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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 1 |
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:0048476 | Holliday junction resolvase complex | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1905347 | endodeoxyribonuclease complex | 4 | 1 |
GO:1905348 | endonuclease complex | 3 | 1 |
Related structures:
AlphaFold database: E9AWZ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000737 | obsolete DNA catabolic process, endonucleolytic | 6 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006302 | double-strand break repair | 6 | 7 |
GO:0006308 | DNA catabolic process | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009056 | catabolic process | 2 | 7 |
GO:0009057 | macromolecule catabolic process | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019439 | aromatic compound catabolic process | 4 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044248 | cellular catabolic process | 3 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 7 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0046700 | heterocycle catabolic process | 4 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 7 |
GO:1901575 | organic substance catabolic process | 3 | 7 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 1 |
GO:0000712 | resolution of meiotic recombination intermediates | 4 | 1 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0031573 | mitotic intra-S DNA damage checkpoint signaling | 7 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 1 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004520 | DNA endonuclease activity | 5 | 7 |
GO:0004536 | DNA nuclease activity | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008821 | crossover junction DNA endonuclease activity | 7 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016889 | DNA endonuclease activity, producing 3'-phosphomonoesters | 6 | 7 |
GO:0016894 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 3'-phosphomonoesters | 6 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0048256 | flap endonuclease activity | 6 | 1 |
GO:0048257 | 3'-flap endonuclease activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1024 | 1028 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.787 |
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 526 | 530 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 1112 | 1114 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 854 | 856 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.222 |
CLV_PCSK_KEX2_1 | 1111 | 1113 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.606 |
CLV_PCSK_PC7_1 | 1108 | 1114 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 1075 | 1079 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 874 | 878 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.581 |
DEG_SCF_FBW7_1 | 1053 | 1060 | PF00400 | 0.358 |
DEG_SCF_FBW7_1 | 393 | 399 | PF00400 | 0.740 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.558 |
DEG_SPOP_SBC_1 | 685 | 689 | PF00917 | 0.676 |
DOC_ANK_TNKS_1 | 261 | 268 | PF00023 | 0.683 |
DOC_ANK_TNKS_1 | 988 | 995 | PF00023 | 0.635 |
DOC_CKS1_1 | 1054 | 1059 | PF01111 | 0.293 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.740 |
DOC_CKS1_1 | 393 | 398 | PF01111 | 0.734 |
DOC_CYCLIN_RxL_1 | 32 | 43 | PF00134 | 0.693 |
DOC_CYCLIN_RxL_1 | 517 | 527 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 290 | 296 | PF00134 | 0.691 |
DOC_MAPK_gen_1 | 1132 | 1138 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 751 | 760 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 431 | 437 | PF00149 | 0.516 |
DOC_PP1_RVXF_1 | 749 | 755 | PF00149 | 0.618 |
DOC_PP1_RVXF_1 | 881 | 888 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.704 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.650 |
DOC_PP2B_LxvP_1 | 294 | 297 | PF13499 | 0.655 |
DOC_PP2B_LxvP_1 | 605 | 608 | PF13499 | 0.654 |
DOC_USP7_MATH_1 | 1091 | 1095 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.803 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 832 | 836 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 929 | 933 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 934 | 938 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 945 | 949 | PF00917 | 0.300 |
DOC_USP7_MATH_2 | 96 | 102 | PF00917 | 0.681 |
DOC_WW_Pin1_4 | 1053 | 1058 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 635 | 640 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 877 | 882 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 923 | 928 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 930 | 935 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 1073 | 1082 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 1086 | 1095 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 1126 | 1135 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 438 | 447 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 480 | 490 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 520 | 525 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 657 | 667 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 673 | 683 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 717 | 725 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 855 | 861 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 869 | 877 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 960 | 970 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 980 | 986 | PF00244 | 0.270 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.721 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BIR_III_2 | 1119 | 1123 | PF00653 | 0.472 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.591 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 966 | 970 | PF00533 | 0.332 |
LIG_BRCT_BRCA1_2 | 966 | 972 | PF00533 | 0.326 |
LIG_Clathr_ClatBox_1 | 417 | 421 | PF01394 | 0.585 |
LIG_deltaCOP1_diTrp_1 | 302 | 308 | PF00928 | 0.644 |
LIG_FHA_1 | 1137 | 1143 | PF00498 | 0.424 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.636 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.617 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.681 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.711 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.632 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.686 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.633 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.520 |
LIG_FHA_1 | 898 | 904 | PF00498 | 0.213 |
LIG_FHA_1 | 963 | 969 | PF00498 | 0.499 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.745 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.721 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.576 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.740 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.620 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.584 |
LIG_FHA_2 | 547 | 553 | PF00498 | 0.442 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.578 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.332 |
LIG_FHA_2 | 914 | 920 | PF00498 | 0.435 |
LIG_LIR_Apic_2 | 389 | 393 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 967 | 978 | PF02991 | 0.441 |
LIG_LIR_LC3C_4 | 850 | 853 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 1097 | 1103 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 880 | 885 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 967 | 973 | PF02991 | 0.441 |
LIG_NRBOX | 1091 | 1097 | PF00104 | 0.404 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.589 |
LIG_PCNA_yPIPBox_3 | 406 | 417 | PF02747 | 0.524 |
LIG_PDZ_Class_3 | 1143 | 1148 | PF00595 | 0.527 |
LIG_Pex14_1 | 304 | 308 | PF04695 | 0.652 |
LIG_Pex14_1 | 756 | 760 | PF04695 | 0.425 |
LIG_RPA_C_Fungi | 655 | 667 | PF08784 | 0.512 |
LIG_SH2_CRK | 1100 | 1104 | PF00017 | 0.460 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.656 |
LIG_SH2_NCK_1 | 579 | 583 | PF00017 | 0.629 |
LIG_SH2_PTP2 | 1135 | 1138 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 870 | 873 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 1135 | 1138 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.309 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.716 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.783 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.674 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.661 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.657 |
LIG_SH3_3 | 664 | 670 | PF00018 | 0.745 |
LIG_SH3_3 | 680 | 686 | PF00018 | 0.540 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.660 |
LIG_SH3_3 | 792 | 798 | PF00018 | 0.211 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.744 |
LIG_SH3_3 | 928 | 934 | PF00018 | 0.304 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.649 |
LIG_SUMO_SIM_anti_2 | 411 | 418 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 801 | 807 | PF11976 | 0.332 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.683 |
LIG_TRAF2_1 | 740 | 743 | PF00917 | 0.581 |
LIG_TRAF2_1 | 809 | 812 | PF00917 | 0.402 |
LIG_WW_3 | 252 | 256 | PF00397 | 0.467 |
LIG_WW_3 | 628 | 632 | PF00397 | 0.632 |
MOD_CDC14_SPxK_1 | 199 | 202 | PF00782 | 0.601 |
MOD_CDC14_SPxK_1 | 628 | 631 | PF00782 | 0.629 |
MOD_CDC14_SPxK_1 | 880 | 883 | PF00782 | 0.441 |
MOD_CDK_SPxK_1 | 196 | 202 | PF00069 | 0.611 |
MOD_CDK_SPxK_1 | 625 | 631 | PF00069 | 0.630 |
MOD_CDK_SPxK_1 | 877 | 883 | PF00069 | 0.441 |
MOD_CK1_1 | 1094 | 1100 | PF00069 | 0.444 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.668 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.641 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.718 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.749 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.561 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.695 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.700 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.598 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.632 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.609 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.645 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.617 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.562 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.562 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.677 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.609 |
MOD_CK1_1 | 835 | 841 | PF00069 | 0.311 |
MOD_CK1_1 | 996 | 1002 | PF00069 | 0.513 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.677 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.737 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.713 |
MOD_CK2_1 | 806 | 812 | PF00069 | 0.336 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.380 |
MOD_CK2_1 | 930 | 936 | PF00069 | 0.350 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 925 | 929 | PF00069 | 0.441 |
MOD_GlcNHglycan | 1003 | 1007 | PF01048 | 0.601 |
MOD_GlcNHglycan | 1015 | 1018 | PF01048 | 0.638 |
MOD_GlcNHglycan | 1035 | 1038 | PF01048 | 0.621 |
MOD_GlcNHglycan | 1065 | 1068 | PF01048 | 0.422 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.529 |
MOD_GlcNHglycan | 1088 | 1091 | PF01048 | 0.523 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.643 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.637 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.679 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.494 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.711 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.563 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.663 |
MOD_GlcNHglycan | 429 | 433 | PF01048 | 0.631 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.706 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.544 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.711 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.637 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.685 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.560 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.663 |
MOD_GlcNHglycan | 618 | 623 | PF01048 | 0.699 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.706 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.583 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.685 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.594 |
MOD_GlcNHglycan | 693 | 696 | PF01048 | 0.729 |
MOD_GlcNHglycan | 764 | 767 | PF01048 | 0.659 |
MOD_GlcNHglycan | 772 | 775 | PF01048 | 0.626 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.489 |
MOD_GlcNHglycan | 897 | 900 | PF01048 | 0.328 |
MOD_GlcNHglycan | 936 | 939 | PF01048 | 0.448 |
MOD_GlcNHglycan | 943 | 946 | PF01048 | 0.342 |
MOD_GlcNHglycan | 995 | 998 | PF01048 | 0.592 |
MOD_GSK3_1 | 1053 | 1060 | PF00069 | 0.393 |
