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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WXM7
Term | Name | Level | Count |
---|---|---|---|
GO:0006479 | protein methylation | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0008213 | protein alkylation | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016571 | histone methylation | 5 | 1 |
GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032259 | methylation | 2 | 2 |
GO:0034968 | histone lysine methylation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 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 | 2 |
GO:0008168 | methyltransferase activity | 4 | 2 |
GO:0008170 | N-methyltransferase activity | 5 | 1 |
GO:0008276 | protein methyltransferase activity | 3 | 1 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 2 |
GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
GO:0042054 | histone methyltransferase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 493 | 497 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 551 | 555 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 621 | 625 | PF00656 | 0.473 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 601 | 603 | PF00082 | 0.328 |
CLV_PCSK_PC7_1 | 245 | 251 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 597 | 603 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.364 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.571 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.512 |
DEG_SCF_FBW7_1 | 822 | 829 | PF00400 | 0.554 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.641 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.566 |
DEG_SPOP_SBC_1 | 459 | 463 | PF00917 | 0.613 |
DOC_ANK_TNKS_1 | 513 | 520 | PF00023 | 0.573 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.507 |
DOC_CYCLIN_RxL_1 | 227 | 240 | PF00134 | 0.549 |
DOC_CYCLIN_RxL_1 | 734 | 742 | PF00134 | 0.362 |
DOC_CYCLIN_yCln2_LP_2 | 437 | 440 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 219 | 226 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 249 | 259 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 755 | 763 | PF00069 | 0.352 |
DOC_PP1_RVXF_1 | 364 | 371 | PF00149 | 0.518 |
DOC_PP2B_LxvP_1 | 437 | 440 | PF13499 | 0.546 |
DOC_PP2B_LxvP_1 | 806 | 809 | PF13499 | 0.520 |
DOC_PP2B_PxIxI_1 | 758 | 764 | PF00149 | 0.364 |
DOC_PP4_FxxP_1 | 787 | 790 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.752 |
DOC_USP7_MATH_2 | 473 | 479 | PF00917 | 0.486 |
DOC_USP7_UBL2_3 | 210 | 214 | PF12436 | 0.552 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 811 | 816 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 822 | 827 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 360 | 365 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 514 | 521 | PF00244 | 0.790 |
LIG_14-3-3_CanoR_1 | 536 | 543 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 589 | 593 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 616 | 621 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 836 | 841 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 475 | 491 | PF00022 | 0.465 |
LIG_APCC_ABBA_1 | 678 | 683 | PF00400 | 0.447 |
LIG_BIR_III_2 | 496 | 500 | PF00653 | 0.581 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.406 |
LIG_EVH1_2 | 807 | 811 | PF00568 | 0.404 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.579 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.606 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.663 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.657 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.475 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.701 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.712 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.679 |
LIG_FHA_2 | 723 | 729 | PF00498 | 0.639 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.470 |
LIG_GSK3_LRP6_1 | 439 | 444 | PF00069 | 0.544 |
LIG_Integrin_RGD_1 | 449 | 451 | PF01839 | 0.565 |
LIG_LIR_Apic_2 | 263 | 268 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 133 | 144 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 369 | 378 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 568 | 577 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 651 | 661 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 721 | 730 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 369 | 373 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 590 | 595 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 651 | 657 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 665 | 669 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 721 | 727 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 742 | 746 | PF02991 | 0.364 |
LIG_LYPXL_S_1 | 321 | 325 | PF13949 | 0.356 |
LIG_LYPXL_yS_3 | 322 | 325 | PF13949 | 0.363 |
LIG_NRBOX | 606 | 612 | PF00104 | 0.485 |
LIG_SH2_GRB2like | 686 | 689 | PF00017 | 0.434 |
LIG_SH2_NCK_1 | 280 | 284 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 724 | 728 | PF00017 | 0.448 |
LIG_SH2_SRC | 280 | 283 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 709 | 713 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 669 | 672 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 686 | 689 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 802 | 805 | PF00017 | 0.309 |
LIG_SH3_1 | 802 | 808 | PF00018 | 0.351 |
LIG_SH3_3 | 345 | 351 | PF00018 | 0.710 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.441 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.696 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.625 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.710 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.712 |
LIG_SH3_3 | 713 | 719 | PF00018 | 0.502 |
LIG_SH3_3 | 769 | 775 | PF00018 | 0.695 |
LIG_SH3_3 | 802 | 808 | PF00018 | 0.413 |
LIG_SH3_CIN85_PxpxPR_1 | 528 | 533 | PF14604 | 0.565 |
LIG_SUMO_SIM_anti_2 | 491 | 496 | PF11976 | 0.550 |
LIG_SUMO_SIM_anti_2 | 578 | 585 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 490 | 496 | PF11976 | 0.574 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.604 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.489 |
LIG_TRAF2_1 | 715 | 718 | PF00917 | 0.485 |
LIG_TRAF2_1 | 829 | 832 | PF00917 | 0.546 |
LIG_TYR_ITIM | 722 | 727 | PF00017 | 0.359 |
MOD_CDC14_SPxK_1 | 814 | 817 | PF00782 | 0.594 |
MOD_CDK_SPK_2 | 565 | 570 | PF00069 | 0.535 |
MOD_CDK_SPxK_1 | 811 | 817 | PF00069 | 0.586 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.744 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.607 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.648 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.714 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.352 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.465 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.600 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.746 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.636 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.712 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.570 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.682 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.650 |
