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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WTI0
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 11 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 11 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 11 |
GO:0032259 | methylation | 2 | 3 |
GO:0035556 | intracellular signal transduction | 3 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0006810 | transport | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005092 | GDP-dissociation inhibitor activity | 3 | 11 |
GO:0008168 | methyltransferase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
GO:0030234 | enzyme regulator activity | 2 | 11 |
GO:0030695 | GTPase regulator activity | 4 | 11 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 11 |
GO:0098772 | molecular function regulator activity | 1 | 11 |
GO:0140677 | molecular function activator activity | 2 | 11 |
GO:0005093 | Rab GDP-dissociation inhibitor activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 834 | 838 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 657 | 659 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 938 | 940 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 418 | 422 | PF00082 | 0.296 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 1006 | 1008 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 1006 | 1008 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 498 | 500 | PF00082 | 0.255 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 80 | 86 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 1006 | 1010 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 767 | 771 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 940 | 944 | PF00082 | 0.445 |
DEG_APCC_DBOX_1 | 358 | 366 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.475 |
DEG_APCC_DBOX_1 | 65 | 73 | PF00400 | 0.474 |
DEG_APCC_DBOX_1 | 656 | 664 | PF00400 | 0.486 |
DEG_APCC_DBOX_1 | 717 | 725 | PF00400 | 0.660 |
DEG_SCF_FBW7_1 | 957 | 964 | PF00400 | 0.581 |
DEG_SPOP_SBC_1 | 472 | 476 | PF00917 | 0.494 |
DEG_SPOP_SBC_1 | 587 | 591 | PF00917 | 0.529 |
DOC_CDC14_PxL_1 | 981 | 989 | PF14671 | 0.402 |
DOC_CKS1_1 | 687 | 692 | PF01111 | 0.573 |
DOC_CYCLIN_RxL_1 | 418 | 425 | PF00134 | 0.457 |
DOC_CYCLIN_RxL_1 | 454 | 465 | PF00134 | 0.517 |
DOC_MAPK_DCC_7 | 71 | 79 | PF00069 | 0.484 |
DOC_MAPK_DCC_7 | 904 | 913 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 1006 | 1014 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.287 |
DOC_MAPK_gen_1 | 498 | 504 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 657 | 665 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 71 | 79 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 812 | 819 | PF00149 | 0.445 |
DOC_PP2B_LxvP_1 | 1012 | 1015 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.279 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.501 |
DOC_PP2B_PxIxI_1 | 402 | 408 | PF00149 | 0.401 |
DOC_PP4_FxxP_1 | 1038 | 1041 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 400 | 403 | PF00568 | 0.401 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 753 | 757 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 952 | 956 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 961 | 965 | PF00917 | 0.540 |
DOC_USP7_MATH_2 | 910 | 916 | PF00917 | 0.498 |
DOC_USP7_UBL2_3 | 742 | 746 | PF12436 | 0.654 |
DOC_USP7_UBL2_3 | 98 | 102 | PF12436 | 0.297 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 686 | 691 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 755 | 760 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 950 | 955 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 957 | 962 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 484 | 488 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 645 | 653 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 657 | 661 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 918 | 922 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 974 | 982 | PF00244 | 0.532 |
LIG_Actin_WH2_2 | 642 | 659 | PF00022 | 0.455 |
LIG_AP2alpha_1 | 7 | 11 | PF02296 | 0.525 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.538 |
LIG_BIR_III_2 | 951 | 955 | PF00653 | 0.656 |
LIG_BIR_III_4 | 1010 | 1014 | PF00653 | 0.473 |
LIG_BIR_III_4 | 3 | 7 | PF00653 | 0.549 |
LIG_BIR_III_4 | 327 | 331 | PF00653 | 0.410 |
LIG_BIR_III_4 | 837 | 841 | PF00653 | 0.561 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 975 | 979 | PF00533 | 0.545 |
LIG_CtBP_PxDLS_1 | 690 | 694 | PF00389 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 705 | 710 | PF00928 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 916 | 925 | PF00928 | 0.536 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.297 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.464 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.457 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.433 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.589 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.528 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.720 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.421 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.452 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.522 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.369 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.398 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.415 |
LIG_FHA_2 | 687 | 693 | PF00498 | 0.538 |
LIG_FHA_2 | 946 | 952 | PF00498 | 0.724 |
LIG_GBD_Chelix_1 | 247 | 255 | PF00786 | 0.356 |
LIG_IRF3_LxIS_1 | 21 | 28 | PF10401 | 0.435 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.386 |
LIG_LIR_Apic_2 | 38 | 44 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 398 | 403 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 878 | 884 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 916 | 922 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 236 | 247 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 278 | 286 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 336 | 343 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 627 | 636 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 705 | 715 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 976 | 987 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 1002 | 1008 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 647 | 653 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 670 | 676 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 705 | 711 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 976 | 982 | PF02991 | 0.489 |
LIG_LYPXL_SIV_4 | 1004 | 1012 | PF13949 | 0.410 |
LIG_LYPXL_yS_3 | 300 | 303 | PF13949 | 0.382 |
LIG_MAD2 | 1007 | 1015 | PF02301 | 0.462 |
LIG_MYND_1 | 985 | 989 | PF01753 | 0.491 |
LIG_NRBOX | 250 | 256 | PF00104 | 0.391 |
LIG_NRBOX | 558 | 564 | PF00104 | 0.457 |
LIG_PCNA_yPIPBox_3 | 549 | 563 | PF02747 | 0.533 |
LIG_PCNA_yPIPBox_3 | 856 | 867 | PF02747 | 0.440 |
LIG_Pex14_1 | 650 | 654 | PF04695 | 0.442 |
LIG_Pex14_1 | 706 | 710 | PF04695 | 0.475 |
LIG_Pex14_1 | 919 | 923 | PF04695 | 0.544 |
LIG_Pex14_2 | 7 | 11 | PF04695 | 0.525 |
LIG_PTB_Apo_2 | 987 | 994 | PF02174 | 0.501 |
LIG_PTB_Phospho_1 | 987 | 993 | PF10480 | 0.502 |
LIG_REV1ctd_RIR_1 | 279 | 288 | PF16727 | 0.332 |
LIG_SH2_CRK | 1005 | 1009 | PF00017 | 0.490 |
LIG_SH2_CRK | 1036 | 1040 | PF00017 | 0.466 |
LIG_SH2_CRK | 229 | 233 | PF00017 | 0.426 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.443 |
LIG_SH2_CRK | 673 | 677 | PF00017 | 0.526 |
LIG_SH2_CRK | 708 | 712 | PF00017 | 0.506 |
LIG_SH2_CRK | 881 | 885 | PF00017 | 0.429 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.326 |
LIG_SH2_GRB2like | 935 | 938 | PF00017 | 0.464 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 797 | 801 | PF00017 | 0.581 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.384 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.384 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 373 | 377 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 797 | 801 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 871 | 875 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 885 | 889 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 388 | 391 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 797 | 800 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 866 | 869 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 871 | 874 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 881 | 884 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 997 | 1000 | PF00017 | 0.353 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.494 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.497 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.682 |
LIG_SH3_3 | 904 | 910 | PF00018 | 0.568 |
LIG_SH3_3 | 979 | 985 | PF00018 | 0.360 |
LIG_SUMO_SIM_anti_2 | 230 | 236 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 572 | 578 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 230 | 236 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 572 | 578 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 787 | 793 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 909 | 917 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 980 | 986 | PF11976 | 0.435 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.515 |
LIG_TRAF2_1 | 689 | 692 | PF00917 | 0.291 |
LIG_TYR_ITIM | 290 | 295 | PF00017 | 0.406 |
LIG_TYR_ITIM | 883 | 888 | PF00017 | 0.385 |
LIG_WRC_WIRS_1 | 377 | 382 | PF05994 | 0.536 |
LIG_WRC_WIRS_1 | 397 | 402 | PF05994 | 0.401 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.497 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.553 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.526 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.595 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.574 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.429 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.499 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.297 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.493 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.575 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.437 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.441 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.588 |
MOD_CK2_1 | 930 | 936 | PF00069 | 0.643 |
MOD_CK2_1 | 952 | 958 | PF00069 | 0.591 |
MOD_Cter_Amidation | 210 | 213 | PF01082 | 0.466 |
MOD_GlcNHglycan | 1021 | 1024 | PF01048 | 0.712 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.551 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.247 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.370 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.363 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.370 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.540 |
MOD_GlcNHglycan | 568 | 572 | PF01048 | 0.450 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.323 |
MOD_GlcNHglycan | 727 | 731 | PF01048 | 0.647 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.554 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.589 |
MOD_GlcNHglycan | 932 | 935 | PF01048 | 0.443 |
MOD_GlcNHglycan | 963 | 966 | PF01048 | 0.562 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.544 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.498 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.494 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.522 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.532 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.618 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.682 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.572 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.710 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.298 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.469 |
MOD_GSK3_1 | 953 | 960 | PF00069 | 0.785 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.322 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.506 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.631 |
MOD_N-GLC_2 | 642 | 644 | PF02516 | 0.255 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.392 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.308 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.499 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.432 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.422 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.561 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.569 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.531 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.428 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.412 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.533 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.483 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.474 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.359 |
MOD_NEK2_2 | 925 | 930 | PF00069 | 0.482 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.527 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.536 |
MOD_PIKK_1 | 856 | 862 | PF00454 | 0.444 |
MOD_PK_1 | 112 | 118 | PF00069 | 0.355 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.297 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.504 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.493 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.423 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.381 |
MOD_PKA_2 | 831 | 837 | PF00069 | 0.593 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.297 |
MOD_PKA_2 | 917 | 923 | PF00069 | 0.546 |
MOD_PKA_2 | 973 | 979 | PF00069 | 0.547 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.470 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.516 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.514 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.565 |
MOD_Plk_1 | 925 | 931 | PF00069 | 0.435 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.297 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.459 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.455 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.403 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.485 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.426 |
MOD_Plk_4 | 773 | 779 | PF00069 | 0.419 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.326 |
MOD_Plk_4 | 983 | 989 | PF00069 | 0.377 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.373 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.497 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.442 |
MOD_ProDKin_1 | 686 | 692 | PF00069 | 0.571 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.658 |
MOD_ProDKin_1 | 755 | 761 | PF00069 | 0.665 |
MOD_ProDKin_1 | 950 | 956 | PF00069 | 0.658 |
MOD_ProDKin_1 | 957 | 963 | PF00069 | 0.675 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.538 |
MOD_SUMO_for_1 | 875 | 878 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 619 | 628 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 666 | 671 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 933 | 942 | PF00179 | 0.411 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.343 |
TRG_DiLeu_BaEn_1 | 977 | 982 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 983 | 988 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 926 | 932 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 41 | 46 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 433 | 438 | PF01217 | 0.536 |
TRG_DiLeu_BaLyEn_6 | 717 | 722 | PF01217 | 0.655 |
TRG_ENDOCYTIC_2 | 1005 | 1008 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 1036 | 1039 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 885 | 888 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 418 | 421 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 499 | 501 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 65 | 68 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 656 | 658 | PF00400 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 457 | 462 | PF00026 | 0.230 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXX4 | Leptomonas seymouri | 65% | 100% |
A0A0S4JKJ3 | Bodo saltans | 36% | 100% |
A0A1X0NTW1 | Trypanosomatidae | 37% | 100% |
A0A3R7KR10 | Trypanosoma rangeli | 40% | 100% |
A4H854 | Leishmania braziliensis | 83% | 100% |
A4HWH9 | Leishmania infantum | 100% | 100% |
C9ZXW9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AQ80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QFA2 | Leishmania major | 92% | 99% |