Helicases, Helicase-like
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000109 | nucleotide-excision repair complex | 3 | 1 |
GO:0000112 | nucleotide-excision repair factor 3 complex | 4 | 1 |
GO:0005667 | transcription regulator complex | 2 | 1 |
GO:0005675 | transcription factor TFIIH holo complex | 4 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0032993 | protein-DNA complex | 2 | 1 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 1 |
GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 1 |
GO:0097550 | transcription preinitiation complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 1 |
GO:1902911 | protein kinase complex | 5 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4I6A0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006352 | DNA-templated transcription initiation | 6 | 1 |
GO:0006367 | transcription initiation at RNA polymerase II promoter | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0033683 | obsolete nucleotide-excision repair, DNA incision | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003678 | DNA helicase activity | 3 | 1 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 1 |
GO:0043138 | 3'-5' DNA helicase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 877 | 881 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 820 | 822 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 882 | 884 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 890 | 892 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 901 | 903 | PF00675 | 0.623 |
CLV_PCSK_FUR_1 | 134 | 138 | PF00082 | 0.500 |
CLV_PCSK_FUR_1 | 821 | 825 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.199 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 673 | 675 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 735 | 737 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 822 | 824 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 890 | 892 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 899 | 901 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 903 | 905 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.204 |
CLV_PCSK_PC1ET2_1 | 673 | 675 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 735 | 737 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 822 | 824 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 899 | 901 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 903 | 905 | PF00082 | 0.685 |
CLV_PCSK_PC7_1 | 132 | 138 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 819 | 825 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.289 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 515 | 523 | PF00400 | 0.399 |
DEG_APCC_DBOX_1 | 636 | 644 | PF00400 | 0.393 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.621 |
DEG_SCF_FBW7_1 | 180 | 186 | PF00400 | 0.500 |
DOC_CDC14_PxL_1 | 279 | 287 | PF14671 | 0.233 |
DOC_CKS1_1 | 180 | 185 | PF01111 | 0.495 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.200 |
DOC_CKS1_1 | 401 | 406 | PF01111 | 0.353 |
DOC_CYCLIN_RxL_1 | 102 | 110 | PF00134 | 0.457 |
DOC_MAPK_DCC_7 | 277 | 287 | PF00069 | 0.276 |
DOC_MAPK_DCC_7 | 757 | 767 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 105 | 111 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 515 | 522 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 615 | 622 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 757 | 767 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 922 | 930 | PF00069 | 0.338 |
DOC_MAPK_MEF2A_6 | 515 | 524 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 760 | 767 | PF00069 | 0.429 |
DOC_MAPK_NFAT4_5 | 515 | 523 | PF00069 | 0.412 |
DOC_MAPK_RevD_3 | 807 | 822 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 458 | 465 | PF00149 | 0.494 |
DOC_PP1_RVXF_1 | 815 | 821 | PF00149 | 0.434 |
DOC_PP2B_LxvP_1 | 384 | 387 | PF13499 | 0.366 |
DOC_PP4_FxxP_1 | 539 | 542 | PF00568 | 0.399 |
DOC_PP4_FxxP_1 | 638 | 641 | PF00568 | 0.311 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.367 |
DOC_USP7_UBL2_3 | 899 | 903 | PF12436 | 0.617 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 775 | 780 | PF00397 | 0.293 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 543 | 550 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 629 | 638 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 757 | 763 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 823 | 831 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 944 | 950 | PF00244 | 0.477 |
LIG_Actin_WH2_2 | 274 | 291 | PF00022 | 0.234 |
LIG_Actin_WH2_2 | 409 | 425 | PF00022 | 0.272 |
LIG_Actin_WH2_2 | 616 | 631 | PF00022 | 0.348 |
LIG_Actin_WH2_2 | 9 | 25 | PF00022 | 0.366 |
LIG_APCC_ABBA_1 | 166 | 171 | PF00400 | 0.390 |
LIG_APCC_ABBA_1 | 362 | 367 | PF00400 | 0.233 |
LIG_APCC_ABBA_1 | 472 | 477 | PF00400 | 0.445 |
LIG_APCC_ABBA_1 | 522 | 527 | PF00400 | 0.412 |
LIG_APCC_ABBA_1 | 592 | 597 | PF00400 | 0.291 |
LIG_BIR_III_2 | 153 | 157 | PF00653 | 0.655 |
LIG_BIR_III_2 | 776 | 780 | PF00653 | 0.295 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.633 |
LIG_BRCT_BRCA1_1 | 565 | 569 | PF00533 | 0.269 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.366 |
LIG_deltaCOP1_diTrp_1 | 52 | 59 | PF00928 | 0.233 |
LIG_EH_1 | 431 | 435 | PF12763 | 0.355 |
LIG_eIF4E_1 | 348 | 354 | PF01652 | 0.366 |
LIG_eIF4E_1 | 842 | 848 | PF01652 | 0.257 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.284 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.298 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.440 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.330 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.588 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.466 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.298 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.366 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.231 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.233 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.357 |
