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: A4HIG1
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 | 454 | 458 | PF00656 | 0.388 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 681 | 685 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.359 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 746 | 748 | PF00675 | 0.641 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.763 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 744 | 746 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 744 | 746 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.788 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 893 | 897 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 302 | 310 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 354 | 362 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 644 | 652 | PF00400 | 0.462 |
DEG_MDM2_SWIB_1 | 977 | 985 | PF02201 | 0.460 |
DOC_CDC14_PxL_1 | 358 | 366 | PF14671 | 0.502 |
DOC_CKS1_1 | 821 | 826 | PF01111 | 0.356 |
DOC_CKS1_1 | 991 | 996 | PF01111 | 0.527 |
DOC_CYCLIN_RxL_1 | 166 | 173 | PF00134 | 0.409 |
DOC_CYCLIN_RxL_1 | 291 | 299 | PF00134 | 0.458 |
DOC_CYCLIN_yCln2_LP_2 | 270 | 276 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 333 | 339 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 444 | 450 | PF00134 | 0.348 |
DOC_CYCLIN_yCln2_LP_2 | 604 | 610 | PF00134 | 0.335 |
DOC_MAPK_DCC_7 | 269 | 279 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 744 | 754 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 395 | 402 | PF00069 | 0.446 |
DOC_MAPK_NFAT4_5 | 395 | 403 | PF00069 | 0.443 |
DOC_MAPK_RevD_3 | 280 | 295 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.458 |
DOC_PP1_RVXF_1 | 865 | 871 | PF00149 | 0.488 |
DOC_PP2B_LxvP_1 | 796 | 799 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.447 |
DOC_SPAK_OSR1_1 | 224 | 228 | PF12202 | 0.490 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 895 | 899 | PF00917 | 0.667 |
DOC_USP7_MATH_2 | 624 | 630 | PF00917 | 0.427 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 620 | 625 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 780 | 785 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 820 | 825 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 837 | 842 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 965 | 970 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 990 | 995 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 28 | 35 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 295 | 304 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 386 | 394 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 408 | 413 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 496 | 500 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 537 | 547 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 795 | 799 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 929 | 935 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 944 | 949 | PF00244 | 0.551 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.608 |
LIG_BRCT_BRCA1_1 | 967 | 971 | PF00533 | 0.474 |
LIG_Clathr_ClatBox_1 | 306 | 310 | PF01394 | 0.502 |
LIG_DLG_GKlike_1 | 408 | 415 | PF00625 | 0.492 |
LIG_EH_1 | 605 | 609 | PF12763 | 0.364 |
LIG_eIF4E_1 | 161 | 167 | PF01652 | 0.409 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.447 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.412 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.418 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.549 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.760 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.434 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.496 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.495 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.477 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.285 |
LIG_FHA_1 | 974 | 980 | PF00498 | 0.550 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.454 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.751 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.602 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.625 |
LIG_FHA_2 | 832 | 838 | PF00498 | 0.429 |
LIG_FHA_2 | 892 | 898 | PF00498 | 0.632 |
LIG_GBD_Chelix_1 | 555 | 563 | PF00786 | 0.302 |
LIG_LIR_Apic_2 | 158 | 164 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 278 | 284 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 902 | 906 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 325 | 333 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 411 | 418 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 667 | 678 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 932 | 941 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 381 | 385 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 609 | 613 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 667 | 673 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 697 | 702 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 932 | 937 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 968 | 974 | PF02991 | 0.466 |
LIG_MLH1_MIPbox_1 | 967 | 971 | PF16413 | 0.498 |
LIG_NRBOX | 292 | 298 | PF00104 | 0.444 |
LIG_NRBOX | 460 | 466 | PF00104 | 0.497 |
LIG_NRBOX | 668 | 674 | PF00104 | 0.398 |
LIG_PCNA_PIPBox_1 | 844 | 853 | PF02747 | 0.505 |
LIG_PCNA_yPIPBox_3 | 395 | 406 | PF02747 | 0.359 |
LIG_Pex14_1 | 318 | 322 | PF04695 | 0.447 |
LIG_Pex14_2 | 322 | 326 | PF04695 | 0.447 |
LIG_Pex14_2 | 977 | 981 | PF04695 | 0.473 |
LIG_PTB_Apo_2 | 964 | 971 | PF02174 | 0.590 |
LIG_PTB_Phospho_1 | 964 | 970 | PF10480 | 0.590 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.398 |
LIG_SH2_CRK | 710 | 714 | PF00017 | 0.428 |
LIG_SH2_CRK | 821 | 825 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 965 | 968 | PF00017 | 0.577 |
LIG_SH2_SRC | 965 | 968 | PF00017 | 0.577 |
LIG_SH2_STAT3 | 954 | 957 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 965 | 968 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 970 | 973 | PF00017 | 0.465 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.429 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.513 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.514 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.368 |
LIG_SH3_3 | 963 | 969 | PF00018 | 0.471 |
LIG_SUMO_SIM_par_1 | 230 | 238 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 647 | 653 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 827 | 834 | PF11976 | 0.415 |
LIG_TRAF2_1 | 511 | 514 | PF00917 | 0.650 |
LIG_TRAF2_2 | 66 | 71 | PF00917 | 0.499 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.530 |
LIG_TYR_ITIM | 708 | 713 | PF00017 | 0.448 |
LIG_UBA3_1 | 82 | 91 | PF00899 | 0.445 |
LIG_WRC_WIRS_1 | 974 | 979 | PF05994 | 0.554 |
MOD_CDC14_SPxK_1 | 283 | 286 | PF00782 | 0.459 |
MOD_CDC14_SPxK_1 | 697 | 700 | PF00782 | 0.361 |
MOD_CDK_SPxK_1 | 280 | 286 | PF00069 | 0.459 |
MOD_CDK_SPxK_1 | 694 | 700 | PF00069 | 0.385 |
MOD_CDK_SPxK_1 | 738 | 744 | PF00069 | 0.624 |
MOD_CDK_SPxK_1 | 990 | 996 | PF00069 | 0.418 |
MOD_CDK_SPxxK_3 | 738 | 745 | PF00069 | 0.625 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.565 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.509 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.637 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.593 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.650 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.712 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.447 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.490 |
