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 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q8I2
Term | Name | Level | Count |
---|---|---|---|
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:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 12 |
GO:0006270 | DNA replication initiation | 5 | 12 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010639 | negative regulation of organelle organization | 6 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0032392 | DNA geometric change | 7 | 12 |
GO:0032508 | DNA duplex unwinding | 8 | 12 |
GO:0032780 | negative regulation of ATP-dependent activity | 4 | 12 |
GO:0033043 | regulation of organelle organization | 5 | 12 |
GO:0033044 | regulation of chromosome organization | 6 | 12 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043086 | negative regulation of catalytic activity | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043462 | regulation of ATP-dependent activity | 3 | 12 |
GO:0044092 | negative regulation of molecular function | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0048519 | negative regulation of biological process | 3 | 12 |
GO:0048523 | negative regulation of cellular process | 4 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050790 | regulation of catalytic activity | 3 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051095 | regulation of helicase activity | 4 | 12 |
GO:0051097 | negative regulation of helicase activity | 5 | 12 |
GO:0051128 | regulation of cellular component organization | 4 | 12 |
GO:0051129 | negative regulation of cellular component organization | 5 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0065009 | regulation of molecular function | 2 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1902292 | cell cycle DNA replication initiation | 3 | 2 |
GO:1902315 | nuclear cell cycle DNA replication initiation | 4 | 2 |
GO:1902975 | mitotic DNA replication initiation | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
GO:1905462 | regulation of DNA duplex unwinding | 7 | 12 |
GO:1905463 | negative regulation of DNA duplex unwinding | 8 | 12 |
GO:1905774 | regulation of DNA helicase activity | 5 | 12 |
GO:1905775 | negative regulation of DNA helicase activity | 6 | 12 |
GO:2001251 | negative regulation of chromosome organization | 7 | 12 |
GO:0007049 | cell cycle | 2 | 10 |
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:0003697 | single-stranded DNA binding | 5 | 2 |
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:0016462 | pyrophosphatase activity | 5 | 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:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.785 |
CLV_C14_Caspase3-7 | 767 | 771 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 877 | 879 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 947 | 949 | PF00675 | 0.565 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.198 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 752 | 754 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 947 | 949 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.653 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 732 | 736 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 782 | 786 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.554 |
CLV_Separin_Metazoa | 210 | 214 | PF03568 | 0.395 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.591 |
DEG_APCC_DBOX_1 | 678 | 686 | PF00400 | 0.457 |
DEG_ODPH_VHL_1 | 502 | 514 | PF01847 | 0.458 |
DEG_SCF_FBW7_1 | 672 | 678 | PF00400 | 0.447 |
DOC_CKS1_1 | 672 | 677 | PF01111 | 0.454 |
DOC_CYCLIN_RxL_1 | 490 | 501 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 296 | 304 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 316 | 325 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 410 | 419 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 426 | 435 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 535 | 542 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 892 | 899 | PF00069 | 0.508 |
DOC_MAPK_HePTP_8 | 506 | 518 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 297 | 306 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 319 | 327 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 509 | 518 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 535 | 544 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 687 | 694 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 815 | 823 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 892 | 899 | PF00069 | 0.516 |
DOC_MAPK_NFAT4_5 | 509 | 517 | PF00069 | 0.449 |
