG_NLS_MonoCore_2 | 144 | 149 | PF00514 | 0.705 |
TRG_NLS_MonoExtC_3 | 143 | 148 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 144 | 149 | PF00514 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 61 | 66 | PF00026 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 621 | 625 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 97 | 102 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILT4 | Leptomonas seymouri | 54% | 100% |
A0A3S7X9A6 | Leishmania donovani | 92% | 100% |
A4HMM7 | Leishmania braziliensis | 78% | 100% |
A4IBA5 | Leishmania infantum | 92% | 100% |
E9B685 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |