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: A4I0Z0
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 | 1039 | 1043 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.801 |
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 537 | 541 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 827 | 831 | PF00656 | 0.384 |
CLV_NRD_NRD_1 | 1115 | 1117 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 856 | 858 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 876 | 878 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 991 | 993 | PF00675 | 0.499 |
CLV_PCSK_FUR_1 | 988 | 992 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 1114 | 1116 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 876 | 878 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 990 | 992 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.665 |
CLV_PCSK_PC1ET2_1 | 467 | 469 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 1111 | 1117 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 1078 | 1082 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 876 | 880 | PF00082 | 0.453 |
DEG_APCC_DBOX_1 | 59 | 67 | PF00400 | 0.549 |
DEG_SCF_FBW7_1 | 395 | 401 | PF00400 | 0.771 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.545 |
DEG_SPOP_SBC_1 | 525 | 529 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 686 | 690 | PF00917 | 0.671 |
DOC_ANK_TNKS_1 | 1037 | 1044 | PF00023 | 0.518 |
DOC_ANK_TNKS_1 | 260 | 267 | PF00023 | 0.720 |
DOC_ANK_TNKS_1 | 488 | 495 | PF00023 | 0.641 |
DOC_ANK_TNKS_1 | 991 | 998 | PF00023 | 0.646 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.693 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.768 |
DOC_CYCLIN_RxL_1 | 32 | 42 | PF00134 | 0.680 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 302 | PF00134 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 607 | 613 | PF00134 | 0.745 |
DOC_MAPK_gen_1 | 1135 | 1141 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 753 | 762 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 241 | 248 | PF00069 | 0.574 |
DOC_PP1_RVXF_1 | 751 | 757 | PF00149 | 0.558 |
DOC_PP1_RVXF_1 | 883 | 890 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.736 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.670 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.752 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.663 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 641 | 645 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 834 | 838 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 897 | 901 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 936 | 940 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 947 | 951 | PF00917 | 0.340 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 702 | 707 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 808 | 813 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 879 | 884 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 925 | 930 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 931 | 936 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 1076 | 1085 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 1089 | 1098 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 112 | 120 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 1129 | 1138 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 325 | 334 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 462 | 466 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 482 | 490 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 556 | 564 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 662 | 672 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 719 | 728 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 835 | 845 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 857 | 863 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 871 | 879 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 962 | 972 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 982 | 988 | PF00244 | 0.279 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.734 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.689 |
LIG_BIR_III_2 | 1122 | 1126 | PF00653 | 0.499 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.689 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.595 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.576 |
LIG_BRCT_BRCA1_1 | 968 | 972 | PF00533 | 0.335 |
LIG_BRCT_BRCA1_2 | 968 | 974 | PF00533 | 0.330 |
LIG_Clathr_ClatBox_1 | 419 | 423 | PF01394 | 0.580 |
LIG_deltaCOP1_diTrp_1 | 304 | 310 | PF00928 | 0.659 |
LIG_FHA_1 | 1050 | 1056 | PF00498 | 0.485 |
LIG_FHA_1 | 1140 | 1146 | PF00498 | 0.485 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.645 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.602 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.703 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.565 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.619 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.747 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.656 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.751 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.557 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.578 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.526 |
LIG_FHA_1 | 965 | 971 | PF00498 | 0.485 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.753 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.715 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.593 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.717 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.771 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.738 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.469 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.681 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.590 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.633 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.358 |
LIG_FHA_2 | 857 | 863 | PF00498 | 0.335 |
LIG_FHA_2 | 916 | 922 | PF00498 | 0.389 |
LIG_GBD_Chelix_1 | 886 | 894 | PF00786 | 0.278 |
LIG_Integrin_RGD_1 | 219 | 221 | PF01839 | 0.594 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 340 | 347 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 92 | 103 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 969 | 980 | PF02991 | 0.453 |
LIG_LIR_LC3C_4 | 852 | 855 | PF02991 | 0.335 |
LIG_LIR_LC3C_4 | 892 | 896 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 1100 | 1106 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 882 | 887 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 92 | 98 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 969 | 975 | PF02991 | 0.453 |