DOC_MAPK_RevD_3 | 323 | 336 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 780 | 787 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 475 | 478 | PF13499 | 0.418 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 930 | 934 | PF00917 | 0.553 |
DOC_USP7_UBL2_3 | 557 | 561 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 296 | 306 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 410 | 416 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 467 | 475 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 572 | 579 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 697 | 702 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 831 | 839 | PF00244 | 0.458 |
LIG_Actin_WH2_2 | 855 | 872 | PF00022 | 0.517 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.533 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.680 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 662 | 666 | PF00533 | 0.458 |
LIG_BRCT_BRCA1_1 | 760 | 764 | PF00533 | 0.621 |
LIG_BRCT_BRCA1_1 | 788 | 792 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 942 | 946 | PF00533 | 0.410 |
LIG_Clathr_ClatBox_1 | 326 | 330 | PF01394 | 0.447 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.533 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.453 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.447 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.393 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.485 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.440 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.455 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.447 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.627 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.533 |
LIG_FHA_1 | 883 | 889 | PF00498 | 0.500 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.394 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.533 |
LIG_FHA_2 | 711 | 717 | PF00498 | 0.539 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.498 |
LIG_FHA_2 | 844 | 850 | PF00498 | 0.533 |
LIG_GBD_Chelix_1 | 203 | 211 | PF00786 | 0.427 |
LIG_Integrin_RGD_1 | 186 | 188 | PF01839 | 0.594 |
LIG_Integrin_RGD_1 | 363 | 365 | PF01839 | 0.231 |
LIG_Integrin_RGD_1 | 537 | 539 | PF01839 | 0.247 |
LIG_LIR_Apic_2 | 173 | 179 | PF02991 | 0.716 |
LIG_LIR_Apic_2 | 65 | 69 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 253 | 261 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 553 | 563 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 610 | 619 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 678 | 686 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 288 | 292 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 317 | 321 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 789 | 795 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 874 | 880 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 949 | 953 | PF02991 | 0.413 |
LIG_LYPXL_S_1 | 339 | 343 | PF13949 | 0.247 |
LIG_LYPXL_yS_3 | 340 | 343 | PF13949 | 0.447 |
LIG_NRBOX | 513 | 519 | PF00104 | 0.458 |
LIG_PCNA_PIPBox_1 | 934 | 943 | PF02747 | 0.535 |
LIG_PCNA_yPIPBox_3 | 197 | 207 | PF02747 | 0.429 |
LIG_PCNA_yPIPBox_3 | 773 | 784 | PF02747 | 0.392 |
LIG_PCNA_yPIPBox_3 | 934 | 948 | PF02747 | 0.540 |
LIG_PDZ_Class_1 | 964 | 969 | PF00595 | 0.454 |
LIG_Pex14_2 | 680 | 684 | PF04695 | 0.447 |
LIG_Pex14_2 | 857 | 861 | PF04695 | 0.447 |
LIG_PTB_Apo_2 | 215 | 222 | PF02174 | 0.315 |
LIG_PTB_Phospho_1 | 215 | 221 | PF10480 | 0.315 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.496 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.447 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.450 |
LIG_SH2_CRK | 950 | 954 | PF00017 | 0.408 |
LIG_SH2_GRB2like | 224 | 227 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 941 | 945 | PF00017 | 0.528 |
LIG_SH2_PTP2 | 807 | 810 | PF00017 | 0.533 |
LIG_SH2_SRC | 355 | 358 | PF00017 | 0.471 |
LIG_SH2_SRC | 660 | 663 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 928 | 932 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 783 | 786 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 844 | 847 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 928 | 931 | PF00017 | 0.557 |
LIG_SH3_1 | 335 | 341 | PF00018 | 0.447 |
LIG_SH3_2 | 27 | 32 | PF14604 | 0.739 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.737 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.458 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.438 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.447 |
