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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 8 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A0A3Q8IBS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 9 |
GO:0006505 | GPI anchor metabolic process | 6 | 9 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 9 |
GO:0006629 | lipid metabolic process | 3 | 9 |
GO:0006643 | membrane lipid metabolic process | 4 | 9 |
GO:0006644 | phospholipid metabolic process | 4 | 9 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 9 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 9 |
GO:0006664 | glycolipid metabolic process | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008610 | lipid biosynthetic process | 4 | 9 |
GO:0008654 | phospholipid biosynthetic process | 5 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009247 | glycolipid biosynthetic process | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0019637 | organophosphate metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0044255 | cellular lipid metabolic process | 3 | 9 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 9 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 9 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 9 |
GO:0046486 | glycerolipid metabolic process | 4 | 9 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090407 | organophosphate biosynthetic process | 4 | 9 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 9 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
GO:1903509 | liposaccharide metabolic process | 4 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016780 | phosphotransferase activity, for other substituted phosphate groups | 4 | 8 |
GO:0051377 | mannose-ethanolamine phosphotransferase activity | 5 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.353 |
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 869 | 873 | PF00656 | 0.721 |
CLV_MEL_PAP_1 | 560 | 566 | PF00089 | 0.326 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 728 | 730 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 571 | 573 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 728 | 730 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 193 | 195 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 189 | 195 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 940 | 944 | PF00082 | 0.391 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.390 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.421 |
DEG_SPOP_SBC_1 | 720 | 724 | PF00917 | 0.544 |
DOC_CKS1_1 | 184 | 189 | PF01111 | 0.464 |
DOC_CYCLIN_RxL_1 | 937 | 944 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 403 | 409 | PF00134 | 0.354 |
DOC_CYCLIN_yCln2_LP_2 | 625 | 631 | PF00134 | 0.655 |
DOC_CYCLIN_yCln2_LP_2 | 652 | 658 | PF00134 | 0.682 |
DOC_CYCLIN_yCln2_LP_2 | 845 | 851 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 189 | 198 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 442 | 451 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 659 | 667 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 414 | 421 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 522 | 530 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 611 | 618 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 659 | 667 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 762 | 771 | PF00069 | 0.503 |
DOC_MAPK_NFAT4_5 | 611 | 619 | PF00069 | 0.694 |
DOC_PP1_RVXF_1 | 938 | 944 | PF00149 | 0.325 |
DOC_PP1_SILK_1 | 161 | 166 | PF00149 | 0.386 |
DOC_PP2B_LxvP_1 | 625 | 628 | PF13499 | 0.661 |
DOC_PP2B_LxvP_1 | 652 | 655 | PF13499 | 0.674 |
DOC_PP2B_LxvP_1 | 845 | 848 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 891 | 894 | PF13499 | 0.710 |
DOC_PP2B_PxIxI_1 | 459 | 465 | PF00149 | 0.478 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 720 | 724 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 898 | 902 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 973 | 977 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 112 | 122 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 292 | 297 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 38 | 44 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 386 | 392 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 459 | 465 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 476 | 485 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 522 | 530 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 531 | 536 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 595 | 602 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 733 | 738 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 880 | 889 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 897 | 906 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 268 | 285 | PF00022 | 0.325 |
LIG_BIR_III_4 | 88 | 92 | PF00653 | 0.535 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.560 |
LIG_BRCT_BRCA1_1 | 837 | 841 | PF00533 | 0.417 |
LIG_Clathr_ClatBox_1 | 58 | 62 | PF01394 | 0.335 |
LIG_Clathr_ClatBox_1 | 782 | 786 | PF01394 | 0.625 |
LIG_CSL_BTD_1 | 502 | 505 | PF09270 | 0.564 |
LIG_deltaCOP1_diTrp_1 | 176 | 183 | PF00928 | 0.359 |
LIG_EH_1 | 267 | 271 | PF12763 | 0.360 |
LIG_eIF4E_1 | 19 | 25 | PF01652 | 0.491 |
LIG_eIF4E_1 | 830 | 836 | PF01652 | 0.397 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.386 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.435 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.295 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.353 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.302 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.399 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.391 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.395 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.670 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.668 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.630 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.438 |
LIG_FHA_1 | 788 | 794 | PF00498 | 0.491 |
LIG_FHA_1 | 886 | 892 | PF00498 | 0.746 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.397 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.441 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.706 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.511 |
LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 176 | 187 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 367 | 378 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 744 | 753 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 798 | 805 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 838 | 849 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 907 | 915 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 612 | 618 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 744 | 749 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 798 | 803 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 838 | 844 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 907 | 912 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 920 | 925 | PF02991 | 0.289 |
LIG_NRBOX | 525 | 531 | PF00104 | 0.457 |
LIG_NRBOX | 551 | 557 | PF00104 | 0.450 |
LIG_NRBOX | 778 | 784 | PF00104 | 0.485 |
LIG_Pex14_1 | 179 | 183 | PF04695 | 0.365 |
LIG_Pex14_1 | 672 | 676 | PF04695 | 0.613 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.397 |
LIG_Pex14_2 | 536 | 540 | PF04695 | 0.577 |
LIG_Pex14_2 | 800 | 804 | PF04695 | 0.430 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.397 |
LIG_SH2_CRK | 696 | 700 | PF00017 | 0.561 |
LIG_SH2_CRK | 746 | 750 | PF00017 | 0.394 |
LIG_SH2_CRK | 909 | 913 | PF00017 | 0.491 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.437 |
LIG_SH2_GRB2like | 409 | 412 | PF00017 | 0.420 |
LIG_SH2_PTP2 | 911 | 914 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 746 | 750 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 909 | 913 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 748 | 751 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 909 | 912 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 925 | 928 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.397 |
LIG_SH3_1 | 181 | 187 | PF00018 | 0.444 |
LIG_SH3_1 | 575 | 581 | PF00018 | 0.612 |
LIG_SH3_2 | 184 | 189 | PF14604 | 0.464 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.444 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.360 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.708 |
LIG_SH3_3 | 886 | 892 | PF00018 | 0.708 |
LIG_SH3_3 | 933 | 939 | PF00018 | 0.394 |
LIG_SH3_3 | 966 | 972 | PF00018 | 0.725 |
LIG_SH3_CIN85_PxpxPR_1 | 892 | 897 | PF14604 | 0.598 |
LIG_Sin3_3 | 843 | 850 | PF02671 | 0.388 |
LIG_SUMO_SIM_anti_2 | 298 | 305 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 398 | 403 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 418 | 423 | PF11976 | 0.380 |
LIG_SUMO_SIM_anti_2 | 524 | 530 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 54 | 60 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 298 | 305 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 56 | 62 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 683 | 688 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 904 | 910 | PF11976 | 0.386 |
LIG_SUMO_SIM_par_1 | 944 | 951 | PF11976 | 0.438 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.409 |
LIG_TRAF2_1 | 875 | 878 | PF00917 | 0.803 |
LIG_TRFH_1 | 844 | 848 | PF08558 | 0.391 |
LIG_TYR_ITSM | 905 | 912 | PF00017 | 0.388 |
LIG_WRC_WIRS_1 | 198 | 203 | PF05994 | 0.360 |
MOD_CDK_SPxK_1 | 183 | 189 | PF00069 | 0.455 |
MOD_CDK_SPxxK_3 | 183 | 190 | PF00069 | 0.454 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.352 |
MOD_CDK_SPxxK_3 | 501 | 508 | PF00069 | 0.557 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.397 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.339 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.389 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.317 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.418 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.426 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.438 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.632 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.610 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.461 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.499 |
MOD_CK1_1 | 885 | 891 | PF00069 | 0.745 |
MOD_CK1_1 | 917 | 923 | PF00069 | 0.500 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.324 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.397 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.405 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.376 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.499 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.613 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.592 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.525 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.630 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.639 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.665 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.621 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.547 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.492 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.422 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.427 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.494 |
MOD_GlcNHglycan | 797 | 800 | PF01048 | 0.429 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.460 |
MOD_GlcNHglycan | 900 | 903 | PF01048 | 0.470 |
MOD_GlcNHglycan | 916 | 919 | PF01048 | 0.312 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.401 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.295 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.470 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.429 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.293 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.399 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.388 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.387 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.420 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.746 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.666 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.743 |
MOD_GSK3_1 | 771 | 778 | PF00069 | 0.450 |
MOD_GSK3_1 | 811 | 818 | PF00069 | 0.395 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.775 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.565 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.501 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.613 |
MOD_N-GLC_1 | 866 | 871 | PF02516 | 0.409 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.365 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.363 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.294 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.376 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.453 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.384 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.420 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.488 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.357 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.339 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.359 |
MOD_NEK2_1 | 753 | 758 | PF00069 | 0.392 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.417 |
MOD_NEK2_1 | 771 | 776 | PF00069 | 0.391 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.429 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.417 |
MOD_NEK2_1 | 914 | 919 | PF00069 | 0.501 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.393 |
MOD_NEK2_2 | 610 | 615 | PF00069 | 0.628 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.403 |
MOD_PIKK_1 | 787 | 793 | PF00454 | 0.525 |
MOD_PK_1 | 115 | 121 | PF00069 | 0.392 |
MOD_PK_1 | 531 | 537 | PF00069 | 0.426 |
MOD_PKA_1 | 571 | 577 | PF00069 | 0.708 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.459 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.350 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.301 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.379 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.682 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.414 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.603 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.686 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.759 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.610 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.618 |
MOD_PKA_2 | 732 | 738 | PF00069 | 0.715 |
MOD_PKB_1 | 290 | 298 | PF00069 | 0.397 |
MOD_PKB_1 | 731 | 739 | PF00069 | 0.670 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.384 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.374 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.403 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.330 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.375 |
MOD_Plk_1 | 866 | 872 | PF00069 | 0.612 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.341 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.379 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.368 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.403 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.354 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.342 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.330 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.369 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.403 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.326 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.307 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.693 |
MOD_Plk_4 | 681 | 687 | PF00069 | 0.606 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.721 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.491 |
MOD_Plk_4 | 817 | 823 | PF00069 | 0.384 |
MOD_Plk_4 | 907 | 913 | PF00069 | 0.402 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.455 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.373 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.475 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.554 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.687 |
MOD_SUMO_rev_2 | 446 | 452 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 547 | 552 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_2 | 320 | 326 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 703 | 708 | PF01217 | 0.622 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.674 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 909 | 912 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 571 | 573 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 728 | 731 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 287 | 291 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEK1 | Leptomonas seymouri | 61% | 100% |
A0A1X0NIL0 | Trypanosomatidae | 38% | 100% |
A0A3R7MBN8 | Trypanosoma rangeli | 33% | 100% |
A4HD90 | Leishmania braziliensis | 79% | 100% |
E9AH45 | Leishmania infantum | 99% | 100% |
E9AWM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAU7 | Leishmania major | 92% | 100% |