Helicases, ATP-dependent RNA helicase
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005654 | nucleoplasm | 2 | 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 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XB63
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006401 | RNA catabolic process | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009057 | macromolecule catabolic process | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0019439 | aromatic compound catabolic process | 4 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 12 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046700 | heterocycle catabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
GO:0000460 | maturation of 5.8S rRNA | 9 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003724 | RNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 34 | 38 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 656 | 660 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 732 | 734 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.247 |
CLV_PCSK_FUR_1 | 13 | 17 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 732 | 734 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 908 | 910 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 943 | 945 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 355 | 357 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 492 | 494 | PF00082 | 0.301 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 732 | 734 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 943 | 945 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 805 | 809 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 852 | 856 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 885 | 889 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 934 | 938 | PF00082 | 0.258 |
CLV_Separin_Metazoa | 118 | 122 | PF03568 | 0.447 |
CLV_Separin_Metazoa | 129 | 133 | PF03568 | 0.447 |
CLV_Separin_Metazoa | 912 | 916 | PF03568 | 0.491 |
DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.510 |
DOC_ANK_TNKS_1 | 921 | 928 | PF00023 | 0.447 |
DOC_CYCLIN_RxL_1 | 380 | 390 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 432 | 440 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 515 | 523 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 662 | 670 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 15 | 24 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 290 | 298 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 370 | 377 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.503 |
DOC_PP1_RVXF_1 | 148 | 155 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 312 | 318 | PF00149 | 0.412 |
DOC_PP1_RVXF_1 | 381 | 387 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 398 | 405 | PF00149 | 0.447 |
DOC_PP1_RVXF_1 | 942 | 949 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.447 |
DOC_PP4_FxxP_1 | 594 | 597 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 833 | 836 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 839 | 842 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 925 | 929 | PF00917 | 0.458 |
DOC_USP7_UBL2_3 | 730 | 734 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 826 | 831 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 920 | 925 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 493 | 501 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 570 | 577 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 852 | 857 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 915 | 924 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 116 | 134 | PF00022 | 0.447 |
LIG_Actin_WH2_2 | 766 | 783 | PF00022 | 0.364 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.457 |
LIG_Clathr_ClatBox_1 | 479 | 483 | PF01394 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 576 | 585 | PF00928 | 0.488 |
LIG_FAT_LD_1 | 910 | 918 | PF03623 | 0.508 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.453 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.447 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.458 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.510 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.447 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.512 |
LIG_FHA_1 | 719 | 725 | PF00498 | 0.458 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.447 |
LIG_FHA_1 | 798 | 804 | PF00498 | 0.447 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.447 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.634 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.418 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.316 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.447 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.300 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.533 |
LIG_FHA_2 | 788 | 794 | PF00498 | 0.447 |
LIG_FHA_2 | 895 | 901 | PF00498 | 0.537 |
LIG_LIR_Apic_2 | 831 | 836 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 838 | 842 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 215 | 223 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 422 | 430 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 472 | 480 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 494 | 501 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 638 | 647 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 91 | 100 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 472 | 476 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 638 | 644 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 726 | 731 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 801 | 807 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.440 |
LIG_LYPXL_S_1 | 292 | 296 | PF13949 | 0.331 |
LIG_LYPXL_yS_3 | 293 | 296 | PF13949 | 0.332 |
LIG_NRBOX | 798 | 804 | PF00104 | 0.447 |
LIG_PDZ_Class_2 | 949 | 954 | PF00595 | 0.381 |
LIG_Pex14_2 | 555 | 559 | PF04695 | 0.436 |
LIG_Pex14_2 | 90 | 94 | PF04695 | 0.447 |
LIG_PTB_Apo_2 | 588 | 595 | PF02174 | 0.552 |
LIG_PTB_Apo_2 | 81 | 88 | PF02174 | 0.447 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.390 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.325 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.447 |
LIG_SH2_SRC | 208 | 211 | PF00017 | 0.336 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 772 | 775 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 881 | 884 | PF00017 | 0.488 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 155 | 163 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 371 | 377 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 714 | 719 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 812 | 821 | PF11976 | 0.447 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.496 |
LIG_TRAF2_1 | 506 | 509 | PF00917 | 0.516 |
LIG_TRAF2_1 | 867 | 870 | PF00917 | 0.399 |
LIG_TYR_ITIM | 471 | 476 | PF00017 | 0.329 |
LIG_TYR_ITSM | 196 | 203 | PF00017 | 0.393 |
LIG_UBA3_1 | 217 | 224 | PF00899 | 0.450 |
LIG_UBA3_1 | 280 | 285 | PF00899 | 0.380 |
