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 | 2 |
GO:1990112 | RQC complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QHT0
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0072344 | rescue of stalled ribosome | 6 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1990116 | ribosome-associated ubiquitin-dependent protein catabolic process | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 2 |
GO:0043023 | ribosomal large subunit binding | 4 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 393 | 397 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 1160 | 1162 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 558 | 560 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 904 | 906 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 907 | 909 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 943 | 945 | PF00675 | 0.677 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.173 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 904 | 906 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 955 | 957 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 401 | 403 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.292 |
CLV_PCSK_PC1ET2_1 | 904 | 906 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 955 | 957 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 466 | 472 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 1122 | 1126 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 1161 | 1165 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 843 | 847 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 897 | 901 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 769 | 777 | PF00400 | 0.643 |
DEG_APCC_DBOX_1 | 934 | 942 | PF00400 | 0.587 |
DEG_Kelch_Keap1_1 | 502 | 507 | PF01344 | 0.389 |
DEG_SCF_FBW7_1 | 860 | 867 | PF00400 | 0.633 |
DEG_SCF_TRCP1_1 | 782 | 787 | PF00400 | 0.521 |
DOC_ANK_TNKS_1 | 470 | 477 | PF00023 | 0.467 |
DOC_CKS1_1 | 861 | 866 | PF01111 | 0.631 |
DOC_CKS1_1 | 969 | 974 | PF01111 | 0.787 |
DOC_CYCLIN_RxL_1 | 1122 | 1134 | PF00134 | 0.335 |
DOC_MAPK_DCC_7 | 1214 | 1222 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 139 | 149 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 231 | 240 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 3 | 11 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 47 | 53 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 816 | 823 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 490 | 497 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 1216 | 1223 | PF00149 | 0.562 |
DOC_PP1_RVXF_1 | 237 | 243 | PF00149 | 0.292 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.500 |
DOC_PP2B_PxIxI_1 | 1101 | 1107 | PF00149 | 0.335 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.451 |
DOC_USP7_MATH_1 | 1020 | 1024 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 1058 | 1062 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 762 | 766 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 780 | 784 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.748 |
DOC_USP7_UBL2_3 | 1165 | 1169 | PF12436 | 0.725 |
DOC_USP7_UBL2_3 | 403 | 407 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 572 | 576 | PF12436 | 0.386 |
DOC_USP7_UBL2_3 | 843 | 847 | PF12436 | 0.616 |
DOC_USP7_UBL2_3 | 909 | 913 | PF12436 | 0.522 |
DOC_WW_Pin1_4 | 1178 | 1183 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 1184 | 1189 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 776 | 781 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 860 | 865 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 886 | 891 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 968 | 973 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 12 | 16 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 284 | 294 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 376 | 380 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 590 | 598 | PF00244 | 0.259 |
LIG_14-3-3_CanoR_1 | 682 | 691 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 816 | 822 | PF00244 | 0.607 |
LIG_APCC_ABBA_1 | 619 | 624 | PF00400 | 0.289 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.508 |
LIG_Clathr_ClatBox_1 | 237 | 241 | PF01394 | 0.292 |
LIG_EH1_1 | 131 | 139 | PF00400 | 0.436 |
LIG_eIF4E_1 | 132 | 138 | PF01652 | 0.436 |
LIG_eIF4E_1 | 481 | 487 | PF01652 | 0.436 |
LIG_FHA_1 | 1204 | 1210 | PF00498 | 0.528 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.627 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.554 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.494 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.506 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.273 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.349 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.491 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.531 |
LIG_FHA_2 | 1040 | 1046 | PF00498 | 0.733 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.436 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.499 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.434 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.466 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.271 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.292 |
