Unlikely to be a membrane protein.
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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3S7X433
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 22 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 22 |
GO:0004386 | helicase activity | 2 | 22 |
GO:0005488 | binding | 1 | 22 |
GO:0005524 | ATP binding | 5 | 22 |
GO:0017076 | purine nucleotide binding | 4 | 22 |
GO:0030554 | adenyl nucleotide binding | 5 | 22 |
GO:0032553 | ribonucleotide binding | 3 | 22 |
GO:0032555 | purine ribonucleotide binding | 4 | 22 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 22 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 22 |
GO:0036094 | small molecule binding | 2 | 22 |
GO:0043167 | ion binding | 2 | 22 |
GO:0043168 | anion binding | 3 | 22 |
GO:0097159 | organic cyclic compound binding | 2 | 22 |
GO:0097367 | carbohydrate derivative binding | 2 | 22 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 22 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:1901265 | nucleoside phosphate binding | 3 | 22 |
GO:1901363 | heterocyclic compound binding | 2 | 22 |
GO:0003723 | RNA binding | 4 | 3 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.207 |
CLV_NRD_NRD_1 | 828 | 830 | PF00675 | 0.304 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.209 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 828 | 830 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.189 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.467 |
CLV_Separin_Metazoa | 836 | 840 | PF03568 | 0.409 |
DEG_APCC_DBOX_1 | 827 | 835 | PF00400 | 0.315 |
DEG_COP1_1 | 729 | 737 | PF00400 | 0.337 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.447 |
DEG_SPOP_SBC_1 | 573 | 577 | PF00917 | 0.307 |
DOC_CYCLIN_RxL_1 | 538 | 549 | PF00134 | 0.286 |
DOC_CYCLIN_RxL_1 | 94 | 106 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.415 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 75 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 117 | 124 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 52 | 61 | PF00069 | 0.456 |
DOC_MAPK_HePTP_8 | 65 | 77 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 68 | 77 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 775 | 783 | PF00069 | 0.277 |
DOC_MAPK_RevD_3 | 366 | 382 | PF00069 | 0.415 |
DOC_MAPK_RevD_3 | 814 | 829 | PF00069 | 0.436 |
DOC_PIKK_1 | 444 | 451 | PF02985 | 0.316 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 905 | 908 | PF00568 | 0.471 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 874 | 878 | PF00917 | 0.437 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.273 |
DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 770 | 775 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 517 | 527 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 828 | 838 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 839 | 847 | PF00244 | 0.308 |
LIG_Actin_WH2_2 | 824 | 841 | PF00022 | 0.357 |
LIG_APCC_ABBA_1 | 725 | 730 | PF00400 | 0.331 |
LIG_BIR_III_2 | 328 | 332 | PF00653 | 0.518 |
LIG_Clathr_ClatBox_1 | 626 | 630 | PF01394 | 0.427 |
LIG_deltaCOP1_diTrp_1 | 222 | 228 | PF00928 | 0.419 |
LIG_EH1_1 | 776 | 784 | PF00400 | 0.279 |
LIG_eIF4E_1 | 283 | 289 | PF01652 | 0.425 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.410 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.408 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.417 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.395 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.459 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.417 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.482 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.538 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.349 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.294 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.401 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.319 |
LIG_FHA_1 | 871 | 877 | PF00498 | 0.319 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.435 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.392 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.407 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.283 |
LIG_FHA_2 | 790 | 796 | PF00498 | 0.367 |
LIG_FHA_2 | 884 | 890 | PF00498 | 0.339 |
LIG_GBD_Chelix_1 | 284 | 292 | PF00786 | 0.293 |
LIG_GBD_Chelix_1 | 371 | 379 | PF00786 | 0.226 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.370 |
LIG_GBD_Chelix_1 | 899 | 907 | PF00786 | 0.456 |
LIG_Integrin_RGD_1 | 145 | 147 | PF01839 | 0.219 |
LIG_LIR_Apic_2 | 259 | 264 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 904 | 908 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 160 | 169 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 174 | 185 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 651 | 659 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 797 | 807 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 811 | 820 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 849 | 859 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 877 | 887 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 533 | 539 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 651 | 655 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 671 | 675 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 797 | 803 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 811 | 816 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 849 | 855 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 877 | 882 | PF02991 | 0.395 |