LIG_FHA_2 | 776 | 782 | PF00498 | 0.286 |
LIG_IBAR_NPY_1 | 448 | 450 | PF08397 | 0.247 |
LIG_Integrin_RGD_1 | 714 | 716 | PF01839 | 0.301 |
LIG_LIR_Apic_2 | 398 | 404 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 207 | 217 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 377 | 388 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.235 |
LIG_LIR_Gen_1 | 566 | 574 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 588 | 595 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 667 | 677 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 716 | 725 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 778 | 788 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 839 | 849 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 189 | 195 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 410 | 416 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 566 | 570 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 716 | 722 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 778 | 783 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 839 | 845 | PF02991 | 0.300 |
LIG_LYPXL_S_1 | 191 | 195 | PF13949 | 0.494 |
LIG_LYPXL_yS_3 | 192 | 195 | PF13949 | 0.494 |
LIG_PCNA_yPIPBox_3 | 228 | 239 | PF02747 | 0.347 |
LIG_Pex14_1 | 665 | 669 | PF04695 | 0.282 |
LIG_Pex14_2 | 212 | 216 | PF04695 | 0.457 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.233 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.312 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.355 |
LIG_SH2_CRK | 702 | 706 | PF00017 | 0.332 |
LIG_SH2_GRB2like | 430 | 433 | PF00017 | 0.272 |
LIG_SH2_GRB2like | 849 | 852 | PF00017 | 0.403 |
LIG_SH2_NCK_1 | 849 | 853 | PF00017 | 0.393 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 55 | 58 | PF00017 | 0.254 |
LIG_SH2_PTP2 | 772 | 775 | PF00017 | 0.288 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.272 |
LIG_SH2_SRC | 702 | 705 | PF00017 | 0.421 |
LIG_SH2_SRC | 849 | 852 | PF00017 | 0.403 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.541 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 618 | 622 | PF00017 | 0.327 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 298 | 301 | PF00017 | 0.210 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.207 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.178 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 719 | 722 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 755 | 758 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 861 | 864 | PF00017 | 0.326 |
LIG_SH3_2 | 867 | 872 | PF14604 | 0.337 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.642 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.306 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.412 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.281 |
LIG_SH3_3 | 736 | 742 | PF00018 | 0.455 |
LIG_SH3_3 | 796 | 802 | PF00018 | 0.447 |
LIG_SH3_3 | 864 | 870 | PF00018 | 0.326 |
LIG_SUMO_SIM_anti_2 | 223 | 228 | PF11976 | 0.506 |
LIG_SUMO_SIM_anti_2 | 302 | 311 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 619 | 624 | PF11976 | 0.322 |
LIG_SUMO_SIM_anti_2 | 926 | 932 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 302 | 311 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 313 | 318 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 341 | 347 | PF11976 | 0.223 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.298 |
LIG_TRAF2_1 | 895 | 898 | PF00917 | 0.512 |
LIG_TYR_ITIM | 261 | 266 | PF00017 | 0.312 |
LIG_UBA3_1 | 238 | 247 | PF00899 | 0.254 |
LIG_UBA3_1 | 451 | 460 | PF00899 | 0.326 |
LIG_UBA3_1 | 606 | 615 | PF00899 | 0.326 |
LIG_UBA3_1 | 668 | 673 | PF00899 | 0.338 |
LIG_UBA3_1 | 75 | 81 | PF00899 | 0.366 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.233 |
LIG_WRC_WIRS_1 | 508 | 513 | PF05994 | 0.298 |
LIG_WRC_WIRS_1 | 586 | 591 | PF05994 | 0.380 |
LIG_WW_3 | 887 | 891 | PF00397 | 0.387 |
MOD_CDK_SPxK_1 | 400 | 406 | PF00069 | 0.350 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.366 |
MOD_CDK_SPxxK_3 | 775 | 782 | PF00069 | 0.286 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.560 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.399 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.360 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.233 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.254 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.364 |
MOD_CK1_1 | 935 | 941 | PF00069 | 0.518 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.737 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.676 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.298 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.366 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.256 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.407 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.288 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.353 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.600 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.530 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.364 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.291 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.309 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.421 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.461 |
MOD_GlcNHglycan | 910 | 913 | PF01048 | 0.634 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.581 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.576 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.237 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.272 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.233 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.366 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.242 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.305 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.375 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.382 |
