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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4H3X2
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 | 9 |
GO:0016409 | palmitoyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0008374 | O-acyltransferase activity | 5 | 1 |
GO:0016416 | O-palmitoyltransferase activity | 6 | 1 |
GO:0047965 | glycoprotein O-fatty-acyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
GO:0140103 | catalytic activity, acting on a glycoprotein | 3 | 1 |
GO:0016417 | S-acyltransferase activity | 5 | 2 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 2 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 866 | 870 | PF00656 | 0.748 |
CLV_C14_Caspase3-7 | 958 | 962 | PF00656 | 0.623 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.455 |
CLV_PCSK_FUR_1 | 461 | 465 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.356 |
CLV_Separin_Metazoa | 973 | 977 | PF03568 | 0.651 |
DEG_APCC_DBOX_1 | 1021 | 1029 | PF00400 | 0.664 |
DEG_APCC_DBOX_1 | 861 | 869 | PF00400 | 0.556 |
DEG_APCC_DBOX_1 | 975 | 983 | PF00400 | 0.569 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.604 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.500 |
DOC_CYCLIN_RxL_1 | 195 | 202 | PF00134 | 0.434 |
DOC_CYCLIN_RxL_1 | 402 | 409 | PF00134 | 0.539 |
DOC_CYCLIN_RxL_1 | 471 | 484 | PF00134 | 0.624 |
DOC_CYCLIN_RxL_1 | 651 | 663 | PF00134 | 0.676 |
DOC_CYCLIN_RxL_1 | 790 | 799 | PF00134 | 0.532 |
DOC_CYCLIN_yCln2_LP_2 | 507 | 513 | PF00134 | 0.584 |
DOC_CYCLIN_yCln2_LP_2 | 540 | 546 | PF00134 | 0.279 |
DOC_MAPK_gen_1 | 157 | 164 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 177 | 187 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 157 | 164 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 443 | 450 | PF00069 | 0.676 |
DOC_MAPK_MEF2A_6 | 704 | 713 | PF00069 | 0.342 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.595 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 918 | 922 | PF00917 | 0.676 |
DOC_USP7_UBL2_3 | 439 | 443 | PF12436 | 0.674 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 191 | 200 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 485 | 495 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 565 | 571 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 728 | 737 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 793 | 798 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 836 | 846 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 923 | 929 | PF00244 | 0.758 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.646 |
LIG_APCC_ABBA_1 | 849 | 854 | PF00400 | 0.522 |
LIG_APCC_ABBA_1 | 968 | 973 | PF00400 | 0.704 |
LIG_BIR_III_4 | 211 | 215 | PF00653 | 0.532 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.642 |
LIG_eIF4E_1 | 261 | 267 | PF01652 | 0.577 |
LIG_eIF4E_1 | 441 | 447 | PF01652 | 0.677 |
LIG_eIF4E_1 | 725 | 731 | PF01652 | 0.204 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.744 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.448 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.639 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.595 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.448 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.402 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.377 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.688 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.691 |
LIG_FHA_2 | 1004 | 1010 | PF00498 | 0.703 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.630 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.600 |
LIG_FHA_2 | 632 | 638 | PF00498 | 0.682 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.662 |
LIG_FHA_2 | 794 | 800 | PF00498 | 0.482 |
LIG_FHA_2 | 811 | 817 | PF00498 | 0.581 |
LIG_FHA_2 | 864 | 870 | PF00498 | 0.753 |
LIG_FHA_2 | 978 | 984 | PF00498 | 0.686 |
LIG_GBD_Chelix_1 | 578 | 586 | PF00786 | 0.322 |
LIG_IBAR_NPY_1 | 850 | 852 | PF08397 | 0.654 |
LIG_LIR_Gen_1 | 260 | 267 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 550 | 558 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 621 | 630 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 816 | 826 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 260 | 264 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 550 | 554 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 726 | 730 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 816 | 822 | PF02991 | 0.593 |
LIG_LYPXL_SIV_4 | 223 | 231 | PF13949 | 0.607 |
LIG_LYPXL_yS_3 | 224 | 227 | PF13949 | 0.612 |
LIG_MLH1_MIPbox_1 | 320 | 324 | PF16413 | 0.642 |
LIG_NRBOX | 581 | 587 | PF00104 | 0.322 |
LIG_PCNA_yPIPBox_3 | 157 | 165 | PF02747 | 0.608 |
LIG_Pex14_1 | 572 | 576 | PF04695 | 0.390 |
LIG_Pex14_2 | 434 | 438 | PF04695 | 0.629 |
LIG_Rb_pABgroove_1 | 816 | 824 | PF01858 | 0.618 |
LIG_REV1ctd_RIR_1 | 831 | 840 | PF16727 | 0.532 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.601 |
LIG_SH2_CRK | 644 | 648 | PF00017 | 0.639 |
LIG_SH2_CRK | 768 | 772 | PF00017 | 0.342 |
LIG_SH2_CRK | 844 | 848 | PF00017 | 0.684 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.603 |
LIG_SH2_PTP2 | 623 | 626 | PF00017 | 0.483 |
LIG_SH2_SRC | 789 | 792 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.601 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.220 |
LIG_SH2_STAP1 | 587 | 591 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 723 | 727 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 768 | 772 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.709 |
LIG_SH2_STAT3 | 676 | 679 | PF00017 | 0.525 |
LIG_SH2_STAT3 | 852 | 855 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 1024 | 1027 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 676 | 679 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 810 | 813 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 852 | 855 | PF00017 | 0.621 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.612 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.606 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.465 |
LIG_SH3_3 | 768 | 774 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 349 | 357 | PF11976 | 0.625 |
LIG_SUMO_SIM_anti_2 | 40 | 46 | PF11976 | 0.647 |
LIG_SUMO_SIM_anti_2 | 400 | 405 | PF11976 | 0.491 |
LIG_TRAF2_1 | 1006 | 1009 | PF00917 | 0.708 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.633 |
LIG_TRFH_1 | 19 | 23 | PF08558 | 0.706 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.615 |
LIG_TYR_ITSM | 586 | 593 | PF00017 | 0.355 |
LIG_UBA3_1 | 585 | 594 | PF00899 | 0.358 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.588 |
LIG_WRC_WIRS_1 | 396 | 401 | PF05994 | 0.404 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.619 |
MOD_CDK_SPxK_1 | 25 | 31 | PF00069 | 0.606 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.778 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.689 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.624 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.289 |
