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:0032991 | protein-containing complex | 1 | 2 |
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:0048476 | Holliday junction resolvase complex | 5 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905347 | endodeoxyribonuclease complex | 4 | 2 |
GO:1905348 | endonuclease complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QAH9
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 2 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 2 |
GO:0000712 | resolution of meiotic recombination intermediates | 4 | 2 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 2 |
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:0007093 | mitotic cell cycle checkpoint signaling | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
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:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010948 | negative regulation of cell cycle process | 6 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 7 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 2 |
GO:0031573 | mitotic intra-S DNA damage checkpoint signaling | 7 | 2 |
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:0035556 | intracellular signal transduction | 3 | 2 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 2 |
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:0044773 | mitotic DNA damage checkpoint signaling | 6 | 2 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 2 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0046700 | heterocycle catabolic process | 4 | 7 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0061982 | meiosis I cell cycle process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
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:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 2 |
GO:1903046 | meiotic cell cycle process | 2 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
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:0048256 | flap endonuclease activity | 6 | 2 |
GO:0048257 | 3'-flap endonuclease activity | 7 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 165 | 169 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.781 |
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.635 |
CLV_NRD_NRD_1 | 1116 | 1118 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 857 | 859 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 877 | 879 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 992 | 994 | PF00675 | 0.502 |
CLV_PCSK_FUR_1 | 113 | 117 | PF00082 | 0.562 |
CLV_PCSK_FUR_1 | 989 | 993 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 1115 | 1117 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 778 | 780 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 877 | 879 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 991 | 993 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.652 |
CLV_PCSK_PC7_1 | 1112 | 1118 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 1079 | 1083 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.698 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 877 | 881 | PF00082 | 0.394 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.558 |
DEG_COP1_1 | 827 | 837 | PF00400 | 0.243 |
DEG_SCF_FBW7_1 | 396 | 402 | PF00400 | 0.711 |
DEG_SPOP_SBC_1 | 1045 | 1049 | PF00917 | 0.432 |
DEG_SPOP_SBC_1 | 687 | 691 | PF00917 | 0.661 |
DOC_ANK_TNKS_1 | 261 | 268 | PF00023 | 0.673 |
DOC_ANK_TNKS_1 | 489 | 496 | PF00023 | 0.607 |
DOC_ANK_TNKS_1 | 992 | 999 | PF00023 | 0.577 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.659 |
DOC_CKS1_1 | 396 | 401 | PF01111 | 0.707 |
DOC_CYCLIN_RxL_1 | 32 | 43 | PF00134 | 0.636 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.661 |
DOC_CYCLIN_yCln2_LP_2 | 608 | 614 | PF00134 | 0.626 |
DOC_MAPK_gen_1 | 1136 | 1142 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 754 | 763 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 413 | 421 | PF00069 | 0.521 |
DOC_PP1_RVXF_1 | 575 | 581 | PF00149 | 0.361 |
DOC_PP1_RVXF_1 | 752 | 758 | PF00149 | 0.502 |
DOC_PP1_RVXF_1 | 884 | 891 | PF00149 | 0.388 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.686 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.684 |
DOC_PP2B_LxvP_1 | 608 | 611 | PF13499 | 0.649 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.621 |
DOC_USP7_MATH_1 | 1095 | 1099 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 835 | 839 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 898 | 902 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 932 | 936 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 948 | 952 | PF00917 | 0.315 |
DOC_USP7_MATH_2 | 96 | 102 | PF00917 | 0.651 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 638 | 643 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 703 | 708 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 731 | 736 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 880 | 885 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 926 | 931 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 1077 | 1086 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 1090 | 1099 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 113 | 122 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 1130 | 1139 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 326 | 335 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 503 | 512 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 557 | 565 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 663 | 673 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 720 | 729 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 858 | 864 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 872 | 880 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 963 | 973 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 983 | 989 | PF00244 | 0.462 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.679 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.631 |
LIG_BIR_III_2 | 1123 | 1127 | PF00653 | 0.440 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.631 |
LIG_BIR_III_4 | 168 | 172 | PF00653 | 0.567 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 969 | 973 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_2 | 969 | 975 | PF00533 | 0.307 |
LIG_deltaCOP1_diTrp_1 | 305 | 311 | PF00928 | 0.620 |
LIG_FHA_1 | 1141 | 1147 | PF00498 | 0.423 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.630 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.561 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.672 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.678 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.593 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.607 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.586 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.648 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.527 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.466 |