LIG_UBA3_1 | 365 | 370 | PF00899 | 0.493 |
LIG_UBA3_1 | 798 | 805 | PF00899 | 0.447 |
LIG_UBA3_1 | 876 | 885 | PF00899 | 0.399 |
LIG_WRC_WIRS_1 | 28 | 33 | PF05994 | 0.415 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 466 | 471 | PF05994 | 0.473 |
MOD_CDC14_SPxK_1 | 77 | 80 | PF00782 | 0.447 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.447 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.447 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.452 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.466 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.374 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.483 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.469 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.472 |
MOD_CK1_1 | 857 | 863 | PF00069 | 0.447 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.552 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.698 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.535 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.533 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.447 |
MOD_CK2_1 | 530 | 536 | PF00069 | 0.506 |
MOD_CK2_1 | 788 | 794 | PF00069 | 0.447 |
MOD_CK2_1 | 864 | 870 | PF00069 | 0.463 |
MOD_CK2_1 | 872 | 878 | PF00069 | 0.425 |
MOD_CK2_1 | 894 | 900 | PF00069 | 0.508 |
MOD_Cter_Amidation | 430 | 433 | PF01082 | 0.247 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.247 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.711 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.247 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.247 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.370 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.248 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.244 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.343 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.296 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.324 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.255 |
MOD_GlcNHglycan | 918 | 921 | PF01048 | 0.333 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.670 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.477 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.447 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.447 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.404 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.347 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.435 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.466 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.494 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.398 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.467 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.496 |
MOD_GSK3_1 | 848 | 855 | PF00069 | 0.475 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.533 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.447 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.701 |
MOD_N-GLC_1 | 317 | 322 | PF02516 | 0.416 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.274 |
MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.296 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.447 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.348 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.496 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.453 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.352 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.447 |
MOD_NEK2_1 | 948 | 953 | PF00069 | 0.499 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.447 |
MOD_NEK2_2 | 646 | 651 | PF00069 | 0.469 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.503 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.552 |
MOD_PIKK_1 | 699 | 705 | PF00454 | 0.495 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.447 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.447 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.552 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.478 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.447 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.447 |
MOD_Plk_2-3 | 865 | 871 | PF00069 | 0.472 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.535 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.447 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.447 |
MOD_Plk_4 | 948 | 954 | PF00069 | 0.504 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.552 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.455 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.533 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.447 |
MOD_ProDKin_1 | 826 | 832 | PF00069 | 0.447 |
MOD_ProDKin_1 | 920 | 926 | PF00069 | 0.447 |
MOD_SUMO_for_1 | 301 | 304 | PF00179 | 0.407 |
MOD_SUMO_for_1 | 744 | 747 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 335 | 345 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 503 | 512 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 757 | 763 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 865 | 873 | PF00179 | 0.399 |
TRG_DiLeu_BaEn_1 | 156 | 161 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 282 | 287 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_1 | 321 | 326 | PF01217 | 0.399 |
TRG_DiLeu_BaEn_1 | 794 | 799 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_3 | 758 | 764 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_4 | 339 | 345 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 767 | 769 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 907 | 909 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 278 | 289 | PF08389 | 0.394 |
TRG_NLS_Bipartite_1 | 768 | 785 | PF00514 | 0.370 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 9 | 16 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 844 | 848 | PF00026 | 0.258 |
TRG_Pf-PMV_PEXEL_1 | 908 | 912 | PF00026 | 0.247 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDH1 | Leptomonas seymouri | 88% | 100% |
A0A0S4JCF9 | Bodo saltans | 69% | 100% |
A0A1X0NKW0 | Trypanosomatidae | 76% | 100% |
A0A3R7NR74 | Trypanosoma rangeli | 75% | 100% |
A4HPG6 | Leishmania braziliensis | 91% | 100% |
A4ID88 | Leishmania infantum | 100% | 100% |
D0A3H7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
E9AT78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
F4JAA5 | Arabidopsis thaliana | 35% | 71% |
O13799 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 41% | 93% |
O14232 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 85% |
O59801 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 79% |
P42285 | Homo sapiens | 47% | 92% |
P47047 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 46% | 89% |
Q15477 | Homo sapiens | 36% | 77% |
Q23223 | Caenorhabditis elegans | 43% | 93% |
Q4Q1B9 | Leishmania major | 97% | 100% |
Q9CZU3 | Mus musculus | 47% | 92% |
Q9XIF2 | Arabidopsis thaliana | 42% | 97% |
Q9ZBD8 | Mycobacterium leprae (strain TN) | 29% | 100% |
Q9ZVW2 | Arabidopsis thaliana | 42% | 96% |
V5BPT8 | Trypanosoma cruzi | 74% | 100% |