MOD_CK1_1 | 824 | 830 | PF00069 | 0.584 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.567 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.255 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.535 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.726 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.577 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.748 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.546 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.398 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.491 |
MOD_DYRK1A_RPxSP_1 | 565 | 569 | PF00069 | 0.434 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.714 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.627 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.456 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.432 |
MOD_GlcNHglycan | 310 | 314 | PF01048 | 0.461 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.619 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.481 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.687 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.621 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.379 |
MOD_GlcNHglycan | 507 | 511 | PF01048 | 0.635 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.663 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.578 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.516 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.440 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.684 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.574 |
MOD_GlcNHglycan | 819 | 822 | PF01048 | 0.635 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.664 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.693 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.510 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.683 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.504 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.671 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.436 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.735 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.678 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.577 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.715 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.594 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.417 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.360 |
MOD_GSK3_1 | 718 | 725 | PF00069 | 0.446 |
MOD_GSK3_1 | 770 | 777 | PF00069 | 0.656 |
MOD_GSK3_1 | 811 | 818 | PF00069 | 0.683 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.475 |
MOD_GSK3_1 | 836 | 843 | PF00069 | 0.394 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.782 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.698 |
MOD_N-GLC_1 | 549 | 554 | PF02516 | 0.615 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.270 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.270 |
MOD_N-GLC_2 | 44 | 46 | PF02516 | 0.459 |
MOD_N-GLC_2 | 694 | 696 | PF02516 | 0.270 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.523 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.462 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.450 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.688 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.538 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.270 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.601 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.372 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.740 |
MOD_NEK2_2 | 795 | 800 | PF00069 | 0.363 |
MOD_PIKK_1 | 425 | 431 | PF00454 | 0.819 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.342 |
MOD_PKA_1 | 210 | 216 | PF00069 | 0.650 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.567 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.484 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.574 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.649 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.305 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.442 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.610 |
MOD_PKB_1 | 542 | 550 | PF00069 | 0.530 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.522 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.288 |
MOD_Plk_1 | 682 | 688 | PF00069 | 0.270 |
MOD_Plk_1 | 795 | 801 | PF00069 | 0.532 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.481 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.790 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.371 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.755 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.603 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.289 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.275 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.596 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.424 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.379 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.526 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.594 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.767 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.645 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.827 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.537 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.453 |
MOD_ProDKin_1 | 811 | 817 | PF00069 | 0.599 |
MOD_ProDKin_1 | 822 | 828 | PF00069 | 0.430 |
TRG_DiLeu_BaEn_1 | 369 | 374 | PF01217 | 0.331 |
TRG_DiLeu_BaEn_1 | 788 | 793 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 787 | 792 | PF01217 | 0.454 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 724 | 727 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 743 | 746 | PF00928 | 0.354 |
TRG_ER_diArg_1 | 243 | 246 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 735 | 737 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 842 | 845 | PF00400 | 0.434 |
TRG_NLS_Bipartite_1 | 207 | 223 | PF00514 | 0.485 |
TRG_NLS_MonoExtC_3 | 206 | 211 | PF00514 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEZ6 | Leptomonas seymouri | 49% | 100% |
A0A1X0NYH3 | Trypanosomatidae | 30% | 100% |
A0A3R7KV16 | Trypanosoma rangeli | 30% | 100% |
A4I0D0 | Leishmania infantum | 100% | 100% |
C9ZV40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AW94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QB84 | Leishmania major | 87% | 100% |
V5ARQ1 | Trypanosoma cruzi | 29% | 100% |