LIG_SH3_4 | 773 | 780 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 414 | 420 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 274 | 282 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 395 | 401 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 484 | 489 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 541 | 547 | PF11976 | 0.447 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.659 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.455 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.502 |
LIG_TRAF2_1 | 713 | 716 | PF00917 | 0.508 |
LIG_TYR_ITIM | 252 | 257 | PF00017 | 0.299 |
LIG_UBA3_1 | 485 | 490 | PF00899 | 0.315 |
LIG_UBA3_1 | 517 | 526 | PF00899 | 0.299 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.419 |
LIG_WRC_WIRS_1 | 698 | 703 | PF05994 | 0.275 |
LIG_WW_3 | 28 | 32 | PF00397 | 0.756 |
MOD_CDK_SPxxK_3 | 488 | 495 | PF00069 | 0.419 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.754 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.315 |
MOD_CK1_1 | 671 | 677 | PF00069 | 0.193 |
MOD_CK1_1 | 868 | 874 | PF00069 | 0.400 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.315 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.334 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.386 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.299 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.484 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.484 |
MOD_CK2_1 | 759 | 765 | PF00069 | 0.642 |
MOD_CK2_1 | 868 | 874 | PF00069 | 0.408 |
MOD_CK2_1 | 880 | 886 | PF00069 | 0.445 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.419 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.421 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.315 |
MOD_GlcNHglycan | 870 | 873 | PF01048 | 0.419 |
MOD_GlcNHglycan | 909 | 912 | PF01048 | 0.476 |
MOD_GlcNHglycan | 942 | 945 | PF01048 | 0.528 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.299 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.308 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.299 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.326 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.249 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.299 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.534 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.625 |
MOD_GSK3_1 | 848 | 855 | PF00069 | 0.347 |
MOD_GSK3_1 | 861 | 868 | PF00069 | 0.298 |
MOD_GSK3_1 | 880 | 887 | PF00069 | 0.453 |
MOD_GSK3_1 | 926 | 933 | PF00069 | 0.447 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.301 |
MOD_N-GLC_1 | 736 | 741 | PF02516 | 0.498 |
MOD_N-GLC_1 | 930 | 935 | PF02516 | 0.465 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.445 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.308 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.288 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.530 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.419 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.363 |
MOD_NEK2_2 | 563 | 568 | PF00069 | 0.419 |
MOD_NEK2_2 | 852 | 857 | PF00069 | 0.315 |
MOD_NEK2_2 | 898 | 903 | PF00069 | 0.421 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.299 |
MOD_PIKK_1 | 710 | 716 | PF00454 | 0.473 |
MOD_PIKK_1 | 861 | 867 | PF00454 | 0.374 |
MOD_PIKK_1 | 913 | 919 | PF00454 | 0.514 |
MOD_PIKK_1 | 930 | 936 | PF00454 | 0.421 |
MOD_PKA_1 | 467 | 473 | PF00069 | 0.570 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.746 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.334 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.315 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.315 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.466 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.299 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.326 |
MOD_PKA_2 | 754 | 760 | PF00069 | 0.539 |
MOD_PKA_2 | 793 | 799 | PF00069 | 0.299 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.315 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.436 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.390 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.189 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.404 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.315 |
MOD_Plk_1 | 668 | 674 | PF00069 | 0.193 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.655 |
MOD_Plk_1 | 726 | 732 | PF00069 | 0.485 |
MOD_Plk_1 | 759 | 765 | PF00069 | 0.665 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.343 |
MOD_Plk_2-3 | 613 | 619 | PF00069 | 0.299 |
MOD_Plk_2-3 | 843 | 849 | PF00069 | 0.419 |
MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.419 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.334 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.302 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.303 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.306 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.393 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.275 |
MOD_Plk_4 | 825 | 831 | PF00069 | 0.299 |
MOD_Plk_4 | 852 | 858 | PF00069 | 0.446 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.299 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.419 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.309 |
MOD_SUMO_rev_2 | 231 | 239 | PF00179 | 0.340 |
MOD_SUMO_rev_2 | 505 | 514 | PF00179 | 0.299 |
TRG_DiLeu_BaEn_1 | 595 | 600 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_1 | 715 | 720 | PF01217 | 0.653 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_4 | 52 | 58 | PF01217 | 0.417 |
TRG_DiLeu_BaEn_4 | 715 | 721 | PF01217 | 0.627 |
TRG_DiLeu_BaEn_4 | 726 | 732 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 442 | 447 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 948 | 953 | PF01217 | 0.538 |
TRG_DiLeu_LyEn_5 | 715 | 720 | PF01217 | 0.653 |
TRG_DiLeu_LyEn_5 | 886 | 891 | PF01217 | 0.460 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 783 | 786 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 807 | 810 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 950 | 953 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 730 | 733 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 751 | 753 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 891 | 894 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 946 | 948 | PF00400 | 0.335 |
TRG_ER_FFAT_2 | 921 | 933 | PF00635 | 0.577 |
TRG_NES_CRM1_1 | 681 | 696 | PF08389 | 0.315 |
TRG_NLS_MonoCore_2 | 11 | 16 | PF00514 | 0.719 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.719 |
TRG_NLS_MonoExtN_4 | 11 | 17 | PF00514 | 0.732 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.277 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.373 |
TRG_Pf-PMV_PEXEL_1 | 718 | 723 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 752 | 756 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 951 | 955 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 87% | 98% |
A0A0N1I383 | Leptomonas seymouri | 32% | 95% |
A0A0S4IK09 | Bodo saltans | 64% | 98% |
A0A1X0NZT6 | Trypanosomatidae | 75% | 100% |
A0A3Q8IAX4 | Leishmania donovani | 98% | 100% |
A0A3R7K9K0 | Trypanosoma rangeli | 31% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 76% | 100% |
A0A3S7WY81 | Leishmania donovani | 30% | 100% |
A0A3S7X726 | Leishmania donovani | 32% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 29% | 100% |
A4FUD9 | Bos taurus | 33% | 100% |
A4H5K0 | Leishmania braziliensis | 32% | 100% |
A4HDE7 | Leishmania braziliensis | 30% | 100% |
A4HGC9 | Leishmania braziliensis | 92% | 100% |
A4HLY1 | Leishmania braziliensis | 32% | 100% |
A4I0T0 | Leishmania infantum | 30% | 100% |
A4I3G2 | Leishmania infantum | 98% | 100% |
A4I9B0 | Leishmania infantum | 32% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 34% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 46% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F1M5F3 | Rattus norvegicus | 31% | 86% |
F1N2W9 | Bos taurus | 31% | 85% |
F6RIX4 | Xenopus tropicalis | 30% | 87% |
P25205 | Homo sapiens | 34% | 100% |
P25206 | Mus musculus | 33% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P33991 | Homo sapiens | 31% | 100% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 100% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P49735 | Drosophila melanogaster | 43% | 100% |
P49736 | Homo sapiens | 45% | 100% |
P55861 | Xenopus laevis | 40% | 100% |
P97310 | Mus musculus | 44% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 34% | 100% |
Q21902 | Caenorhabditis elegans | 29% | 100% |
Q28BS0 | Xenopus tropicalis | 34% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 31% | 100% |
Q2KHI9 | Mus musculus | 32% | 85% |
Q2R482 | Oryza sativa subsp. japonica | 46% | 100% |
Q43704 | Zea mays | 34% | 100% |
Q4Q3R6 | Leishmania major | 32% | 100% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q4QI01 | Leishmania major | 31% | 100% |
Q54CP4 | Dictyostelium discoideum | 31% | 100% |
Q5R8G6 | Pongo abelii | 34% | 100% |
Q6DIH3 | Xenopus tropicalis | 42% | 100% |
Q6NRM6 | Xenopus laevis | 30% | 85% |
Q7ZXZ0 | Xenopus laevis | 35% | 100% |
Q9LPD9 | Arabidopsis thaliana | 41% | 100% |
Q9NXL9 | Homo sapiens | 31% | 85% |
Q9SF37 | Arabidopsis thaliana | 31% | 100% |
Q9SX03 | Zea mays | 34% | 100% |
Q9SX04 | Zea mays | 34% | 100% |
Q9V461 | Drosophila melanogaster | 32% | 100% |
Q9VGW6 | Drosophila melanogaster | 31% | 100% |
Q9XYU0 | Drosophila melanogaster | 32% | 100% |
Q9XYU1 | Drosophila melanogaster | 34% | 100% |
V5BQA9 | Trypanosoma cruzi | 80% | 100% |
V5BSG2 | Trypanosoma cruzi | 30% | 100% |