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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QBB9
Term | Name | Level | Count |
---|---|---|---|
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 3 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004527 | exonuclease activity | 5 | 10 |
GO:0004532 | RNA exonuclease activity | 5 | 2 |
GO:0004534 | 5'-3' RNA exonuclease activity | 7 | 2 |
GO:0004540 | RNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1028 | 1032 | PF00656 | 0.640 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.569 |
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.776 |
CLV_C14_Caspase3-7 | 611 | 615 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 1019 | 1021 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 1045 | 1047 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 1052 | 1054 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.248 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 971 | 973 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 974 | 976 | PF00675 | 0.626 |
CLV_PCSK_FUR_1 | 109 | 113 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 1019 | 1021 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 1051 | 1053 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 971 | 973 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 976 | 978 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 693 | 695 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 976 | 978 | PF00082 | 0.607 |
CLV_PCSK_PC7_1 | 109 | 115 | PF00082 | 0.247 |
CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.330 |
CLV_PCSK_PC7_1 | 972 | 978 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 1052 | 1056 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 751 | 755 | PF00082 | 0.558 |
DEG_APCC_DBOX_1 | 1050 | 1058 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.461 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.347 |
DEG_SCF_FBW7_2 | 824 | 830 | PF00400 | 0.678 |
DEG_SPOP_SBC_1 | 583 | 587 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 766 | 770 | PF00917 | 0.680 |
DOC_CDC14_PxL_1 | 554 | 562 | PF14671 | 0.369 |
DOC_CDC14_PxL_1 | 613 | 621 | PF14671 | 0.472 |
DOC_CKS1_1 | 824 | 829 | PF01111 | 0.709 |
DOC_CYCLIN_RxL_1 | 53 | 64 | PF00134 | 0.524 |
DOC_CYCLIN_RxL_1 | 69 | 79 | PF00134 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 649 | 652 | PF00134 | 0.446 |
DOC_MAPK_gen_1 | 1019 | 1027 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 364 | 373 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 636 | 644 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 268 | 275 | PF00069 | 0.603 |
DOC_MAPK_MEF2A_6 | 638 | 646 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 89 | 96 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 908 | 915 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 54 | 61 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 724 | 731 | PF00149 | 0.387 |
DOC_PP1_RVXF_1 | 910 | 916 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 998 | 1001 | PF13499 | 0.537 |
DOC_PP2B_PxIxI_1 | 204 | 210 | PF00149 | 0.478 |
DOC_PP2B_PxIxI_1 | 261 | 267 | PF00149 | 0.447 |
DOC_SPAK_OSR1_1 | 885 | 889 | PF12202 | 0.603 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 985 | 989 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 278 | 282 | PF12436 | 0.663 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 811 | 816 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 823 | 828 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 831 | 836 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 463 | 473 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 591 | 600 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 701 | 710 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 202 | 218 | PF00022 | 0.533 |
LIG_Actin_WH2_2 | 353 | 370 | PF00022 | 0.466 |
LIG_AP2alpha_1 | 14 | 18 | PF02296 | 0.502 |
LIG_AP2alpha_2 | 960 | 962 | PF02296 | 0.593 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.359 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.524 |
LIG_CtBP_PxDLS_1 | 272 | 276 | PF00389 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 351 | 358 | PF00928 | 0.414 |
LIG_deltaCOP1_diTrp_1 | 496 | 499 | PF00928 | 0.571 |
LIG_FAT_LD_1 | 431 | 439 | PF03623 | 0.345 |
LIG_FHA_1 | 1031 | 1037 | PF00498 | 0.684 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.447 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.447 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.447 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.498 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.447 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.512 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.536 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.349 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.400 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.604 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.739 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.572 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.670 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.785 |
LIG_FHA_1 | 928 | 934 | PF00498 | 0.365 |
LIG_FHA_2 | 1035 | 1041 | PF00498 | 0.560 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.467 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.564 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.672 |
LIG_LIR_Apic_2 | 731 | 737 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 934 | 939 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 406 | 414 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 571 | 579 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 705 | 714 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 546 | 551 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 571 | 575 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 702 | 707 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 727 | 733 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 890 | 894 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 960 | 965 | PF02991 | 0.583 |
LIG_MLH1_MIPbox_1 | 354 | 358 | PF16413 | 0.382 |
LIG_NRBOX | 430 | 436 | PF00104 | 0.352 |
LIG_NRBOX | 73 | 79 | PF00104 | 0.465 |
LIG_PAM2_1 | 433 | 445 | PF00658 | 0.461 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.391 |
LIG_Pex14_1 | 536 | 540 | PF04695 | 0.359 |
LIG_Pex14_1 | 548 | 552 | PF04695 | 0.304 |
LIG_Pex14_2 | 14 | 18 | PF04695 | 0.447 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.325 |
LIG_Pex14_2 | 730 | 734 | PF04695 | 0.371 |
LIG_Rb_pABgroove_1 | 69 | 77 | PF01858 | 0.447 |
LIG_SH2_CRK | 566 | 570 | PF00017 | 0.413 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.424 |
LIG_SH2_GRB2like | 733 | 736 | PF00017 | 0.432 |
LIG_SH2_NCK_1 | 936 | 940 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 202 | 205 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 891 | 894 | PF00017 | 0.594 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.532 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.414 |
LIG_SH2_SRC | 936 | 939 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 859 | 862 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 891 | 894 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.449 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.398 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.456 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.600 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.681 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.392 |
LIG_SH3_3 | 813 | 819 | PF00018 | 0.686 |
LIG_SH3_3 | 829 | 835 | PF00018 | 0.719 |
LIG_SH3_5 | 855 | 859 | PF00018 | 0.483 |