MOD_CK1_1 | 650 | 656 | PF00069 | 0.402 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.581 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.409 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.609 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.542 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.815 |
MOD_CK2_1 | 508 | 514 | PF00069 | 0.762 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.447 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.386 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.510 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.671 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.566 |
MOD_CK2_1 | 891 | 897 | PF00069 | 0.552 |
MOD_CK2_1 | 929 | 935 | PF00069 | 0.456 |
MOD_DYRK1A_RPxSP_1 | 694 | 698 | PF00069 | 0.339 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.610 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.247 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.302 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.631 |
MOD_GlcNHglycan | 427 | 431 | PF01048 | 0.394 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.501 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.590 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.312 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.290 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.726 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.506 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.578 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.760 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.693 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.511 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.463 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.635 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.442 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.702 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.694 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.447 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.462 |
MOD_GSK3_1 | 633 | 640 | PF00069 | 0.360 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.523 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.640 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.575 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.527 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.558 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.413 |
MOD_GSK3_1 | 891 | 898 | PF00069 | 0.553 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.562 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.544 |
MOD_N-GLC_1 | 732 | 737 | PF02516 | 0.756 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.448 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.688 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.517 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.530 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.441 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.547 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.478 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.421 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.668 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.409 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.487 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.460 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.460 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.395 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.498 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.713 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.711 |
MOD_NEK2_1 | 810 | 815 | PF00069 | 0.549 |
MOD_NEK2_1 | 831 | 836 | PF00069 | 0.331 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.454 |
MOD_NEK2_1 | 960 | 965 | PF00069 | 0.485 |
MOD_NEK2_1 | 977 | 982 | PF00069 | 0.442 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.519 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.477 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.449 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.734 |
MOD_PIKK_1 | 840 | 846 | PF00454 | 0.335 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.762 |
MOD_PKA_1 | 745 | 751 | PF00069 | 0.715 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.616 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.502 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.492 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.447 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.535 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.536 |
MOD_PKA_2 | 745 | 751 | PF00069 | 0.715 |
MOD_PKA_2 | 794 | 800 | PF00069 | 0.436 |
MOD_PKB_1 | 927 | 935 | PF00069 | 0.464 |
MOD_Plk_1 | 732 | 738 | PF00069 | 0.771 |
MOD_Plk_1 | 977 | 983 | PF00069 | 0.514 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.342 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.490 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.449 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.399 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.358 |
MOD_Plk_4 | 914 | 920 | PF00069 | 0.518 |
MOD_Plk_4 | 960 | 966 | PF00069 | 0.521 |
MOD_Plk_4 | 977 | 983 | PF00069 | 0.459 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.456 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.476 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.476 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.544 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.404 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.699 |
MOD_ProDKin_1 | 620 | 626 | PF00069 | 0.450 |
MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.550 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.729 |
MOD_ProDKin_1 | 780 | 786 | PF00069 | 0.513 |
MOD_ProDKin_1 | 820 | 826 | PF00069 | 0.447 |
MOD_ProDKin_1 | 837 | 843 | PF00069 | 0.446 |
MOD_ProDKin_1 | 965 | 971 | PF00069 | 0.473 |
MOD_ProDKin_1 | 990 | 996 | PF00069 | 0.529 |
MOD_SUMO_for_1 | 268 | 271 | PF00179 | 0.389 |
TRG_DiLeu_BaEn_2 | 665 | 671 | PF01217 | 0.332 |
TRG_DiLeu_BaLyEn_6 | 166 | 171 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 333 | 338 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 599 | 604 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 710 | 713 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 934 | 937 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 736 | 739 | PF00400 | 0.735 |
TRG_ER_diArg_1 | 745 | 747 | PF00400 | 0.700 |
TRG_ER_diArg_1 | 856 | 859 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 927 | 930 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 943 | 946 | PF00400 | 0.482 |
TRG_NES_CRM1_1 | 553 | 566 | PF08389 | 0.447 |
TRG_NLS_MonoCore_2 | 743 | 748 | PF00514 | 0.691 |
TRG_NLS_MonoExtN_4 | 742 | 748 | PF00514 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 17 | 21 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 946 | 950 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMF3 | Leptomonas seymouri | 59% | 91% |
A0A1X0P1S1 | Trypanosomatidae | 43% | 100% |
A0A3R7L9G4 | Trypanosoma rangeli | 44% | 100% |
A0A3S7X3I6 | Leishmania donovani | 79% | 100% |
A4I5Q7 | Leishmania infantum | 78% | 100% |
C9ZR26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9B102 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q764 | Leishmania major | 77% | 100% |