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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q381
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 2 |
GO:0006066 | alcohol metabolic process | 3 | 2 |
GO:0006629 | lipid metabolic process | 3 | 8 |
GO:0006644 | phospholipid metabolic process | 4 | 8 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 8 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016311 | dephosphorylation | 5 | 8 |
GO:0019637 | organophosphate metabolic process | 3 | 8 |
GO:0019751 | polyol metabolic process | 4 | 2 |
GO:0030258 | lipid modification | 4 | 8 |
GO:0043647 | inositol phosphate metabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044255 | cellular lipid metabolic process | 3 | 8 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0044282 | small molecule catabolic process | 3 | 2 |
GO:0046164 | alcohol catabolic process | 4 | 2 |
GO:0046174 | polyol catabolic process | 5 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 8 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 8 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 2 |
GO:0046839 | phospholipid dephosphorylation | 5 | 8 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 2 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 8 |
GO:0071545 | inositol phosphate catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 2 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004439 | phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | 8 | 2 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0034593 | phosphatidylinositol bisphosphate phosphatase activity | 7 | 2 |
GO:0034595 | phosphatidylinositol phosphate 5-phosphatase activity | 7 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
GO:0052866 | phosphatidylinositol phosphate phosphatase activity | 6 | 2 |
GO:0106019 | phosphatidylinositol-4,5-bisphosphate phosphatase activity | 8 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.395 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.808 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 689 | 691 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.692 |
CLV_PCSK_FUR_1 | 533 | 537 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 679 | 681 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 689 | 691 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 61 | 63 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 679 | 681 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.792 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.720 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.615 |
DEG_APCC_DBOX_1 | 129 | 137 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 634 | 642 | PF00400 | 0.448 |
DEG_Kelch_Keap1_1 | 697 | 702 | PF01344 | 0.558 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.774 |
DEG_SPOP_SBC_1 | 620 | 624 | PF00917 | 0.598 |
DOC_CYCLIN_RxL_1 | 632 | 640 | PF00134 | 0.447 |
DOC_CYCLIN_RxL_1 | 689 | 699 | PF00134 | 0.555 |
DOC_CYCLIN_RxL_1 | 81 | 92 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 141 | 147 | PF00134 | 0.443 |
DOC_MAPK_gen_1 | 305 | 312 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 44 | 53 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 734 | 744 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.541 |
DOC_MAPK_HePTP_8 | 345 | 357 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 25 | 33 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 81 | 90 | PF00069 | 0.506 |
DOC_MIT_MIM_1 | 465 | 473 | PF04212 | 0.355 |
DOC_PP1_RVXF_1 | 386 | 393 | PF00149 | 0.366 |
DOC_PP1_RVXF_1 | 541 | 547 | PF00149 | 0.319 |
DOC_PP2B_LxvP_1 | 141 | 144 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 584 | 587 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 704 | 707 | PF13499 | 0.589 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.385 |
DOC_PP4_FxxP_1 | 573 | 576 | PF00568 | 0.602 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.596 |
DOC_SPAK_OSR1_1 | 739 | 743 | PF12202 | 0.399 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.391 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 128 | 137 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 228 | 236 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 333 | 337 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 432 | 437 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 616 | 625 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 729 | 736 | PF00244 | 0.338 |
LIG_AP2alpha_1 | 257 | 261 | PF02296 | 0.362 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.364 |
LIG_BRCT_BRCA1_1 | 569 | 573 | PF00533 | 0.626 |
LIG_Clathr_ClatBox_1 | 87 | 91 | PF01394 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 247 | 257 | PF00928 | 0.406 |
LIG_deltaCOP1_diTrp_1 | 511 | 516 | PF00928 | 0.404 |
LIG_deltaCOP1_diTrp_1 | 537 | 546 | PF00928 | 0.317 |
LIG_eIF4E_1 | 358 | 364 | PF01652 | 0.330 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.316 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.399 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.445 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.381 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.530 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.527 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.454 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.540 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.463 |
LIG_FHA_2 | 555 | 561 | PF00498 | 0.587 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.593 |
LIG_HCF-1_HBM_1 | 456 | 459 | PF13415 | 0.395 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.372 |
LIG_LIR_Apic_2 | 570 | 576 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 656 | 662 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 247 | 258 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 428 | 436 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 486 | 491 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 511 | 520 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 593 | 602 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 721 | 728 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 39 | 43 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 486 | 490 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 504 | 509 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 708 | 713 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 721 | 725 | PF02991 | 0.283 |
LIG_Pex14_1 | 36 | 40 | PF04695 | 0.282 |
LIG_Pex14_1 | 430 | 434 | PF04695 | 0.507 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.362 |
LIG_Pex14_2 | 441 | 445 | PF04695 | 0.562 |
LIG_Pex14_2 | 509 | 513 | PF04695 | 0.405 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.336 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.379 |
LIG_SH2_CRK | 722 | 726 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 487 | 490 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 722 | 726 | PF00017 | 0.382 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.379 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.720 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.578 |
LIG_SUMO_SIM_par_1 | 261 | 267 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 27 | 32 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 743 | 748 | PF11976 | 0.437 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.305 |
LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.588 |
