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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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: A4HCS1
Term | Name | Level | Count |
---|---|---|---|
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006401 | RNA catabolic process | 5 | 1 |
GO:0006402 | mRNA catabolic process | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010629 | negative regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
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:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0004527 | exonuclease activity | 5 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0004532 | RNA exonuclease activity | 5 | 1 |
GO:0004534 | 5'-3' RNA exonuclease activity | 7 | 1 |
GO:0004540 | RNA nuclease activity | 4 | 1 |
GO:0008409 | 5'-3' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016896 | RNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 611 | 615 | PF00656 | 0.618 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 1049 | 1051 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.834 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 974 | 976 | PF00675 | 0.594 |
CLV_PCSK_FUR_1 | 109 | 113 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 1048 | 1050 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.834 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 976 | 978 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 993 | 995 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.360 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 693 | 695 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 976 | 978 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 993 | 995 | PF00082 | 0.418 |
CLV_PCSK_PC7_1 | 109 | 115 | PF00082 | 0.301 |
CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.360 |
CLV_PCSK_PC7_1 | 972 | 978 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.301 |
DEG_APCC_DBOX_1 | 1047 | 1055 | PF00400 | 0.535 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 462 | 470 | PF00400 | 0.435 |
DEG_SCF_FBW7_1 | 789 | 794 | PF00400 | 0.530 |
DEG_SCF_FBW7_2 | 824 | 830 | PF00400 | 0.825 |
DEG_SPOP_SBC_1 | 1027 | 1031 | PF00917 | 0.541 |
DEG_SPOP_SBC_1 | 791 | 795 | PF00917 | 0.573 |
DOC_CDC14_PxL_1 | 554 | 562 | PF14671 | 0.444 |
DOC_CKS1_1 | 824 | 829 | PF01111 | 0.764 |
DOC_CYCLIN_RxL_1 | 69 | 79 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 649 | 652 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 1048 | 1054 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.598 |
DOC_MAPK_gen_1 | 636 | 644 | PF00069 | 0.535 |
DOC_MAPK_MEF2A_6 | 638 | 646 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 89 | 96 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 908 | 915 | PF00069 | 0.525 |
DOC_MAPK_RevD_3 | 939 | 953 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 910 | 916 | PF00149 | 0.479 |
DOC_PP2B_LxvP_1 | 616 | 619 | PF13499 | 0.523 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.496 |
DOC_PP2B_PxIxI_1 | 261 | 267 | PF00149 | 0.501 |
DOC_SPAK_OSR1_1 | 885 | 889 | PF12202 | 0.551 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 766 | 770 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.589 |
DOC_USP7_UBL2_3 | 963 | 967 | PF12436 | 0.547 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 811 | 816 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 823 | 828 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 182 | 190 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 701 | 710 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 202 | 218 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 353 | 370 | PF00022 | 0.506 |
LIG_AP2alpha_1 | 14 | 18 | PF02296 | 0.598 |
LIG_AP2alpha_2 | 960 | 962 | PF02296 | 0.690 |
LIG_BIR_III_4 | 573 | 577 | PF00653 | 0.415 |
LIG_BRCT_BRCA1_1 | 124 | 128 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 351 | 358 | PF00928 | 0.479 |
LIG_deltaCOP1_diTrp_1 | 496 | 499 | PF00928 | 0.608 |
LIG_FAT_LD_1 | 431 | 439 | PF03623 | 0.418 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.501 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.501 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.501 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.560 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.501 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.560 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.424 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.436 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.624 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.798 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.784 |
LIG_FHA_1 | 845 | 851 | PF00498 | 0.620 |
LIG_FHA_2 | 1029 | 1035 | PF00498 | 0.622 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.442 |
LIG_FHA_2 | 818 | 824 | PF00498 | 0.771 |
LIG_LIR_Apic_2 | 731 | 737 | PF02991 | 0.527 |
LIG_LIR_Apic_2 | 934 | 939 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 1004 | 1014 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 406 | 414 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 571 | 579 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 705 | 714 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 1004 | 1010 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 546 | 551 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 571 | 575 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 702 | 707 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 727 | 733 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 781 | 785 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 890 | 894 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 960 | 965 | PF02991 | 0.633 |
LIG_LRP6_Inhibitor_1 | 24 | 30 | PF00058 | 0.217 |
LIG_MLH1_MIPbox_1 | 354 | 358 | PF16413 | 0.425 |
LIG_NRBOX | 430 | 436 | PF00104 | 0.426 |
LIG_NRBOX | 73 | 79 | PF00104 | 0.525 |
LIG_PAM2_1 | 433 | 445 | PF00658 | 0.503 |
LIG_PCNA_yPIPBox_3 | 208 | 216 | PF02747 | 0.480 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.455 |
LIG_Pex14_1 | 536 | 540 | PF04695 | 0.417 |
LIG_Pex14_1 | 548 | 552 | PF04695 | 0.358 |
LIG_Pex14_2 | 14 | 18 | PF04695 | 0.501 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.417 |
LIG_Pex14_2 | 730 | 734 | PF04695 | 0.418 |
LIG_Rb_pABgroove_1 | 69 | 77 | PF01858 | 0.501 |
LIG_RPA_C_Fungi | 577 | 589 | PF08784 | 0.397 |
LIG_SH2_CRK | 1007 | 1011 | PF00017 | 0.533 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.240 |
LIG_SH2_CRK | 566 | 570 | PF00017 | 0.450 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 269 | 273 | PF00017 | 0.463 |
LIG_SH2_PTP2 | 891 | 894 | PF00017 | 0.685 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.438 |
LIG_SH2_SRC | 269 | 272 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 1007 | 1011 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 928 | 932 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 859 | 862 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 891 | 894 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.357 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.374 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.468 |
LIG_SH3_3 | 809 | 815 | PF00018 | 0.735 |
LIG_SH3_5 | 855 | 859 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 654 | 660 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 3 | 8 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 681 | 687 | PF11976 | 0.351 |