LIG_FHA_2 | 730 | 736 | PF00498 | 0.624 |
LIG_FHA_2 | 887 | 893 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 101 | 107 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 129 | 138 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 292 | 303 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 461 | 469 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 638 | 648 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 764 | 774 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 461 | 465 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 638 | 643 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 686 | 692 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 764 | 769 | PF02991 | 0.672 |
LIG_LIR_Nem_3 | 971 | 977 | PF02991 | 0.688 |
LIG_MYND_1 | 774 | 778 | PF01753 | 0.489 |
LIG_NRBOX | 464 | 470 | PF00104 | 0.436 |
LIG_PCNA_yPIPBox_3 | 368 | 381 | PF02747 | 0.451 |
LIG_PDZ_Class_2 | 1219 | 1224 | PF00595 | 0.598 |
LIG_Pex14_1 | 582 | 586 | PF04695 | 0.327 |
LIG_Pex14_1 | 672 | 676 | PF04695 | 0.333 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.436 |
LIG_Pex14_2 | 676 | 680 | PF04695 | 0.335 |
LIG_REV1ctd_RIR_1 | 584 | 594 | PF16727 | 0.313 |
LIG_RPA_C_Fungi | 554 | 566 | PF08784 | 0.543 |
LIG_SH2_CRK | 974 | 978 | PF00017 | 0.692 |
LIG_SH2_GRB2like | 366 | 369 | PF00017 | 0.292 |
LIG_SH2_SRC | 1109 | 1112 | PF00017 | 0.335 |
LIG_SH2_SRC | 705 | 708 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 692 | 696 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 692 | 695 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 914 | 917 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 1083 | 1086 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 1109 | 1112 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.436 |
LIG_SH3_1 | 66 | 72 | PF00018 | 0.271 |
LIG_SH3_2 | 280 | 285 | PF14604 | 0.226 |
LIG_SH3_3 | 1096 | 1102 | PF00018 | 0.289 |
LIG_SH3_3 | 1176 | 1182 | PF00018 | 0.768 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.449 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.240 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.431 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.292 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.592 |
LIG_SH3_3 | 783 | 789 | PF00018 | 0.785 |
LIG_SH3_3 | 800 | 806 | PF00018 | 0.613 |
LIG_SH3_3 | 966 | 972 | PF00018 | 0.747 |
LIG_SUMO_SIM_anti_2 | 492 | 499 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 272 | 277 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 347 | 353 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 513 | 518 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 658 | 665 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 801 | 807 | PF11976 | 0.517 |
LIG_TRAF2_1 | 1023 | 1026 | PF00917 | 0.690 |
LIG_TRAF2_1 | 1032 | 1035 | PF00917 | 0.674 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.271 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.542 |
LIG_TRAF2_1 | 986 | 989 | PF00917 | 0.615 |
LIG_UBA3_1 | 115 | 122 | PF00899 | 0.271 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.384 |
LIG_WRC_WIRS_1 | 763 | 768 | PF05994 | 0.557 |
MOD_CDK_SPK_2 | 886 | 891 | PF00069 | 0.512 |
MOD_CDK_SPxxK_3 | 968 | 975 | PF00069 | 0.595 |
MOD_CK1_1 | 1183 | 1189 | PF00069 | 0.570 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.204 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.313 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.405 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.351 |
MOD_CK1_1 | 997 | 1003 | PF00069 | 0.703 |
MOD_CK2_1 | 1013 | 1019 | PF00069 | 0.652 |
MOD_CK2_1 | 1020 | 1026 | PF00069 | 0.639 |
MOD_CK2_1 | 1039 | 1045 | PF00069 | 0.753 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.271 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.635 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.267 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.335 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.271 |
MOD_CK2_1 | 729 | 735 | PF00069 | 0.654 |
MOD_CK2_1 | 871 | 877 | PF00069 | 0.715 |
MOD_Cter_Amidation | 1159 | 1162 | PF01082 | 0.520 |
MOD_DYRK1A_RPxSP_1 | 1178 | 1182 | PF00069 | 0.544 |
MOD_GlcNHglycan | 1014 | 1018 | PF01048 | 0.645 |
MOD_GlcNHglycan | 1072 | 1075 | PF01048 | 0.600 |
MOD_GlcNHglycan | 1118 | 1121 | PF01048 | 0.204 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.609 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.590 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.580 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.664 |
MOD_GlcNHglycan | 208 | 212 | PF01048 | 0.706 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.388 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.382 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.426 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.422 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.349 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.262 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.714 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.685 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.644 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.706 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.703 |