LIG_TRAF2_1 | 598 | 601 | PF00917 | 0.569 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.338 |
LIG_TYR_ITIM | 720 | 725 | PF00017 | 0.365 |
LIG_UBA3_1 | 317 | 324 | PF00899 | 0.375 |
LIG_WRC_WIRS_1 | 37 | 42 | PF05994 | 0.282 |
LIG_WRC_WIRS_1 | 405 | 410 | PF05994 | 0.436 |
LIG_WRC_WIRS_1 | 433 | 438 | PF05994 | 0.548 |
LIG_WW_1 | 159 | 162 | PF00397 | 0.464 |
LIG_WW_1 | 517 | 520 | PF00397 | 0.326 |
MOD_CDC14_SPxK_1 | 225 | 228 | PF00782 | 0.541 |
MOD_CDK_SPK_2 | 222 | 227 | PF00069 | 0.550 |
MOD_CDK_SPxK_1 | 222 | 228 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 472 | 479 | PF00069 | 0.468 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.563 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.547 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.395 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.457 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.586 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.575 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.502 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.589 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.547 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.529 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.292 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.444 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.395 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.477 |
MOD_CK2_1 | 554 | 560 | PF00069 | 0.577 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.575 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.593 |
MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.551 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.732 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.815 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.563 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.644 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.691 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.768 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.588 |
MOD_GlcNHglycan | 560 | 565 | PF01048 | 0.826 |
MOD_GlcNHglycan | 568 | 572 | PF01048 | 0.788 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.774 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.707 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.757 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.747 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.793 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.596 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.550 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.519 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.478 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.348 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.474 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.538 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.456 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.520 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.364 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.570 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.590 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.478 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.450 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.412 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.493 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.731 |
MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.712 |
MOD_N-GLC_2 | 148 | 150 | PF02516 | 0.616 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.769 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.548 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.363 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.465 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.470 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.352 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.410 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.327 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.473 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.398 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.583 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.365 |
MOD_NEK2_2 | 115 | 120 | PF00069 | 0.499 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.535 |
MOD_NEK2_2 | 664 | 669 | PF00069 | 0.444 |
MOD_NEK2_2 | 724 | 729 | PF00069 | 0.455 |
MOD_OFUCOSY | 661 | 668 | PF10250 | 0.646 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.443 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.576 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.571 |
MOD_PKA_1 | 227 | 233 | PF00069 | 0.505 |
MOD_PKA_1 | 377 | 383 | PF00069 | 0.419 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.540 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.454 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.335 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.336 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.454 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.510 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.396 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.341 |
MOD_PKB_1 | 209 | 217 | PF00069 | 0.606 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.451 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.395 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.539 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.520 |
MOD_Plk_1 | 633 | 639 | PF00069 | 0.560 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.535 |
MOD_Plk_1 | 720 | 726 | PF00069 | 0.370 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.447 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.474 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.332 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.491 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.580 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.528 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.523 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.470 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.527 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 178 | 188 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 249 | 258 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 298 | 307 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 598 | 607 | PF00179 | 0.577 |
TRG_DiLeu_BaEn_1 | 486 | 491 | PF01217 | 0.355 |
TRG_DiLeu_BaEn_1 | 495 | 500 | PF01217 | 0.341 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 83 | 88 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 722 | 725 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 59 | 62 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 736 | 739 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.505 |
TRG_ER_FFAT_2 | 439 | 451 | PF00635 | 0.548 |
TRG_Pf-PMV_PEXEL_1 | 452 | 456 | PF00026 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 547 | 552 | PF00026 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 635 | 640 | PF00026 | 0.791 |
TRG_Pf-PMV_PEXEL_1 | 692 | 696 | PF00026 | 0.756 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDQ6 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IFD8 | Leishmania donovani | 94% | 100% |
A0A422NU02 | Trypanosoma rangeli | 36% | 99% |
A4I9T4 | Leishmania infantum | 94% | 100% |
E9B4U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5B3B9 | Trypanosoma cruzi | 38% | 100% |