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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9N4
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 2 |
GO:0006338 | chromatin remodeling | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003682 | chromatin binding | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 9 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 2 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042393 | histone binding | 3 | 2 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0051213 | dioxygenase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1004 | 1008 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 1020 | 1024 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 1039 | 1043 | PF00656 | 0.452 |
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 646 | 650 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 765 | 769 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 977 | 979 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.787 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 907 | 909 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 977 | 979 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.787 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 583 | 585 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 907 | 909 | PF00082 | 0.635 |
CLV_PCSK_PC7_1 | 409 | 415 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 780 | 788 | PF00400 | 0.629 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.633 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.799 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.743 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.561 |
DOC_CKS1_1 | 38 | 43 | PF01111 | 0.569 |
DOC_CKS1_1 | 398 | 403 | PF01111 | 0.487 |
DOC_MAPK_FxFP_2 | 467 | 470 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 390 | 398 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 408 | 419 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 500 | 510 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 366 | 373 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 501 | 510 | PF00069 | 0.491 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 618 | 625 | PF00149 | 0.476 |
DOC_PP1_SILK_1 | 659 | 664 | PF00149 | 0.414 |
DOC_PP2B_LxvP_1 | 508 | 511 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 467 | 470 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 1021 | 1025 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 976 | 980 | PF00917 | 0.552 |
DOC_USP7_UBL2_3 | 790 | 794 | PF12436 | 0.717 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.626 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 856 | 861 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 439 | 447 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 641 | 646 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 908 | 913 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 977 | 983 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 259 | 275 | PF00022 | 0.568 |
LIG_BIR_III_2 | 934 | 938 | PF00653 | 0.467 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.684 |
LIG_BRCT_BRCA1_1 | 668 | 672 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 938 | 942 | PF00533 | 0.425 |
LIG_Clathr_ClatBox_1 | 403 | 407 | PF01394 | 0.581 |
LIG_deltaCOP1_diTrp_1 | 460 | 467 | PF00928 | 0.476 |
LIG_DLG_GKlike_1 | 641 | 648 | PF00625 | 0.537 |
LIG_FHA_1 | 1001 | 1007 | PF00498 | 0.761 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.731 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.476 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.489 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.480 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.425 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.504 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.476 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.487 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.410 |
LIG_FHA_1 | 845 | 851 | PF00498 | 0.671 |
LIG_FHA_2 | 1018 | 1024 | PF00498 | 0.672 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.537 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.562 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.476 |
LIG_FHA_2 | 729 | 735 | PF00498 | 0.413 |
LIG_FHA_2 | 774 | 780 | PF00498 | 0.615 |
LIG_LIR_Apic_2 | 466 | 470 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 4 | 11 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 460 | 470 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 644 | 649 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 669 | 680 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 939 | 950 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 644 | 648 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 669 | 675 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 939 | 945 | PF02991 | 0.408 |
LIG_LYPXL_S_1 | 468 | 472 | PF13949 | 0.301 |
LIG_LYPXL_yS_3 | 469 | 472 | PF13949 | 0.537 |
LIG_NRBOX | 161 | 167 | PF00104 | 0.544 |
LIG_NRBOX | 529 | 535 | PF00104 | 0.581 |
LIG_PCNA_yPIPBox_3 | 520 | 534 | PF02747 | 0.565 |
LIG_Pex14_2 | 254 | 258 | PF04695 | 0.516 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.537 |
LIG_Pex14_2 | 696 | 700 | PF04695 | 0.537 |
LIG_REV1ctd_RIR_1 | 255 | 265 | PF16727 | 0.437 |
LIG_REV1ctd_RIR_1 | 408 | 418 | PF16727 | 0.470 |
LIG_SH2_NCK_1 | 664 | 668 | PF00017 | 0.581 |
LIG_SH2_PTP2 | 496 | 499 | PF00017 | 0.537 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 982 | 985 | PF00017 | 0.383 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.734 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.735 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.501 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.501 |
LIG_SH3_3 | 799 | 805 | PF00018 | 0.673 |
LIG_SH3_3 | 873 | 879 | PF00018 | 0.479 |
LIG_SH3_3 | 896 | 902 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 155 | 166 | PF11976 | 0.654 |
LIG_SUMO_SIM_anti_2 | 628 | 635 | PF11976 | 0.488 |
LIG_SUMO_SIM_anti_2 | 658 | 663 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 279 | 287 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 529 | 535 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 628 | 635 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 691 | 697 | PF11976 | 0.476 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.581 |
LIG_TRAF2_1 | 731 | 734 | PF00917 | 0.376 |
LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.537 |
LIG_UBA3_1 | 403 | 408 | PF00899 | 0.581 |
LIG_UBA3_1 | 610 | 615 | PF00899 | 0.562 |
LIG_UBA3_1 | 783 | 790 | PF00899 | 0.638 |
LIG_UBA3_1 | 880 | 888 | PF00899 | 0.471 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.521 |
LIG_WW_3 | 510 | 514 | PF00397 | 0.487 |
LIG_WW_3 | 898 | 902 | PF00397 | 0.655 |
MOD_CDC14_SPxK_1 | 859 | 862 | PF00782 | 0.634 |