LIG_LYPXL_yS_3 | 395 | 398 | PF13949 | 0.482 |
LIG_NRBOX | 898 | 904 | PF00104 | 0.266 |
LIG_Pex14_1 | 224 | 228 | PF04695 | 0.450 |
LIG_PTB_Apo_2 | 697 | 704 | PF02174 | 0.267 |
LIG_REV1ctd_RIR_1 | 47 | 56 | PF16727 | 0.500 |
LIG_SH2_CRK | 162 | 166 | PF00017 | 0.415 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.483 |
LIG_SH2_CRK | 438 | 442 | PF00017 | 0.514 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.319 |
LIG_SH2_CRK | 652 | 656 | PF00017 | 0.371 |
LIG_SH2_GRB2like | 717 | 720 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 438 | 442 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 667 | 671 | PF00017 | 0.373 |
LIG_SH2_NCK_1 | 859 | 863 | PF00017 | 0.289 |
LIG_SH2_PTP2 | 813 | 816 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 822 | 825 | PF00017 | 0.437 |
LIG_SH2_SRC | 813 | 816 | PF00017 | 0.421 |
LIG_SH2_SRC | 848 | 851 | PF00017 | 0.349 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 652 | 656 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 848 | 852 | PF00017 | 0.386 |
LIG_SH2_STAT3 | 283 | 286 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 508 | 511 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 53 | 56 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 813 | 816 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 822 | 825 | PF00017 | 0.267 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.420 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.407 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.403 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.310 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.341 |
LIG_SH3_5 | 244 | 248 | PF00018 | 0.315 |
LIG_Sin3_3 | 210 | 217 | PF02671 | 0.434 |
LIG_SUMO_SIM_anti_2 | 195 | 200 | PF11976 | 0.408 |
LIG_SUMO_SIM_anti_2 | 376 | 381 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 565 | 571 | PF11976 | 0.271 |
LIG_SUMO_SIM_anti_2 | 615 | 622 | PF11976 | 0.264 |
LIG_SUMO_SIM_anti_2 | 689 | 695 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 893 | 901 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 101 | 106 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 461 | 467 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 657 | 663 | PF11976 | 0.306 |
LIG_SUMO_SIM_par_1 | 693 | 699 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 70 | 76 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 898 | 904 | PF11976 | 0.473 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.427 |
LIG_TRAF2_1 | 54 | 57 | PF00917 | 0.431 |
LIG_TRAF2_1 | 598 | 601 | PF00917 | 0.350 |
LIG_TRFH_1 | 424 | 428 | PF08558 | 0.299 |
LIG_TRFH_1 | 859 | 863 | PF08558 | 0.379 |
LIG_TYR_ITIM | 393 | 398 | PF00017 | 0.482 |
LIG_TYR_ITIM | 650 | 655 | PF00017 | 0.364 |
LIG_UBA3_1 | 102 | 110 | PF00899 | 0.402 |
LIG_UBA3_1 | 198 | 206 | PF00899 | 0.442 |
LIG_UBA3_1 | 684 | 690 | PF00899 | 0.359 |
LIG_WRC_WIRS_1 | 764 | 769 | PF05994 | 0.251 |
LIG_WRC_WIRS_1 | 790 | 795 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 902 | 907 | PF05994 | 0.405 |
MOD_CDK_SPK_2 | 770 | 775 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 103 | 110 | PF00069 | 0.491 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.450 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.444 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.300 |
MOD_CK1_1 | 637 | 643 | PF00069 | 0.550 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.368 |
MOD_CK1_1 | 766 | 772 | PF00069 | 0.266 |
MOD_CK1_1 | 901 | 907 | PF00069 | 0.305 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.466 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.557 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.428 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.389 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.400 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.480 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.387 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.362 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.484 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.268 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.532 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.416 |
MOD_CK2_1 | 805 | 811 | PF00069 | 0.360 |
MOD_CK2_1 | 883 | 889 | PF00069 | 0.355 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.605 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.230 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.232 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.499 |
MOD_GlcNHglycan | 807 | 810 | PF01048 | 0.305 |
MOD_GlcNHglycan | 831 | 834 | PF01048 | 0.391 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.269 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.426 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.389 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.459 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.522 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.446 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.486 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.290 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.302 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.293 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.463 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.299 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.428 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.493 |
MOD_GSK3_1 | 870 | 877 | PF00069 | 0.310 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.202 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.455 |
MOD_N-GLC_1 | 583 | 588 | PF02516 | 0.554 |