MOD_CK1_1 | 837 | 843 | PF00069 | 0.684 |
MOD_CK1_1 | 883 | 889 | PF00069 | 0.637 |
MOD_CK1_1 | 902 | 908 | PF00069 | 0.680 |
MOD_CK1_1 | 977 | 983 | PF00069 | 0.695 |
MOD_CK2_1 | 1003 | 1009 | PF00069 | 0.706 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.632 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.615 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.518 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.563 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.683 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.722 |
MOD_CK2_1 | 800 | 806 | PF00069 | 0.664 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.761 |
MOD_CK2_1 | 977 | 983 | PF00069 | 0.714 |
MOD_GlcNHglycan | 1030 | 1033 | PF01048 | 0.413 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.591 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.633 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.506 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.639 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.497 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.563 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.545 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.500 |
MOD_GlcNHglycan | 507 | 510 | PF01048 | 0.332 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.470 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.445 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.485 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.405 |
MOD_GlcNHglycan | 886 | 889 | PF01048 | 0.559 |
MOD_GlcNHglycan | 892 | 895 | PF01048 | 0.555 |
MOD_GlcNHglycan | 901 | 904 | PF01048 | 0.562 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.387 |
MOD_GlcNHglycan | 963 | 966 | PF01048 | 0.501 |
MOD_GlcNHglycan | 976 | 979 | PF01048 | 0.408 |
MOD_GSK3_1 | 1024 | 1031 | PF00069 | 0.651 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.668 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.786 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.601 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.813 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.736 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.772 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.672 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.600 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.612 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.296 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.622 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.412 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.275 |
MOD_GSK3_1 | 800 | 807 | PF00069 | 0.678 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.715 |
MOD_GSK3_1 | 895 | 902 | PF00069 | 0.679 |
MOD_LATS_1 | 469 | 475 | PF00433 | 0.539 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.530 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.433 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.455 |
MOD_N-GLC_1 | 793 | 798 | PF02516 | 0.332 |
MOD_N-GLC_2 | 870 | 872 | PF02516 | 0.421 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.627 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.542 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.573 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.601 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.676 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.736 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.376 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.295 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.414 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.400 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.640 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.464 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.317 |
MOD_NEK2_1 | 834 | 839 | PF00069 | 0.631 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.663 |
MOD_NEK2_2 | 618 | 623 | PF00069 | 0.253 |
MOD_NEK2_2 | 92 | 97 | PF00069 | 0.538 |
MOD_NEK2_2 | 924 | 929 | PF00069 | 0.620 |
MOD_PIKK_1 | 1003 | 1009 | PF00454 | 0.714 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.783 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.518 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.579 |
MOD_PIKK_1 | 766 | 772 | PF00454 | 0.400 |
MOD_PIKK_1 | 783 | 789 | PF00454 | 0.358 |
MOD_PIKK_1 | 837 | 843 | PF00454 | 0.691 |
MOD_PIKK_1 | 936 | 942 | PF00454 | 0.761 |
MOD_PK_1 | 37 | 43 | PF00069 | 0.688 |
MOD_PK_1 | 594 | 600 | PF00069 | 0.329 |
MOD_PKA_1 | 556 | 562 | PF00069 | 0.542 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.758 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.630 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.620 |
MOD_PKA_2 | 835 | 841 | PF00069 | 0.549 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.625 |
MOD_Plk_1 | 793 | 799 | PF00069 | 0.545 |
MOD_Plk_1 | 804 | 810 | PF00069 | 0.678 |
MOD_Plk_2-3 | 49 | 55 | PF00069 | 0.630 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.436 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.622 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.700 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.638 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.291 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.354 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.279 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.557 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.570 |
MOD_Plk_4 | 793 | 799 | PF00069 | 0.532 |
MOD_Plk_4 | 805 | 811 | PF00069 | 0.593 |
MOD_Plk_4 | 817 | 823 | PF00069 | 0.505 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.479 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.721 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.754 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.728 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.738 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.482 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.496 |
MOD_SUMO_for_1 | 750 | 753 | PF00179 | 0.193 |
TRG_DiLeu_BaEn_1 | 726 | 731 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 245 | 250 | PF01217 | 0.608 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 590 | 593 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 727 | 730 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 819 | 822 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 461 | 464 | PF00400 | 0.702 |
TRG_NES_CRM1_1 | 787 | 799 | PF08389 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.269 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9Z8 | Leptomonas seymouri | 50% | 97% |
A0A1X0NKY1 | Trypanosomatidae | 32% | 100% |
A0A3S5H5B0 | Leishmania donovani | 68% | 97% |
A4HS47 | Leishmania infantum | 68% | 97% |
C9ZY45 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AK34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 98% |
O97203 | Leishmania major | 67% | 100% |