LIG_SUMO_SIM_anti_2 | 654 | 660 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 3 | 8 | PF11976 | 0.447 |
LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.523 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.690 |
LIG_TRAF2_1 | 697 | 700 | PF00917 | 0.414 |
LIG_TRAF2_1 | 827 | 830 | PF00917 | 0.684 |
LIG_TRAF2_1 | 907 | 910 | PF00917 | 0.632 |
LIG_TYR_ITIM | 570 | 575 | PF00017 | 0.444 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.284 |
LIG_UBA3_1 | 1042 | 1047 | PF00899 | 0.545 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.308 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.468 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.400 |
LIG_WW_3 | 650 | 654 | PF00397 | 0.433 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.284 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.391 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.284 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.348 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.360 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.300 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.640 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.466 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.613 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.616 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.520 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.616 |
MOD_CK1_1 | 834 | 840 | PF00069 | 0.644 |
MOD_CK2_1 | 1034 | 1040 | PF00069 | 0.532 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.284 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.475 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.368 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.774 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.399 |
MOD_CK2_1 | 823 | 829 | PF00069 | 0.705 |
MOD_CK2_1 | 931 | 937 | PF00069 | 0.614 |
MOD_CK2_1 | 985 | 991 | PF00069 | 0.691 |
MOD_Cter_Amidation | 785 | 788 | PF01082 | 0.701 |
MOD_GlcNHglycan | 1002 | 1005 | PF01048 | 0.692 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.420 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.357 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.329 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.393 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.608 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.604 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.568 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.399 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.412 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.324 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.573 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.664 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.495 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.689 |
MOD_GlcNHglycan | 933 | 936 | PF01048 | 0.475 |
MOD_GSK3_1 | 1026 | 1033 | PF00069 | 0.786 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.319 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.308 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.631 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.522 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.497 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.293 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.477 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.283 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.478 |
MOD_GSK3_1 | 760 | 767 | PF00069 | 0.601 |
MOD_GSK3_1 | 774 | 781 | PF00069 | 0.490 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.604 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.655 |
MOD_GSK3_1 | 923 | 930 | PF00069 | 0.641 |
MOD_LATS_1 | 299 | 305 | PF00433 | 0.699 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.308 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.568 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.672 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.454 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.334 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.284 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.333 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.530 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.733 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.380 |
MOD_NEK2_2 | 877 | 882 | PF00069 | 0.472 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.400 |
MOD_PK_1 | 59 | 65 | PF00069 | 0.400 |
MOD_PKA_1 | 1052 | 1058 | PF00069 | 0.514 |
MOD_PKA_1 | 692 | 698 | PF00069 | 0.502 |
MOD_PKA_1 | 787 | 793 | PF00069 | 0.621 |
MOD_PKA_2 | 1052 | 1058 | PF00069 | 0.514 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.360 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.776 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.800 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.597 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.483 |
MOD_PKA_2 | 746 | 752 | PF00069 | 0.615 |
MOD_PKA_2 | 787 | 793 | PF00069 | 0.670 |
MOD_PKB_1 | 580 | 588 | PF00069 | 0.523 |
MOD_Plk_1 | 1030 | 1036 | PF00069 | 0.618 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.484 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.291 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.251 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.370 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.312 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.410 |
MOD_Plk_1 | 924 | 930 | PF00069 | 0.585 |
MOD_Plk_2-3 | 601 | 607 | PF00069 | 0.568 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.284 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.503 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.412 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.406 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.400 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.284 |
MOD_Plk_4 | 657 | 663 | PF00069 | 0.418 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.578 |
MOD_Plk_4 | 887 | 893 | PF00069 | 0.646 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.391 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.779 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.532 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.404 |
MOD_ProDKin_1 | 811 | 817 | PF00069 | 0.685 |
MOD_ProDKin_1 | 823 | 829 | PF00069 | 0.662 |
MOD_ProDKin_1 | 831 | 837 | PF00069 | 0.473 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.284 |
MOD_SUMO_rev_2 | 219 | 225 | PF00179 | 0.284 |
MOD_SUMO_rev_2 | 690 | 695 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 678 | 683 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 1 | 6 | PF01217 | 0.284 |
TRG_DiLeu_BaLyEn_6 | 928 | 933 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 891 | 894 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.288 |
TRG_ER_diArg_1 | 1019 | 1021 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 1051 | 1053 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.813 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 701 | 704 | PF00400 | 0.371 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.697 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 694 | 698 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 963 | 967 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9R9 | Leptomonas seymouri | 68% | 100% |
A0A1X0NX31 | Trypanosomatidae | 37% | 100% |
A0A3Q8IBP8 | Leishmania donovani | 94% | 100% |
A4HCS1 | Leishmania braziliensis | 83% | 100% |
C9ZV53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AH11 | Leishmania infantum | 94% | 100% |
E9AW59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BCF8 | Trypanosoma cruzi | 40% | 100% |