LIG_TRAF2_1 | 425 | 428 | PF00917 | 0.571 |
LIG_TRAF2_1 | 603 | 606 | PF00917 | 0.826 |
LIG_TRAF2_1 | 676 | 679 | PF00917 | 0.463 |
LIG_TRAF2_1 | 697 | 700 | PF00917 | 0.472 |
LIG_TRAF2_1 | 907 | 910 | PF00917 | 0.726 |
LIG_TYR_ITIM | 570 | 575 | PF00017 | 0.438 |
LIG_TYR_ITIM | 91 | 96 | PF00017 | 0.357 |
LIG_UBA3_1 | 1051 | 1055 | PF00899 | 0.524 |
LIG_UBA3_1 | 6 | 12 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.500 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.438 |
LIG_WW_3 | 330 | 334 | PF00397 | 0.613 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.357 |
MOD_CK1_1 | 1023 | 1029 | PF00069 | 0.556 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.357 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.436 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.391 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.379 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.520 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.329 |
MOD_CK1_1 | 765 | 771 | PF00069 | 0.709 |
MOD_CK1_1 | 781 | 787 | PF00069 | 0.570 |
MOD_CK1_1 | 828 | 834 | PF00069 | 0.719 |
MOD_CK1_1 | 902 | 908 | PF00069 | 0.479 |
MOD_CK2_1 | 1026 | 1032 | PF00069 | 0.678 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.357 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.526 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.446 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.412 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.466 |
MOD_CK2_1 | 694 | 700 | PF00069 | 0.440 |
MOD_CK2_1 | 817 | 823 | PF00069 | 0.770 |
MOD_CK2_1 | 985 | 991 | PF00069 | 0.643 |
MOD_Cter_Amidation | 785 | 788 | PF01082 | 0.741 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.454 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.412 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.401 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.376 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.415 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.455 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.393 |
MOD_GlcNHglycan | 754 | 757 | PF01048 | 0.627 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.561 |
MOD_GlcNHglycan | 768 | 771 | PF01048 | 0.442 |
MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.640 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.609 |
MOD_GlcNHglycan | 904 | 907 | PF01048 | 0.680 |
MOD_GlcNHglycan | 933 | 936 | PF01048 | 0.498 |
MOD_GSK3_1 | 1023 | 1030 | PF00069 | 0.796 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.367 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.391 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.367 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.560 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.521 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.345 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.287 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.514 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.313 |
MOD_GSK3_1 | 762 | 769 | PF00069 | 0.670 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.635 |
MOD_GSK3_1 | 807 | 814 | PF00069 | 0.645 |
MOD_GSK3_1 | 980 | 987 | PF00069 | 0.550 |
MOD_LATS_1 | 299 | 305 | PF00433 | 0.834 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.391 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.733 |
MOD_N-GLC_1 | 984 | 989 | PF02516 | 0.557 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.478 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.357 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.400 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.698 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.279 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.444 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.438 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.734 |
MOD_PIKK_1 | 844 | 850 | PF00454 | 0.461 |
MOD_PK_1 | 59 | 65 | PF00069 | 0.438 |
MOD_PKA_1 | 975 | 981 | PF00069 | 0.442 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.240 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.498 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.807 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.326 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.471 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.517 |
MOD_PKB_1 | 180 | 188 | PF00069 | 0.240 |
MOD_PKB_1 | 230 | 238 | PF00069 | 0.326 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.492 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.390 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.312 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.527 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.482 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.309 |
MOD_Plk_1 | 924 | 930 | PF00069 | 0.602 |
MOD_Plk_2-3 | 1028 | 1034 | PF00069 | 0.520 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.357 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.563 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.438 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.452 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.438 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.357 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.446 |
MOD_Plk_4 | 653 | 659 | PF00069 | 0.461 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.307 |
MOD_Plk_4 | 757 | 763 | PF00069 | 0.508 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.654 |
MOD_Plk_4 | 887 | 893 | PF00069 | 0.588 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.806 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.671 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.447 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.691 |
MOD_ProDKin_1 | 811 | 817 | PF00069 | 0.739 |
MOD_ProDKin_1 | 823 | 829 | PF00069 | 0.714 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.550 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.357 |
MOD_SUMO_for_1 | 992 | 995 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 219 | 225 | PF00179 | 0.357 |
MOD_SUMO_rev_2 | 496 | 505 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_1 | 678 | 683 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 1 | 6 | PF01217 | 0.357 |
TRG_DiLeu_BaLyEn_6 | 928 | 933 | PF01217 | 0.551 |
TRG_ENDOCYTIC_2 | 1007 | 1010 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 666 | 669 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 891 | 894 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 1048 | 1050 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 109 | 112 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.838 |
TRG_ER_diArg_1 | 363 | 366 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 580 | 582 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 594 | 596 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 701 | 704 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 850 | 853 | PF00400 | 0.515 |
TRG_NLS_MonoExtC_3 | 10 | 16 | PF00514 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 694 | 698 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9R9 | Leptomonas seymouri | 63% | 100% |
A0A3Q8IBP8 | Leishmania donovani | 84% | 100% |
C9ZV53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AH11 | Leishmania infantum | 84% | 100% |
E9AW59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QBB9 | Leishmania major | 83% | 100% |
V5BCF8 | Trypanosoma cruzi | 41% | 100% |