Proteins belonging to the subfamily G of Eukaryotic ABC transporters. Probably functional as dimers, with broad substrate specificity.. Expanded in Kinetoplastids (also in free-living forms)
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. | yes | yes: 45 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 21 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 31 |
GO:0110165 | cellular anatomical entity | 1 | 31 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0030139 | endocytic vesicle | 7 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 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:0097708 | intracellular vesicle | 5 | 1 |
Related structures:
AlphaFold database: A0A3Q8IA65
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 29 |
GO:0005215 | transporter activity | 1 | 31 |
GO:0005488 | binding | 1 | 29 |
GO:0005524 | ATP binding | 5 | 29 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 31 |
GO:0017076 | purine nucleotide binding | 4 | 29 |
GO:0022804 | active transmembrane transporter activity | 3 | 31 |
GO:0022857 | transmembrane transporter activity | 2 | 31 |
GO:0030554 | adenyl nucleotide binding | 5 | 29 |
GO:0032553 | ribonucleotide binding | 3 | 29 |
GO:0032555 | purine ribonucleotide binding | 4 | 29 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 29 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 29 |
GO:0036094 | small molecule binding | 2 | 29 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 31 |
GO:0043167 | ion binding | 2 | 29 |
GO:0043168 | anion binding | 3 | 29 |
GO:0097159 | organic cyclic compound binding | 2 | 29 |
GO:0097367 | carbohydrate derivative binding | 2 | 29 |
GO:0140359 | ABC-type transporter activity | 3 | 31 |
GO:0140657 | ATP-dependent activity | 1 | 31 |
GO:1901265 | nucleoside phosphate binding | 3 | 29 |
GO:1901363 | heterocyclic compound binding | 2 | 29 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0005319 | lipid transporter activity | 2 | 1 |
GO:0005548 | phospholipid transporter activity | 3 | 1 |
GO:0090556 | phosphatidylserine floppase activity | 4 | 1 |
GO:0140303 | intramembrane lipid transporter activity | 3 | 1 |
GO:0140326 | ATPase-coupled intramembrane lipid transporter activity | 2 | 1 |
GO:0140328 | floppase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 63 | 67 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.510 |
CLV_PCSK_FUR_1 | 130 | 134 | PF00082 | 0.376 |
CLV_PCSK_FUR_1 | 639 | 643 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 178 | 180 | PF00082 | 0.380 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 732 | 736 | PF00082 | 0.495 |
DEG_APCC_DBOX_1 | 641 | 649 | PF00400 | 0.712 |
DEG_MDM2_SWIB_1 | 374 | 382 | PF02201 | 0.639 |
DEG_MDM2_SWIB_1 | 499 | 507 | PF02201 | 0.392 |
DEG_SCF_FBW7_1 | 588 | 594 | PF00400 | 0.524 |
DOC_CKS1_1 | 13 | 18 | PF01111 | 0.827 |
DOC_CKS1_1 | 588 | 593 | PF01111 | 0.471 |
DOC_CKS1_1 | 681 | 686 | PF01111 | 0.766 |
DOC_CKS1_1 | 718 | 723 | PF01111 | 0.789 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.584 |
DOC_CYCLIN_RxL_1 | 69 | 79 | PF00134 | 0.589 |
DOC_MAPK_gen_1 | 375 | 382 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 639 | 647 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 419 | 427 | PF00069 | 0.345 |
DOC_PP1_RVXF_1 | 45 | 52 | PF00149 | 0.643 |
DOC_PP1_RVXF_1 | 642 | 648 | PF00149 | 0.661 |
DOC_PP1_RVXF_1 | 70 | 77 | PF00149 | 0.689 |
DOC_PP1_SILK_1 | 193 | 198 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.560 |
DOC_PP2B_LxvP_1 | 715 | 718 | PF13499 | 0.683 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.831 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 682 | 686 | PF00917 | 0.761 |
DOC_USP7_MATH_2 | 16 | 22 | PF00917 | 0.687 |
DOC_USP7_MATH_2 | 315 | 321 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 649 | 653 | PF12436 | 0.673 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.843 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 587 | 592 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 680 | 685 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.829 |
DOC_WW_Pin1_4 | 717 | 722 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 724 | 729 | PF00397 | 0.796 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 179 | 183 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 391 | 397 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 581 | 585 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 712 | 716 | PF00244 | 0.824 |
LIG_14-3-3_CterR_2 | 737 | 741 | PF00244 | 0.870 |
LIG_Actin_WH2_2 | 612 | 629 | PF00022 | 0.436 |
LIG_APCC_ABBA_1 | 264 | 269 | PF00400 | 0.510 |
LIG_APCC_ABBA_1 | 554 | 559 | PF00400 | 0.380 |
LIG_BRCT_BRCA1_1 | 260 | 264 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.622 |
LIG_deltaCOP1_diTrp_1 | 471 | 478 | PF00928 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 559 | 566 | PF00928 | 0.287 |
LIG_EH_1 | 215 | 219 | PF12763 | 0.631 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.563 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.539 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.589 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.868 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.654 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.538 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.363 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.595 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.823 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.680 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.687 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.553 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.576 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.599 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.365 |
LIG_FHA_2 | 592 | 598 | PF00498 | 0.417 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.842 |
LIG_LIR_Apic_2 | 293 | 299 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 57 | 61 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 395 | 406 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 471 | 482 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 576 | 585 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 615 | 624 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 576 | 582 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 603 | 607 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 615 | 619 | PF02991 | 0.440 |
LIG_MYND_1 | 339 | 343 | PF01753 | 0.686 |
LIG_PCNA_PIPBox_1 | 417 | 426 | PF02747 | 0.445 |
LIG_Pex14_1 | 474 | 478 | PF04695 | 0.470 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.580 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.526 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.396 |
LIG_Pex14_2 | 478 | 482 | PF04695 | 0.356 |
LIG_Pex14_2 | 488 | 492 | PF04695 | 0.319 |
LIG_Pex14_2 | 499 | 503 | PF04695 | 0.392 |
