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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HCT1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0016567 | protein ubiquitination | 7 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0032446 | protein modification by small protein conjugation | 6 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008641 | ubiquitin-like modifier activating enzyme activity | 2 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016877 | ligase activity, forming carbon-sulfur bonds | 3 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0004839 | ubiquitin activating enzyme activity | 3 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016746 | acyltransferase activity | 3 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 1 |
GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1012 | 1016 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.354 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 801 | 803 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 879 | 881 | PF00675 | 0.579 |
CLV_PCSK_KEX2_1 | 1000 | 1002 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 696 | 698 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 801 | 803 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 1000 | 1002 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 696 | 698 | PF00082 | 0.268 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 843 | 845 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 686 | 690 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 870 | 874 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 905 | 909 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 911 | 915 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 957 | 961 | PF00082 | 0.300 |
DEG_APCC_DBOX_1 | 685 | 693 | PF00400 | 0.468 |
DEG_COP1_1 | 215 | 223 | PF00400 | 0.213 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.628 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.370 |
DEG_SPOP_SBC_1 | 854 | 858 | PF00917 | 0.353 |
DOC_CYCLIN_RxL_1 | 551 | 564 | PF00134 | 0.296 |
DOC_CYCLIN_yCln2_LP_2 | 110 | 116 | PF00134 | 0.346 |
DOC_CYCLIN_yCln2_LP_2 | 631 | 637 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 969 | 976 | PF00069 | 0.481 |
DOC_MAPK_HePTP_8 | 565 | 577 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 568 | 577 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 911 | 919 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 969 | 978 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 137 | 143 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.437 |
DOC_PP1_RVXF_1 | 939 | 946 | PF00149 | 0.536 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.346 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.328 |
DOC_PP4_FxxP_1 | 924 | 927 | PF00568 | 0.337 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 936 | 940 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 709 | 713 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 994 | 998 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.353 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 141 | 150 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 490 | 495 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 775 | 783 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 225 | 243 | PF00022 | 0.370 |
LIG_AP2alpha_1 | 681 | 685 | PF02296 | 0.482 |
LIG_APCC_ABBA_1 | 186 | 191 | PF00400 | 0.309 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.294 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.294 |
LIG_Clathr_ClatBox_1 | 285 | 289 | PF01394 | 0.467 |
LIG_Clathr_ClatBox_1 | 863 | 867 | PF01394 | 0.309 |
LIG_eIF4E_1 | 729 | 735 | PF01652 | 0.468 |
LIG_FHA_1 | 1023 | 1029 | PF00498 | 0.482 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.302 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.483 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.457 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.309 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.323 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.318 |
LIG_FHA_1 | 840 | 846 | PF00498 | 0.471 |
LIG_FHA_1 | 854 | 860 | PF00498 | 0.378 |
LIG_FHA_2 | 1010 | 1016 | PF00498 | 0.431 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.213 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.396 |
LIG_FHA_2 | 465 | 471 | PF00498 | 0.295 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.370 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.360 |
LIG_IRF3_LxIS_1 | 947 | 954 | PF10401 | 0.213 |
LIG_KLC1_Yacidic_2 | 893 | 898 | PF13176 | 0.423 |
LIG_LIR_Apic_2 | 583 | 589 | PF02991 | 0.353 |
LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.328 |
LIG_LIR_Apic_2 | 932 | 938 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 1018 | 1028 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 614 | 624 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 912 | 922 | PF02991 | 0.365 |
LIG_LIR_LC3C_4 | 1021 | 1024 | PF02991 | 0.559 |
LIG_LIR_LC3C_4 | 30 | 35 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 1018 | 1023 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 614 | 619 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 912 | 917 | PF02991 | 0.364 |
LIG_NRBOX | 614 | 620 | PF00104 | 0.559 |
LIG_NRBOX | 671 | 677 | PF00104 | 0.554 |
LIG_NRBOX | 868 | 874 | PF00104 | 0.309 |
LIG_NRBOX | 963 | 969 | PF00104 | 0.524 |
LIG_PDZ_Class_2 | 1040 | 1045 | PF00595 | 0.460 |
