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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A0A3S7X2X3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000018 | regulation of DNA recombination | 6 | 1 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006282 | regulation of DNA repair | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010569 | regulation of double-strand break repair via homologous recombination | 7 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0032204 | regulation of telomere maintenance | 6 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033044 | regulation of chromosome organization | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0045910 | negative regulation of DNA recombination | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051129 | negative regulation of cellular component organization | 5 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0080134 | regulation of response to stress | 4 | 1 |
GO:0080135 | regulation of cellular response to stress | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090657 | telomeric loop disassembly | 6 | 1 |
GO:1904429 | regulation of t-circle formation | 5 | 1 |
GO:1904430 | negative regulation of t-circle formation | 6 | 1 |
GO:2000779 | regulation of double-strand break repair | 7 | 1 |
GO:2001020 | obsolete regulation of response to DNA damage stimulus | 5 | 1 |
GO:0006950 | response to stress | 2 | 3 |
GO:0006974 | DNA damage response | 4 | 3 |
GO:0033554 | cellular response to stress | 3 | 3 |
GO:0050896 | response to stimulus | 1 | 3 |
GO:0051716 | cellular response to stimulus | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0070182 | DNA polymerase binding | 4 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 603 | 607 | PF00656 | 0.486 |
CLV_MEL_PAP_1 | 498 | 504 | PF00089 | 0.399 |
CLV_NRD_NRD_1 | 700 | 702 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 628 | 632 | PF00082 | 0.220 |
CLV_PCSK_FUR_1 | 773 | 777 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 700 | 702 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 773 | 775 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.214 |
CLV_PCSK_PC1ET2_1 | 630 | 632 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.178 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 781 | 785 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 881 | 885 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 891 | 895 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 913 | 917 | PF00082 | 0.472 |
DEG_SPOP_SBC_1 | 242 | 246 | PF00917 | 0.484 |
DOC_CYCLIN_RxL_1 | 151 | 161 | PF00134 | 0.378 |
DOC_CYCLIN_RxL_1 | 217 | 228 | PF00134 | 0.431 |
DOC_CYCLIN_RxL_1 | 412 | 423 | PF00134 | 0.455 |
DOC_CYCLIN_RxL_1 | 46 | 57 | PF00134 | 0.322 |
DOC_CYCLIN_RxL_1 | 888 | 897 | PF00134 | 0.456 |
DOC_MAPK_gen_1 | 426 | 435 | PF00069 | 0.339 |
DOC_MAPK_gen_1 | 595 | 604 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 672 | 681 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.245 |
DOC_MAPK_MEF2A_6 | 426 | 435 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 586 | 593 | PF00069 | 0.455 |
DOC_MAPK_NFAT4_5 | 586 | 594 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 545 | 551 | PF00149 | 0.330 |
DOC_PP2B_LxvP_1 | 908 | 911 | PF13499 | 0.506 |
DOC_PP4_FxxP_1 | 560 | 563 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 805 | 809 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 813 | 818 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 894 | 899 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 133 | 143 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 271 | 279 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 374 | 380 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 495 | 499 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 595 | 604 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 703 | 712 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 723 | 733 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 822 | 828 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 573 | 588 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 880 | 897 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 303 | 308 | PF00400 | 0.425 |
LIG_APCC_ABBA_1 | 331 | 336 | PF00400 | 0.362 |
LIG_APCC_ABBAyCdc20_2 | 701 | 707 | PF00400 | 0.349 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 398 | 402 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 860 | 864 | PF00533 | 0.421 |
LIG_EH1_1 | 175 | 183 | PF00400 | 0.420 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.443 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.378 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.365 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.441 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.323 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.472 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.473 |
LIG_FHA_1 | 727 | 733 | PF00498 | 0.671 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.656 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.551 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.477 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.275 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.489 |
LIG_FHA_2 | 648 | 654 | PF00498 | 0.441 |
LIG_FHA_2 | 821 | 827 | PF00498 | 0.731 |
LIG_FHA_2 | 858 | 864 | PF00498 | 0.457 |
LIG_FHA_2 | 917 | 923 | PF00498 | 0.450 |
LIG_LIR_Gen_1 | 327 | 338 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 525 | 533 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 623 | 634 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 702 | 713 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 861 | 872 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 875 | 885 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 926 | 936 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 675 | 680 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 684 | 690 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 702 | 708 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 861 | 867 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 875 | 880 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 926 | 931 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 937 | 942 | PF02991 | 0.346 |
LIG_MYND_1 | 855 | 859 | PF01753 | 0.678 |
LIG_NRBOX | 293 | 299 | PF00104 | 0.454 |
LIG_NRBOX | 904 | 910 | PF00104 | 0.394 |
LIG_PCNA_PIPBox_1 | 379 | 388 | PF02747 | 0.411 |
LIG_PCNA_PIPBox_1 | 529 | 538 | PF02747 | 0.484 |
LIG_PCNA_yPIPBox_3 | 661 | 671 | PF02747 | 0.420 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.486 |
LIG_REV1ctd_RIR_1 | 153 | 161 | PF16727 | 0.504 |
LIG_REV1ctd_RIR_1 | 716 | 727 | PF16727 | 0.537 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.431 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.245 |
LIG_SH2_CRK | 677 | 681 | PF00017 | 0.431 |
LIG_SH2_CRK | 712 | 716 | PF00017 | 0.323 |
LIG_SH2_GRB2like | 619 | 622 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 712 | 716 | PF00017 | 0.339 |
LIG_SH2_NCK_1 | 757 | 761 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 734 | 737 | PF00017 | 0.682 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.451 |
LIG_SH2_SRC | 619 | 622 | PF00017 | 0.520 |
LIG_SH2_SRC | 757 | 760 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 712 | 716 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 943 | 947 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 19 | 22 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 734 | 737 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.420 |
LIG_SH3_2 | 817 | 822 | PF14604 | 0.524 |
LIG_SH3_2 | 851 | 856 | PF14604 | 0.493 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.420 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.420 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.475 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.397 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.420 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.445 |
LIG_SH3_3 | 795 | 801 | PF00018 | 0.648 |
LIG_SH3_3 | 814 | 820 | PF00018 | 0.441 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.621 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.331 |
LIG_SUMO_SIM_anti_2 | 204 | 209 | PF11976 | 0.508 |
LIG_SUMO_SIM_anti_2 | 228 | 235 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 252 | 258 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 678 | 685 | PF11976 | 0.486 |
LIG_TRFH_1 | 212 | 216 | PF08558 | 0.520 |
LIG_TYR_ITIM | 732 | 737 | PF00017 | 0.697 |
LIG_UBA3_1 | 331 | 337 | PF00899 | 0.318 |
LIG_UBA3_1 | 552 | 557 | PF00899 | 0.462 |
LIG_UBA3_1 | 625 | 630 | PF00899 | 0.420 |
LIG_WRC_WIRS_1 | 573 | 578 | PF05994 | 0.423 |
MOD_CDC14_SPxK_1 | 583 | 586 | PF00782 | 0.520 |
MOD_CDK_SPxK_1 | 580 | 586 | PF00069 | 0.520 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.491 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.486 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.519 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.498 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.582 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.571 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.480 |
MOD_CK1_1 | 824 | 830 | PF00069 | 0.652 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.375 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.465 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.480 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.730 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.707 |
MOD_CK2_1 | 857 | 863 | PF00069 | 0.431 |
MOD_CK2_1 | 916 | 922 | PF00069 | 0.478 |
MOD_Cter_Amidation | 720 | 723 | PF01082 | 0.354 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.307 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.269 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.320 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.291 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.584 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.314 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.392 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.272 |
MOD_GlcNHglycan | 6 | 10 | PF01048 | 0.458 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.588 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.532 |
MOD_GlcNHglycan | 823 | 826 | PF01048 | 0.641 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.502 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.421 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.441 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.566 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.535 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.347 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.307 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.521 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.520 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.410 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.505 |
MOD_GSK3_1 | 820 | 827 | PF00069 | 0.702 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.655 |
MOD_LATS_1 | 645 | 651 | PF00433 | 0.515 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.233 |
MOD_N-GLC_2 | 664 | 666 | PF02516 | 0.231 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.441 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.467 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.424 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.321 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.498 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.411 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.311 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.298 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.371 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.314 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.355 |
MOD_NEK2_1 | 690 | 695 | PF00069 | 0.507 |
MOD_NEK2_1 | 842 | 847 | PF00069 | 0.695 |
MOD_NEK2_1 | 893 | 898 | PF00069 | 0.601 |
MOD_NEK2_1 | 946 | 951 | PF00069 | 0.520 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.403 |
MOD_NEK2_2 | 911 | 916 | PF00069 | 0.444 |
MOD_NEK2_2 | 923 | 928 | PF00069 | 0.343 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.512 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.497 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.548 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.437 |
MOD_PKA_1 | 106 | 112 | PF00069 | 0.520 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.524 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.553 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.378 |
MOD_PKA_2 | 699 | 705 | PF00069 | 0.410 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.616 |
MOD_PKA_2 | 724 | 730 | PF00069 | 0.631 |
MOD_PKA_2 | 821 | 827 | PF00069 | 0.757 |
MOD_PKA_2 | 836 | 842 | PF00069 | 0.669 |
MOD_PKB_1 | 701 | 709 | PF00069 | 0.424 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.484 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.399 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.395 |
MOD_Plk_1 | 828 | 834 | PF00069 | 0.792 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.508 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.462 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.332 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.462 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.379 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.478 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.417 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.456 |
MOD_Plk_4 | 828 | 834 | PF00069 | 0.735 |
MOD_Plk_4 | 923 | 929 | PF00069 | 0.572 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.476 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.473 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.624 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.335 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.306 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.431 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.520 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.614 |
MOD_ProDKin_1 | 813 | 819 | PF00069 | 0.488 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.669 |
MOD_ProDKin_1 | 894 | 900 | PF00069 | 0.500 |
MOD_SUMO_rev_2 | 540 | 549 | PF00179 | 0.520 |
MOD_SUMO_rev_2 | 554 | 559 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 778 | 786 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_2 | 862 | 868 | PF01217 | 0.400 |
TRG_DiLeu_BaEn_4 | 937 | 943 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 889 | 894 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 904 | 909 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 526 | 529 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 677 | 680 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 712 | 715 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 734 | 737 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 877 | 880 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 943 | 946 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 700 | 703 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 722 | 725 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 773 | 776 | PF00400 | 0.563 |
TRG_NES_CRM1_1 | 384 | 398 | PF08389 | 0.370 |
TRG_Pf-PMV_PEXEL_1 | 933 | 937 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 940 | 945 | PF00026 | 0.517 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K3 | Leptomonas seymouri | 70% | 99% |
A0A0P0V4R0 | Oryza sativa subsp. japonica | 35% | 94% |
A0A0S4KH73 | Bodo saltans | 39% | 92% |
A0A1X0P9Z9 | Trypanosomatidae | 47% | 98% |
A0A3R7MDU1 | Trypanosoma rangeli | 56% | 98% |
A0A3R7RLU2 | Trypanosoma rangeli | 24% | 93% |
A0A3S7WYU3 | Leishmania donovani | 24% | 100% |
A1CJ34 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 26% | 100% |
A1D8E4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 100% |
A2QY22 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 27% | 100% |
A3LN13 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 24% | 100% |
A4HDT9 | Leishmania braziliensis | 25% | 100% |
A4HHR4 | Leishmania braziliensis | 86% | 100% |
A4I136 | Leishmania infantum | 24% | 100% |
A4I4X4 | Leishmania infantum | 100% | 100% |
A4K436 | Bos taurus | 34% | 78% |
A5DNW6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 100% |
A5DUW8 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 24% | 100% |
A8MPP1 | Homo sapiens | 27% | 100% |
A8WS58 | Caenorhabditis briggsae | 32% | 96% |
B0W9F4 | Culex quinquefasciatus | 32% | 97% |
B3MSG8 | Drosophila ananassae | 32% | 96% |
B3NSW1 | Drosophila erecta | 33% | 97% |
B4GU19 | Drosophila persimilis | 33% | 94% |
B4I0K4 | Drosophila sechellia | 32% | 99% |
B4JNS2 | Drosophila grimshawi | 33% | 97% |
B4L1Z2 | Drosophila mojavensis | 32% | 94% |
B4M891 | Drosophila virilis | 32% | 95% |
B4NDG5 | Drosophila willistoni | 33% | 95% |
B4PZB4 | Drosophila yakuba | 34% | 97% |
C9ZKX7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 99% |
E9AEC8 | Leishmania major | 93% | 100% |
E9ALF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AX74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
F1R345 | Danio rerio | 29% | 100% |
F4HQE2 | Arabidopsis thaliana | 34% | 92% |
O14147 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
P06839 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P0C928 | Danio rerio | 32% | 81% |
Q0VGM9 | Mus musculus | 34% | 79% |
Q16X92 | Aedes aegypti | 33% | 94% |
Q1E5T3 | Coccidioides immitis (strain RS) | 28% | 100% |
Q21489 | Caenorhabditis elegans | 24% | 100% |
Q29FS3 | Drosophila pseudoobscura pseudoobscura | 33% | 94% |
Q2U587 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 100% |
Q3YK19 | Gallus gallus | 29% | 76% |
Q4QAA2 | Leishmania major | 25% | 100% |
Q4WWE9 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
Q55G81 | Dictyostelium discoideum | 26% | 100% |
Q5AD67 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 26% | 100% |
Q5RE34 | Pongo abelii | 32% | 73% |
Q5RJZ1 | Rattus norvegicus | 33% | 75% |
Q6AXC6 | Mus musculus | 28% | 100% |
Q6BZD9 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 100% |
Q6CAX3 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 26% | 100% |
Q6CIF0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
Q6FKT4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 100% |
Q6H1L8 | Mus spretus | 34% | 79% |
Q7QEI1 | Anopheles gambiae | 33% | 96% |
Q92771 | Homo sapiens | 27% | 100% |
Q93575 | Caenorhabditis elegans | 31% | 96% |
Q96FC9 | Homo sapiens | 28% | 98% |
Q9BX63 | Homo sapiens | 29% | 76% |
Q9NZ71 | Homo sapiens | 33% | 78% |
Q9W484 | Drosophila melanogaster | 33% | 97% |
V5B587 | Trypanosoma cruzi | 24% | 100% |
V5BAP9 | Trypanosoma cruzi | 28% | 100% |
V5BX91 | Trypanosoma cruzi | 50% | 100% |