MOD_LATS_1 | 873 | 879 | PF00433 | 0.490 |
MOD_N-GLC_2 | 320 | 322 | PF02516 | 0.254 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.465 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.670 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.406 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.581 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.468 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.210 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.240 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.253 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.317 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.259 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.366 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.366 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.479 |
MOD_NEK2_2 | 624 | 629 | PF00069 | 0.308 |
MOD_NEK2_2 | 664 | 669 | PF00069 | 0.416 |
MOD_PIKK_1 | 836 | 842 | PF00454 | 0.349 |
MOD_PKA_1 | 136 | 142 | PF00069 | 0.509 |
MOD_PKA_1 | 823 | 829 | PF00069 | 0.370 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.231 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.703 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.246 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.568 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.312 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.252 |
MOD_PKA_2 | 628 | 634 | PF00069 | 0.521 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.336 |
MOD_PKA_2 | 823 | 829 | PF00069 | 0.370 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.353 |
MOD_PKB_1 | 134 | 142 | PF00069 | 0.498 |
MOD_PKB_1 | 821 | 829 | PF00069 | 0.317 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.489 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.386 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.353 |
MOD_Plk_1 | 833 | 839 | PF00069 | 0.310 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.399 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.521 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.242 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.318 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.249 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.252 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.366 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.307 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.299 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.447 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.366 |
MOD_Plk_4 | 715 | 721 | PF00069 | 0.356 |
MOD_Plk_4 | 833 | 839 | PF00069 | 0.316 |
MOD_Plk_4 | 926 | 932 | PF00069 | 0.372 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.670 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.583 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.233 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.344 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.421 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.233 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.233 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.298 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.369 |
MOD_ProDKin_1 | 775 | 781 | PF00069 | 0.288 |
MOD_SUMO_for_1 | 931 | 934 | PF00179 | 0.394 |
MOD_SUMO_rev_2 | 241 | 248 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 597 | 607 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 667 | 675 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_1 | 84 | 89 | PF01217 | 0.366 |
TRG_DiLeu_BaEn_3 | 670 | 676 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 301 | 306 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.366 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 719 | 722 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 842 | 845 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 861 | 864 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 816 | 819 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 820 | 823 | PF00400 | 0.338 |
TRG_ER_diArg_1 | 889 | 891 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 901 | 904 | PF00400 | 0.649 |
TRG_ER_FFAT_2 | 41 | 50 | PF00635 | 0.203 |
TRG_NES_CRM1_1 | 453 | 467 | PF08389 | 0.332 |
TRG_NLS_Bipartite_1 | 890 | 908 | PF00514 | 0.678 |
TRG_NLS_MonoCore_2 | 820 | 825 | PF00514 | 0.452 |
TRG_NLS_MonoCore_2 | 901 | 906 | PF00514 | 0.490 |
TRG_NLS_MonoExtC_3 | 902 | 907 | PF00514 | 0.532 |
TRG_NLS_MonoExtN_4 | 819 | 826 | PF00514 | 0.463 |
TRG_NLS_MonoExtN_4 | 899 | 906 | PF00514 | 0.772 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.233 |
TRG_Pf-PMV_PEXEL_1 | 846 | 850 | PF00026 | 0.341 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3J1 | Leptomonas seymouri | 71% | 98% |
A0A1X0P8K5 | Trypanosomatidae | 53% | 100% |
A0A3Q8IF99 | Leishmania donovani | 100% | 100% |
A0A3R7KPC7 | Trypanosoma rangeli | 55% | 100% |
A4HIX1 | Leishmania braziliensis | 84% | 100% |
D0A541 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B1F5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P0C8H0 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 37% | 100% |
P0C8H1 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 38% | 100% |
P0C8H2 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 38% | 100% |
P0C8H3 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 38% | 100% |
Q4Q6Q7 | Leishmania major | 93% | 100% |
Q65143 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 38% | 100% |
V5B0I9 | Trypanosoma cruzi | 56% | 100% |