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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005694 | chromosome | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X3I6
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003678 | DNA helicase activity | 3 | 2 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 2 |
GO:0009378 | four-way junction helicase activity | 4 | 1 |
GO:0043138 | 3'-5' DNA helicase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.400 |
CLV_C14_Caspase3-7 | 835 | 839 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.739 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 750 | 752 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 872 | 874 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 748 | 750 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 12 | 18 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 549 | 553 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 649 | 653 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 872 | 876 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 943 | 947 | PF00082 | 0.506 |
DEG_APCC_DBOX_1 | 302 | 310 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 354 | 362 | PF00400 | 0.468 |
DEG_APCC_DBOX_1 | 648 | 656 | PF00400 | 0.420 |
DEG_MDM2_SWIB_1 | 982 | 990 | PF02201 | 0.464 |
DOC_CDC14_PxL_1 | 358 | 366 | PF14671 | 0.420 |
DOC_CYCLIN_RxL_1 | 291 | 299 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 338 | 344 | PF00134 | 0.526 |
DOC_CYCLIN_yCln2_LP_2 | 444 | 450 | PF00134 | 0.355 |
DOC_CYCLIN_yCln2_LP_2 | 608 | 614 | PF00134 | 0.336 |
DOC_MAPK_FxFP_2 | 161 | 164 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 131 | 139 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 825 | 834 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 133 | 141 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 395 | 402 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 828 | 836 | PF00069 | 0.383 |
DOC_MAPK_NFAT4_5 | 395 | 403 | PF00069 | 0.460 |
DOC_MAPK_RevD_3 | 280 | 295 | PF00069 | 0.532 |
DOC_PP1_RVXF_1 | 155 | 162 | PF00149 | 0.471 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.805 |
DOC_PP2B_LxvP_1 | 699 | 702 | PF13499 | 0.468 |
DOC_PP2B_LxvP_1 | 801 | 804 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 996 | 999 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 161 | 164 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.449 |
DOC_SPAK_OSR1_1 | 224 | 228 | PF12202 | 0.492 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 851 | 855 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.537 |
DOC_USP7_MATH_2 | 628 | 634 | PF00917 | 0.418 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 742 | 747 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 785 | 790 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 842 | 847 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 970 | 975 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 997 | 1002 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 181 | 187 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 431 | 438 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 51 | 58 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 636 | 646 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 828 | 836 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 872 | 878 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 934 | 940 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 949 | 954 | PF00244 | 0.595 |
LIG_AP2alpha_2 | 392 | 394 | PF02296 | 0.353 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_BIR_III_4 | 505 | 509 | PF00653 | 0.639 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 484 | 488 | PF00533 | 0.658 |
LIG_BRCT_BRCA1_1 | 972 | 976 | PF00533 | 0.484 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.507 |
LIG_DLG_GKlike_1 | 408 | 415 | PF00625 | 0.542 |
LIG_EH_1 | 609 | 613 | PF12763 | 0.365 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.449 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.440 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.564 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.511 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.585 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.488 |
LIG_FHA_1 | 979 | 985 | PF00498 | 0.553 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.742 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.333 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.466 |
LIG_GBD_Chelix_1 | 559 | 567 | PF00786 | 0.307 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.469 |
LIG_LIR_Apic_2 | 278 | 284 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 907 | 911 | PF02991 | 0.617 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 325 | 333 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 411 | 418 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 671 | 682 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 937 | 946 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 613 | 617 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 713 | 717 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 937 | 942 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 973 | 979 | PF02991 | 0.476 |
LIG_MAD2 | 265 | 273 | PF02301 | 0.471 |
LIG_MLH1_MIPbox_1 | 972 | 976 | PF16413 | 0.509 |
LIG_NRBOX | 460 | 466 | PF00104 | 0.506 |
LIG_NRBOX | 672 | 678 | PF00104 | 0.394 |
LIG_NRBOX | 941 | 947 | PF00104 | 0.574 |
LIG_PCNA_PIPBox_1 | 849 | 858 | PF02747 | 0.503 |
LIG_Pex14_1 | 318 | 322 | PF04695 | 0.449 |
LIG_Pex14_2 | 322 | 326 | PF04695 | 0.449 |
LIG_Pex14_2 | 982 | 986 | PF04695 | 0.476 |
LIG_PTB_Apo_2 | 969 | 976 | PF02174 | 0.595 |
LIG_PTB_Phospho_1 | 969 | 975 | PF10480 | 0.597 |
LIG_SH2_CRK | 714 | 718 | PF00017 | 0.429 |
LIG_SH2_GRB2like | 970 | 973 | PF00017 | 0.583 |
LIG_SH2_SRC | 970 | 973 | PF00017 | 0.608 |
LIG_SH2_STAT3 | 806 | 809 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 959 | 962 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 970 | 973 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 975 | 978 | PF00017 | 0.506 |
LIG_SH3_1 | 786 | 792 | PF00018 | 0.365 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.512 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.492 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.732 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.581 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.712 |
LIG_SH3_3 | 679 | 685 | PF00018 | 0.624 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.396 |
LIG_SH3_3 | 968 | 974 | PF00018 | 0.477 |
LIG_SH3_3 | 987 | 993 | PF00018 | 0.472 |
LIG_SH3_4 | 131 | 138 | PF00018 | 0.383 |
LIG_SUMO_SIM_par_1 | 230 | 238 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 651 | 656 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 832 | 839 | PF11976 | 0.387 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.523 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.456 |
LIG_TYR_ITIM | 712 | 717 | PF00017 | 0.449 |
LIG_UBA3_1 | 82 | 91 | PF00899 | 0.457 |
LIG_WRC_WIRS_1 | 979 | 984 | PF05994 | 0.562 |
MOD_CDC14_SPxK_1 | 283 | 286 | PF00782 | 0.449 |
MOD_CDC14_SPxK_1 | 695 | 698 | PF00782 | 0.492 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.449 |
MOD_CDK_SPxK_1 | 692 | 698 | PF00069 | 0.508 |
MOD_CDK_SPxK_1 | 742 | 748 | PF00069 | 0.736 |
MOD_CDK_SPxxK_3 | 742 | 749 | PF00069 | 0.644 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.598 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.484 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.541 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.684 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.732 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.449 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.675 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.432 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.582 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.708 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.449 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.387 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.529 |
MOD_CK2_1 | 836 | 842 | PF00069 | 0.471 |
MOD_CK2_1 | 934 | 940 | PF00069 | 0.484 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.647 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.573 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.310 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.268 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.271 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.247 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.706 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.307 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.630 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.604 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.479 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.596 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.622 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.805 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.307 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.292 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.739 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.436 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.517 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.684 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.504 |
MOD_GlcNHglycan | 817 | 820 | PF01048 | 0.601 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.419 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.577 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.486 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.394 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.511 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.425 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.555 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.706 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.541 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.466 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.418 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.289 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.753 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.504 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.530 |
MOD_GSK3_1 | 978 | 985 | PF00069 | 0.607 |
MOD_LATS_1 | 10 | 16 | PF00433 | 0.595 |
MOD_N-GLC_1 | 736 | 741 | PF02516 | 0.665 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.384 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.705 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.536 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.518 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.532 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.532 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.532 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.363 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.441 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.518 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.395 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.440 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.405 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.368 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.539 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.671 |
MOD_NEK2_1 | 758 | 763 | PF00069 | 0.561 |
MOD_NEK2_1 | 815 | 820 | PF00069 | 0.527 |
MOD_NEK2_1 | 965 | 970 | PF00069 | 0.474 |
MOD_NEK2_1 | 982 | 987 | PF00069 | 0.526 |
MOD_OFUCOSY | 115 | 122 | PF10250 | 0.317 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.486 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.474 |
MOD_PIKK_1 | 537 | 543 | PF00454 | 0.485 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.451 |
MOD_PK_1 | 873 | 879 | PF00069 | 0.399 |
MOD_PKA_1 | 12 | 18 | PF00069 | 0.747 |
MOD_PKA_1 | 749 | 755 | PF00069 | 0.722 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.507 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.449 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.510 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.724 |
MOD_PKA_2 | 827 | 833 | PF00069 | 0.436 |
MOD_PKA_2 | 879 | 885 | PF00069 | 0.519 |
MOD_PKB_1 | 932 | 940 | PF00069 | 0.497 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.664 |
MOD_Plk_1 | 982 | 988 | PF00069 | 0.526 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.492 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.454 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.381 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.337 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.387 |
MOD_Plk_4 | 919 | 925 | PF00069 | 0.552 |
MOD_Plk_4 | 965 | 971 | PF00069 | 0.492 |
MOD_Plk_4 | 982 | 988 | PF00069 | 0.593 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.462 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.449 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.449 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.584 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.736 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.663 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.403 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.693 |
MOD_ProDKin_1 | 742 | 748 | PF00069 | 0.734 |
MOD_ProDKin_1 | 785 | 791 | PF00069 | 0.503 |
MOD_ProDKin_1 | 842 | 848 | PF00069 | 0.454 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.644 |
MOD_ProDKin_1 | 970 | 976 | PF00069 | 0.479 |
MOD_ProDKin_1 | 997 | 1003 | PF00069 | 0.609 |
TRG_DiLeu_BaEn_2 | 669 | 675 | PF01217 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 166 | 171 | PF01217 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 939 | 942 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 749 | 751 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 861 | 864 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 871 | 873 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 932 | 935 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 948 | 951 | PF00400 | 0.508 |
TRG_NES_CRM1_1 | 557 | 570 | PF08389 | 0.449 |
TRG_NLS_MonoCore_2 | 747 | 752 | PF00514 | 0.725 |
TRG_NLS_MonoExtN_4 | 746 | 752 | PF00514 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.267 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 951 | 955 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMF3 | Leptomonas seymouri | 58% | 91% |
A0A1X0P1S1 | Trypanosomatidae | 43% | 100% |
A0A3R7L9G4 | Trypanosoma rangeli | 43% | 100% |
A4HIG1 | Leishmania braziliensis | 79% | 100% |
A4I5Q7 | Leishmania infantum | 99% | 100% |
C9ZR26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B102 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q764 | Leishmania major | 92% | 100% |