Proteases, prolyl oligopeptidase
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005829 | cytosol | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4ICB5
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004175 | endopeptidase activity | 4 | 11 |
GO:0004252 | serine-type endopeptidase activity | 5 | 11 |
GO:0008233 | peptidase activity | 3 | 11 |
GO:0008236 | serine-type peptidase activity | 4 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0017171 | serine hydrolase activity | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:0070012 | oligopeptidase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.280 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.280 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.218 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.297 |
DEG_Kelch_Keap1_1 | 157 | 162 | PF01344 | 0.515 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.520 |
DEG_SCF_FBW7_1 | 472 | 479 | PF00400 | 0.336 |
DOC_CDC14_PxL_1 | 186 | 194 | PF14671 | 0.498 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 484 | 493 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.547 |
DOC_CYCLIN_yCln2_LP_2 | 653 | 659 | PF00134 | 0.400 |
DOC_MAPK_gen_1 | 274 | 282 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 368 | 374 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 385 | 391 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 106 | 114 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 310 | 318 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 341 | 349 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 165 | 171 | PF00149 | 0.520 |
DOC_PP1_RVXF_1 | 273 | 280 | PF00149 | 0.580 |
DOC_PP1_RVXF_1 | 480 | 486 | PF00149 | 0.317 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.499 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.340 |
DOC_PP2B_PxIxI_1 | 620 | 626 | PF00149 | 0.340 |
DOC_PP4_FxxP_1 | 113 | 116 | PF00568 | 0.468 |
DOC_PP4_FxxP_1 | 396 | 399 | PF00568 | 0.468 |
DOC_PP4_FxxP_1 | 669 | 672 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 399 | 403 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 671 | 675 | PF12436 | 0.321 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.321 |
LIG_14-3-3_CanoR_1 | 65 | 72 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.487 |
LIG_APCC_ABBA_1 | 345 | 350 | PF00400 | 0.498 |
LIG_APCC_ABBA_1 | 414 | 419 | PF00400 | 0.407 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.498 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.547 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.434 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.493 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.291 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.391 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.521 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.317 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.498 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.536 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.516 |
LIG_FHA_2 | 647 | 653 | PF00498 | 0.420 |
LIG_HCF-1_HBM_1 | 243 | 246 | PF13415 | 0.538 |
LIG_LIR_Apic_2 | 111 | 116 | PF02991 | 0.481 |
LIG_LIR_Apic_2 | 394 | 399 | PF02991 | 0.468 |
LIG_LIR_Apic_2 | 591 | 596 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 148 | 158 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 428 | 437 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 563 | 572 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 681 | 691 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 563 | 568 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 599 | 605 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 606 | 611 | PF02991 | 0.305 |
LIG_LYPXL_S_1 | 4 | 8 | PF13949 | 0.388 |
LIG_LYPXL_yS_3 | 189 | 192 | PF13949 | 0.498 |
LIG_LYPXL_yS_3 | 5 | 8 | PF13949 | 0.374 |
LIG_LYPXL_yS_3 | 620 | 623 | PF13949 | 0.321 |
LIG_PAM2_1 | 76 | 88 | PF00658 | 0.547 |
LIG_PCNA_yPIPBox_3 | 571 | 582 | PF02747 | 0.335 |
LIG_Pex14_1 | 589 | 593 | PF04695 | 0.321 |
LIG_REV1ctd_RIR_1 | 182 | 189 | PF16727 | 0.468 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.571 |
LIG_SH2_CRK | 608 | 612 | PF00017 | 0.297 |
LIG_SH2_PTP2 | 152 | 155 | PF00017 | 0.547 |
LIG_SH2_PTP2 | 290 | 293 | PF00017 | 0.418 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.446 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.418 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 684 | 688 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.313 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.479 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.440 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.379 |
LIG_SH3_4 | 671 | 678 | PF00018 | 0.321 |
LIG_SUMO_SIM_anti_2 | 220 | 227 | PF11976 | 0.498 |
LIG_SUMO_SIM_anti_2 | 342 | 348 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 622 | 627 | PF11976 | 0.321 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.515 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.520 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.520 |
LIG_TRAF2_1 | 596 | 599 | PF00917 | 0.388 |
LIG_TYR_ITIM | 618 | 623 | PF00017 | 0.340 |
LIG_UBA3_1 | 260 | 265 | PF00899 | 0.520 |
LIG_UBA3_1 | 299 | 306 | PF00899 | 0.496 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.554 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.487 |
MOD_CDC14_SPxK_1 | 479 | 482 | PF00782 | 0.374 |