LIG_Pex14_2 | 524 | 528 | PF04695 | 0.294 |
LIG_Pex14_2 | 616 | 620 | PF04695 | 0.457 |
LIG_Pex14_2 | 681 | 685 | PF04695 | 0.461 |
LIG_Pex14_2 | 910 | 914 | PF04695 | 0.464 |
LIG_PTB_Apo_2 | 522 | 529 | PF02174 | 0.328 |
LIG_REV1ctd_RIR_1 | 71 | 76 | PF16727 | 0.346 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.346 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.328 |
LIG_SH2_CRK | 739 | 743 | PF00017 | 0.500 |
LIG_SH2_CRK | 832 | 836 | PF00017 | 0.464 |
LIG_SH2_CRK | 935 | 939 | PF00017 | 0.461 |
LIG_SH2_GRB2like | 120 | 123 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 586 | 590 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 832 | 836 | PF00017 | 0.438 |
LIG_SH2_NCK_1 | 935 | 939 | PF00017 | 0.528 |
LIG_SH2_SRC | 547 | 550 | PF00017 | 0.309 |
LIG_SH2_SRC | 586 | 589 | PF00017 | 0.389 |
LIG_SH2_SRC | 677 | 680 | PF00017 | 0.559 |
LIG_SH2_SRC | 896 | 899 | PF00017 | 0.646 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 582 | 586 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 972 | 976 | PF00017 | 0.559 |
LIG_SH2_STAT3 | 12 | 15 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 434 | 437 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 1019 | 1022 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 871 | 874 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 896 | 899 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 988 | 991 | PF00017 | 0.559 |
LIG_SH3_2 | 414 | 419 | PF14604 | 0.336 |
LIG_SH3_3 | 1031 | 1037 | PF00018 | 0.470 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.374 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.294 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.437 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.502 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.392 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.559 |
LIG_SH3_3 | 708 | 714 | PF00018 | 0.457 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.518 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.262 |
LIG_Sin3_3 | 1020 | 1027 | PF02671 | 0.559 |
LIG_SUMO_SIM_anti_2 | 160 | 168 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 29 | 36 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 183 | 191 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 251 | 258 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 62 | 68 | PF11976 | 0.439 |
LIG_TRAF2_1 | 361 | 364 | PF00917 | 0.294 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.437 |
LIG_TRAF2_1 | 747 | 750 | PF00917 | 0.524 |
LIG_TRAF2_1 | 899 | 902 | PF00917 | 0.579 |
LIG_TRFH_1 | 73 | 77 | PF08558 | 0.328 |
LIG_TRFH_1 | 739 | 743 | PF08558 | 0.478 |
LIG_TYR_ITIM | 1017 | 1022 | PF00017 | 0.559 |
LIG_TYR_ITIM | 869 | 874 | PF00017 | 0.353 |
LIG_UBA3_1 | 688 | 696 | PF00899 | 0.468 |
LIG_UBA3_1 | 978 | 985 | PF00899 | 0.457 |
LIG_ULM_U2AF65_1 | 941 | 946 | PF00076 | 0.461 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.437 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.485 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.422 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.491 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.294 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.328 |
MOD_CK1_1 | 778 | 784 | PF00069 | 0.555 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.440 |
MOD_CK1_1 | 858 | 864 | PF00069 | 0.353 |
MOD_CK2_1 | 1005 | 1011 | PF00069 | 0.485 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.353 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.165 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.437 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.309 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.369 |
MOD_CK2_1 | 744 | 750 | PF00069 | 0.485 |
MOD_CK2_1 | 887 | 893 | PF00069 | 0.538 |
MOD_CMANNOS | 945 | 948 | PF00535 | 0.355 |
MOD_Cter_Amidation | 266 | 269 | PF01082 | 0.370 |
MOD_Cter_Amidation | 939 | 942 | PF01082 | 0.495 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.370 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.213 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.437 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.423 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.216 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.294 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.673 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.580 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.327 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.238 |
MOD_GlcNHglycan | 784 | 787 | PF01048 | 0.343 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.511 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.481 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.586 |
MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.505 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.483 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.315 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.248 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.294 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.603 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.309 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.328 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.294 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.561 |
MOD_GSK3_1 | 770 | 777 | PF00069 | 0.540 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.522 |