MOD_GSK3_1 | 1091 | 1098 | PF00069 | 0.504 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.551 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.655 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.748 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.763 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.624 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.820 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.780 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.534 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.635 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.721 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.600 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.632 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.496 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.442 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.642 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.702 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.772 |
MOD_GSK3_1 | 802 | 809 | PF00069 | 0.444 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.303 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.475 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.738 |
MOD_GSK3_1 | 913 | 920 | PF00069 | 0.507 |
MOD_GSK3_1 | 921 | 928 | PF00069 | 0.347 |
MOD_GSK3_1 | 930 | 937 | PF00069 | 0.349 |
MOD_GSK3_1 | 941 | 948 | PF00069 | 0.339 |
MOD_GSK3_1 | 958 | 965 | PF00069 | 0.484 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.674 |
MOD_LATS_1 | 1071 | 1077 | PF00433 | 0.487 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.545 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.705 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.657 |
MOD_N-GLC_1 | 962 | 967 | PF02516 | 0.381 |
MOD_N-GLC_2 | 1059 | 1061 | PF02516 | 0.457 |
MOD_N-GLC_2 | 555 | 557 | PF02516 | 0.387 |
MOD_NEK2_1 | 1095 | 1100 | PF00069 | 0.499 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.617 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.673 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.672 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.653 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.628 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.511 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.580 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.573 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.496 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.551 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.335 |
MOD_NEK2_1 | 973 | 978 | PF00069 | 0.502 |
MOD_NEK2_2 | 371 | 376 | PF00069 | 0.612 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.479 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.653 |
MOD_PIKK_1 | 702 | 708 | PF00454 | 0.592 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.678 |
MOD_PIKK_1 | 917 | 923 | PF00454 | 0.381 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.598 |
MOD_PKA_2 | 1125 | 1131 | PF00069 | 0.447 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.714 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.644 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.529 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.559 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.509 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.605 |
MOD_PKA_2 | 656 | 662 | PF00069 | 0.547 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.721 |
MOD_PKA_2 | 762 | 768 | PF00069 | 0.563 |
MOD_PKA_2 | 854 | 860 | PF00069 | 0.335 |
MOD_PKA_2 | 868 | 874 | PF00069 | 0.331 |
MOD_PKA_2 | 961 | 967 | PF00069 | 0.332 |
MOD_PKB_1 | 319 | 327 | PF00069 | 0.658 |
MOD_PKB_1 | 939 | 947 | PF00069 | 0.441 |
MOD_PKB_1 | 960 | 968 | PF00069 | 0.441 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.545 |
MOD_Plk_1 | 861 | 867 | PF00069 | 0.332 |
MOD_Plk_2-3 | 286 | 292 | PF00069 | 0.521 |
MOD_Plk_2-3 | 451 | 457 | PF00069 | 0.682 |
MOD_Plk_2-3 | 98 | 104 | PF00069 | 0.543 |
MOD_Plk_4 | 1091 | 1097 | PF00069 | 0.447 |
MOD_Plk_4 | 1099 | 1105 | PF00069 | 0.373 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.628 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.332 |
MOD_Plk_4 | 847 | 853 | PF00069 | 0.332 |
MOD_ProDKin_1 | 1053 | 1059 | PF00069 | 0.355 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.521 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.684 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.606 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.620 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.703 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.574 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.570 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.623 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.695 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.783 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.572 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.675 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.644 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.630 |
MOD_ProDKin_1 | 635 | 641 | PF00069 | 0.655 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.550 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.578 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.303 |
MOD_ProDKin_1 | 877 | 883 | PF00069 | 0.332 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.753 |
MOD_ProDKin_1 | 923 | 929 | PF00069 | 0.334 |
MOD_ProDKin_1 | 930 | 936 | PF00069 | 0.328 |
MOD_SUMO_rev_2 | 850 | 858 | PF00179 | 0.332 |
TRG_DiLeu_BaEn_1 | 409 | 414 | PF01217 | 0.585 |
TRG_DiLeu_BaEn_1 | 872 | 877 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_2 | 965 | 971 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.689 |
TRG_DiLeu_LyEn_5 | 872 | 877 | PF01217 | 0.332 |
TRG_ENDOCYTIC_2 | 1100 | 1103 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 1135 | 1138 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 1110 | 1113 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 751 | 754 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 874 | 876 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 939 | 942 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 959 | 962 | PF00400 | 0.339 |
TRG_NLS_MonoExtC_3 | 318 | 323 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 317 | 324 | PF00514 | 0.661 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEQ9 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IEY2 | Leishmania donovani | 83% | 100% |
A4HDI9 | Leishmania braziliensis | 65% | 99% |
A4I0Z0 | Leishmania infantum | 84% | 100% |
Q4QAH9 | Leishmania major | 82% | 100% |