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: A4HMM7
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 | 314 | 318 | PF00656 | 0.685 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.424 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.635 |
DEG_APCC_DBOX_1 | 528 | 536 | PF00400 | 0.513 |
DEG_SPOP_SBC_1 | 587 | 591 | PF00917 | 0.383 |
DOC_ANK_TNKS_1 | 76 | 83 | PF00023 | 0.567 |
DOC_CDC14_PxL_1 | 9 | 17 | PF14671 | 0.673 |
DOC_PP2B_LxvP_1 | 522 | 525 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 617 | 620 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.660 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.829 |
LIG_14-3-3_CanoR_1 | 228 | 235 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 529 | 533 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 675 | 681 | PF00244 | 0.524 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 589 | 593 | PF00533 | 0.261 |
LIG_BRCT_BRCA1_1 | 660 | 664 | PF00533 | 0.513 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.492 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.353 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.411 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.515 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.606 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.710 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.518 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.716 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.411 |
LIG_FHA_2 | 646 | 652 | PF00498 | 0.411 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.507 |
LIG_GBD_Chelix_1 | 407 | 415 | PF00786 | 0.513 |
LIG_GBD_Chelix_1 | 489 | 497 | PF00786 | 0.474 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 335 | 344 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 455 | 464 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 491 | 502 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 612 | 620 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 491 | 497 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 612 | 617 | PF02991 | 0.513 |
LIG_NRBOX | 492 | 498 | PF00104 | 0.513 |
LIG_REV1ctd_RIR_1 | 543 | 551 | PF16727 | 0.513 |
LIG_SH2_GRB2like | 595 | 598 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 595 | 599 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.387 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.675 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.411 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 638 | 643 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 655 | 661 | PF11976 | 0.369 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.690 |
LIG_WRC_WIRS_1 | 489 | 494 | PF05994 | 0.513 |
MOD_CDC14_SPxK_1 | 153 | 156 | PF00782 | 0.558 |
MOD_CDK_SPxK_1 | 150 | 156 | PF00069 | 0.543 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.777 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.742 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.721 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.782 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.637 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.373 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.733 |
MOD_CK2_1 | 410 | 416 | PF00069 | 0.411 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.265 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.521 |
MOD_CMANNOS | 606 | 609 | PF00535 | 0.513 |
MOD_Cter_Amidation | 174 | 177 | PF01082 | 0.594 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.713 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.781 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.821 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.713 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.807 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.689 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.609 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.370 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.294 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.351 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.416 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.272 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.433 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.413 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.411 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.739 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.672 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.612 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.323 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.515 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.411 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.220 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.446 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.411 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.436 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.499 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.523 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.678 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.711 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.741 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.509 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.537 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.507 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.411 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.499 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.420 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.323 |
MOD_NEK2_1 | 653 | 658 | PF00069 | 0.375 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.411 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.694 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.339 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.597 |
MOD_PKA_1 | 228 | 234 | PF00069 | 0.585 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.664 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.677 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.836 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.411 |
MOD_PKA_2 | 528 | 534 | PF00069 | 0.351 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.358 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.513 |
MOD_PKB_1 | 454 | 462 | PF00069 | 0.323 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.261 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.452 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.680 |
MOD_Plk_2-3 | 645 | 651 | PF00069 | 0.411 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.411 |
MOD_Plk_4 | 488 | 494 | PF00069 | 0.411 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.416 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.362 |
MOD_Plk_4 | 676 | 682 | PF00069 | 0.411 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.521 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.556 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.711 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.695 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.763 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 78 | 81 | PF00179 | 0.571 |
MOD_SUMO_for_1 | 99 | 102 | PF00179 | 0.429 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 453 | 456 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.568 |
TRG_NES_CRM1_1 | 84 | 96 | PF08389 | 0.521 |
TRG_NLS_Bipartite_1 | 132 | 150 | PF00514 | 0.488 |
TRG_NLS_MonoExtC_3 | 122 | 128 | PF00514 | 0.456 |
TRG_NLS_MonoExtC_3 | 144 | 149 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 145 | 150 | PF00514 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 61 | 66 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 624 | 628 | PF00026 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 97 | 102 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILT4 | Leptomonas seymouri | 51% | 100% |
A0A3S7X9A6 | Leishmania donovani | 78% | 100% |
A4IBA5 | Leishmania infantum | 78% | 100% |
E9AF29 | Leishmania major | 78% | 100% |
E9B685 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |