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: A0A3S7X1Q1
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 | 0.546 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.441 |
CLV_PCSK_FUR_1 | 680 | 684 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 55 | 57 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.562 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.623 |
DEG_SIAH_1 | 270 | 278 | PF03145 | 0.567 |
DOC_CKS1_1 | 376 | 381 | PF01111 | 0.541 |
DOC_CKS1_1 | 557 | 562 | PF01111 | 0.545 |
DOC_CYCLIN_RxL_1 | 609 | 621 | PF00134 | 0.457 |
DOC_MAPK_MEF2A_6 | 145 | 152 | PF00069 | 0.551 |
DOC_MAPK_NFAT4_5 | 145 | 153 | PF00069 | 0.610 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.541 |
DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.606 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 156 | 163 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 571 | 576 | PF00244 | 0.489 |
LIG_APCC_ABBA_1 | 314 | 319 | PF00400 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 109 | 116 | PF00928 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 194 | 200 | PF00928 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 294 | 299 | PF00928 | 0.516 |
LIG_EH1_1 | 459 | 467 | PF00400 | 0.614 |
LIG_eIF4E_1 | 460 | 466 | PF01652 | 0.614 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.577 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.614 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.533 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.539 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.427 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.622 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.524 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.606 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.557 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.463 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.548 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.556 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.562 |
LIG_FHA_2 | 603 | 609 | PF00498 | 0.457 |
LIG_GBD_Chelix_1 | 349 | 357 | PF00786 | 0.254 |
LIG_HCF-1_HBM_1 | 16 | 19 | PF13415 | 0.535 |
LIG_HCF-1_HBM_1 | 41 | 44 | PF13415 | 0.610 |
LIG_LIR_Apic_2 | 531 | 537 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 572 | 579 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 653 | 663 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 386 | 392 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 490 | 496 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 580 | 585 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 653 | 659 | PF02991 | 0.442 |
LIG_LYPXL_yS_3 | 44 | 47 | PF13949 | 0.614 |
LIG_MYND_1 | 537 | 541 | PF01753 | 0.510 |
LIG_NRBOX | 253 | 259 | PF00104 | 0.614 |
LIG_PDZ_Class_3 | 681 | 686 | PF00595 | 0.482 |
LIG_Pex14_1 | 246 | 250 | PF04695 | 0.533 |
LIG_Pex14_1 | 272 | 276 | PF04695 | 0.533 |
LIG_Pex14_2 | 673 | 677 | PF04695 | 0.477 |
LIG_PTB_Apo_2 | 167 | 174 | PF02174 | 0.533 |
LIG_PTB_Apo_2 | 249 | 256 | PF02174 | 0.533 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.533 |
LIG_SH2_CRK | 496 | 500 | PF00017 | 0.614 |
LIG_SH2_GRB2like | 250 | 253 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 233 | 237 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 412 | 416 | PF00017 | 0.614 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.529 |
LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.611 |
LIG_SH2_SRC | 575 | 578 | PF00017 | 0.493 |
LIG_SH2_SRC | 656 | 659 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 656 | 659 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.533 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.605 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.518 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.437 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.584 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 102 | 109 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.614 |
LIG_SUMO_SIM_par_1 | 371 | 378 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 522 | 528 | PF11976 | 0.579 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.614 |
LIG_TYR_ITIM | 573 | 578 | PF00017 | 0.492 |
LIG_UBA3_1 | 254 | 262 | PF00899 | 0.390 |
LIG_UBA3_1 | 358 | 364 | PF00899 | 0.338 |
LIG_UBA3_1 | 47 | 55 | PF00899 | 0.376 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.562 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.386 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.359 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.430 |
MOD_CK2_1 | 548 | 554 | PF00069 | 0.600 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.597 |
MOD_CK2_1 | 602 | 608 | PF00069 | 0.464 |
MOD_CMANNOS | 296 | 299 | PF00535 | 0.411 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.413 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.487 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.628 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.472 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.439 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.462 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.349 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.390 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.390 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.517 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.578 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.506 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.489 |
MOD_N-GLC_1 | 644 | 649 | PF02516 | 0.546 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.388 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.485 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.543 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.491 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.451 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.444 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.554 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.547 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.578 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.380 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.379 |
MOD_PKB_1 | 54 | 62 | PF00069 | 0.376 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.489 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.499 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.492 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.462 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.504 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.559 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.552 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.479 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.489 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.496 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.539 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.514 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.396 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.376 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.501 |
MOD_SUMO_for_1 | 97 | 100 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_1 | 87 | 92 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 656 | 659 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 679 | 682 | PF00400 | 0.454 |
TRG_NLS_MonoExtN_4 | 52 | 58 | PF00514 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I036 | Leptomonas seymouri | 80% | 100% |
A0A1X0NRA9 | Trypanosomatidae | 55% | 100% |
A0A422N0C2 | Trypanosoma rangeli | 56% | 100% |
A4I3S2 | Leishmania infantum | 100% | 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 | 56% | 100% |