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: A4H5S2
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 | 779 | 783 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 987 | 991 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 1132 | 1134 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 893 | 895 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 932 | 934 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 833 | 835 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 893 | 895 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 932 | 934 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 951 | 953 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 893 | 895 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 944 | 946 | PF00082 | 0.558 |
CLV_PCSK_PC7_1 | 466 | 472 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 1019 | 1023 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 1095 | 1099 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 886 | 890 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 894 | 898 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 984 | 988 | PF00082 | 0.491 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.414 |
DEG_APCC_DBOX_1 | 769 | 777 | PF00400 | 0.631 |
DEG_Kelch_actinfilin_1 | 1074 | 1078 | PF01344 | 0.178 |
DEG_SCF_FBW7_1 | 849 | 856 | PF00400 | 0.587 |
DOC_ANK_TNKS_1 | 470 | 477 | PF00023 | 0.398 |
DOC_CKS1_1 | 850 | 855 | PF01111 | 0.587 |
DOC_CYCLIN_RxL_1 | 1095 | 1107 | PF00134 | 0.271 |
DOC_MAPK_FxFP_2 | 198 | 201 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 233 | 243 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 611 | 621 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 490 | 497 | PF00069 | 0.296 |
DOC_PP2B_LxvP_1 | 199 | 202 | PF13499 | 0.392 |
DOC_PP2B_PxIxI_1 | 1074 | 1080 | PF00149 | 0.271 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.347 |
DOC_USP7_MATH_1 | 1026 | 1030 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 1043 | 1047 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 1117 | 1121 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 839 | 843 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 953 | 957 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 992 | 996 | PF00917 | 0.580 |
DOC_USP7_UBL2_3 | 1134 | 1138 | PF12436 | 0.691 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.437 |
DOC_USP7_UBL2_3 | 572 | 576 | PF12436 | 0.384 |
DOC_USP7_UBL2_3 | 886 | 890 | PF12436 | 0.474 |
DOC_USP7_UBL2_3 | 893 | 897 | PF12436 | 0.443 |
DOC_USP7_UBL2_3 | 898 | 902 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 1031 | 1036 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 1152 | 1157 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 1176 | 1181 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 849 | 854 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 857 | 862 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 1176 | 1180 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 186 | 195 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 281 | 285 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 376 | 380 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.239 |
LIG_14-3-3_CanoR_1 | 578 | 583 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 590 | 598 | PF00244 | 0.230 |
LIG_14-3-3_CanoR_1 | 682 | 691 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 731 | 736 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 816 | 822 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 952 | 958 | PF00244 | 0.448 |
LIG_AP2alpha_2 | 764 | 766 | PF02296 | 0.468 |
LIG_APCC_ABBA_1 | 619 | 624 | PF00400 | 0.255 |
LIG_BIR_III_2 | 782 | 786 | PF00653 | 0.495 |
LIG_BIR_III_4 | 205 | 209 | PF00653 | 0.532 |
LIG_BRCT_BRCA1_1 | 1049 | 1053 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 1192 | 1196 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.482 |
LIG_EH1_1 | 131 | 139 | PF00400 | 0.414 |
LIG_eIF4E_1 | 132 | 138 | PF01652 | 0.414 |
LIG_eIF4E_1 | 481 | 487 | PF01652 | 0.332 |
LIG_FHA_1 | 1085 | 1091 | PF00498 | 0.259 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.470 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.363 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.438 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.242 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.312 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.459 |
LIG_FHA_1 | 743 | 749 | PF00498 | 0.666 |
LIG_FHA_1 | 796 | 802 | PF00498 | 0.575 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.729 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.508 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.414 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.450 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.425 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.239 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.370 |
LIG_FHA_2 | 730 | 736 | PF00498 | 0.614 |
LIG_FHA_2 | 985 | 991 | PF00498 | 0.729 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 289 | 300 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 461 | 469 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 581 | 589 | PF02991 | 0.238 |
