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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3Q8IAZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006399 | tRNA metabolic process | 7 | 12 |
GO:0006400 | tRNA modification | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008033 | tRNA processing | 8 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 11 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0042274 | ribosomal small subunit biogenesis | 5 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044085 | cellular component biogenesis | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051391 | tRNA acetylation | 7 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1990884 | RNA acetylation | 6 | 12 |
GO:1904812 | rRNA acetylation involved in maturation of SSU-rRNA | 8 | 1 |
GO:1990882 | rRNA acetylation | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008080 | N-acetyltransferase activity | 6 | 12 |
GO:0016407 | acetyltransferase activity | 5 | 12 |
GO:0016410 | N-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0000049 | tRNA binding | 5 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:1990883 | rRNA cytidine N-acetyltransferase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1045 | 1049 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 893 | 897 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 1015 | 1017 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.268 |
CLV_PCSK_KEX2_1 | 1063 | 1065 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 973 | 975 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 1063 | 1065 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 281 | 283 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.263 |
CLV_PCSK_PC1ET2_1 | 973 | 975 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 1010 | 1014 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 1016 | 1020 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 1026 | 1030 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 670 | 674 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 886 | 890 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 936 | 940 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 955 | 959 | PF00082 | 0.302 |
DEG_APCC_DBOX_1 | 1046 | 1054 | PF00400 | 0.642 |
DEG_SCF_FBW7_2 | 716 | 722 | PF00400 | 0.470 |
DEG_SPOP_SBC_1 | 563 | 567 | PF00917 | 0.554 |
DOC_CDC14_PxL_1 | 873 | 881 | PF14671 | 0.336 |
DOC_CKS1_1 | 716 | 721 | PF01111 | 0.467 |
DOC_CYCLIN_RxL_1 | 19 | 31 | PF00134 | 0.461 |
DOC_CYCLIN_RxL_1 | 471 | 482 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 881 | 893 | PF00134 | 0.402 |
DOC_CYCLIN_RxL_1 | 933 | 944 | PF00134 | 0.422 |
DOC_CYCLIN_yCln2_LP_2 | 793 | 799 | PF00134 | 0.359 |
DOC_MAPK_gen_1 | 21 | 29 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 369 | 377 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 746 | 753 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 75 | 81 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 143 | 152 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 21 | 29 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 34 | 42 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 360 | 367 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 746 | 755 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 788 | 795 | PF00069 | 0.343 |
DOC_PP1_RVXF_1 | 879 | 885 | PF00149 | 0.294 |
DOC_PP2B_LxvP_1 | 793 | 796 | PF13499 | 0.317 |
DOC_PP4_FxxP_1 | 1054 | 1057 | PF00568 | 0.658 |
DOC_PP4_FxxP_1 | 889 | 892 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 1032 | 1036 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 983 | 987 | PF00917 | 0.608 |
DOC_USP7_UBL2_3 | 1013 | 1017 | PF12436 | 0.672 |
DOC_USP7_UBL2_3 | 1059 | 1063 | PF12436 | 0.613 |
DOC_USP7_UBL2_3 | 109 | 113 | PF12436 | 0.458 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 471 | 475 | PF12436 | 0.527 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.461 |
DOC_USP7_UBL2_3 | 955 | 959 | PF12436 | 0.383 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 153 | 159 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 171 | 180 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 428 | 433 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 520 | 525 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 649 | 654 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 860 | 867 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 9 | 14 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 945 | 953 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 1015 | 1032 | PF00022 | 0.612 |
LIG_APCC_ABBA_1 | 365 | 370 | PF00400 | 0.439 |
LIG_APCC_ABBAyCdc20_2 | 364 | 370 | PF00400 | 0.439 |
LIG_BIR_III_4 | 542 | 546 | PF00653 | 0.449 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 862 | 866 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_2 | 354 | 360 | PF00533 | 0.535 |
LIG_Clathr_ClatBox_1 | 476 | 480 | PF01394 | 0.449 |
LIG_eIF4E_1 | 883 | 889 | PF01652 | 0.357 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.449 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.379 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.493 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.460 |
LIG_FHA_1 | 736 | 742 | PF00498 | 0.490 |
LIG_FHA_1 | 862 | 868 | PF00498 | 0.271 |
LIG_FHA_1 | 893 | 899 | PF00498 | 0.387 |
LIG_FHA_1 | 916 | 922 | PF00498 | 0.450 |
LIG_FHA_1 | 930 | 936 | PF00498 | 0.382 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.554 |
LIG_FHA_2 | 1043 | 1049 | PF00498 | 0.685 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.560 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.465 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.395 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.459 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.395 |