MOD_GlcNHglycan | 963 | 966 | PF01048 | 0.671 |
MOD_GSK3_1 | 1054 | 1061 | PF00069 | 0.644 |
MOD_GSK3_1 | 1180 | 1187 | PF00069 | 0.627 |
MOD_GSK3_1 | 1189 | 1196 | PF00069 | 0.456 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.654 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.315 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.333 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.285 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.617 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.575 |
MOD_GSK3_1 | 860 | 867 | PF00069 | 0.645 |
MOD_N-GLC_1 | 897 | 902 | PF02516 | 0.578 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.289 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.342 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.271 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.330 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.394 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.305 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.271 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.349 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.271 |
MOD_NEK2_2 | 1081 | 1086 | PF00069 | 0.335 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.386 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.363 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.335 |
MOD_PIKK_1 | 691 | 697 | PF00454 | 0.271 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.320 |
MOD_PK_1 | 87 | 93 | PF00069 | 0.271 |
MOD_PKA_1 | 1161 | 1167 | PF00069 | 0.546 |
MOD_PKA_1 | 402 | 408 | PF00069 | 0.281 |
MOD_PKA_1 | 682 | 688 | PF00069 | 0.335 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.271 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.271 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.364 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.404 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.350 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.289 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.271 |
MOD_PKA_2 | 850 | 856 | PF00069 | 0.625 |
MOD_PKB_1 | 1178 | 1186 | PF00069 | 0.541 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.651 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.521 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.340 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.333 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.271 |
MOD_Plk_2-3 | 804 | 810 | PF00069 | 0.596 |
MOD_Plk_4 | 1193 | 1199 | PF00069 | 0.530 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.303 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.369 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.396 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.426 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.301 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.477 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.615 |
MOD_ProDKin_1 | 1178 | 1184 | PF00069 | 0.652 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.271 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.406 |
MOD_ProDKin_1 | 776 | 782 | PF00069 | 0.593 |
MOD_ProDKin_1 | 860 | 866 | PF00069 | 0.640 |
MOD_ProDKin_1 | 886 | 892 | PF00069 | 0.617 |
MOD_ProDKin_1 | 968 | 974 | PF00069 | 0.783 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.527 |
MOD_SUMO_for_1 | 433 | 436 | PF00179 | 0.302 |
MOD_SUMO_rev_2 | 143 | 151 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 408 | 414 | PF00179 | 0.339 |
MOD_SUMO_rev_2 | 677 | 685 | PF00179 | 0.276 |
TRG_DiLeu_BaEn_1 | 233 | 238 | PF01217 | 0.445 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.271 |
TRG_DiLeu_BaEn_1 | 772 | 777 | PF01217 | 0.546 |
TRG_DiLeu_BaLyEn_6 | 23 | 28 | PF01217 | 0.289 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 974 | 977 | PF00928 | 0.692 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.271 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.271 |
TRG_NLS_MonoExtC_3 | 469 | 475 | PF00514 | 0.349 |
TRG_NLS_MonoExtC_3 | 903 | 908 | PF00514 | 0.501 |
TRG_NLS_MonoExtN_4 | 838 | 844 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 901 | 908 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 228 | 232 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 908 | 912 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 922 | 927 | PF00026 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2W4 | Leptomonas seymouri | 59% | 98% |
A0A1X0NMG1 | Trypanosomatidae | 45% | 100% |
A0A3Q8I8L7 | Leishmania donovani | 91% | 100% |
A0A422MXM2 | Trypanosoma rangeli | 44% | 100% |
A4H5S2 | Leishmania braziliensis | 78% | 100% |
A4HU15 | Leishmania infantum | 91% | 100% |
D0A9I3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AMU6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5B6T4 | Trypanosoma cruzi | 43% | 100% |