LIG_LIR_Gen_1 | 638 | 648 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 764 | 774 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 1050 | 1056 | PF02991 | 0.179 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 378 | 382 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 581 | 586 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 638 | 643 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 686 | 692 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 764 | 769 | PF02991 | 0.666 |
LIG_NRBOX | 464 | 470 | PF00104 | 0.338 |
LIG_NRBOX | 923 | 929 | PF00104 | 0.393 |
LIG_PCNA_yPIPBox_3 | 142 | 155 | PF02747 | 0.474 |
LIG_PCNA_yPIPBox_3 | 916 | 928 | PF02747 | 0.416 |
LIG_PDZ_Class_2 | 1193 | 1198 | PF00595 | 0.563 |
LIG_Pex14_1 | 582 | 586 | PF04695 | 0.295 |
LIG_Pex14_1 | 672 | 676 | PF04695 | 0.296 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.414 |
LIG_Pex14_2 | 676 | 680 | PF04695 | 0.271 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.457 |
LIG_PTB_Phospho_1 | 149 | 155 | PF10480 | 0.458 |
LIG_REV1ctd_RIR_1 | 584 | 594 | PF16727 | 0.257 |
LIG_SH2_SRC | 1082 | 1085 | PF00017 | 0.271 |
LIG_SH2_STAP1 | 1082 | 1086 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 692 | 696 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 692 | 695 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 903 | 906 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 1056 | 1059 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 1182 | 1185 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.417 |
LIG_SH3_1 | 1133 | 1139 | PF00018 | 0.507 |
LIG_SH3_1 | 66 | 72 | PF00018 | 0.414 |
LIG_SH3_3 | 1069 | 1075 | PF00018 | 0.255 |
LIG_SH3_3 | 1133 | 1139 | PF00018 | 0.521 |
LIG_SH3_3 | 1150 | 1156 | PF00018 | 0.736 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.423 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.665 |
LIG_SH3_3 | 650 | 656 | PF00018 | 0.431 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.414 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.577 |
LIG_SH3_3 | 800 | 806 | PF00018 | 0.568 |
LIG_SH3_3 | 991 | 997 | PF00018 | 0.591 |
LIG_SH3_4 | 1138 | 1145 | PF00018 | 0.505 |
LIG_SUMO_SIM_anti_2 | 492 | 499 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 1075 | 1081 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 347 | 353 | PF11976 | 0.562 |
LIG_SUMO_SIM_par_1 | 797 | 804 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 855 | 860 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 964 | 974 | PF11976 | 0.491 |
LIG_TRAF2_1 | 1006 | 1009 | PF00917 | 0.619 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.414 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.535 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.408 |
LIG_TRAF2_1 | 997 | 1000 | PF00917 | 0.633 |
LIG_UBA3_1 | 115 | 122 | PF00899 | 0.414 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.397 |
LIG_WRC_WIRS_1 | 371 | 376 | PF05994 | 0.270 |
MOD_CDK_SPK_2 | 652 | 657 | PF00069 | 0.178 |
MOD_CK1_1 | 1121 | 1127 | PF00069 | 0.685 |
MOD_CK1_1 | 1155 | 1161 | PF00069 | 0.526 |
MOD_CK1_1 | 1163 | 1169 | PF00069 | 0.402 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.568 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.257 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.334 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.441 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.482 |
MOD_CK1_1 | 973 | 979 | PF00069 | 0.636 |
MOD_CK2_1 | 1011 | 1017 | PF00069 | 0.720 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.370 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.414 |
MOD_CK2_1 | 1138 | 1144 | PF00069 | 0.504 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.489 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.585 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.375 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.260 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.370 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.239 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.661 |
MOD_CK2_1 | 784 | 790 | PF00069 | 0.488 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.711 |
MOD_CK2_1 | 953 | 959 | PF00069 | 0.503 |
MOD_Cter_Amidation | 831 | 834 | PF01082 | 0.484 |
MOD_GlcNHglycan | 1045 | 1048 | PF01048 | 0.597 |
MOD_GlcNHglycan | 1123 | 1126 | PF01048 | 0.684 |
MOD_GlcNHglycan | 1127 | 1130 | PF01048 | 0.658 |
MOD_GlcNHglycan | 1157 | 1160 | PF01048 | 0.619 |
MOD_GlcNHglycan | 1162 | 1165 | PF01048 | 0.573 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.536 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.599 |
MOD_GlcNHglycan | 205 | 209 | PF01048 | 0.670 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.453 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.266 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.209 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.263 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.232 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.606 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.689 |
MOD_GlcNHglycan | 993 | 997 | PF01048 | 0.647 |
MOD_GSK3_1 | 1027 | 1034 | PF00069 | 0.634 |
MOD_GSK3_1 | 1043 | 1050 | PF00069 | 0.332 |
MOD_GSK3_1 | 1117 | 1124 | PF00069 | 0.690 |
MOD_GSK3_1 | 1163 | 1170 | PF00069 | 0.418 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.642 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.412 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.431 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.371 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.251 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.568 |
MOD_GSK3_1 | 849 | 856 | PF00069 | 0.626 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.528 |
MOD_N-GLC_1 | 1167 | 1172 | PF02516 | 0.306 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.344 |
MOD_N-GLC_1 | 886 | 891 | PF02516 | 0.488 |
MOD_N-GLC_1 | 984 | 989 | PF02516 | 0.553 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.370 |
MOD_NEK2_1 | 1175 | 1180 | PF00069 | 0.331 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.425 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.376 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.303 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.492 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.436 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.327 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.432 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.239 |
MOD_NEK2_1 | 776 | 781 | PF00069 | 0.486 |
MOD_NEK2_2 | 1054 | 1059 | PF00069 | 0.271 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.348 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.271 |
MOD_PIKK_1 | 691 | 697 | PF00454 | 0.239 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.445 |
MOD_PIKK_1 | 875 | 881 | PF00454 | 0.566 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.366 |
MOD_PK_1 | 87 | 93 | PF00069 | 0.414 |
MOD_PKA_1 | 402 | 408 | PF00069 | 0.415 |
MOD_PKA_1 | 682 | 688 | PF00069 | 0.271 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.414 |
MOD_PKA_2 | 1175 | 1181 | PF00069 | 0.565 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.409 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.444 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.320 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.323 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.239 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.525 |
MOD_PKA_2 | 839 | 845 | PF00069 | 0.571 |
MOD_Plk_1 | 1167 | 1173 | PF00069 | 0.305 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.422 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.641 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.453 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.302 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.420 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.414 |
MOD_Plk_1 | 984 | 990 | PF00069 | 0.543 |
MOD_Plk_2-3 | 804 | 810 | PF00069 | 0.559 |
MOD_Plk_4 | 1167 | 1173 | PF00069 | 0.498 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.487 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.352 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.351 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.496 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.463 |
MOD_Plk_4 | 701 | 707 | PF00069 | 0.239 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.566 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.597 |
MOD_Plk_4 | 797 | 803 | PF00069 | 0.415 |
MOD_Plk_4 | 920 | 926 | PF00069 | 0.410 |
MOD_ProDKin_1 | 1031 | 1037 | PF00069 | 0.463 |
MOD_ProDKin_1 | 1152 | 1158 | PF00069 | 0.573 |
MOD_ProDKin_1 | 1176 | 1182 | PF00069 | 0.343 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.292 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.374 |
MOD_ProDKin_1 | 849 | 855 | PF00069 | 0.622 |
MOD_ProDKin_1 | 857 | 863 | PF00069 | 0.642 |
MOD_SUMO_for_1 | 227 | 230 | PF00179 | 0.495 |
MOD_SUMO_for_1 | 235 | 238 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 406 | 414 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 567 | 574 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 677 | 685 | PF00179 | 0.244 |
TRG_DiLeu_BaEn_1 | 145 | 150 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 230 | 235 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.309 |
TRG_DiLeu_BaEn_1 | 772 | 777 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.289 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 769 | 771 | PF00400 | 0.532 |
TRG_NLS_MonoCore_2 | 1133 | 1138 | PF00514 | 0.510 |
TRG_NLS_MonoExtC_3 | 1132 | 1137 | PF00514 | 0.521 |
TRG_NLS_MonoExtC_3 | 469 | 475 | PF00514 | 0.425 |
TRG_NLS_MonoExtC_3 | 892 | 897 | PF00514 | 0.447 |
TRG_NLS_MonoExtN_4 | 1132 | 1138 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 890 | 897 | PF00514 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2W4 | Leptomonas seymouri | 60% | 95% |
A0A1X0NMG1 | Trypanosomatidae | 45% | 100% |
A0A3Q8I8L7 | Leishmania donovani | 77% | 98% |
A0A422MXM2 | Trypanosoma rangeli | 44% | 100% |
A4HU15 | Leishmania infantum | 78% | 98% |
D0A9I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AMU6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QHT0 | Leishmania major | 78% | 100% |
V5B6T4 | Trypanosoma cruzi | 43% | 100% |