MOD_N-GLC_2 | 293 | 295 | PF02516 | 0.310 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.472 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.467 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.365 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.322 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.486 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.393 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.376 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.282 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.326 |
MOD_NEK2_1 | 803 | 808 | PF00069 | 0.368 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.356 |
MOD_NEK2_1 | 855 | 860 | PF00069 | 0.201 |
MOD_NEK2_2 | 874 | 879 | PF00069 | 0.434 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.455 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.496 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.494 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.506 |
MOD_PIKK_1 | 483 | 489 | PF00454 | 0.360 |
MOD_PIKK_1 | 782 | 788 | PF00454 | 0.387 |
MOD_PK_1 | 132 | 138 | PF00069 | 0.384 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.384 |
MOD_PKA_1 | 829 | 835 | PF00069 | 0.430 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.422 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.404 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.507 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.385 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.423 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.438 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.478 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.430 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.321 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.457 |
MOD_Plk_1 | 729 | 735 | PF00069 | 0.337 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.480 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.418 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.373 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.448 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.440 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.293 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.483 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.277 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.391 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.520 |
MOD_Plk_4 | 874 | 880 | PF00069 | 0.421 |
MOD_Plk_4 | 898 | 904 | PF00069 | 0.329 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.491 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.317 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.279 |
MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.324 |
MOD_ProDKin_1 | 770 | 776 | PF00069 | 0.395 |
MOD_SUMO_for_1 | 665 | 668 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 104 | 112 | PF00179 | 0.482 |
TRG_DiLeu_BaEn_1 | 680 | 685 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_2 | 667 | 673 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 842 | 847 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 790 | 793 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 813 | 816 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 822 | 825 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 827 | 829 | PF00400 | 0.287 |
TRG_NES_CRM1_1 | 33 | 48 | PF08389 | 0.373 |
TRG_NLS_MonoCore_2 | 380 | 385 | PF00514 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 100 | 104 | PF00026 | 0.215 |
TRG_Pf-PMV_PEXEL_1 | 676 | 680 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 845 | 849 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P949 | Leptomonas seymouri | 33% | 71% |
A0A0N1IMH3 | Leptomonas seymouri | 88% | 76% |
A0A0S4J9K2 | Bodo saltans | 37% | 85% |
A0A0S4JFJ8 | Bodo saltans | 25% | 73% |
A0A0S4JM26 | Bodo saltans | 22% | 95% |
A0A0S4KI38 | Bodo saltans | 59% | 80% |
A0A1X0NJ25 | Trypanosomatidae | 68% | 83% |
A0A1X0P5Z5 | Trypanosomatidae | 34% | 79% |
A0A3Q8IWG4 | Leishmania donovani | 25% | 100% |
A0A3R7KS57 | Trypanosoma rangeli | 26% | 72% |
A0A3R7RLJ0 | Trypanosoma rangeli | 34% | 74% |
A0A3S7X9A0 | Leishmania donovani | 33% | 100% |
A0A422P032 | Trypanosoma rangeli | 64% | 84% |
A4HJ00 | Leishmania braziliensis | 93% | 100% |
A4HMQ1 | Leishmania braziliensis | 34% | 100% |
A4HN04 | Leishmania braziliensis | 21% | 100% |
A4HQ83 | Leishmania braziliensis | 26% | 100% |
A4I6B7 | Leishmania infantum | 100% | 100% |
A4IDY1 | Leishmania infantum | 25% | 100% |
B8A4F4 | Danio rerio | 28% | 68% |
C9ZN47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 84% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AF51 | Leishmania major | 34% | 100% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B1H5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9B6A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
F4IM84 | Arabidopsis thaliana | 27% | 82% |
O70133 | Mus musculus | 27% | 66% |
P24785 | Drosophila melanogaster | 26% | 71% |
P43329 | Escherichia coli (strain K12) | 24% | 70% |
P45018 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 70% |
Q08211 | Homo sapiens | 27% | 72% |
Q14147 | Homo sapiens | 25% | 80% |
Q16JS8 | Aedes aegypti | 25% | 66% |
Q28141 | Bos taurus | 26% | 71% |
Q4Q0J4 | Leishmania major | 29% | 100% |
Q4Q6N9 | Leishmania major | 98% | 100% |
Q5R874 | Pongo abelii | 27% | 72% |
Q68FK8 | Xenopus laevis | 25% | 72% |
Q9DBV3 | Mus musculus | 25% | 80% |
V5B7H6 | Trypanosoma cruzi | 25% | 84% |
V5BDX9 | Trypanosoma cruzi | 65% | 79% |
V5BTH4 | Trypanosoma cruzi | 35% | 73% |