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: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990112 | RQC complex | 2 | 1 |
Related structures:
AlphaFold database: E9AMU6
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0072344 | rescue of stalled ribosome | 6 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1990116 | ribosome-associated ubiquitin-dependent protein catabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0043023 | ribosomal large subunit binding | 4 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 367 | 371 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 735 | 739 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 1124 | 1126 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 744 | 746 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 910 | 912 | PF00675 | 0.698 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.194 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 910 | 912 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 922 | 924 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 922 | 924 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 440 | 446 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 1086 | 1090 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 1125 | 1129 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 810 | 814 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 872 | 876 | PF00082 | 0.533 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.505 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 743 | 751 | PF00400 | 0.714 |
DEG_APCC_DBOX_1 | 901 | 909 | PF00400 | 0.653 |
DEG_SCF_FBW7_1 | 827 | 834 | PF00400 | 0.797 |
DOC_ANK_TNKS_1 | 444 | 451 | PF00023 | 0.513 |
DOC_CKS1_1 | 828 | 833 | PF01111 | 0.796 |
DOC_CKS1_1 | 936 | 941 | PF01111 | 0.799 |
DOC_CYCLIN_RxL_1 | 1086 | 1098 | PF00134 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 751 | 757 | PF00134 | 0.612 |
DOC_MAPK_DCC_7 | 1179 | 1187 | PF00069 | 0.623 |
DOC_MAPK_FxFP_2 | 175 | 178 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 139 | 149 | PF00069 | 0.658 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 585 | 595 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 790 | 797 | PF00069 | 0.668 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.661 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 464 | 471 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 1181 | 1188 | PF00149 | 0.620 |
DOC_PP1_RVXF_1 | 211 | 217 | PF00149 | 0.402 |
DOC_PP1_RVXF_1 | 557 | 564 | PF00149 | 0.188 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.609 |
DOC_PP2B_PxIxI_1 | 1065 | 1071 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.530 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.506 |
DOC_USP7_MATH_1 | 1017 | 1021 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 1034 | 1038 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 1158 | 1162 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 736 | 740 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 769 | 773 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 817 | 821 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 984 | 988 | PF00917 | 0.780 |
DOC_USP7_UBL2_3 | 1129 | 1133 | PF12436 | 0.773 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.480 |
DOC_USP7_UBL2_3 | 377 | 381 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 534 | 538 | PF12436 | 0.516 |
DOC_USP7_UBL2_3 | 546 | 550 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 810 | 814 | PF12436 | 0.693 |
DOC_USP7_UBL2_3 | 864 | 868 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 871 | 875 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 876 | 880 | PF12436 | 0.576 |
DOC_WW_Pin1_4 | 1143 | 1148 | PF00397 | 0.810 |
DOC_WW_Pin1_4 | 1149 | 1154 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 750 | 755 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 827 | 832 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 935 | 940 | PF00397 | 0.788 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 258 | 268 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 350 | 354 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 464 | 470 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 564 | 572 | PF00244 | 0.322 |
LIG_14-3-3_CanoR_1 | 656 | 665 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 705 | 710 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.691 |
LIG_APCC_ABBA_1 | 593 | 598 | PF00400 | 0.355 |
LIG_BIR_III_4 | 182 | 186 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.372 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.546 |
LIG_Clathr_ClatBox_1 | 211 | 215 | PF01394 | 0.402 |
LIG_EH1_1 | 131 | 139 | PF00400 | 0.482 |
LIG_eIF4E_1 | 132 | 138 | PF01652 | 0.482 |
LIG_eIF4E_1 | 455 | 461 | PF01652 | 0.482 |
LIG_FHA_1 | 1065 | 1071 | PF00498 | 0.413 |
LIG_FHA_1 | 1076 | 1082 | PF00498 | 0.360 |
LIG_FHA_1 | 1169 | 1175 | PF00498 | 0.592 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.562 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.535 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.544 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.338 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.408 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.530 |
LIG_FHA_1 | 832 | 838 | PF00498 | 0.785 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.562 |
LIG_FHA_2 | 1004 | 1010 | PF00498 | 0.775 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.482 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.521 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.480 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.335 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.402 |
LIG_FHA_2 | 704 | 710 | PF00498 | 0.673 |
LIG_FHA_2 | 865 | 871 | PF00498 | 0.467 |
LIG_LIR_Apic_2 | 101 | 107 | PF02991 | 0.530 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 266 | 277 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 435 | 443 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 558 | 567 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 612 | 622 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 738 | 748 | PF02991 | 0.767 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 351 | 356 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 612 | 617 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 738 | 743 | PF02991 | 0.739 |
LIG_NRBOX | 438 | 444 | PF00104 | 0.482 |
LIG_PCNA_yPIPBox_3 | 342 | 355 | PF02747 | 0.530 |
LIG_PDZ_Class_2 | 1184 | 1189 | PF00595 | 0.649 |
LIG_Pex14_1 | 556 | 560 | PF04695 | 0.393 |
LIG_Pex14_1 | 646 | 650 | PF04695 | 0.395 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.482 |
LIG_Pex14_2 | 650 | 654 | PF04695 | 0.480 |
LIG_PTB_Apo_2 | 126 | 133 | PF02174 | 0.377 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.529 |
LIG_PTB_Phospho_1 | 126 | 132 | PF10480 | 0.377 |
LIG_PTB_Phospho_1 | 149 | 155 | PF10480 | 0.529 |
LIG_SH2_GRB2like | 340 | 343 | PF00017 | 0.530 |
LIG_SH2_SRC | 1073 | 1076 | PF00017 | 0.480 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.395 |
LIG_SH2_SRC | 679 | 682 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 666 | 670 | PF00017 | 0.408 |
LIG_SH2_STAT3 | 666 | 669 | PF00017 | 0.408 |
LIG_SH2_STAT3 | 881 | 884 | PF00017 | 0.584 |
LIG_SH2_STAT3 | 937 | 940 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 1047 | 1050 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 702 | 705 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 937 | 940 | PF00017 | 0.492 |
LIG_SH3_1 | 66 | 72 | PF00018 | 0.482 |
LIG_SH3_2 | 254 | 259 | PF14604 | 0.447 |
LIG_SH3_3 | 1060 | 1066 | PF00018 | 0.355 |
LIG_SH3_3 | 1141 | 1147 | PF00018 | 0.804 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.512 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.447 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.574 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.551 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.482 |
LIG_SH3_3 | 704 | 710 | PF00018 | 0.652 |
LIG_SH3_3 | 774 | 780 | PF00018 | 0.726 |
LIG_SH3_4 | 296 | 303 | PF00018 | 0.460 |
LIG_SUMO_SIM_anti_2 | 466 | 472 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 952 | 965 | PF11976 | 0.733 |
LIG_SUMO_SIM_par_1 | 1066 | 1072 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 246 | 251 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 321 | 327 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 487 | 492 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 632 | 639 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 775 | 781 | PF11976 | 0.729 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.482 |
LIG_TRAF2_1 | 987 | 990 | PF00917 | 0.741 |
LIG_TRAF2_1 | 996 | 999 | PF00917 | 0.814 |
LIG_UBA3_1 | 115 | 122 | PF00899 | 0.482 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.553 |
LIG_WRC_WIRS_1 | 737 | 742 | PF05994 | 0.692 |
MOD_CDK_SPxxK_3 | 935 | 942 | PF00069 | 0.709 |
MOD_CK1_1 | 1148 | 1154 | PF00069 | 0.683 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.572 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.424 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.513 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.644 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.558 |
MOD_CK1_1 | 964 | 970 | PF00069 | 0.727 |
MOD_CK2_1 | 1003 | 1009 | PF00069 | 0.787 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.482 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.471 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.586 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.335 |
MOD_CK2_1 | 703 | 709 | PF00069 | 0.675 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.598 |
MOD_CK2_1 | 838 | 844 | PF00069 | 0.757 |
MOD_CK2_1 | 864 | 870 | PF00069 | 0.438 |
MOD_CK2_1 | 984 | 990 | PF00069 | 0.698 |
MOD_Cter_Amidation | 1123 | 1126 | PF01082 | 0.597 |
MOD_DYRK1A_RPxSP_1 | 1143 | 1147 | PF00069 | 0.615 |
MOD_GlcNHglycan | 1036 | 1039 | PF01048 | 0.633 |
