Proteases, X-pro, dipeptidyl-peptidase,serine peptidase,Clan SC, family S15
| 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. | yes | yes: 15 |
| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4I3S2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006470 | protein dephosphorylation | 5 | 1 |
| GO:0006793 | phosphorus metabolic process | 3 | 1 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016311 | dephosphorylation | 5 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0036211 | protein modification process | 4 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 9 |
| GO:0008233 | peptidase activity | 3 | 9 |
| GO:0008238 | exopeptidase activity | 4 | 9 |
| GO:0008239 | dipeptidyl-peptidase activity | 5 | 9 |
| GO:0016787 | hydrolase activity | 2 | 9 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
| GO:0004721 | phosphoprotein phosphatase activity | 3 | 2 |
| GO:0004725 | protein tyrosine phosphatase activity | 4 | 2 |
| GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
| GO:0016791 | phosphatase activity | 5 | 2 |
| GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.446 |
| CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.257 |
| CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.506 |
| CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.240 |
| CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.427 |
| CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.341 |
| CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.338 |
| CLV_PCSK_FUR_1 | 680 | 684 | PF00082 | 0.453 |
| CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.257 |
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.506 |
| CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.237 |
| CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.402 |
| CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.341 |
| CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.338 |
| CLV_PCSK_PC1ET2_1 | 55 | 57 | PF00082 | 0.237 |
| CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.360 |
| CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.360 |
| CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.288 |
| CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.250 |
| CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.460 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.518 |
| DEG_SIAH_1 | 270 | 278 | PF03145 | 0.472 |
| DOC_CKS1_1 | 376 | 381 | PF01111 | 0.440 |
| DOC_CKS1_1 | 557 | 562 | PF01111 | 0.438 |
| DOC_CYCLIN_RxL_1 | 609 | 621 | PF00134 | 0.354 |
| DOC_MAPK_MEF2A_6 | 145 | 152 | PF00069 | 0.457 |
| DOC_MAPK_NFAT4_5 | 145 | 153 | PF00069 | 0.519 |
| DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.466 |
| DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.440 |
| DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.421 |
| DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.532 |
| DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.514 |
| DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.482 |
| DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.393 |
| DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.444 |
| DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.440 |
| DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.395 |
| LIG_14-3-3_CanoR_1 | 156 | 163 | PF00244 | 0.440 |
| LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.436 |
| LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.440 |
| LIG_14-3-3_CanoR_1 | 571 | 576 | PF00244 | 0.382 |
| LIG_APCC_ABBA_1 | 314 | 319 | PF00400 | 0.362 |
| LIG_deltaCOP1_diTrp_1 | 109 | 116 | PF00928 | 0.440 |
| LIG_deltaCOP1_diTrp_1 | 194 | 200 | PF00928 | 0.440 |
| LIG_deltaCOP1_diTrp_1 | 294 | 299 | PF00928 | 0.422 |
| LIG_EH1_1 | 459 | 467 | PF00400 | 0.523 |
| LIG_eIF4E_1 | 460 | 466 | PF01652 | 0.523 |
| LIG_FHA_1 | 10 | 16 | PF00498 | 0.476 |
| LIG_FHA_1 | 116 | 122 | PF00498 | 0.523 |
| LIG_FHA_1 | 156 | 162 | PF00498 | 0.440 |
| LIG_FHA_1 | 249 | 255 | PF00498 | 0.440 |