LIG_NRBOX | 1094 | 1100 | PF00104 | 0.409 |
LIG_NRBOX | 414 | 420 | PF00104 | 0.602 |
LIG_PDZ_Class_3 | 1146 | 1151 | PF00595 | 0.569 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.668 |
LIG_Pex14_1 | 758 | 762 | PF04695 | 0.404 |
LIG_SH2_CRK | 1103 | 1107 | PF00017 | 0.497 |
LIG_SH2_CRK | 638 | 642 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 581 | 585 | PF00017 | 0.671 |
LIG_SH2_PTP2 | 1138 | 1141 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 872 | 875 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 1138 | 1141 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.313 |
LIG_SH3_2 | 236 | 241 | PF14604 | 0.666 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.731 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.809 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.723 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.667 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.650 |
LIG_SH3_3 | 655 | 661 | PF00018 | 0.600 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.755 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.578 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.729 |
LIG_SH3_3 | 930 | 936 | PF00018 | 0.310 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 1052 | 1057 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 411 | 420 | PF11976 | 0.650 |
LIG_SUMO_SIM_par_1 | 803 | 809 | PF11976 | 0.335 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.697 |
LIG_TRAF2_1 | 742 | 745 | PF00917 | 0.586 |
LIG_UBA3_1 | 783 | 789 | PF00899 | 0.278 |
LIG_Vh1_VBS_1 | 495 | 513 | PF01044 | 0.564 |
LIG_WW_3 | 630 | 634 | PF00397 | 0.641 |
MOD_CDC14_SPxK_1 | 109 | 112 | PF00782 | 0.642 |
MOD_CDC14_SPxK_1 | 198 | 201 | PF00782 | 0.568 |
MOD_CDC14_SPxK_1 | 630 | 633 | PF00782 | 0.642 |
MOD_CDC14_SPxK_1 | 882 | 885 | PF00782 | 0.453 |
MOD_CDK_SPK_2 | 116 | 121 | PF00069 | 0.581 |
MOD_CDK_SPK_2 | 517 | 522 | PF00069 | 0.588 |
MOD_CDK_SPxK_1 | 106 | 112 | PF00069 | 0.637 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.580 |
MOD_CDK_SPxK_1 | 267 | 273 | PF00069 | 0.665 |
MOD_CDK_SPxK_1 | 627 | 633 | PF00069 | 0.644 |
MOD_CDK_SPxK_1 | 879 | 885 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 234 | 241 | PF00069 | 0.670 |
MOD_CK1_1 | 1097 | 1103 | PF00069 | 0.490 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.674 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.657 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.586 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.606 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.753 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.735 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.731 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.725 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.613 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.711 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.752 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.627 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.602 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.756 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.648 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.624 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.766 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.746 |
MOD_CK1_1 | 715 | 721 | PF00069 | 0.640 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.642 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.703 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.715 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.578 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.577 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.724 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.768 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.741 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.659 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.335 |
MOD_Cter_Amidation | 775 | 778 | PF01082 | 0.653 |
MOD_DYRK1A_RPxSP_1 | 927 | 931 | PF00069 | 0.453 |
MOD_GlcNHglycan | 1017 | 1021 | PF01048 | 0.664 |
MOD_GlcNHglycan | 1038 | 1041 | PF01048 | 0.627 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.521 |
MOD_GlcNHglycan | 1068 | 1071 | PF01048 | 0.423 |
MOD_GlcNHglycan | 1091 | 1094 | PF01048 | 0.556 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.659 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.688 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.643 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.612 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.667 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.726 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.640 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.659 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.647 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.576 |
MOD_GlcNHglycan | 469 | 473 | PF01048 | 0.692 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.692 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.655 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.527 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.682 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.639 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.604 |
MOD_GlcNHglycan | 612 | 616 | PF01048 | 0.646 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.700 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.669 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.677 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.727 |
MOD_GlcNHglycan | 766 | 769 | PF01048 | 0.672 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.684 |
MOD_GlcNHglycan | 836 | 839 | PF01048 | 0.471 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.636 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.331 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.424 |
MOD_GlcNHglycan | 945 | 948 | PF01048 | 0.359 |
MOD_GlcNHglycan | 998 | 1001 | PF01048 | 0.586 |
MOD_GSK3_1 | 1060 | 1067 | PF00069 | 0.585 |