MOD_GlcNHglycan | 1118 | 1121 | PF01048 | 0.733 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.669 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.339 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.334 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.326 |
MOD_GlcNHglycan | 717 | 720 | PF01048 | 0.783 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.706 |
MOD_GlcNHglycan | 771 | 774 | PF01048 | 0.564 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.701 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.757 |
MOD_GlcNHglycan | 930 | 933 | PF01048 | 0.710 |
MOD_GSK3_1 | 1064 | 1071 | PF00069 | 0.319 |
MOD_GSK3_1 | 1143 | 1150 | PF00069 | 0.748 |
MOD_GSK3_1 | 1154 | 1161 | PF00069 | 0.578 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.514 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.525 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.493 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.777 |
MOD_GSK3_1 | 827 | 834 | PF00069 | 0.724 |
MOD_N-GLC_1 | 928 | 933 | PF02516 | 0.546 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.496 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.531 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.507 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.523 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.482 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.534 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.507 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.335 |
MOD_NEK2_2 | 1045 | 1050 | PF00069 | 0.480 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.377 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.542 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.480 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.335 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.517 |
MOD_PIKK_1 | 853 | 859 | PF00454 | 0.699 |
MOD_PK_1 | 87 | 93 | PF00069 | 0.482 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.490 |
MOD_PKA_1 | 656 | 662 | PF00069 | 0.480 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.482 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.482 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.586 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.562 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.418 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.496 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.335 |
MOD_PKA_2 | 817 | 823 | PF00069 | 0.749 |
MOD_PKB_1 | 1143 | 1151 | PF00069 | 0.617 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.638 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.526 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.418 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.525 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.482 |
MOD_Plk_2-3 | 778 | 784 | PF00069 | 0.694 |
MOD_Plk_4 | 1158 | 1164 | PF00069 | 0.593 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.530 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.545 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.572 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.518 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.487 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.775 |
MOD_ProDKin_1 | 1143 | 1149 | PF00069 | 0.812 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.488 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.482 |
MOD_ProDKin_1 | 750 | 756 | PF00069 | 0.711 |
MOD_ProDKin_1 | 827 | 833 | PF00069 | 0.720 |
MOD_ProDKin_1 | 935 | 941 | PF00069 | 0.794 |
MOD_SUMO_for_1 | 204 | 207 | PF00179 | 0.559 |
MOD_SUMO_for_1 | 407 | 410 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 382 | 388 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 651 | 659 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 865 | 874 | PF00179 | 0.420 |
TRG_DiLeu_BaEn_1 | 145 | 150 | PF01217 | 0.546 |
TRG_DiLeu_BaEn_1 | 207 | 212 | PF01217 | 0.575 |
TRG_DiLeu_BaEn_1 | 421 | 426 | PF01217 | 0.482 |
TRG_DiLeu_BaEn_1 | 746 | 751 | PF01217 | 0.655 |
TRG_DiLeu_BaEn_3 | 170 | 176 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.482 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 584 | 586 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 743 | 745 | PF00400 | 0.669 |
TRG_NLS_Bipartite_1 | 790 | 811 | PF00514 | 0.483 |
TRG_NLS_MonoExtC_3 | 1124 | 1129 | PF00514 | 0.577 |
TRG_NLS_MonoExtC_3 | 443 | 449 | PF00514 | 0.534 |
TRG_NLS_MonoExtC_3 | 871 | 876 | PF00514 | 0.554 |
TRG_NLS_MonoExtN_4 | 805 | 811 | PF00514 | 0.721 |
TRG_NLS_MonoExtN_4 | 871 | 876 | PF00514 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 889 | 894 | PF00026 | 0.710 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2W4 | Leptomonas seymouri | 60% | 95% |
A0A1X0NMG1 | Trypanosomatidae | 47% | 100% |
A0A3Q8I8L7 | Leishmania donovani | 87% | 97% |
A0A422MXM2 | Trypanosoma rangeli | 47% | 100% |
A4H5S2 | Leishmania braziliensis | 77% | 98% |
A4HU15 | Leishmania infantum | 87% | 97% |
D0A9I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q4QHT0 | Leishmania major | 86% | 100% |
V5B6T4 | Trypanosoma cruzi | 45% | 100% |