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: A0A3S7X9A6
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 | 201 | 205 | PF00656 | 0.755 |
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.348 |
CLV_Separin_Metazoa | 467 | 471 | PF03568 | 0.389 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.621 |
DEG_APCC_DBOX_1 | 526 | 534 | PF00400 | 0.513 |
DEG_SCF_TRCP1_1 | 514 | 519 | PF00400 | 0.397 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.635 |
DEG_SPOP_SBC_1 | 585 | 589 | PF00917 | 0.416 |
DOC_ANK_TNKS_1 | 76 | 83 | PF00023 | 0.564 |
DOC_CDC14_PxL_1 | 9 | 17 | PF14671 | 0.674 |
DOC_MAPK_MEF2A_6 | 517 | 524 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 538 | 545 | PF00149 | 0.389 |
DOC_PP1_RVXF_1 | 656 | 663 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 520 | 523 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 615 | 618 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.343 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.733 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.840 |
LIG_14-3-3_CanoR_1 | 527 | 531 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 673 | 679 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 2 | 18 | PF00022 | 0.641 |
LIG_Actin_WH2_2 | 455 | 472 | PF00022 | 0.436 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.513 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.513 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.387 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.411 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.459 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.594 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.705 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.389 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.411 |
LIG_FHA_2 | 644 | 650 | PF00498 | 0.411 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.503 |
LIG_GBD_Chelix_1 | 405 | 413 | PF00786 | 0.513 |
LIG_GBD_Chelix_1 | 487 | 495 | PF00786 | 0.474 |
LIG_LIR_Apic_2 | 476 | 482 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 453 | 462 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 489 | 500 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 610 | 618 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 610 | 615 | PF02991 | 0.513 |
LIG_NRBOX | 490 | 496 | PF00104 | 0.513 |
LIG_REV1ctd_RIR_1 | 541 | 549 | PF16727 | 0.513 |
LIG_SH2_GRB2like | 593 | 596 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 593 | 597 | PF00017 | 0.513 |
LIG_SH2_STAP1 | 389 | 393 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 557 | 561 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.411 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.658 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.630 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.411 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.419 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 636 | 641 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 422 | 428 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 646 | 656 | PF11976 | 0.424 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.487 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.389 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.513 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.728 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.775 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.732 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.742 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.823 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.769 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.443 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.434 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.681 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.769 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.362 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.389 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.436 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.517 |
MOD_CMANNOS | 604 | 607 | PF00535 | 0.513 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.757 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.821 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.845 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.410 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.303 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.388 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.306 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.364 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.384 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.730 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.722 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.831 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.436 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.515 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.279 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.478 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.437 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.411 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.671 |
MOD_N-GLC_1 | 594 | 599 | PF02516 | 0.513 |
MOD_N-GLC_1 | 633 | 638 | PF02516 | 0.455 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.703 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.826 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.509 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.521 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.485 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.389 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.393 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.411 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.513 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.408 |
MOD_NEK2_1 | 678 | 683 | PF00069 | 0.404 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.691 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.679 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.780 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.769 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.383 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.411 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.363 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.461 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.513 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.455 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.681 |
MOD_Plk_2-3 | 643 | 649 | PF00069 | 0.411 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.593 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.500 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.411 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.411 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.416 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.411 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.411 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.502 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.709 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.808 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.513 |
MOD_SUMO_for_1 | 78 | 81 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.593 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.514 |
TRG_DiLeu_LyEn_5 | 100 | 105 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.619 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.560 |
TRG_NES_CRM1_1 | 84 | 96 | PF08389 | 0.514 |
TRG_NLS_MonoCore_2 | 144 | 149 | PF00514 | 0.688 |
TRG_NLS_MonoExtC_3 | 143 | 148 | PF00514 | 0.680 |
TRG_NLS_MonoExtN_4 | 144 | 149 | PF00514 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 103 | 107 | PF00026 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 61 | 66 | PF00026 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 622 | 626 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 97 | 102 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILT4 | Leptomonas seymouri | 54% | 100% |
A4HMM7 | Leishmania braziliensis | 78% | 100% |
A4IBA5 | Leishmania infantum | 99% | 100% |
E9AF29 | Leishmania major | 92% | 100% |
E9B685 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |