DNA repair, DNA repair and recombination ,mitochondrial
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
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: A4HUU4
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 17 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 17 |
GO:0006259 | DNA metabolic process | 4 | 17 |
GO:0006281 | DNA repair | 5 | 17 |
GO:0006310 | DNA recombination | 5 | 17 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 17 |
GO:0006807 | nitrogen compound metabolic process | 2 | 17 |
GO:0006950 | response to stress | 2 | 17 |
GO:0006974 | DNA damage response | 4 | 17 |
GO:0006996 | organelle organization | 4 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0016043 | cellular component organization | 3 | 17 |
GO:0032200 | telomere organization | 6 | 17 |
GO:0033554 | cellular response to stress | 3 | 17 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 17 |
GO:0043170 | macromolecule metabolic process | 3 | 17 |
GO:0044237 | cellular metabolic process | 2 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 17 |
GO:0046483 | heterocycle metabolic process | 3 | 17 |
GO:0050896 | response to stimulus | 1 | 17 |
GO:0051276 | chromosome organization | 5 | 17 |
GO:0051716 | cellular response to stimulus | 2 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
GO:0071840 | cellular component organization or biogenesis | 2 | 17 |
GO:0090304 | nucleic acid metabolic process | 4 | 17 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 17 |
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 | 17 |
GO:0003678 | DNA helicase activity | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004386 | helicase activity | 2 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 17 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
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 | 181 | 185 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 822 | 826 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 840 | 844 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 945 | 949 | PF00656 | 0.758 |
CLV_C14_Caspase3-7 | 953 | 957 | PF00656 | 0.733 |
CLV_MEL_PAP_1 | 847 | 853 | PF00089 | 0.761 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 888 | 890 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 946 | 948 | PF00675 | 0.682 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.739 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 763 | 765 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 780 | 782 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 888 | 890 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 946 | 948 | PF00082 | 0.682 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 763 | 765 | PF00082 | 0.517 |
CLV_PCSK_PC7_1 | 242 | 248 | PF00082 | 0.407 |
CLV_PCSK_PC7_1 | 6 | 12 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 472 | 476 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 744 | 748 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 780 | 784 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 899 | 903 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.540 |
DEG_APCC_DBOX_1 | 779 | 787 | PF00400 | 0.636 |
DEG_SCF_FBW7_2 | 545 | 551 | PF00400 | 0.447 |
DOC_CKS1_1 | 545 | 550 | PF01111 | 0.456 |
DOC_CYCLIN_RxL_1 | 469 | 478 | PF00134 | 0.458 |
DOC_CYCLIN_RxL_1 | 91 | 102 | PF00134 | 0.534 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 576 | 585 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 402 | PF00134 | 0.509 |
DOC_MAPK_gen_1 | 215 | 222 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 570 | 577 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 741 | 751 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 215 | 222 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 358 | 365 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 744 | 751 | PF00069 | 0.543 |
DOC_MAPK_NFAT4_5 | 744 | 752 | PF00069 | 0.451 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.587 |
DOC_PP2B_LxvP_1 | 479 | 482 | PF13499 | 0.491 |
DOC_PP4_MxPP_1 | 502 | 505 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 806 | 810 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 923 | 927 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 935 | 939 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 982 | 986 | PF00917 | 0.725 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.369 |
DOC_USP7_UBL2_3 | 556 | 560 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 911 | 915 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 800 | 805 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 978 | 983 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 122 | 132 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 138 | 145 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 370 | 377 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 483 | 487 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 775 | 780 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 965 | 970 | PF00244 | 0.745 |
LIG_Actin_WH2_2 | 241 | 256 | PF00022 | 0.325 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.591 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.300 |
LIG_BRCT_BRCA1_2 | 352 | 358 | PF00533 | 0.369 |
LIG_CtBP_PxDLS_1 | 672 | 676 | PF00389 | 0.397 |
LIG_DLG_GKlike_1 | 775 | 782 | PF00625 | 0.561 |
LIG_EH1_1 | 496 | 504 | PF00400 | 0.516 |
LIG_EVH1_2 | 649 | 653 | PF00568 | 0.347 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.477 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.608 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.679 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.640 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.300 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.306 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.380 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.575 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.405 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.473 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.457 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.466 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.502 |
LIG_FHA_1 | 857 | 863 | PF00498 | 0.526 |
LIG_FHA_1 | 865 | 871 | PF00498 | 0.457 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.626 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.697 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.506 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.534 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.423 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.473 |
LIG_FHA_2 | 532 | 538 | PF00498 | 0.451 |
LIG_FHA_2 | 590 | 596 | PF00498 | 0.394 |
LIG_FHA_2 | 748 | 754 | PF00498 | 0.519 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 293 | 302 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 338 | 345 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.717 |
LIG_LIR_Gen_1 | 517 | 526 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 293 | 297 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.711 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 618 | 623 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 661 | 666 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.436 |
LIG_NBox_RRM_1 | 739 | 749 | PF00076 | 0.366 |
LIG_NRBOX | 778 | 784 | PF00104 | 0.548 |
LIG_PCNA_PIPBox_1 | 634 | 643 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 587 | 600 | PF02747 | 0.421 |
LIG_Pex14_2 | 356 | 360 | PF04695 | 0.306 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.570 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.348 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.450 |
LIG_SH2_SRC | 493 | 496 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 294 | 298 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 677 | 681 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 553 | 556 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.333 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.642 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.291 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.516 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.389 |
LIG_SH3_3 | 630 | 636 | PF00018 | 0.395 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.327 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.371 |
LIG_SH3_3 | 917 | 923 | PF00018 | 0.660 |
LIG_SUMO_SIM_anti_2 | 295 | 301 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 295 | 301 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 433 | 438 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 449 | 459 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 794 | 799 | PF11976 | 0.667 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.340 |
LIG_TYR_ITIM | 73 | 78 | PF00017 | 0.452 |
LIG_WRC_WIRS_1 | 722 | 727 | PF05994 | 0.414 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.577 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.647 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.301 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.451 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.670 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.451 |
MOD_CK1_1 | 589 | 595 | PF00069 | 0.362 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.388 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.435 |
MOD_CK1_1 | 814 | 820 | PF00069 | 0.782 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.441 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.682 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.515 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.627 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.632 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.508 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.380 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.376 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.432 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.659 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.431 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.515 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.564 |
MOD_CK2_1 | 821 | 827 | PF00069 | 0.753 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.793 |
MOD_Cter_Amidation | 8 | 11 | PF01082 | 0.539 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.537 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.516 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.605 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.301 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.458 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.745 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.416 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.544 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.726 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.718 |
MOD_GlcNHglycan | 808 | 811 | PF01048 | 0.509 |
MOD_GlcNHglycan | 812 | 816 | PF01048 | 0.654 |
MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.806 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.742 |
MOD_GlcNHglycan | 877 | 880 | PF01048 | 0.635 |
MOD_GlcNHglycan | 925 | 928 | PF01048 | 0.727 |
MOD_GlcNHglycan | 930 | 933 | PF01048 | 0.724 |
MOD_GlcNHglycan | 937 | 940 | PF01048 | 0.677 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.742 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.456 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.526 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.536 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.341 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.450 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.380 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.478 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.660 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.405 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.464 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.450 |
MOD_GSK3_1 | 785 | 792 | PF00069 | 0.621 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.670 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.751 |
MOD_GSK3_1 | 838 | 845 | PF00069 | 0.725 |
MOD_GSK3_1 | 937 | 944 | PF00069 | 0.727 |
MOD_GSK3_1 | 978 | 985 | PF00069 | 0.649 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.544 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.409 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.378 |
MOD_N-GLC_1 | 732 | 737 | PF02516 | 0.353 |
MOD_N-GLC_1 | 765 | 770 | PF02516 | 0.542 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.632 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.273 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.281 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.324 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.394 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.475 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.479 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.668 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.442 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.403 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.358 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.372 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.433 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.686 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.731 |
MOD_NEK2_1 | 811 | 816 | PF00069 | 0.486 |
MOD_NEK2_1 | 970 | 975 | PF00069 | 0.723 |
MOD_NEK2_2 | 269 | 274 | PF00069 | 0.326 |
MOD_NEK2_2 | 677 | 682 | PF00069 | 0.340 |
MOD_NEK2_2 | 765 | 770 | PF00069 | 0.555 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.789 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.340 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.470 |
MOD_PK_1 | 163 | 169 | PF00069 | 0.574 |
MOD_PK_1 | 171 | 177 | PF00069 | 0.607 |
MOD_PK_1 | 609 | 615 | PF00069 | 0.466 |
MOD_PK_1 | 965 | 971 | PF00069 | 0.648 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.627 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.778 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.638 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.441 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.379 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.747 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.540 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.507 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.590 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.390 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.550 |
MOD_PKB_1 | 169 | 177 | PF00069 | 0.638 |
MOD_PKB_1 | 773 | 781 | PF00069 | 0.567 |
MOD_PKB_1 | 907 | 915 | PF00069 | 0.724 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.677 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.278 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.342 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.706 |
MOD_Plk_1 | 600 | 606 | PF00069 | 0.514 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.650 |
MOD_Plk_1 | 651 | 657 | PF00069 | 0.474 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.529 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.390 |
MOD_Plk_1 | 732 | 738 | PF00069 | 0.415 |
MOD_Plk_1 | 765 | 771 | PF00069 | 0.543 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.378 |
MOD_Plk_2-3 | 864 | 870 | PF00069 | 0.598 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.543 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.592 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.311 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.291 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.363 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.472 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.391 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.686 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.431 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.466 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.403 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.387 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.485 |
MOD_Plk_4 | 725 | 731 | PF00069 | 0.452 |
MOD_Plk_4 | 765 | 771 | PF00069 | 0.550 |
MOD_Plk_4 | 880 | 886 | PF00069 | 0.561 |
MOD_Plk_4 | 965 | 971 | PF00069 | 0.719 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.750 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.362 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.447 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.449 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.544 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.423 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.658 |
MOD_ProDKin_1 | 800 | 806 | PF00069 | 0.556 |
MOD_ProDKin_1 | 978 | 984 | PF00069 | 0.592 |
MOD_SUMO_for_1 | 608 | 611 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 209 | 217 | PF00179 | 0.387 |
TRG_DiLeu_BaEn_1 | 521 | 526 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 778 | 783 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 620 | 623 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 708 | 711 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.422 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.737 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 772 | 775 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 779 | 781 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 888 | 891 | PF00400 | 0.565 |
TRG_NES_CRM1_1 | 685 | 696 | PF08389 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 472 | 476 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 780 | 784 | PF00026 | 0.631 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q4 | Leptomonas seymouri | 75% | 87% |
A0A0S4ITU4 | Bodo saltans | 46% | 100% |
A0A0S4IUA9 | Bodo saltans | 39% | 100% |
A0A1X0NV89 | Trypanosomatidae | 66% | 100% |
A0A1X0NVS9 | Trypanosomatidae | 39% | 94% |
A0A3R7MZY3 | Trypanosoma rangeli | 41% | 94% |
A0A3S7WRL1 | Leishmania donovani | 100% | 100% |
A0A422NYP6 | Trypanosoma rangeli | 68% | 100% |
A4H6F0 | Leishmania braziliensis | 86% | 100% |
D0A7L1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
D0A7L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 95% |
D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ANH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
Q384Y0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 41% | 95% |
Q384Y1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 61% | 100% |
Q4QH47 | Leishmania major | 95% | 100% |
V5BW80 | Trypanosoma cruzi | 70% | 100% |