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. | yes | yes: 9 |
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 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A0A3S5H5B0
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0018345 | protein palmitoylation | 6 | 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:0043543 | protein acylation | 5 | 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 | 8 |
GO:0008374 | O-acyltransferase activity | 5 | 2 |
GO:0016409 | palmitoyltransferase activity | 5 | 8 |
GO:0016416 | O-palmitoyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
GO:0047965 | glycoprotein O-fatty-acyltransferase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
GO:0140103 | catalytic activity, acting on a glycoprotein | 3 | 2 |
GO:0016417 | S-acyltransferase activity | 5 | 1 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 1 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 882 | 886 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 1020 | 1022 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 680 | 682 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 727 | 729 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 1020 | 1022 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 556 | 562 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.178 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 809 | 813 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 847 | 851 | PF00082 | 0.406 |
CLV_Separin_Metazoa | 1009 | 1013 | PF03568 | 0.570 |
CLV_Separin_Metazoa | 229 | 233 | PF03568 | 0.476 |
DEG_APCC_DBOX_1 | 1052 | 1060 | PF00400 | 0.587 |
DEG_APCC_DBOX_1 | 654 | 662 | PF00400 | 0.614 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.602 |
DEG_SPOP_SBC_1 | 146 | 150 | PF00917 | 0.629 |
DEG_SPOP_SBC_1 | 913 | 917 | PF00917 | 0.685 |
DOC_ANK_TNKS_1 | 312 | 319 | PF00023 | 0.620 |
DOC_CYCLIN_RxL_1 | 402 | 409 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 474 | 484 | PF00134 | 0.579 |
DOC_CYCLIN_RxL_1 | 652 | 662 | PF00134 | 0.645 |
DOC_CYCLIN_RxL_1 | 805 | 817 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.585 |
DOC_CYCLIN_yCln2_LP_2 | 610 | 616 | PF00134 | 0.258 |
DOC_MAPK_gen_1 | 1020 | 1026 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 494 | 504 | PF00069 | 0.605 |
DOC_MAPK_MEF2A_6 | 157 | 164 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 443 | 450 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 497 | 504 | PF00069 | 0.620 |
DOC_MAPK_MEF2A_6 | 506 | 515 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 535 | 543 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 703 | 712 | PF00069 | 0.351 |
DOC_MAPK_NFAT4_5 | 703 | 711 | PF00069 | 0.313 |
DOC_PP1_RVXF_1 | 807 | 814 | PF00149 | 0.457 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.661 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.585 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.266 |
DOC_PP2B_LxvP_1 | 940 | 943 | PF13499 | 0.695 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 747 | 751 | PF00917 | 0.216 |
DOC_USP7_MATH_1 | 951 | 955 | PF00917 | 0.679 |
DOC_USP7_UBL2_3 | 439 | 443 | PF12436 | 0.649 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 728 | 734 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 779 | 785 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 809 | 814 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 833 | 838 | PF00244 | 0.623 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.678 |
LIG_APCC_ABBA_1 | 1004 | 1009 | PF00400 | 0.607 |
LIG_BIR_III_4 | 211 | 215 | PF00653 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 569 | 576 | PF00928 | 0.291 |
LIG_eIF4E_1 | 261 | 267 | PF01652 | 0.538 |
LIG_eIF4E_1 | 441 | 447 | PF01652 | 0.647 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.709 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.351 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.326 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.565 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.272 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.184 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.671 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.661 |
LIG_FHA_2 | 1035 | 1041 | PF00498 | 0.648 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.583 |
LIG_FHA_2 | 631 | 637 | PF00498 | 0.654 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.623 |
LIG_FHA_2 | 810 | 816 | PF00498 | 0.457 |
LIG_FHA_2 | 880 | 886 | PF00498 | 0.688 |
LIG_GBD_Chelix_1 | 1002 | 1010 | PF00786 | 0.385 |
LIG_GBD_Chelix_1 | 796 | 804 | PF00786 | 0.313 |
LIG_IBAR_NPY_1 | 866 | 868 | PF08397 | 0.660 |
LIG_LIR_Apic_2 | 607 | 612 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 783 | 792 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 832 | 842 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 687 | 692 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 725 | 729 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 775 | 780 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 783 | 787 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 812 | 816 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 832 | 838 | PF02991 | 0.561 |
LIG_LYPXL_SIV_4 | 223 | 231 | PF13949 | 0.564 |
LIG_LYPXL_yS_3 | 224 | 227 | PF13949 | 0.568 |
LIG_PCNA_yPIPBox_3 | 157 | 165 | PF02747 | 0.574 |
LIG_PCNA_yPIPBox_3 | 191 | 200 | PF02747 | 0.472 |
LIG_PCNA_yPIPBox_3 | 703 | 716 | PF02747 | 0.324 |
LIG_Pex14_1 | 572 | 576 | PF04695 | 0.340 |
LIG_Rb_pABgroove_1 | 832 | 840 | PF01858 | 0.643 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.567 |
LIG_SH2_CRK | 643 | 647 | PF00017 | 0.601 |
LIG_SH2_CRK | 726 | 730 | PF00017 | 0.272 |
LIG_SH2_CRK | 784 | 788 | PF00017 | 0.351 |
LIG_SH2_CRK | 860 | 864 | PF00017 | 0.668 |
LIG_SH2_GRB2like | 692 | 695 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 483 | 487 | PF00017 | 0.561 |
LIG_SH2_PTP2 | 551 | 554 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 623 | 626 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.578 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 653 | 657 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 659 | 663 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 722 | 726 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 784 | 788 | PF00017 | 0.351 |
LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.680 |
LIG_SH2_STAT3 | 591 | 594 | PF00017 | 0.421 |
LIG_SH2_STAT3 | 675 | 678 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 868 | 871 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 1055 | 1058 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 826 | 829 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 868 | 871 | PF00017 | 0.663 |
LIG_SH3_2 | 302 | 307 | PF14604 | 0.687 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.568 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.674 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.651 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.603 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.457 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.357 |
LIG_SUMO_SIM_anti_2 | 1022 | 1028 | PF11976 | 0.589 |
LIG_SUMO_SIM_anti_2 | 40 | 46 | PF11976 | 0.618 |
LIG_SUMO_SIM_anti_2 | 400 | 405 | PF11976 | 0.500 |
