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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 1 |
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: E9AXT7
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 9 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 13 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0051213 | dioxygenase activity | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0042393 | histone binding | 3 | 1 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1005 | 1009 | PF00656 | 0.565 |
CLV_C14_Caspase3-7 | 1021 | 1025 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 1040 | 1044 | PF00656 | 0.465 |
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 645 | 649 | PF00656 | 0.419 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 977 | 979 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 907 | 909 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 977 | 979 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 412 | 414 | PF00082 | 0.233 |
CLV_PCSK_PC1ET2_1 | 582 | 584 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 907 | 909 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 408 | 414 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.226 |
CLV_PCSK_SKI1_1 | 780 | 784 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.536 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.647 |
DEG_SPOP_SBC_1 | 126 | 130 | PF00917 | 0.749 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.678 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.479 |
DEG_SPOP_SBC_1 | 801 | 805 | PF00917 | 0.427 |
DOC_CKS1_1 | 397 | 402 | PF01111 | 0.426 |
DOC_MAPK_FxFP_2 | 466 | 469 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 389 | 397 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 407 | 418 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 499 | 509 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 365 | 372 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 411 | 420 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 500 | 509 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 502 | 510 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 235 | 242 | PF00149 | 0.310 |
DOC_PP1_RVXF_1 | 617 | 624 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.417 |
DOC_PP4_FxxP_1 | 466 | 469 | PF00568 | 0.417 |
DOC_USP7_MATH_1 | 1022 | 1026 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 976 | 980 | PF00917 | 0.461 |
DOC_USP7_UBL2_3 | 48 | 52 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 789 | 793 | PF12436 | 0.467 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 768 | 773 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 856 | 861 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 152 | 161 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 438 | 446 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 548 | 557 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 640 | 645 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 977 | 983 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 258 | 274 | PF00022 | 0.502 |
LIG_BIR_III_2 | 934 | 938 | PF00653 | 0.314 |
LIG_BIR_III_4 | 953 | 957 | PF00653 | 0.370 |
LIG_BRCT_BRCA1_1 | 667 | 671 | PF00533 | 0.417 |
LIG_BRCT_BRCA1_1 | 938 | 942 | PF00533 | 0.330 |
LIG_Clathr_ClatBox_1 | 402 | 406 | PF01394 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 459 | 466 | PF00928 | 0.417 |
LIG_DLG_GKlike_1 | 640 | 647 | PF00625 | 0.481 |
LIG_FHA_1 | 1002 | 1008 | PF00498 | 0.701 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.439 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.441 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.426 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.505 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.469 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.417 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.426 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.410 |
LIG_FHA_1 | 769 | 775 | PF00498 | 0.627 |
LIG_FHA_1 | 808 | 814 | PF00498 | 0.593 |
LIG_FHA_1 | 845 | 851 | PF00498 | 0.593 |
LIG_FHA_2 | 1019 | 1025 | PF00498 | 0.524 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.514 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.522 |
LIG_FHA_2 | 685 | 691 | PF00498 | 0.435 |
LIG_FHA_2 | 728 | 734 | PF00498 | 0.356 |
LIG_FHA_2 | 773 | 779 | PF00498 | 0.504 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.499 |
LIG_Integrin_RGD_1 | 1034 | 1036 | PF01839 | 0.469 |
LIG_LIR_Apic_2 | 465 | 469 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 4 | 11 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 459 | 469 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 643 | 648 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 668 | 679 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 939 | 950 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 668 | 674 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 939 | 945 | PF02991 | 0.316 |
LIG_LYPXL_S_1 | 467 | 471 | PF13949 | 0.239 |
LIG_LYPXL_yS_3 | 468 | 471 | PF13949 | 0.481 |
LIG_NRBOX | 160 | 166 | PF00104 | 0.485 |
LIG_NRBOX | 528 | 534 | PF00104 | 0.442 |
LIG_PCNA_yPIPBox_3 | 519 | 533 | PF02747 | 0.527 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.468 |
LIG_Pex14_2 | 466 | 470 | PF04695 | 0.502 |
LIG_Pex14_2 | 695 | 699 | PF04695 | 0.481 |
LIG_REV1ctd_RIR_1 | 254 | 264 | PF16727 | 0.346 |
LIG_REV1ctd_RIR_1 | 407 | 417 | PF16727 | 0.413 |
LIG_SH2_NCK_1 | 663 | 667 | PF00017 | 0.466 |
LIG_SH2_PTP2 | 495 | 498 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 744 | 747 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 949 | 952 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 982 | 985 | PF00017 | 0.292 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.671 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.439 |
LIG_SH3_3 | 510 | 516 | PF00018 | 0.464 |
LIG_SH3_3 | 873 | 879 | PF00018 | 0.404 |
LIG_SH3_3 | 896 | 902 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 155 | 165 | PF11976 | 0.613 |
LIG_SUMO_SIM_anti_2 | 627 | 634 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 278 | 286 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 37 | 43 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 528 | 534 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 627 | 634 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 690 | 696 | PF11976 | 0.446 |
LIG_TRAF2_1 | 537 | 540 | PF00917 | 0.442 |
LIG_TRAF2_1 | 730 | 733 | PF00917 | 0.292 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.658 |
LIG_TYR_ITIM | 493 | 498 | PF00017 | 0.481 |
LIG_UBA3_1 | 402 | 407 | PF00899 | 0.442 |
LIG_UBA3_1 | 609 | 614 | PF00899 | 0.522 |
LIG_UBA3_1 | 880 | 888 | PF00899 | 0.328 |
LIG_WRC_WIRS_1 | 463 | 468 | PF05994 | 0.472 |
LIG_WW_3 | 509 | 513 | PF00397 | 0.459 |
LIG_WW_3 | 898 | 902 | PF00397 | 0.452 |
MOD_CDC14_SPxK_1 | 859 | 862 | PF00782 | 0.563 |