| LIG_FHA_1 | 303 | 309 | PF00498 | 0.319 |
| LIG_FHA_1 | 369 | 375 | PF00498 | 0.586 |
| LIG_FHA_1 | 426 | 432 | PF00498 | 0.431 |
| LIG_FHA_1 | 457 | 463 | PF00498 | 0.525 |
| LIG_FHA_1 | 521 | 527 | PF00498 | 0.448 |
| LIG_FHA_1 | 584 | 590 | PF00498 | 0.365 |
| LIG_FHA_2 | 19 | 25 | PF00498 | 0.450 |
| LIG_FHA_2 | 302 | 308 | PF00498 | 0.414 |
| LIG_FHA_2 | 392 | 398 | PF00498 | 0.473 |
| LIG_FHA_2 | 603 | 609 | PF00498 | 0.351 |
| LIG_HCF-1_HBM_1 | 16 | 19 | PF13415 | 0.435 |
| LIG_HCF-1_HBM_1 | 41 | 44 | PF13415 | 0.519 |
| LIG_LIR_Apic_2 | 531 | 537 | PF02991 | 0.375 |
| LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.354 |
| LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.457 |
| LIG_LIR_Gen_1 | 572 | 579 | PF02991 | 0.372 |
| LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.303 |
| LIG_LIR_Gen_1 | 653 | 663 | PF02991 | 0.336 |
| LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.452 |
| LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.328 |
| LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.479 |
| LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.500 |
| LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.399 |
| LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.580 |
| LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.461 |
| LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.418 |
| LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.486 |
| LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.296 |
| LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.342 |
| LIG_LYPXL_yS_3 | 44 | 47 | PF13949 | 0.523 |
| LIG_MYND_1 | 537 | 541 | PF01753 | 0.373 |
| LIG_NRBOX | 253 | 259 | PF00104 | 0.523 |
| LIG_PDZ_Class_3 | 681 | 686 | PF00595 | 0.380 |
| LIG_Pex14_1 | 246 | 250 | PF04695 | 0.440 |
| LIG_Pex14_1 | 272 | 276 | PF04695 | 0.440 |
| LIG_Pex14_2 | 673 | 677 | PF04695 | 0.374 |
| LIG_PTB_Apo_2 | 167 | 174 | PF02174 | 0.440 |
| LIG_PTB_Apo_2 | 249 | 256 | PF02174 | 0.440 |
| LIG_SH2_CRK | 233 | 237 | PF00017 | 0.455 |
| LIG_SH2_CRK | 496 | 500 | PF00017 | 0.523 |
| LIG_SH2_GRB2like | 250 | 253 | PF00017 | 0.440 |
| LIG_SH2_NCK_1 | 233 | 237 | PF00017 | 0.444 |
| LIG_SH2_NCK_1 | 412 | 416 | PF00017 | 0.523 |
| LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.431 |
| LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.487 |
| LIG_SH2_SRC | 575 | 578 | PF00017 | 0.390 |
| LIG_SH2_SRC | 656 | 659 | PF00017 | 0.349 |
| LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.440 |
| LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.440 |
| LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.391 |
| LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.440 |
| LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.431 |
| LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.440 |
| LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.437 |
| LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.536 |
| LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.508 |
| LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.440 |
| LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.399 |
| LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.333 |
| LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.479 |
| LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.440 |
| LIG_SH3_3 | 373 | 379 | PF00018 | 0.506 |
| LIG_SH3_3 | 535 | 541 | PF00018 | 0.548 |
| LIG_SH3_3 | 543 | 549 | PF00018 | 0.511 |
| LIG_SH3_3 | 554 | 560 | PF00018 | 0.313 |
| LIG_SH3_3 | 632 | 638 | PF00018 | 0.495 |
| LIG_SUMO_SIM_anti_2 | 102 | 109 | PF11976 | 0.457 |
| LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.523 |
| LIG_SUMO_SIM_par_1 | 371 | 378 | PF11976 | 0.487 |
| LIG_SUMO_SIM_par_1 | 522 | 528 | PF11976 | 0.501 |
| LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.523 |
| LIG_TYR_ITIM | 573 | 578 | PF00017 | 0.388 |
| LIG_UBA3_1 | 254 | 262 | PF00899 | 0.288 |
| LIG_UBA3_1 | 358 | 364 | PF00899 | 0.233 |