LIG_FHA_2 | 663 | 669 | PF00498 | 0.549 |
LIG_FHA_2 | 841 | 847 | PF00498 | 0.316 |
LIG_FHA_2 | 863 | 869 | PF00498 | 0.305 |
LIG_FHA_2 | 915 | 921 | PF00498 | 0.387 |
LIG_IRF3_LxIS_1 | 38 | 45 | PF10401 | 0.499 |
LIG_LIR_Apic_2 | 1052 | 1057 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 346 | 354 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 578 | 585 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 621 | 632 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 722 | 733 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 92 | 99 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 126 | 130 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 578 | 583 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 621 | 627 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 722 | 728 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 749 | 753 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.449 |
LIG_MAD2 | 631 | 639 | PF02301 | 0.449 |
LIG_NRBOX | 472 | 478 | PF00104 | 0.449 |
LIG_NRP_CendR_1 | 1063 | 1065 | PF00754 | 0.733 |
LIG_PCNA_PIPBox_1 | 155 | 164 | PF02747 | 0.449 |
LIG_Pex14_2 | 184 | 188 | PF04695 | 0.449 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.554 |
LIG_RPA_C_Fungi | 435 | 447 | PF08784 | 0.449 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.302 |
LIG_SH2_CRK | 510 | 514 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 313 | 316 | PF00017 | 0.302 |
LIG_SH2_GRB2like | 501 | 504 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 725 | 729 | PF00017 | 0.317 |
LIG_SH2_PTP2 | 750 | 753 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 530 | 533 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 754 | 757 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 730 | 733 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 750 | 753 | PF00017 | 0.118 |
LIG_SH2_STAT5 | 754 | 757 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 883 | 886 | PF00017 | 0.315 |
LIG_SH3_1 | 462 | 468 | PF00018 | 0.302 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.302 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.410 |
LIG_SUMO_SIM_anti_2 | 270 | 277 | PF11976 | 0.368 |
LIG_SUMO_SIM_par_1 | 146 | 151 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 412 | 419 | PF11976 | 0.422 |
LIG_SxIP_EBH_1 | 744 | 756 | PF03271 | 0.371 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.302 |
LIG_TRAF2_1 | 917 | 920 | PF00917 | 0.379 |
LIG_TRFH_1 | 776 | 780 | PF08558 | 0.552 |
LIG_UBA3_1 | 13 | 21 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 149 | 154 | PF05994 | 0.371 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.302 |
MOD_CK1_1 | 1034 | 1040 | PF00069 | 0.675 |
MOD_CK1_1 | 1041 | 1047 | PF00069 | 0.631 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.564 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.317 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.430 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.405 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.353 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.434 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.390 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.334 |
MOD_CK1_1 | 821 | 827 | PF00069 | 0.389 |
MOD_CK1_1 | 928 | 934 | PF00069 | 0.415 |
MOD_CK1_1 | 944 | 950 | PF00069 | 0.359 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.377 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.302 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.302 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.302 |
MOD_CK2_1 | 492 | 498 | PF00069 | 0.440 |
MOD_CK2_1 | 662 | 668 | PF00069 | 0.441 |
MOD_CK2_1 | 862 | 868 | PF00069 | 0.314 |
MOD_CK2_1 | 914 | 920 | PF00069 | 0.387 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.387 |
MOD_Cter_Amidation | 971 | 974 | PF01082 | 0.559 |
MOD_GlcNHglycan | 1036 | 1039 | PF01048 | 0.658 |
MOD_GlcNHglycan | 1040 | 1043 | PF01048 | 0.634 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.311 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.422 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.302 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.330 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.521 |
MOD_GlcNHglycan | 557 | 561 | PF01048 | 0.379 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.356 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.415 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.317 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.359 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.230 |
MOD_GlcNHglycan | 699 | 703 | PF01048 | 0.391 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.441 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.386 |
MOD_GlcNHglycan | 927 | 930 | PF01048 | 0.315 |
MOD_GlcNHglycan | 985 | 988 | PF01048 | 0.701 |
MOD_GSK3_1 | 1030 | 1037 | PF00069 | 0.666 |
MOD_GSK3_1 | 1038 | 1045 | PF00069 | 0.609 |
MOD_GSK3_1 | 1055 | 1062 | PF00069 | 0.612 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.302 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.380 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.501 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.541 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.380 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.377 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.393 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.317 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.463 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.549 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.381 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.390 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.326 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.290 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.317 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.378 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.201 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.302 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.289 |