MOD_GSK3_1 | 1094 | 1101 | PF00069 | 0.532 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.697 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.678 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.626 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.800 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.789 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.682 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.770 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.746 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.622 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.633 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.653 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.447 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.570 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.657 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.676 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.782 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.619 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.453 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.499 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.730 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.264 |
MOD_GSK3_1 | 915 | 922 | PF00069 | 0.505 |
MOD_GSK3_1 | 923 | 930 | PF00069 | 0.330 |
MOD_GSK3_1 | 943 | 950 | PF00069 | 0.480 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.385 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.663 |
MOD_LATS_1 | 1074 | 1080 | PF00433 | 0.495 |
MOD_N-GLC_1 | 424 | 429 | PF02516 | 0.706 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.668 |
MOD_N-GLC_1 | 964 | 969 | PF02516 | 0.389 |
MOD_N-GLC_2 | 1062 | 1064 | PF02516 | 0.459 |
MOD_N-GLC_2 | 542 | 544 | PF02516 | 0.573 |
MOD_NEK2_1 | 1049 | 1054 | PF00069 | 0.483 |
MOD_NEK2_1 | 1098 | 1103 | PF00069 | 0.538 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.628 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.693 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.668 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.708 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.609 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.575 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.711 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.511 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.590 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.537 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.482 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.606 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.335 |
MOD_NEK2_1 | 975 | 980 | PF00069 | 0.548 |
MOD_NEK2_2 | 548 | 553 | PF00069 | 0.469 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.630 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.579 |
MOD_PIKK_1 | 639 | 645 | PF00454 | 0.720 |
MOD_PIKK_1 | 704 | 710 | PF00454 | 0.644 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.667 |
MOD_PIKK_1 | 919 | 925 | PF00454 | 0.389 |
MOD_PKA_2 | 1128 | 1134 | PF00069 | 0.493 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.726 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.651 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.634 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.654 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.488 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.741 |
MOD_PKA_2 | 764 | 770 | PF00069 | 0.562 |
MOD_PKA_2 | 834 | 840 | PF00069 | 0.278 |
MOD_PKA_2 | 856 | 862 | PF00069 | 0.335 |
MOD_PKA_2 | 870 | 876 | PF00069 | 0.335 |
MOD_PKA_2 | 963 | 969 | PF00069 | 0.354 |
MOD_PKB_1 | 112 | 120 | PF00069 | 0.669 |
MOD_PKB_1 | 217 | 225 | PF00069 | 0.681 |
MOD_PKB_1 | 321 | 329 | PF00069 | 0.666 |
MOD_PKB_1 | 637 | 645 | PF00069 | 0.598 |
MOD_PKB_1 | 941 | 949 | PF00069 | 0.453 |
MOD_PKB_1 | 962 | 970 | PF00069 | 0.453 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.601 |
MOD_Plk_1 | 863 | 869 | PF00069 | 0.350 |
MOD_Plk_2-3 | 453 | 459 | PF00069 | 0.717 |
MOD_Plk_4 | 1094 | 1100 | PF00069 | 0.454 |
MOD_Plk_4 | 1102 | 1108 | PF00069 | 0.407 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.572 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.570 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.610 |
MOD_Plk_4 | 644 | 650 | PF00069 | 0.644 |
MOD_Plk_4 | 793 | 799 | PF00069 | 0.343 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.335 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.515 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.666 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.620 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.630 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.743 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.525 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.686 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.724 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.756 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.786 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.553 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.742 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.632 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.654 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.679 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.630 |
MOD_ProDKin_1 | 702 | 708 | PF00069 | 0.467 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.717 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.654 |
MOD_ProDKin_1 | 808 | 814 | PF00069 | 0.306 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.735 |
MOD_ProDKin_1 | 879 | 885 | PF00069 | 0.335 |
MOD_ProDKin_1 | 925 | 931 | PF00069 | 0.447 |
MOD_SUMO_rev_2 | 852 | 860 | PF00179 | 0.335 |
TRG_DiLeu_BaEn_1 | 411 | 416 | PF01217 | 0.618 |
TRG_DiLeu_BaEn_1 | 874 | 879 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_2 | 967 | 973 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_4 | 411 | 417 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.704 |
TRG_DiLeu_LyEn_5 | 874 | 879 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 1103 | 1106 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 1138 | 1141 | PF00928 | 0.563 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 1113 | 1116 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 216 | 219 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.805 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 699 | 702 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 753 | 756 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 876 | 878 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 910 | 913 | PF00400 | 0.246 |
TRG_ER_diArg_1 | 941 | 944 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 961 | 964 | PF00400 | 0.225 |
TRG_ER_diArg_1 | 987 | 990 | PF00400 | 0.427 |
TRG_NLS_MonoExtC_3 | 320 | 325 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 319 | 326 | PF00514 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEQ9 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IEY2 | Leishmania donovani | 99% | 100% |
A4HDI9 | Leishmania braziliensis | 65% | 99% |
E9AWZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QAH9 | Leishmania major | 87% | 100% |