MOD_CDK_SPxK_1 | 856 | 862 | PF00069 | 0.672 |
MOD_CK1_1 | 1000 | 1006 | PF00069 | 0.642 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.775 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.724 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.577 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.533 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.507 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.519 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.562 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.645 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.485 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.729 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.768 |
MOD_CK1_1 | 817 | 823 | PF00069 | 0.737 |
MOD_CK1_1 | 993 | 999 | PF00069 | 0.583 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.392 |
MOD_CK2_1 | 995 | 1001 | PF00069 | 0.619 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.777 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.754 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.618 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.446 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.590 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.680 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.301 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.209 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.336 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.369 |
MOD_GlcNHglycan | 599 | 603 | PF01048 | 0.388 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.596 |
MOD_GlcNHglycan | 819 | 822 | PF01048 | 0.710 |
MOD_GlcNHglycan | 954 | 957 | PF01048 | 0.647 |
MOD_GlcNHglycan | 997 | 1000 | PF01048 | 0.689 |
MOD_GSK3_1 | 1017 | 1024 | PF00069 | 0.718 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.607 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.643 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.573 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.550 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.704 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.574 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.616 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.512 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.478 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.746 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.519 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.513 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.487 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.737 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.738 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.727 |
MOD_GSK3_1 | 990 | 997 | PF00069 | 0.531 |
MOD_LATS_1 | 113 | 119 | PF00433 | 0.727 |
MOD_LATS_1 | 639 | 645 | PF00433 | 0.525 |
MOD_LATS_1 | 792 | 798 | PF00433 | 0.664 |
MOD_N-GLC_1 | 625 | 630 | PF02516 | 0.276 |
MOD_N-GLC_1 | 952 | 957 | PF02516 | 0.476 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.791 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.606 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.583 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.661 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.801 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.452 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.358 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.471 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.476 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.544 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.482 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.501 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.484 |
MOD_NEK2_1 | 952 | 957 | PF00069 | 0.530 |
MOD_NEK2_1 | 991 | 996 | PF00069 | 0.570 |
MOD_NEK2_2 | 667 | 672 | PF00069 | 0.537 |
MOD_NEK2_2 | 976 | 981 | PF00069 | 0.538 |
MOD_OFUCOSY | 980 | 985 | PF10250 | 0.498 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.645 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.739 |
MOD_PIKK_1 | 574 | 580 | PF00454 | 0.673 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.627 |
MOD_PK_1 | 657 | 663 | PF00069 | 0.414 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.501 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.575 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.510 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.468 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.794 |
MOD_PKA_2 | 962 | 968 | PF00069 | 0.581 |
MOD_PKA_2 | 976 | 982 | PF00069 | 0.402 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.468 |
MOD_Plk_2-3 | 1005 | 1011 | PF00069 | 0.680 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.538 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.519 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.537 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.516 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.484 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.487 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.799 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.674 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.672 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.656 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.739 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.487 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.470 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.730 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.536 |
MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.678 |
MOD_ProDKin_1 | 856 | 862 | PF00069 | 0.672 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_1 | 460 | 465 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_2 | 301 | 307 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.752 |
TRG_DiLeu_BaLyEn_6 | 563 | 568 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 876 | 881 | PF01217 | 0.603 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 645 | 648 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 966 | 969 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 499 | 501 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 976 | 978 | PF00400 | 0.561 |
TRG_NLS_MonoExtN_4 | 409 | 416 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE28 | Leptomonas seymouri | 65% | 100% |
A0A0S4JP66 | Bodo saltans | 41% | 94% |
A0A1X0NY53 | Trypanosomatidae | 55% | 100% |
A0A3S7WZF4 | Leishmania donovani | 93% | 100% |
A0A422P4R6 | Trypanosoma rangeli | 57% | 100% |
A4HEA7 | Leishmania braziliensis | 83% | 100% |
A4I1Q3 | Leishmania infantum | 93% | 100% |
C9ZKA7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AXT7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DIY2 | Trypanosoma cruzi | 56% | 100% |