LIG_FHA_1 | 966 | 972 | PF00498 | 0.388 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.705 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.658 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.565 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.673 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.711 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.669 |
LIG_FHA_2 | 550 | 556 | PF00498 | 0.432 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.653 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.573 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.613 |
LIG_FHA_2 | 826 | 832 | PF00498 | 0.315 |
LIG_FHA_2 | 858 | 864 | PF00498 | 0.312 |
LIG_FHA_2 | 917 | 923 | PF00498 | 0.340 |
LIG_LIR_Apic_2 | 290 | 296 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 341 | 348 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 970 | 981 | PF02991 | 0.388 |
LIG_LIR_LC3C_4 | 853 | 856 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 1101 | 1107 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.744 |
LIG_LIR_Nem_3 | 883 | 888 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 970 | 976 | PF02991 | 0.388 |
LIG_NRBOX | 1095 | 1101 | PF00104 | 0.380 |
LIG_NRBOX | 415 | 421 | PF00104 | 0.592 |
LIG_PDZ_Class_3 | 1147 | 1152 | PF00595 | 0.506 |
LIG_Pex14_1 | 307 | 311 | PF04695 | 0.623 |
LIG_Pex14_1 | 759 | 763 | PF04695 | 0.391 |
LIG_PTB_Apo_2 | 49 | 56 | PF02174 | 0.505 |
LIG_SH2_CRK | 1104 | 1108 | PF00017 | 0.424 |
LIG_SH2_CRK | 639 | 643 | PF00017 | 0.629 |
LIG_SH2_NCK_1 | 582 | 586 | PF00017 | 0.578 |
LIG_SH2_PTP2 | 1139 | 1142 | PF00017 | 0.484 |
LIG_SH2_STAT3 | 873 | 876 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 1139 | 1142 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.291 |
LIG_SH3_2 | 237 | 242 | PF14604 | 0.636 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.703 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.730 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.670 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.658 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.633 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.607 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.611 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.593 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.649 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.580 |
LIG_SH3_3 | 667 | 673 | PF00018 | 0.810 |
LIG_SH3_3 | 674 | 680 | PF00018 | 0.652 |
LIG_SH3_3 | 701 | 707 | PF00018 | 0.689 |
LIG_SH3_3 | 829 | 835 | PF00018 | 0.243 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.768 |
LIG_SUMO_SIM_anti_2 | 414 | 421 | PF11976 | 0.607 |
LIG_SUMO_SIM_par_1 | 804 | 810 | PF11976 | 0.312 |
LIG_TRAF2_1 | 743 | 746 | PF00917 | 0.543 |
LIG_TRAF2_1 | 812 | 815 | PF00917 | 0.315 |
LIG_UBA3_1 | 1056 | 1063 | PF00899 | 0.338 |
LIG_WW_3 | 631 | 635 | PF00397 | 0.621 |
MOD_CDC14_SPxK_1 | 199 | 202 | PF00782 | 0.569 |
MOD_CDC14_SPxK_1 | 631 | 634 | PF00782 | 0.620 |
MOD_CDC14_SPxK_1 | 883 | 886 | PF00782 | 0.388 |
MOD_CDK_SPK_2 | 392 | 397 | PF00069 | 0.561 |
MOD_CDK_SPxK_1 | 196 | 202 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 628 | 634 | PF00069 | 0.620 |
MOD_CDK_SPxK_1 | 880 | 886 | PF00069 | 0.388 |
MOD_CDK_SPxxK_3 | 235 | 242 | PF00069 | 0.639 |
MOD_CK1_1 | 1046 | 1052 | PF00069 | 0.423 |
MOD_CK1_1 | 1098 | 1104 | PF00069 | 0.414 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.693 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.635 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.725 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.715 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.737 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.684 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.657 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.583 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.585 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.601 |
MOD_CK1_1 | 567 | 573 | PF00069 | 0.604 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.518 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.611 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.548 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.668 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.579 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.689 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.549 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.296 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.673 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.688 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.706 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.705 |
MOD_CK2_1 | 549 | 555 | PF00069 | 0.416 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.620 |
MOD_CK2_1 | 809 | 815 | PF00069 | 0.321 |
MOD_CK2_1 | 933 | 939 | PF00069 | 0.315 |
MOD_Cter_Amidation | 776 | 779 | PF01082 | 0.653 |
MOD_DYRK1A_RPxSP_1 | 928 | 932 | PF00069 | 0.388 |
MOD_GlcNHglycan | 1018 | 1022 | PF01048 | 0.606 |
MOD_GlcNHglycan | 1069 | 1072 | PF01048 | 0.399 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.535 |
MOD_GlcNHglycan | 1092 | 1095 | PF01048 | 0.484 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.584 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.663 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.570 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.613 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.717 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.596 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.822 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.672 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.517 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.744 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.511 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.721 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.591 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.668 |
MOD_GlcNHglycan | 604 | 607 | PF01048 | 0.528 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.655 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.693 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.572 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.789 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.453 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.612 |
MOD_GlcNHglycan | 775 | 778 | PF01048 | 0.565 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.486 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.544 |
MOD_GlcNHglycan | 900 | 903 | PF01048 | 0.333 |
MOD_GlcNHglycan | 939 | 942 | PF01048 | 0.402 |