MOD_CDK_SPxK_1 | 476 | 482 | PF00069 | 0.374 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.546 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.479 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.486 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.328 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.520 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.473 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.498 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.540 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.460 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.571 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.389 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.338 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.306 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.338 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.450 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.426 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.527 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.521 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.524 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.477 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.451 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.403 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.358 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.402 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.241 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.329 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.268 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.520 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.293 |
MOD_N-GLC_2 | 253 | 255 | PF02516 | 0.288 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.501 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.524 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.543 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.482 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.359 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.312 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.329 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.329 |
MOD_NEK2_2 | 412 | 417 | PF00069 | 0.572 |
MOD_NEK2_2 | 636 | 641 | PF00069 | 0.340 |
MOD_PK_1 | 312 | 318 | PF00069 | 0.497 |
MOD_PKA_1 | 452 | 458 | PF00069 | 0.486 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.432 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.508 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.460 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.367 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.493 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.427 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.504 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.471 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.461 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.494 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.414 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.396 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.488 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.408 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.345 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.321 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.321 |
MOD_SUMO_rev_2 | 271 | 276 | PF00179 | 0.578 |
MOD_SUMO_rev_2 | 30 | 40 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 319 | 326 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 350 | 355 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_2 | 35 | 41 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 684 | 687 | PF00928 | 0.305 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.338 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J4 | Leptomonas seymouri | 26% | 95% |
A0A0N0P803 | Leptomonas seymouri | 78% | 100% |
A0A0N1PDP3 | Leptomonas seymouri | 21% | 80% |
A0A0S4IIS9 | Bodo saltans | 59% | 100% |
A0A1X0NKN5 | Trypanosomatidae | 24% | 76% |
A0A1X0NLB6 | Trypanosomatidae | 62% | 100% |
A0A3Q8IGZ3 | Leishmania donovani | 25% | 95% |
A0A3Q8IJI4 | Leishmania donovani | 100% | 100% |
A0A3S5H5P5 | Leishmania donovani | 22% | 77% |
A0A422N761 | Trypanosoma rangeli | 24% | 98% |
A4H4J9 | Leishmania braziliensis | 21% | 100% |
A4H5Q8 | Leishmania braziliensis | 24% | 100% |
A4HQJ7 | Leishmania braziliensis | 82% | 100% |
A4HSS5 | Leishmania infantum | 22% | 77% |
A4HTZ8 | Leishmania infantum | 25% | 100% |
C9ZTC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 21% | 77% |
D0A3P6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E2JFG1 | Amanita bisporigera | 39% | 92% |
E2JFG2 | Amanita bisporigera | 37% | 95% |
E9AKR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AUB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
H2E7Q7 | Galerina marginata (strain CBS 339.88) | 37% | 94% |
H2E7Q8 | Galerina marginata (strain CBS 339.88) | 36% | 95% |
O07834 | Pseudoxanthomonas mexicana | 28% | 96% |
O70196 | Rattus norvegicus | 43% | 98% |
P23687 | Sus scrofa | 44% | 98% |
P24555 | Escherichia coli (strain K12) | 25% | 100% |
P27028 | Elizabethkingia meningoseptica | 37% | 99% |
P27195 | Elizabethkingia miricola | 37% | 99% |
P48147 | Homo sapiens | 44% | 98% |
P55627 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 22% | 92% |
P55656 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 22% | 99% |
Q06903 | Aeromonas hydrophila | 38% | 100% |
Q4Q080 | Leishmania major | 96% | 100% |
Q4QHU7 | Leishmania major | 25% | 100% |
Q4QJ45 | Leishmania major | 22% | 100% |
Q59536 | Moraxella lacunata | 25% | 100% |
Q86AS5 | Dictyostelium discoideum | 36% | 92% |
Q9QUR6 | Mus musculus | 44% | 98% |
Q9XTA2 | Bos taurus | 43% | 98% |
V5B5S3 | Trypanosoma cruzi | 24% | 81% |
V5B860 | Trypanosoma cruzi | 25% | 97% |
V5BM62 | Trypanosoma cruzi | 65% | 100% |