LIG_SUMO_SIM_anti_2 | 444 | 450 | PF11976 | 0.629 |
LIG_SUMO_SIM_anti_2 | 512 | 519 | PF11976 | 0.457 |
LIG_SUMO_SIM_anti_2 | 95 | 100 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 512 | 519 | PF11976 | 0.457 |
LIG_TRAF2_1 | 1037 | 1040 | PF00917 | 0.656 |
LIG_TRAF2_1 | 967 | 970 | PF00917 | 0.706 |
LIG_TRFH_1 | 19 | 23 | PF08558 | 0.606 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.452 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.429 |
LIG_WRC_WIRS_1 | 595 | 600 | PF05994 | 0.533 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.471 |
MOD_CDC14_SPxK_1 | 472 | 475 | PF00782 | 0.497 |
MOD_CDK_SPxK_1 | 469 | 475 | PF00069 | 0.517 |
MOD_CK1_1 | 1013 | 1019 | PF00069 | 0.531 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.656 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.651 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.380 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.468 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.523 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.468 |
MOD_CK1_1 | 853 | 859 | PF00069 | 0.589 |
MOD_CK2_1 | 1034 | 1040 | PF00069 | 0.578 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.505 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.571 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.649 |
MOD_CK2_1 | 816 | 822 | PF00069 | 0.576 |
MOD_CK2_1 | 972 | 978 | PF00069 | 0.729 |
MOD_Cter_Amidation | 1018 | 1021 | PF01082 | 0.465 |
MOD_GlcNHglycan | 1012 | 1015 | PF01048 | 0.421 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.723 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.730 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.617 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.721 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.632 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.481 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.328 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.506 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.650 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.503 |
MOD_GlcNHglycan | 739 | 742 | PF01048 | 0.339 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.455 |
MOD_GlcNHglycan | 901 | 904 | PF01048 | 0.635 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.646 |
MOD_GlcNHglycan | 953 | 956 | PF01048 | 0.653 |
MOD_GlcNHglycan | 972 | 975 | PF01048 | 0.579 |
MOD_GlcNHglycan | 998 | 1002 | PF01048 | 0.591 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.663 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.433 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.724 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.643 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.589 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.442 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.586 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.465 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.655 |
MOD_GSK3_1 | 829 | 836 | PF00069 | 0.471 |
MOD_GSK3_1 | 914 | 921 | PF00069 | 0.618 |
MOD_LATS_1 | 35 | 41 | PF00433 | 0.514 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.606 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.644 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.544 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.498 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.520 |
MOD_N-GLC_1 | 809 | 814 | PF02516 | 0.351 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.541 |
MOD_NEK2_1 | 1010 | 1015 | PF00069 | 0.522 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.442 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.313 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.352 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.574 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.551 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.719 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.351 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.348 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.489 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.362 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.392 |
MOD_NEK2_1 | 772 | 777 | PF00069 | 0.400 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.426 |
MOD_NEK2_1 | 850 | 855 | PF00069 | 0.528 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.619 |
MOD_PIKK_1 | 1034 | 1040 | PF00454 | 0.578 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.471 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.351 |
MOD_PIKK_1 | 799 | 805 | PF00454 | 0.351 |
MOD_PIKK_1 | 853 | 859 | PF00454 | 0.595 |
MOD_PIKK_1 | 972 | 978 | PF00454 | 0.698 |
MOD_PK_1 | 37 | 43 | PF00069 | 0.583 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.576 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.700 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.491 |
MOD_PKA_2 | 737 | 743 | PF00069 | 0.313 |
MOD_PKA_2 | 970 | 976 | PF00069 | 0.578 |
MOD_PKB_1 | 559 | 567 | PF00069 | 0.586 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.628 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.236 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.534 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.481 |
MOD_Plk_1 | 809 | 815 | PF00069 | 0.351 |
MOD_Plk_1 | 820 | 826 | PF00069 | 0.580 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.491 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.600 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.300 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.428 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.348 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.186 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.347 |
MOD_Plk_4 | 821 | 827 | PF00069 | 0.494 |
MOD_Plk_4 | 833 | 839 | PF00069 | 0.448 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.292 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.692 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.647 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.292 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.441 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.490 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.531 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.490 |
TRG_DiLeu_BaEn_1 | 725 | 730 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.588 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 726 | 729 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 784 | 787 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 835 | 838 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 559 | 561 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 679 | 681 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 726 | 728 | PF00400 | 0.313 |
TRG_ER_diArg_1 | 777 | 779 | PF00400 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 465 | 470 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 762 | 766 | PF00026 | 0.258 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9Z8 | Leptomonas seymouri | 50% | 100% |
A0A1X0NKY1 | Trypanosomatidae | 30% | 100% |
A4H3X2 | Leishmania braziliensis | 68% | 96% |
A4HS47 | Leishmania infantum | 100% | 100% |
E9AK34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 98% |
O97203 | Leishmania major | 90% | 100% |