MOD_CDK_SPxK_1 | 856 | 862 | PF00069 | 0.604 |
MOD_CK1_1 | 1001 | 1007 | PF00069 | 0.561 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.574 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.543 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.754 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.542 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.530 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.446 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.470 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.522 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.571 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.476 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.683 |
MOD_CK1_1 | 799 | 805 | PF00069 | 0.646 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.604 |
MOD_CK1_1 | 993 | 999 | PF00069 | 0.491 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.401 |
MOD_CK2_1 | 727 | 733 | PF00069 | 0.336 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.612 |
MOD_CK2_1 | 996 | 1002 | PF00069 | 0.537 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.719 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.705 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.744 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.575 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.352 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.567 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.577 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.250 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.179 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.283 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.242 |
MOD_GlcNHglycan | 598 | 602 | PF01048 | 0.338 |
MOD_GlcNHglycan | 819 | 822 | PF01048 | 0.640 |
MOD_GlcNHglycan | 953 | 957 | PF01048 | 0.613 |
MOD_GlcNHglycan | 998 | 1001 | PF01048 | 0.619 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.660 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.696 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.522 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.649 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.617 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.451 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.445 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.649 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.471 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.489 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.443 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.596 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.644 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.699 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.713 |
MOD_GSK3_1 | 990 | 997 | PF00069 | 0.434 |
MOD_LATS_1 | 113 | 119 | PF00433 | 0.582 |
MOD_LATS_1 | 638 | 644 | PF00433 | 0.420 |
MOD_LATS_1 | 791 | 797 | PF00433 | 0.464 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.521 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.217 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.609 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.633 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.411 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.415 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.448 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.429 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.517 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.423 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.467 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.440 |
MOD_NEK2_1 | 952 | 957 | PF00069 | 0.432 |
MOD_NEK2_1 | 991 | 996 | PF00069 | 0.467 |
MOD_NEK2_2 | 666 | 671 | PF00069 | 0.481 |
MOD_NEK2_2 | 976 | 981 | PF00069 | 0.446 |
MOD_OFUCOSY | 980 | 985 | PF10250 | 0.433 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.546 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.617 |
MOD_PIKK_1 | 56 | 62 | PF00454 | 0.586 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.609 |
MOD_PIKK_1 | 819 | 825 | PF00454 | 0.462 |
MOD_PKA_1 | 438 | 444 | PF00069 | 0.439 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.381 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.454 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.417 |
MOD_PKA_2 | 807 | 813 | PF00069 | 0.536 |
MOD_PKA_2 | 962 | 968 | PF00069 | 0.492 |
MOD_PKA_2 | 976 | 982 | PF00069 | 0.318 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.496 |
MOD_Plk_1 | 1035 | 1041 | PF00069 | 0.666 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.474 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.411 |
MOD_Plk_2-3 | 1006 | 1012 | PF00069 | 0.591 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.484 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.481 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.521 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.481 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.424 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.426 |
MOD_Plk_4 | 802 | 808 | PF00069 | 0.511 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.614 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.426 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.448 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.642 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.637 |
MOD_ProDKin_1 | 768 | 774 | PF00069 | 0.472 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.506 |
MOD_ProDKin_1 | 856 | 862 | PF00069 | 0.604 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.487 |
TRG_DiLeu_BaEn_1 | 459 | 464 | PF01217 | 0.426 |
TRG_DiLeu_BaEn_2 | 300 | 306 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 562 | 567 | PF01217 | 0.351 |
TRG_DiLeu_BaLyEn_6 | 876 | 881 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 955 | 960 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 644 | 647 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 966 | 969 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 758 | 761 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 976 | 978 | PF00400 | 0.464 |
TRG_NLS_MonoExtN_4 | 408 | 415 | PF00514 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 237 | 242 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 948 | 953 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE28 | Leptomonas seymouri | 65% | 100% |
A0A0S4JP66 | Bodo saltans | 41% | 94% |
A0A1X0NY53 | Trypanosomatidae | 55% | 100% |
A0A3S7WZF4 | Leishmania donovani | 92% | 100% |
A0A422P4R6 | Trypanosoma rangeli | 58% | 100% |
A4HEA7 | Leishmania braziliensis | 85% | 100% |
A4I1Q3 | Leishmania infantum | 92% | 100% |
C9ZKA7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AZN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4Q9N4 | Leishmania major | 91% | 100% |
V5DIY2 | Trypanosoma cruzi | 55% | 100% |