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: 3, no: 2 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HJH4
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0008270 | zinc ion binding | 6 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0046914 | transition metal ion binding | 5 | 6 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 633 | 637 | PF00656 | 0.780 |
CLV_C14_Caspase3-7 | 657 | 661 | PF00656 | 0.772 |
CLV_C14_Caspase3-7 | 987 | 991 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 1097 | 1099 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.572 |
CLV_PCSK_KEX2_1 | 1097 | 1099 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 771 | 773 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 667 | 669 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 771 | 773 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 1077 | 1081 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 924 | 928 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.411 |
DEG_SPOP_SBC_1 | 569 | 573 | PF00917 | 0.638 |
DOC_CYCLIN_RxL_1 | 921 | 931 | PF00134 | 0.359 |
DOC_CYCLIN_yCln2_LP_2 | 1010 | 1016 | PF00134 | 0.642 |
DOC_CYCLIN_yCln2_LP_2 | 352 | 358 | PF00134 | 0.364 |
DOC_CYCLIN_yCln2_LP_2 | 359 | 365 | PF00134 | 0.386 |
DOC_MAPK_DCC_7 | 736 | 746 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 114 | 123 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 139 | 146 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 848 | 856 | PF00069 | 0.351 |
DOC_MAPK_MEF2A_6 | 899 | 908 | PF00069 | 0.551 |
DOC_MAPK_NFAT4_5 | 139 | 147 | PF00069 | 0.312 |
DOC_PP1_RVXF_1 | 340 | 346 | PF00149 | 0.366 |
DOC_PP2B_LxvP_1 | 352 | 355 | PF13499 | 0.364 |
DOC_PP2B_LxvP_1 | 359 | 362 | PF13499 | 0.386 |
DOC_PP2B_LxvP_1 | 744 | 747 | PF13499 | 0.551 |
DOC_PP4_FxxP_1 | 1079 | 1082 | PF00568 | 0.772 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.641 |
DOC_PP4_FxxP_1 | 756 | 759 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 1049 | 1053 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.853 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.739 |
DOC_WW_Pin1_4 | 1022 | 1027 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 1040 | 1045 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 1050 | 1055 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 719 | 724 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 890 | 895 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 937 | 942 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.457 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 298 | 305 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.235 |
LIG_14-3-3_CanoR_1 | 568 | 578 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 594 | 599 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 398 | 414 | PF00022 | 0.575 |
LIG_APCC_ABBA_1 | 331 | 336 | PF00400 | 0.292 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.442 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 566 | 570 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 752 | 756 | PF00533 | 0.551 |
LIG_CaM_NSCaTE_8 | 407 | 414 | PF13499 | 0.635 |
LIG_Clathr_ClatBox_1 | 132 | 136 | PF01394 | 0.325 |
LIG_CSL_BTD_1 | 386 | 389 | PF09270 | 0.598 |
LIG_deltaCOP1_diTrp_1 | 384 | 387 | PF00928 | 0.688 |
LIG_EH1_1 | 899 | 907 | PF00400 | 0.435 |
LIG_eIF4E_1 | 859 | 865 | PF01652 | 0.412 |
LIG_eIF4E_1 | 921 | 927 | PF01652 | 0.406 |
LIG_FHA_1 | 1009 | 1015 | PF00498 | 0.652 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.349 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.523 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.429 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.249 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.463 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.551 |
LIG_FHA_1 | 853 | 859 | PF00498 | 0.399 |
LIG_FHA_1 | 928 | 934 | PF00498 | 0.470 |
LIG_FHA_1 | 937 | 943 | PF00498 | 0.359 |
LIG_FHA_1 | 951 | 957 | PF00498 | 0.263 |
LIG_FHA_1 | 978 | 984 | PF00498 | 0.691 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.449 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.434 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.425 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.763 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.507 |
LIG_FHA_2 | 826 | 832 | PF00498 | 0.440 |
LIG_FHA_2 | 985 | 991 | PF00498 | 0.673 |
LIG_FHA_2 | 998 | 1004 | PF00498 | 0.664 |
LIG_HCF-1_HBM_1 | 172 | 175 | PF13415 | 0.456 |
LIG_Integrin_RGD_1 | 975 | 977 | PF01839 | 0.472 |
LIG_LIR_Apic_2 | 1076 | 1082 | PF02991 | 0.773 |
LIG_LIR_Apic_2 | 1092 | 1096 | PF02991 | 0.644 |
LIG_LIR_Apic_2 | 384 | 390 | PF02991 | 0.760 |
LIG_LIR_Apic_2 | 523 | 528 | PF02991 | 0.652 |
LIG_LIR_Apic_2 | 753 | 759 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 172 | 179 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 201 | 212 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 220 | 225 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 254 | 265 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 291 | 302 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 728 | 737 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 835 | 846 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 728 | 734 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 835 | 841 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 960 | 964 | PF02991 | 0.413 |
LIG_NRBOX | 860 | 866 | PF00104 | 0.412 |
LIG_NRBOX | 922 | 928 | PF00104 | 0.306 |
LIG_OCRL_FandH_1 | 895 | 907 | PF00620 | 0.435 |
LIG_PCNA_PIPBox_1 | 190 | 199 | PF02747 | 0.360 |
LIG_PCNA_PIPBox_1 | 417 | 426 | PF02747 | 0.536 |
LIG_PCNA_yPIPBox_3 | 270 | 283 | PF02747 | 0.465 |
LIG_PCNA_yPIPBox_3 | 870 | 878 | PF02747 | 0.502 |
LIG_Pex14_2 | 811 | 815 | PF04695 | 0.349 |
LIG_PROFILIN_1 | 1035 | 1041 | PF00235 | 0.638 |
LIG_PTAP_UEV_1 | 1056 | 1061 | PF05743 | 0.658 |
LIG_Rb_pABgroove_1 | 262 | 270 | PF01858 | 0.352 |
LIG_SH2_CRK | 1093 | 1097 | PF00017 | 0.764 |
LIG_SH2_CRK | 838 | 842 | PF00017 | 0.462 |
LIG_SH2_CRK | 859 | 863 | PF00017 | 0.249 |
LIG_SH2_CRK | 868 | 872 | PF00017 | 0.227 |
LIG_SH2_GRB2like | 868 | 871 | PF00017 | 0.249 |
LIG_SH2_PTP2 | 294 | 297 | PF00017 | 0.394 |
LIG_SH2_SRC | 966 | 969 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 1075 | 1079 | PF00017 | 0.780 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 868 | 872 | PF00017 | 0.249 |
LIG_SH2_STAT3 | 415 | 418 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 1075 | 1078 | PF00017 | 0.776 |
LIG_SH2_STAT5 | 1093 | 1096 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 859 | 862 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 897 | 900 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 921 | 924 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 925 | 928 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 966 | 969 | PF00017 | 0.639 |
LIG_SH3_3 | 1032 | 1038 | PF00018 | 0.764 |
LIG_SH3_3 | 1041 | 1047 | PF00018 | 0.711 |
LIG_SH3_3 | 1051 | 1057 | PF00018 | 0.631 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.617 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.654 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.667 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.719 |
LIG_SUMO_SIM_par_1 | 130 | 137 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 952 | 960 | PF11976 | 0.302 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.768 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.464 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.762 |
LIG_TRAF2_1 | 669 | 672 | PF00917 | 0.782 |
LIG_TRAF2_1 | 723 | 726 | PF00917 | 0.703 |
LIG_TYR_ITIM | 866 | 871 | PF00017 | 0.249 |
LIG_UBA3_1 | 120 | 129 | PF00899 | 0.654 |
LIG_WW_1 | 894 | 897 | PF00397 | 0.523 |
LIG_WW_3 | 1094 | 1098 | PF00397 | 0.702 |
MOD_CDK_SPK_2 | 104 | 109 | PF00069 | 0.529 |
MOD_CDK_SPK_2 | 95 | 100 | PF00069 | 0.560 |
MOD_CK1_1 | 1022 | 1028 | PF00069 | 0.545 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.570 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.514 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.510 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.592 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.547 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.571 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.691 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.694 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.598 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.767 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.787 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.718 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.576 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.576 |
MOD_CK1_1 | 949 | 955 | PF00069 | 0.412 |
MOD_CK2_1 | 1065 | 1071 | PF00069 | 0.658 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.617 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.525 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.687 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.644 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.720 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.543 |
MOD_CK2_1 | 825 | 831 | PF00069 | 0.410 |
MOD_DYRK1A_RPxSP_1 | 31 | 35 | PF00069 | 0.697 |
MOD_GlcNHglycan | 1022 | 1025 | PF01048 | 0.544 |
MOD_GlcNHglycan | 1031 | 1034 | PF01048 | 0.559 |
MOD_GlcNHglycan | 1067 | 1070 | PF01048 | 0.690 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.533 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.582 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.490 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.572 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.698 |
MOD_GlcNHglycan | 269 | 273 | PF01048 | 0.583 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.535 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.758 |
MOD_GlcNHglycan | 474 | 478 | PF01048 | 0.666 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.672 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.625 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.654 |
MOD_GlcNHglycan | 585 | 589 | PF01048 | 0.597 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.612 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.709 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.605 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.683 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.587 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.412 |
MOD_GlcNHglycan | 834 | 837 | PF01048 | 0.576 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.716 |
MOD_GSK3_1 | 1008 | 1015 | PF00069 | 0.625 |
MOD_GSK3_1 | 1016 | 1023 | PF00069 | 0.589 |
MOD_GSK3_1 | 1055 | 1062 | PF00069 | 0.630 |
MOD_GSK3_1 | 1073 | 1080 | PF00069 | 0.534 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.523 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.506 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.607 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.570 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.525 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.746 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.667 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.739 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.665 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.754 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.620 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.597 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.620 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.592 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.617 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.524 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.499 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.387 |
MOD_GSK3_1 | 984 | 991 | PF00069 | 0.565 |
MOD_LATS_1 | 196 | 202 | PF00433 | 0.437 |
MOD_LATS_1 | 582 | 588 | PF00433 | 0.538 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.641 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.540 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.736 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.623 |
MOD_N-GLC_2 | 778 | 780 | PF02516 | 0.412 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.558 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.608 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.647 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.531 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.623 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.508 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.396 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.537 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.590 |
MOD_NEK2_1 | 797 | 802 | PF00069 | 0.565 |
MOD_NEK2_1 | 832 | 837 | PF00069 | 0.460 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.199 |
MOD_NEK2_1 | 926 | 931 | PF00069 | 0.537 |
MOD_NEK2_1 | 950 | 955 | PF00069 | 0.249 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.533 |
MOD_NEK2_2 | 750 | 755 | PF00069 | 0.468 |
MOD_NEK2_2 | 842 | 847 | PF00069 | 0.512 |
MOD_PIKK_1 | 1008 | 1014 | PF00454 | 0.606 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.614 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.538 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.581 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.590 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.562 |
MOD_PIKK_1 | 798 | 804 | PF00454 | 0.562 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.494 |
MOD_PIKK_1 | 876 | 882 | PF00454 | 0.520 |
MOD_PK_1 | 594 | 600 | PF00069 | 0.479 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.586 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.658 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.531 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.366 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.579 |
MOD_PKB_1 | 57 | 65 | PF00069 | 0.608 |
MOD_PKB_1 | 764 | 772 | PF00069 | 0.412 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.479 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.684 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.562 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.518 |
MOD_Plk_2-3 | 246 | 252 | PF00069 | 0.541 |
MOD_Plk_4 | 1005 | 1011 | PF00069 | 0.590 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.682 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.533 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.369 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.497 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.424 |
MOD_Plk_4 | 842 | 848 | PF00069 | 0.546 |
MOD_Plk_4 | 852 | 858 | PF00069 | 0.337 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.287 |
MOD_ProDKin_1 | 1022 | 1028 | PF00069 | 0.634 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.528 |
MOD_ProDKin_1 | 1040 | 1046 | PF00069 | 0.606 |
MOD_ProDKin_1 | 1050 | 1056 | PF00069 | 0.562 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.554 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.702 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.533 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.777 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.510 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.564 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.546 |
MOD_ProDKin_1 | 719 | 725 | PF00069 | 0.495 |
MOD_ProDKin_1 | 890 | 896 | PF00069 | 0.379 |
MOD_ProDKin_1 | 937 | 943 | PF00069 | 0.518 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.555 |
TRG_DiLeu_BaEn_1 | 119 | 124 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 352 | 357 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 740 | 745 | PF01217 | 0.412 |
TRG_DiLeu_LyEn_5 | 938 | 943 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 838 | 841 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 843 | 846 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 868 | 871 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 874 | 877 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 964 | 967 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 1096 | 1098 | PF00400 | 0.706 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 618 | 621 | PF00400 | 0.684 |
TRG_NLS_MonoExtC_3 | 393 | 399 | PF00514 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ISP6 | Leishmania donovani | 63% | 85% |
A4I6W7 | Leishmania infantum | 63% | 85% |
E9B1Z1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 86% |
Q4Q670 | Leishmania major | 62% | 100% |