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 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0048476 | Holliday junction resolvase complex | 5 | 1 |
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: A4HDI9
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:0006310 | DNA recombination | 5 | 3 |
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: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 | 283 | 287 | PF00656 | 0.773 |
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 1066 | 1068 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 1108 | 1110 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 769 | 771 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 848 | 850 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 868 | 870 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 983 | 985 | PF00675 | 0.493 |
CLV_PCSK_FUR_1 | 980 | 984 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 1066 | 1068 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 1107 | 1109 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 769 | 771 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 868 | 870 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 982 | 984 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.652 |
CLV_PCSK_PC7_1 | 1104 | 1110 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 1071 | 1075 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 629 | 633 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 868 | 872 | PF00082 | 0.394 |
DEG_APCC_DBOX_1 | 208 | 216 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.546 |
DEG_Kelch_Keap1_1 | 537 | 542 | PF01344 | 0.497 |
DEG_SCF_FBW7_1 | 1049 | 1056 | PF00400 | 0.341 |
DEG_SCF_FBW7_1 | 392 | 398 | PF00400 | 0.679 |
DEG_SPOP_SBC_1 | 336 | 340 | PF00917 | 0.551 |
DOC_ANK_TNKS_1 | 983 | 990 | PF00023 | 0.572 |
DOC_CKS1_1 | 392 | 397 | PF01111 | 0.674 |
DOC_CKS1_1 | 714 | 719 | PF01111 | 0.539 |
DOC_CYCLIN_RxL_1 | 32 | 42 | PF00134 | 0.599 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 302 | PF00134 | 0.639 |
DOC_MAPK_gen_1 | 1128 | 1134 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 749 | 758 | PF00069 | 0.479 |
DOC_PP1_RVXF_1 | 747 | 753 | PF00149 | 0.507 |
DOC_PP1_RVXF_1 | 875 | 882 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.685 |
DOC_PP4_FxxP_1 | 108 | 111 | PF00568 | 0.515 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.516 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 588 | 591 | PF00568 | 0.542 |
DOC_USP7_MATH_1 | 1040 | 1044 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 1087 | 1091 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 637 | 641 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 928 | 932 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 939 | 943 | PF00917 | 0.315 |
DOC_USP7_MATH_2 | 804 | 810 | PF00917 | 0.219 |
DOC_USP7_MATH_2 | 96 | 102 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 1049 | 1054 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 683 | 688 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 800 | 805 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 871 | 876 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 919 | 924 | PF00397 | 0.374 |
LIG_14-3-3_CanoR_1 | 1069 | 1078 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 1082 | 1091 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 1122 | 1131 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 128 | 132 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 184 | 188 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 437 | 446 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 470 | 480 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 510 | 519 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 553 | 561 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 622 | 627 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 658 | 668 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 671 | 680 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 849 | 855 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 919 | 923 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 954 | 964 | PF00244 | 0.505 |
LIG_APCC_ABBA_1 | 483 | 488 | PF00400 | 0.508 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BIR_III_2 | 1115 | 1119 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.665 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 960 | 964 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_2 | 960 | 966 | PF00533 | 0.307 |
LIG_Clathr_ClatBox_1 | 516 | 520 | PF01394 | 0.525 |
LIG_CtBP_PxDLS_1 | 426 | 430 | PF00389 | 0.539 |
LIG_EVH1_2 | 584 | 588 | PF00568 | 0.525 |
LIG_FHA_1 | 1070 | 1076 | PF00498 | 0.323 |
LIG_FHA_1 | 1133 | 1139 | PF00498 | 0.435 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.518 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.652 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.646 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.549 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.613 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.508 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.584 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.577 |
LIG_FHA_1 | 957 | 963 | PF00498 | 0.388 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.681 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.574 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.580 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.627 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.688 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.679 |
LIG_FHA_2 | 445 | 451 | PF00498 | 0.678 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.561 |
LIG_FHA_2 | 849 | 855 | PF00498 | 0.312 |
LIG_LIR_Apic_2 | 106 | 111 | PF02991 | 0.616 |
LIG_LIR_Apic_2 | 388 | 392 | PF02991 | 0.548 |
LIG_LIR_Apic_2 | 587 | 591 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 1072 | 1081 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 298 | 305 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 490 | 497 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 961 | 972 | PF02991 | 0.388 |
LIG_LIR_LC3C_4 | 844 | 847 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 1022 | 1028 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 874 | 879 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 961 | 967 | PF02991 | 0.388 |
LIG_MYND_1 | 235 | 239 | PF01753 | 0.545 |
LIG_NRBOX | 1087 | 1093 | PF00104 | 0.379 |
LIG_NRBOX | 411 | 417 | PF00104 | 0.583 |
LIG_PCNA_yPIPBox_3 | 404 | 416 | PF02747 | 0.522 |
LIG_Pex14_1 | 754 | 758 | PF04695 | 0.388 |
LIG_Pex14_2 | 705 | 709 | PF04695 | 0.440 |
LIG_PTAP_UEV_1 | 717 | 722 | PF05743 | 0.543 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.627 |
LIG_SH2_NCK_1 | 578 | 582 | PF00017 | 0.625 |
LIG_SH2_PTP2 | 1131 | 1134 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 864 | 867 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 1131 | 1134 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 903 | 906 | PF00017 | 0.231 |
LIG_SH3_1 | 185 | 191 | PF00018 | 0.539 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.709 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.723 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.638 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.605 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.596 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.543 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.824 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.727 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.610 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.731 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.648 |
LIG_SUMO_SIM_par_1 | 1047 | 1052 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 795 | 801 | PF11976 | 0.312 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.646 |
LIG_TRAF2_1 | 803 | 806 | PF00917 | 0.315 |
LIG_WRC_WIRS_1 | 480 | 485 | PF05994 | 0.516 |
LIG_WW_2 | 159 | 162 | PF00397 | 0.549 |
LIG_WW_3 | 626 | 630 | PF00397 | 0.606 |
MOD_CDC14_SPxK_1 | 110 | 113 | PF00782 | 0.582 |
MOD_CDC14_SPxK_1 | 198 | 201 | PF00782 | 0.568 |
MOD_CDC14_SPxK_1 | 626 | 629 | PF00782 | 0.604 |
MOD_CDC14_SPxK_1 | 874 | 877 | PF00782 | 0.388 |
MOD_CDK_SPxK_1 | 107 | 113 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.567 |
MOD_CDK_SPxK_1 | 337 | 343 | PF00069 | 0.546 |
MOD_CDK_SPxK_1 | 623 | 629 | PF00069 | 0.605 |
MOD_CDK_SPxK_1 | 871 | 877 | PF00069 | 0.388 |
MOD_CDK_SPxxK_3 | 337 | 344 | PF00069 | 0.547 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.678 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.556 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.742 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.546 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.667 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.480 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.752 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.656 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.557 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.567 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.617 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.664 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.761 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.654 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.696 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.293 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.536 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.296 |
MOD_CK2_1 | 1044 | 1050 | PF00069 | 0.387 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.521 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.554 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.696 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.676 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.717 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.527 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.557 |
MOD_CK2_1 | 800 | 806 | PF00069 | 0.321 |
MOD_CK2_1 | 924 | 930 | PF00069 | 0.315 |
MOD_CK2_1 | 954 | 960 | PF00069 | 0.291 |
MOD_Cter_Amidation | 767 | 770 | PF01082 | 0.630 |
MOD_DYRK1A_RPxSP_1 | 919 | 923 | PF00069 | 0.388 |
MOD_GlcNHglycan | 1010 | 1013 | PF01048 | 0.576 |
MOD_GlcNHglycan | 1042 | 1045 | PF01048 | 0.471 |
MOD_GlcNHglycan | 1061 | 1064 | PF01048 | 0.390 |
MOD_GlcNHglycan | 1084 | 1087 | PF01048 | 0.482 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.611 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.704 |
MOD_GlcNHglycan | 281 | 285 | PF01048 | 0.595 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.771 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.677 |
MOD_GlcNHglycan | 420 | 424 | PF01048 | 0.588 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.620 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.501 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.611 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.513 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.633 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.645 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.649 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.653 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.673 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.721 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.634 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.423 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.231 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.310 |
MOD_GlcNHglycan | 930 | 933 | PF01048 | 0.402 |
MOD_GlcNHglycan | 937 | 940 | PF01048 | 0.316 |
MOD_GlcNHglycan | 994 | 997 | PF01048 | 0.558 |
MOD_GSK3_1 | 1040 | 1047 | PF00069 | 0.469 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.497 |
MOD_GSK3_1 | 1087 | 1094 | PF00069 | 0.462 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.553 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.628 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.656 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.648 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.571 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.569 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.800 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.753 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.759 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.673 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.619 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.595 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.656 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.791 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.557 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.524 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.628 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.388 |