MOD_GlcNHglycan | 946 | 949 | PF01048 | 0.316 |
MOD_GlcNHglycan | 999 | 1002 | PF01048 | 0.560 |
MOD_GSK3_1 | 1057 | 1064 | PF00069 | 0.500 |
MOD_GSK3_1 | 1095 | 1102 | PF00069 | 0.462 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.580 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.659 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.558 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.815 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.792 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.649 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.783 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.758 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.562 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.602 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.417 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.527 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.611 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.658 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.814 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.560 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.388 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.322 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.497 |
MOD_GSK3_1 | 924 | 931 | PF00069 | 0.313 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.231 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.707 |
MOD_GSK3_1 | 944 | 951 | PF00069 | 0.454 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.315 |
MOD_LATS_1 | 1075 | 1081 | PF00433 | 0.451 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.562 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.676 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.550 |
MOD_N-GLC_1 | 602 | 607 | PF02516 | 0.615 |
MOD_N-GLC_1 | 965 | 970 | PF02516 | 0.340 |
MOD_NEK2_1 | 1038 | 1043 | PF00069 | 0.627 |
MOD_NEK2_1 | 1057 | 1062 | PF00069 | 0.370 |
MOD_NEK2_1 | 1099 | 1104 | PF00069 | 0.469 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.642 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.683 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.684 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.595 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.722 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.611 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.578 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.561 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.552 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.438 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.542 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.731 |
MOD_NEK2_1 | 864 | 869 | PF00069 | 0.312 |
MOD_NEK2_1 | 976 | 981 | PF00069 | 0.456 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.584 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.614 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.493 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.669 |
MOD_PIKK_1 | 705 | 711 | PF00454 | 0.548 |
MOD_PIKK_1 | 920 | 926 | PF00454 | 0.340 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.576 |
MOD_PKA_2 | 1038 | 1044 | PF00069 | 0.486 |
MOD_PKA_2 | 1129 | 1135 | PF00069 | 0.430 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.669 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.545 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.457 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.592 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.612 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.312 |
MOD_PKA_2 | 871 | 877 | PF00069 | 0.353 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.324 |
MOD_PKB_1 | 113 | 121 | PF00069 | 0.627 |
MOD_PKB_1 | 218 | 226 | PF00069 | 0.647 |
MOD_PKB_1 | 322 | 330 | PF00069 | 0.652 |
MOD_PKB_1 | 942 | 950 | PF00069 | 0.388 |
MOD_PKB_1 | 963 | 971 | PF00069 | 0.388 |
MOD_Plk_1 | 864 | 870 | PF00069 | 0.312 |
MOD_Plk_2-3 | 454 | 460 | PF00069 | 0.664 |
MOD_Plk_4 | 1095 | 1101 | PF00069 | 0.438 |
MOD_Plk_4 | 1103 | 1109 | PF00069 | 0.415 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.632 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.587 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.613 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.322 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.312 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.607 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.597 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.618 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.705 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.569 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.764 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.661 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.750 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.759 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.535 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.654 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.572 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.620 |
MOD_ProDKin_1 | 638 | 644 | PF00069 | 0.628 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.619 |
MOD_ProDKin_1 | 703 | 709 | PF00069 | 0.619 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.549 |
MOD_ProDKin_1 | 731 | 737 | PF00069 | 0.478 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.717 |
MOD_ProDKin_1 | 880 | 886 | PF00069 | 0.312 |
MOD_ProDKin_1 | 926 | 932 | PF00069 | 0.361 |
MOD_SUMO_rev_2 | 853 | 861 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_1 | 412 | 417 | PF01217 | 0.592 |
TRG_DiLeu_BaEn_1 | 875 | 880 | PF01217 | 0.312 |
TRG_DiLeu_BaEn_2 | 968 | 974 | PF01217 | 0.312 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.666 |
TRG_DiLeu_LyEn_5 | 875 | 880 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 1104 | 1107 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 1139 | 1142 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 1114 | 1117 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 700 | 703 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 754 | 757 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 877 | 879 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 942 | 945 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 962 | 965 | PF00400 | 0.183 |
TRG_ER_diArg_1 | 988 | 991 | PF00400 | 0.443 |
TRG_NLS_MonoExtC_3 | 321 | 326 | PF00514 | 0.649 |
TRG_NLS_MonoExtN_4 | 320 | 327 | PF00514 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEQ9 | Leptomonas seymouri | 39% | 100% |
A0A3Q8IEY2 | Leishmania donovani | 87% | 100% |
A4HDI9 | Leishmania braziliensis | 65% | 100% |
A4I0Z0 | Leishmania infantum | 87% | 100% |
E9AWZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |