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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005657 | replication fork | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H6F0
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 15 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 15 |
GO:0006259 | DNA metabolic process | 4 | 15 |
GO:0006281 | DNA repair | 5 | 15 |
GO:0006310 | DNA recombination | 5 | 15 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 15 |
GO:0006807 | nitrogen compound metabolic process | 2 | 15 |
GO:0006950 | response to stress | 2 | 15 |
GO:0006974 | DNA damage response | 4 | 15 |
GO:0006996 | organelle organization | 4 | 15 |
GO:0008152 | metabolic process | 1 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0016043 | cellular component organization | 3 | 15 |
GO:0032200 | telomere organization | 6 | 15 |
GO:0033554 | cellular response to stress | 3 | 15 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 15 |
GO:0043170 | macromolecule metabolic process | 3 | 15 |
GO:0044237 | cellular metabolic process | 2 | 15 |
GO:0044238 | primary metabolic process | 2 | 15 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 15 |
GO:0046483 | heterocycle metabolic process | 3 | 15 |
GO:0050896 | response to stimulus | 1 | 15 |
GO:0051276 | chromosome organization | 5 | 15 |
GO:0051716 | cellular response to stimulus | 2 | 15 |
GO:0071704 | organic substance metabolic process | 2 | 15 |
GO:0071840 | cellular component organization or biogenesis | 2 | 15 |
GO:0090304 | nucleic acid metabolic process | 4 | 15 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 15 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003678 | DNA helicase activity | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0004386 | helicase activity | 2 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 15 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 15 |
GO:0016887 | ATP hydrolysis activity | 7 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 15 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0000287 | magnesium ion binding | 5 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.794 |
CLV_C14_Caspase3-7 | 485 | 489 | PF00656 | 0.509 |
CLV_C14_Caspase3-7 | 903 | 907 | PF00656 | 0.771 |
CLV_MEL_PAP_1 | 928 | 934 | PF00089 | 0.753 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 1027 | 1029 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 855 | 857 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 861 | 863 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 969 | 971 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 988 | 990 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 1027 | 1029 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 854 | 856 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 861 | 863 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 969 | 971 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 988 | 990 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 695 | 697 | PF00082 | 0.252 |
CLV_PCSK_PC1ET2_1 | 844 | 846 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.630 |
CLV_PCSK_PC7_1 | 323 | 329 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 581 | 585 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 825 | 829 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 861 | 865 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 980 | 984 | PF00082 | 0.535 |
DEG_APCC_DBOX_1 | 563 | 571 | PF00400 | 0.542 |
DEG_APCC_DBOX_1 | 860 | 868 | PF00400 | 0.679 |
DEG_SCF_FBW7_1 | 14 | 20 | PF00400 | 0.566 |
DEG_SCF_FBW7_2 | 626 | 632 | PF00400 | 0.443 |
DEG_SPOP_SBC_1 | 1060 | 1064 | PF00917 | 0.470 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.566 |
DOC_CKS1_1 | 626 | 631 | PF01111 | 0.450 |
DOC_CYCLIN_RxL_1 | 173 | 184 | PF00134 | 0.542 |
DOC_CYCLIN_RxL_1 | 550 | 559 | PF00134 | 0.463 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 657 | 666 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 480 | 483 | PF00134 | 0.521 |
DOC_MAPK_DCC_7 | 641 | 650 | PF00069 | 0.288 |
DOC_MAPK_gen_1 | 296 | 303 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 651 | 658 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 822 | 832 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 296 | 303 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 439 | 446 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 825 | 832 | PF00069 | 0.454 |
DOC_MAPK_NFAT4_5 | 825 | 833 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 174 | 181 | PF00149 | 0.423 |
DOC_PP2B_LxvP_1 | 480 | 483 | PF13499 | 0.592 |
DOC_PP2B_LxvP_1 | 560 | 563 | PF13499 | 0.482 |
DOC_PP4_MxPP_1 | 583 | 586 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 1004 | 1008 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 1059 | 1063 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 887 | 891 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 900 | 904 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 439 | 443 | PF12436 | 0.373 |
DOC_USP7_UBL2_3 | 992 | 996 | PF12436 | 0.709 |
DOC_WW_Pin1_4 | 1000 | 1005 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.800 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 625 | 630 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 872 | 877 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 1046 | 1051 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 163 | 172 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 253 | 258 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 335 | 344 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 368 | 375 | PF00244 | 0.191 |
LIG_14-3-3_CanoR_1 | 451 | 458 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 550 | 556 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 564 | 568 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 659 | 667 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 855 | 861 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 902 | 911 | PF00244 | 0.642 |
LIG_Actin_WH2_2 | 322 | 337 | PF00022 | 0.312 |
LIG_Actin_WH2_2 | 460 | 477 | PF00022 | 0.361 |
LIG_BIR_III_2 | 18 | 22 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 740 | 744 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_2 | 433 | 439 | PF00533 | 0.373 |
LIG_CORNRBOX | 218 | 226 | PF00104 | 0.280 |
LIG_CtBP_PxDLS_1 | 753 | 757 | PF00389 | 0.385 |
LIG_DLG_GKlike_1 | 856 | 863 | PF00625 | 0.583 |
LIG_EH1_1 | 577 | 585 | PF00400 | 0.513 |
LIG_EVH1_2 | 730 | 734 | PF00568 | 0.351 |
LIG_FHA_1 | 1062 | 1068 | PF00498 | 0.637 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.460 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.630 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.694 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.298 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.313 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.370 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.576 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.656 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.415 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.481 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.444 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.447 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.510 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.781 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.689 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.376 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.532 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.431 |
LIG_FHA_2 | 537 | 543 | PF00498 | 0.471 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.433 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.537 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.381 |
LIG_FHA_2 | 829 | 835 | PF00498 | 0.521 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 374 | 383 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 389 | 398 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 419 | 426 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 598 | 607 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 389 | 394 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 419 | 423 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 598 | 603 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 699 | 704 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 741 | 747 | PF02991 | 0.389 |
LIG_NBox_RRM_1 | 820 | 830 | PF00076 | 0.373 |
LIG_NRBOX | 859 | 865 | PF00104 | 0.583 |
LIG_PCNA_PIPBox_1 | 715 | 724 | PF02747 | 0.362 |
LIG_PCNA_yPIPBox_3 | 668 | 681 | PF02747 | 0.407 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.313 |
LIG_SH2_CRK | 157 | 161 | PF00017 | 0.447 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.335 |
LIG_SH2_SRC | 574 | 577 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 758 | 762 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 789 | 792 | PF00017 | 0.338 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.665 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.682 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.289 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.551 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.388 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.388 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.327 |
LIG_SH3_3 | 792 | 798 | PF00018 | 0.379 |
LIG_SH3_3 | 998 | 1004 | PF00018 | 0.671 |
LIG_SUMO_SIM_anti_2 | 1062 | 1069 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 376 | 382 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 376 | 382 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 514 | 519 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 530 | 540 | PF11976 | 0.361 |
LIG_SUMO_SIM_par_1 | 875 | 880 | PF11976 | 0.666 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.575 |
LIG_TYR_ITIM | 155 | 160 | PF00017 | 0.443 |
LIG_TYR_ITIM | 373 | 378 | PF00017 | 0.328 |
LIG_WRC_WIRS_1 | 803 | 808 | PF05994 | 0.413 |
MOD_CK1_1 | 1021 | 1027 | PF00069 | 0.664 |
MOD_CK1_1 | 1063 | 1069 | PF00069 | 0.739 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.642 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.439 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.660 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.681 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.300 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.767 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.455 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.456 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.356 |
MOD_CK1_1 | 746 | 752 | PF00069 | 0.378 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.424 |
MOD_CK1_1 | 880 | 886 | PF00069 | 0.710 |
MOD_CK1_1 | 898 | 904 | PF00069 | 0.575 |
MOD_CK1_1 | 923 | 929 | PF00069 | 0.677 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.660 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.730 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.672 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.370 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.365 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.430 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.740 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.414 |
MOD_CK2_1 | 902 | 908 | PF00069 | 0.687 |
MOD_Cter_Amidation | 1025 | 1028 | PF01082 | 0.510 |
MOD_GlcNHglycan | 1005 | 1009 | PF01048 | 0.755 |
MOD_GlcNHglycan | 1011 | 1014 | PF01048 | 0.755 |
MOD_GlcNHglycan | 1020 | 1023 | PF01048 | 0.755 |
MOD_GlcNHglycan | 1024 | 1027 | PF01048 | 0.772 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.689 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.624 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.300 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.530 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.455 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.663 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.412 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.671 |
MOD_GlcNHglycan | 840 | 843 | PF01048 | 0.508 |
MOD_GlcNHglycan | 870 | 873 | PF01048 | 0.733 |
MOD_GlcNHglycan | 879 | 882 | PF01048 | 0.712 |
MOD_GlcNHglycan | 914 | 917 | PF01048 | 0.770 |
MOD_GlcNHglycan | 938 | 941 | PF01048 | 0.740 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.747 |
MOD_GSK3_1 | 1000 | 1007 | PF00069 | 0.579 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.752 |
MOD_GSK3_1 | 1059 | 1066 | PF00069 | 0.655 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.707 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.658 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.744 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.445 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.549 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.582 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.572 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.249 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.348 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.450 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.390 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.490 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.399 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.402 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.709 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.649 |
MOD_GSK3_1 | 898 | 905 | PF00069 | 0.690 |
MOD_GSK3_1 | 988 | 995 | PF00069 | 0.535 |
MOD_LATS_1 | 990 | 996 | PF00433 | 0.468 |
MOD_N-GLC_1 | 1018 | 1023 | PF02516 | 0.761 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.558 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.595 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.459 |
MOD_N-GLC_1 | 660 | 665 | PF02516 | 0.417 |
MOD_N-GLC_1 | 667 | 672 | PF02516 | 0.376 |
MOD_N-GLC_1 | 846 | 851 | PF02516 | 0.549 |
MOD_N-GLC_1 | 872 | 877 | PF02516 | 0.586 |
MOD_N-GLC_1 | 920 | 925 | PF02516 | 0.494 |
MOD_N-GLC_1 | 936 | 941 | PF02516 | 0.583 |
MOD_N-GLC_1 | 992 | 997 | PF02516 | 0.710 |
MOD_NEK2_1 | 1051 | 1056 | PF00069 | 0.729 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.621 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.671 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.316 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.326 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.288 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.398 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.467 |
MOD_NEK2_1 | 536 | 541 | PF00069 | 0.467 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.427 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.412 |
MOD_NEK2_1 | 776 | 781 | PF00069 | 0.369 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.381 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.446 |
MOD_NEK2_1 | 877 | 882 | PF00069 | 0.739 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.325 |
MOD_NEK2_2 | 758 | 763 | PF00069 | 0.346 |
MOD_NEK2_2 | 846 | 851 | PF00069 | 0.549 |
MOD_PIKK_1 | 445 | 451 | PF00454 | 0.347 |
MOD_PK_1 | 1046 | 1052 | PF00069 | 0.651 |
MOD_PK_1 | 245 | 251 | PF00069 | 0.591 |
MOD_PK_1 | 253 | 259 | PF00069 | 0.623 |
MOD_PKA_1 | 368 | 374 | PF00069 | 0.342 |
MOD_PKA_1 | 988 | 994 | PF00069 | 0.540 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.751 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.574 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.377 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.690 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.438 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.395 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.553 |
MOD_PKA_2 | 563 | 569 | PF00069 | 0.504 |
MOD_PKA_2 | 988 | 994 | PF00069 | 0.580 |
MOD_PKB_1 | 202 | 210 | PF00069 | 0.542 |
MOD_PKB_1 | 251 | 259 | PF00069 | 0.652 |
MOD_PKB_1 | 333 | 341 | PF00069 | 0.191 |
MOD_PKB_1 | 854 | 862 | PF00069 | 0.579 |
MOD_PKB_1 | 902 | 910 | PF00069 | 0.507 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.673 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.526 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.384 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.392 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.702 |
MOD_Plk_1 | 381 | 387 | PF00069 | 0.283 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.349 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.508 |
MOD_Plk_1 | 732 | 738 | PF00069 | 0.495 |
MOD_Plk_1 | 776 | 782 | PF00069 | 0.396 |
MOD_Plk_1 | 846 | 852 | PF00069 | 0.550 |
MOD_Plk_2-3 | 62 | 68 | PF00069 | 0.562 |
MOD_Plk_4 | 1046 | 1052 | PF00069 | 0.714 |
MOD_Plk_4 | 1063 | 1069 | PF00069 | 0.723 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.642 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.483 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.556 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.602 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.308 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.325 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.297 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.351 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.467 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.404 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.436 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.379 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.390 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.390 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.552 |
MOD_Plk_4 | 961 | 967 | PF00069 | 0.562 |
MOD_ProDKin_1 | 1000 | 1006 | PF00069 | 0.517 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.798 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.349 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.468 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.544 |
MOD_ProDKin_1 | 625 | 631 | PF00069 | 0.425 |
MOD_ProDKin_1 | 872 | 878 | PF00069 | 0.658 |
MOD_SUMO_for_1 | 689 | 692 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 290 | 298 | PF00179 | 0.377 |
MOD_SUMO_rev_2 | 472 | 477 | PF00179 | 0.473 |
TRG_DiLeu_BaEn_1 | 602 | 607 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 859 | 864 | PF01217 | 0.659 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 701 | 704 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 789 | 792 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 327 | 329 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 853 | 856 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 860 | 862 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 969 | 972 | PF00400 | 0.570 |
TRG_NES_CRM1_1 | 766 | 777 | PF08389 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 553 | 557 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 861 | 865 | PF00026 | 0.678 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q4 | Leptomonas seymouri | 74% | 94% |
A0A0S4IUA9 | Bodo saltans | 40% | 100% |
A0A1X0NV89 | Trypanosomatidae | 68% | 100% |
A0A1X0NVS9 | Trypanosomatidae | 37% | 100% |
A0A3S7WRL1 | Leishmania donovani | 86% | 100% |
A0A422NYP6 | Trypanosoma rangeli | 67% | 100% |
A4HUU4 | Leishmania infantum | 86% | 100% |
D0A7L1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
D0A7L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9ANH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q384Y0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 40% | 100% |
Q384Y1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 66% | 100% |
Q4QH47 | Leishmania major | 84% | 100% |
V5BW80 | Trypanosoma cruzi | 67% | 100% |