MOD_GSK3_1 | 925 | 932 | PF00069 | 0.420 |
MOD_LATS_1 | 169 | 175 | PF00433 | 0.302 |
MOD_LATS_1 | 451 | 457 | PF00433 | 0.449 |
MOD_N-GLC_1 | 1038 | 1043 | PF02516 | 0.743 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.302 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.302 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.372 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.387 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.302 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.305 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.449 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.367 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.302 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.331 |
MOD_NEK2_1 | 804 | 809 | PF00069 | 0.310 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.302 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.302 |
MOD_NEK2_2 | 154 | 159 | PF00069 | 0.302 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.382 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.556 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.302 |
MOD_PIKK_1 | 929 | 935 | PF00454 | 0.422 |
MOD_PKA_1 | 1059 | 1065 | PF00069 | 0.757 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.359 |
MOD_PKA_1 | 675 | 681 | PF00069 | 0.422 |
MOD_PKA_1 | 746 | 752 | PF00069 | 0.371 |
MOD_PKA_2 | 1046 | 1052 | PF00069 | 0.631 |
MOD_PKA_2 | 1055 | 1061 | PF00069 | 0.665 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.526 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.471 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.302 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.388 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.354 |
MOD_PKA_2 | 675 | 681 | PF00069 | 0.367 |
MOD_PKA_2 | 944 | 950 | PF00069 | 0.422 |
MOD_PKB_1 | 171 | 179 | PF00069 | 0.417 |
MOD_PKB_1 | 293 | 301 | PF00069 | 0.302 |
MOD_PKB_1 | 858 | 866 | PF00069 | 0.422 |
MOD_PKB_1 | 974 | 982 | PF00069 | 0.579 |
MOD_Plk_1 | 1024 | 1030 | PF00069 | 0.577 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.399 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.336 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.464 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.302 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.369 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.377 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.302 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.399 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.328 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.369 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.371 |
MOD_Plk_4 | 804 | 810 | PF00069 | 0.314 |
MOD_Plk_4 | 862 | 868 | PF00069 | 0.296 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.363 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.302 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.302 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.509 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.343 |
MOD_SUMO_rev_2 | 663 | 672 | PF00179 | 0.448 |
TRG_AP2beta_CARGO_1 | 621 | 631 | PF09066 | 0.302 |
TRG_DiLeu_BaLyEn_6 | 716 | 721 | PF01217 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 785 | 790 | PF01217 | 0.328 |
TRG_DiLeu_BaLyEn_6 | 973 | 978 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.412 |
TRG_ENDOCYTIC_2 | 725 | 728 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.235 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 858 | 861 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 974 | 977 | PF00400 | 0.473 |
TRG_NES_CRM1_1 | 726 | 740 | PF08389 | 0.422 |
TRG_NLS_Bipartite_1 | 958 | 977 | PF00514 | 0.444 |
TRG_NLS_MonoExtC_3 | 674 | 680 | PF00514 | 0.235 |
TRG_NLS_MonoExtN_4 | 1013 | 1020 | PF00514 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 1026 | 1031 | PF00026 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 156 | 160 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 335 | 339 | PF00026 | 0.295 |
TRG_Pf-PMV_PEXEL_1 | 450 | 454 | PF00026 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 779 | 784 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 798 | 803 | PF00026 | 0.140 |
TRG_Pf-PMV_PEXEL_1 | 976 | 980 | PF00026 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8D1 | Leptomonas seymouri | 81% | 98% |
A0A0S4J7H9 | Bodo saltans | 59% | 100% |
A0A1X0NTC6 | Trypanosomatidae | 63% | 100% |
A0A422NAR4 | Trypanosoma rangeli | 64% | 100% |
A1RY08 | Thermofilum pendens (strain DSM 2475 / Hrk 5) | 27% | 100% |
A4H984 | Leishmania braziliensis | 89% | 100% |
A4HXK2 | Leishmania infantum | 100% | 100% |
C9ZP92 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E9AR97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
O01757 | Caenorhabditis elegans | 40% | 100% |
P53914 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 41% | 100% |
P87115 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
Q4QE66 | Leishmania major | 95% | 100% |
Q55EJ3 | Dictyostelium discoideum | 41% | 100% |
Q8K224 | Mus musculus | 41% | 100% |
Q9H0A0 | Homo sapiens | 43% | 100% |
Q9M2Q4 | Arabidopsis thaliana | 39% | 100% |
Q9W3C1 | Drosophila melanogaster | 40% | 100% |
Q9XIK4 | Arabidopsis thaliana | 39% | 100% |
V5BJF5 | Trypanosoma cruzi | 64% | 100% |