MOD_GSK3_1 | 824 | 831 | PF00069 | 0.268 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.322 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.225 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.723 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.259 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.454 |
MOD_GSK3_1 | 952 | 959 | PF00069 | 0.315 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.469 |
MOD_N-GLC_2 | 1055 | 1057 | PF02516 | 0.414 |
MOD_N-GLC_2 | 30 | 32 | PF02516 | 0.484 |
MOD_N-GLC_2 | 554 | 556 | PF02516 | 0.376 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.554 |
MOD_NEK2_1 | 1091 | 1096 | PF00069 | 0.476 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.537 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.688 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.600 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.610 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.577 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.637 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.559 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.561 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.446 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.547 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.523 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.574 |
MOD_NEK2_1 | 826 | 831 | PF00069 | 0.385 |
MOD_NEK2_1 | 855 | 860 | PF00069 | 0.312 |
MOD_NEK2_1 | 967 | 972 | PF00069 | 0.444 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.554 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.611 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.565 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.565 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.667 |
MOD_PIKK_1 | 700 | 706 | PF00454 | 0.598 |
MOD_PIKK_1 | 90 | 96 | PF00454 | 0.685 |
MOD_PIKK_1 | 967 | 973 | PF00454 | 0.284 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.571 |
MOD_PKA_1 | 849 | 855 | PF00069 | 0.231 |
MOD_PKA_2 | 1121 | 1127 | PF00069 | 0.444 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.584 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.557 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.555 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.545 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.619 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.467 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.574 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.628 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.312 |
MOD_PKA_2 | 918 | 924 | PF00069 | 0.231 |
MOD_PKA_2 | 955 | 961 | PF00069 | 0.324 |
MOD_PKB_1 | 1067 | 1075 | PF00069 | 0.317 |
MOD_PKB_1 | 316 | 324 | PF00069 | 0.651 |
MOD_PKB_1 | 633 | 641 | PF00069 | 0.581 |
MOD_PKB_1 | 933 | 941 | PF00069 | 0.388 |
MOD_PKB_1 | 954 | 962 | PF00069 | 0.388 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.464 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.439 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.556 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.518 |
MOD_Plk_1 | 855 | 861 | PF00069 | 0.312 |
MOD_Plk_4 | 1044 | 1050 | PF00069 | 0.387 |
MOD_Plk_4 | 1087 | 1093 | PF00069 | 0.437 |
MOD_Plk_4 | 1095 | 1101 | PF00069 | 0.424 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.504 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.620 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.559 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.529 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.322 |
MOD_Plk_4 | 841 | 847 | PF00069 | 0.312 |
MOD_ProDKin_1 | 1049 | 1055 | PF00069 | 0.339 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.489 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.604 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.562 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.522 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.756 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.584 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.541 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.630 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.586 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.579 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.605 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.627 |
MOD_ProDKin_1 | 683 | 689 | PF00069 | 0.638 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.665 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.619 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.496 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.543 |
MOD_ProDKin_1 | 800 | 806 | PF00069 | 0.285 |
MOD_ProDKin_1 | 871 | 877 | PF00069 | 0.312 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.704 |
MOD_ProDKin_1 | 919 | 925 | PF00069 | 0.374 |
MOD_SUMO_rev_2 | 844 | 852 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.579 |
TRG_DiLeu_BaEn_1 | 866 | 871 | PF01217 | 0.312 |
TRG_DiLeu_BaEn_2 | 959 | 965 | PF01217 | 0.312 |
TRG_DiLeu_LyEn_5 | 866 | 871 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 1096 | 1099 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 1131 | 1134 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.543 |
TRG_ER_diArg_1 | 1066 | 1069 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 1106 | 1109 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 749 | 752 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 868 | 870 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 933 | 936 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 953 | 956 | PF00400 | 0.183 |
TRG_ER_diArg_1 | 981 | 984 | PF00400 | 0.469 |
TRG_NLS_MonoExtC_3 | 317 | 322 | PF00514 | 0.650 |
TRG_NLS_MonoExtN_4 | 316 | 323 | PF00514 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEQ9 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IEY2 | Leishmania donovani | 65% | 99% |
A4I0Z0 | Leishmania infantum | 65% | 99% |
E9AWZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4QAH9 | Leishmania major | 65% | 100% |