| LIG_UBA3_1 | 47 | 55 | PF00899 | 0.275 |
| MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.448 |
| MOD_CK2_1 | 225 | 231 | PF00069 | 0.284 |
| MOD_CK2_1 | 391 | 397 | PF00069 | 0.428 |
| MOD_CK2_1 | 548 | 554 | PF00069 | 0.423 |
| MOD_CK2_1 | 564 | 570 | PF00069 | 0.431 |
| MOD_CK2_1 | 602 | 608 | PF00069 | 0.359 |
| MOD_CMANNOS | 296 | 299 | PF00535 | 0.310 |
| MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.335 |
| MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.400 |
| MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.547 |
| MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.377 |
| MOD_GSK3_1 | 366 | 373 | PF00069 | 0.395 |
| MOD_GSK3_1 | 411 | 418 | PF00069 | 0.380 |
| MOD_GSK3_1 | 425 | 432 | PF00069 | 0.311 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.302 |
| MOD_GSK3_1 | 516 | 523 | PF00069 | 0.343 |
| MOD_GSK3_1 | 555 | 562 | PF00069 | 0.418 |
| MOD_GSK3_1 | 603 | 610 | PF00069 | 0.377 |
| MOD_GSK3_1 | 621 | 628 | PF00069 | 0.424 |
| MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.391 |
| MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.406 |
| MOD_NEK2_1 | 124 | 129 | PF00069 | 0.285 |
| MOD_NEK2_1 | 150 | 155 | PF00069 | 0.352 |
| MOD_NEK2_1 | 408 | 413 | PF00069 | 0.451 |
| MOD_NEK2_1 | 429 | 434 | PF00069 | 0.386 |
| MOD_NEK2_1 | 615 | 620 | PF00069 | 0.325 |
| MOD_NEK2_1 | 633 | 638 | PF00069 | 0.459 |
| MOD_NEK2_1 | 673 | 678 | PF00069 | 0.420 |
| MOD_PIKK_1 | 646 | 652 | PF00454 | 0.441 |
| MOD_PIKK_1 | 9 | 15 | PF00454 | 0.477 |
| MOD_PKA_2 | 155 | 161 | PF00069 | 0.275 |
| MOD_PKA_2 | 456 | 462 | PF00069 | 0.275 |
| MOD_PKB_1 | 54 | 62 | PF00069 | 0.275 |
| MOD_Plk_1 | 231 | 237 | PF00069 | 0.391 |
| MOD_Plk_1 | 318 | 324 | PF00069 | 0.403 |
| MOD_Plk_1 | 521 | 527 | PF00069 | 0.405 |
| MOD_Plk_1 | 569 | 575 | PF00069 | 0.386 |
| MOD_Plk_1 | 603 | 609 | PF00069 | 0.384 |
| MOD_Plk_1 | 613 | 619 | PF00069 | 0.358 |
| MOD_Plk_1 | 673 | 679 | PF00069 | 0.411 |
| MOD_Plk_4 | 345 | 351 | PF00069 | 0.381 |
| MOD_Plk_4 | 370 | 376 | PF00069 | 0.391 |
| MOD_Plk_4 | 521 | 527 | PF00069 | 0.399 |
| MOD_Plk_4 | 559 | 565 | PF00069 | 0.369 |
| MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.394 |
| MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.281 |
| MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.275 |
| MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.395 |
| MOD_SUMO_for_1 | 97 | 100 | PF00179 | 0.391 |
| TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.275 |
| TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.263 |
| TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.431 |
| TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.296 |
| TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.391 |
| TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.391 |
| TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.390 |
| TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.326 |
| TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.334 |
| TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.534 |
| TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.300 |
| TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.275 |
| TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.410 |
| TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.349 |
| TRG_NLS_MonoExtN_4 | 52 | 58 | PF00514 | 0.391 |
| TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.314 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I036 | Leptomonas seymouri | 80% | 100% |
| A0A1X0NRA9 | Trypanosomatidae | 55% | 100% |
| A0A3S7X1Q1 | Leishmania donovani | 100% | 100% |
| A0A422N0C2 | Trypanosoma rangeli | 56% | 100% |
| E9B014 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| Q4Q871 | Leishmania major | 96% | 100% |
| Q82MI6 | Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) | 22% | 100% |
| Q9L9D7 | Rhodococcus sp. (strain MB1 Bresler) | 23% | 100% |
| V5BL63 | Trypanosoma cruzi | 57% | 100% |