MOD_GSK3_1 | 793 | 800 | PF00069 | 0.563 |
MOD_GSK3_1 | 854 | 861 | PF00069 | 0.308 |
MOD_GSK3_1 | 905 | 912 | PF00069 | 0.515 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.437 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.294 |
MOD_N-GLC_1 | 839 | 844 | PF02516 | 0.359 |
MOD_NEK2_1 | 1022 | 1027 | PF00069 | 0.468 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.294 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.294 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.640 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.294 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.482 |
MOD_NEK2_1 | 703 | 708 | PF00069 | 0.451 |
MOD_NEK2_1 | 839 | 844 | PF00069 | 0.529 |
MOD_NEK2_1 | 853 | 858 | PF00069 | 0.285 |
MOD_NEK2_1 | 909 | 914 | PF00069 | 0.491 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.309 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.437 |
MOD_NEK2_2 | 52 | 57 | PF00069 | 0.353 |
MOD_NEK2_2 | 594 | 599 | PF00069 | 0.294 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.328 |
MOD_PIKK_1 | 775 | 781 | PF00454 | 0.518 |
MOD_PIKK_1 | 793 | 799 | PF00454 | 0.438 |
MOD_PK_1 | 490 | 496 | PF00069 | 0.437 |
MOD_PKA_1 | 1000 | 1006 | PF00069 | 0.511 |
MOD_PKA_2 | 1000 | 1006 | PF00069 | 0.511 |
MOD_PKA_2 | 774 | 780 | PF00069 | 0.399 |
MOD_PKA_2 | 879 | 885 | PF00069 | 0.504 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.294 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.370 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.488 |
MOD_Plk_1 | 748 | 754 | PF00069 | 0.445 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.429 |
MOD_Plk_2-3 | 468 | 474 | PF00069 | 0.309 |
MOD_Plk_2-3 | 695 | 701 | PF00069 | 0.399 |
MOD_Plk_4 | 1009 | 1015 | PF00069 | 0.422 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.323 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.426 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.420 |
MOD_Plk_4 | 855 | 861 | PF00069 | 0.363 |
MOD_Plk_4 | 905 | 911 | PF00069 | 0.366 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.358 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.265 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.353 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.294 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.361 |
MOD_SUMO_for_1 | 663 | 666 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 133 | 140 | PF00179 | 0.213 |
MOD_SUMO_rev_2 | 289 | 295 | PF00179 | 0.298 |
TRG_DiLeu_BaEn_1 | 902 | 907 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_1 | 963 | 968 | PF01217 | 0.511 |
TRG_DiLeu_BaEn_2 | 93 | 99 | PF01217 | 0.309 |
TRG_DiLeu_BaEn_2 | 972 | 978 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_4 | 667 | 673 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.346 |
TRG_DiLeu_BaLyEn_6 | 555 | 560 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 671 | 676 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 1019 | 1022 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 871 | 874 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 988 | 991 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 801 | 804 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 827 | 830 | PF00400 | 0.551 |
TRG_NES_CRM1_1 | 614 | 626 | PF08389 | 0.511 |
TRG_NLS_MonoExtC_3 | 264 | 269 | PF00514 | 0.370 |
TRG_NLS_MonoExtN_4 | 938 | 945 | PF00514 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 273 | 277 | PF00026 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 551 | 556 | PF00026 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 557 | 561 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 674 | 678 | PF00026 | 0.268 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0Q7 | Leptomonas seymouri | 78% | 100% |
A0A0N1IJ85 | Leptomonas seymouri | 30% | 90% |
A0A0S4IRG8 | Bodo saltans | 44% | 100% |
A0A0S4JDE8 | Bodo saltans | 30% | 85% |
A0A1X0NX04 | Trypanosomatidae | 55% | 97% |
A0A1X0P5N5 | Trypanosomatidae | 29% | 86% |
A0A3Q8IIG4 | Leishmania donovani | 29% | 91% |
A0A3R7MAM2 | Trypanosoma rangeli | 30% | 86% |
A0A3R7MK28 | Trypanosoma rangeli | 56% | 100% |
A0A3S7WXL3 | Leishmania donovani | 89% | 100% |
A0AVT1 | Homo sapiens | 33% | 99% |
A3KMV5 | Bos taurus | 36% | 99% |
A4HMX3 | Leishmania braziliensis | 29% | 91% |
A4I0A5 | Leishmania infantum | 89% | 100% |
A4IBJ4 | Leishmania infantum | 29% | 91% |
C9ZV28 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 99% |
C9ZZ47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 86% |
E9AFD0 | Leishmania major | 28% | 100% |
E9AW70 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B6I5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
O94609 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P20973 | Triticum aestivum | 34% | 99% |
P22314 | Homo sapiens | 36% | 99% |
P22515 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 100% |
P31251 | Triticum aestivum | 34% | 99% |
P31252 | Triticum aestivum | 32% | 99% |
P31254 | Mus musculus | 36% | 99% |
P41226 | Homo sapiens | 30% | 100% |
P52495 | Candida albicans (strain WO-1) | 36% | 100% |
P92974 | Arabidopsis thaliana | 33% | 97% |
P93028 | Arabidopsis thaliana | 33% | 97% |
Q02053 | Mus musculus | 36% | 99% |
Q29504 | Oryctolagus cuniculus | 36% | 99% |
Q55C16 | Dictyostelium discoideum | 35% | 100% |
Q5U300 | Rattus norvegicus | 36% | 99% |
Q8C7R4 | Mus musculus | 33% | 99% |
Q9NF77 | Leishmania major | 89% | 100% |
V5BB41 | Trypanosoma cruzi | 56% | 100% |