LIG_Pex14_2 | 516 | 520 | PF04695 | 0.406 |
LIG_Pex14_2 | 575 | 579 | PF04695 | 0.319 |
LIG_PTB_Apo_2 | 121 | 128 | PF02174 | 0.534 |
LIG_PTB_Apo_2 | 426 | 433 | PF02174 | 0.363 |
LIG_PTB_Apo_2 | 508 | 515 | PF02174 | 0.411 |
LIG_PTB_Phospho_1 | 121 | 127 | PF10480 | 0.559 |
LIG_PTB_Phospho_1 | 508 | 514 | PF10480 | 0.411 |
LIG_Rb_pABgroove_1 | 261 | 269 | PF01858 | 0.600 |
LIG_REV1ctd_RIR_1 | 521 | 529 | PF16727 | 0.600 |
LIG_SH2_CRK | 131 | 135 | PF00017 | 0.512 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.504 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.554 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.648 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.612 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.631 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.413 |
LIG_SH2_SRC | 622 | 625 | PF00017 | 0.482 |
LIG_SH2_SRC | 724 | 727 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.582 |
LIG_SH2_STAT3 | 137 | 140 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.698 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.779 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.560 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.802 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.592 |
LIG_SH3_3 | 585 | 591 | PF00018 | 0.461 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.642 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.850 |
LIG_SH3_3 | 715 | 721 | PF00018 | 0.843 |
LIG_SH3_3 | 722 | 728 | PF00018 | 0.816 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.530 |
LIG_SUMO_SIM_anti_2 | 580 | 586 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 615 | 621 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 345 | 353 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 713 | 720 | PF11976 | 0.863 |
LIG_SUMO_SIM_par_1 | 726 | 733 | PF11976 | 0.822 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.631 |
LIG_TYR_ITIM | 485 | 490 | PF00017 | 0.401 |
LIG_TYR_ITIM | 69 | 74 | PF00017 | 0.644 |
LIG_UBA3_1 | 101 | 108 | PF00899 | 0.536 |
LIG_UBA3_1 | 189 | 197 | PF00899 | 0.576 |
LIG_UBA3_1 | 240 | 246 | PF00899 | 0.547 |
LIG_UBA3_1 | 266 | 275 | PF00899 | 0.512 |
LIG_UBA3_1 | 74 | 83 | PF00899 | 0.631 |
LIG_WRC_WIRS_1 | 520 | 525 | PF05994 | 0.542 |
LIG_WW_3 | 298 | 302 | PF00397 | 0.510 |
MOD_CDK_SPK_2 | 146 | 151 | PF00069 | 0.536 |
MOD_CDK_SPK_2 | 654 | 659 | PF00069 | 0.590 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.803 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.504 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.493 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.677 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.685 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.794 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.519 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.530 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.835 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.685 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.874 |
MOD_CMANNOS | 323 | 326 | PF00535 | 0.336 |
MOD_CMANNOS | 610 | 613 | PF00535 | 0.569 |
MOD_DYRK1A_RPxSP_1 | 654 | 658 | PF00069 | 0.624 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.417 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.329 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.534 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.455 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.325 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.354 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.799 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.542 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.815 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.598 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.574 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.661 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.489 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.764 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.666 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.813 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.813 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.512 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.382 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.356 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.335 |
MOD_N-GLC_2 | 365 | 367 | PF02516 | 0.353 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.577 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.541 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.546 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.563 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.407 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.352 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.369 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.401 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.796 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.541 |
MOD_NEK2_2 | 630 | 635 | PF00069 | 0.392 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.597 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.633 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.611 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.541 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.494 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.869 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.843 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.546 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.549 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.498 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.360 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.461 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.549 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.265 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.394 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.491 |
MOD_Plk_4 | 612 | 618 | PF00069 | 0.365 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.276 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.813 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.573 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.832 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.539 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.843 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.532 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.504 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.814 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.642 |
MOD_ProDKin_1 | 587 | 593 | PF00069 | 0.470 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.590 |
MOD_ProDKin_1 | 680 | 686 | PF00069 | 0.756 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.829 |
MOD_ProDKin_1 | 717 | 723 | PF00069 | 0.786 |
MOD_ProDKin_1 | 724 | 730 | PF00069 | 0.796 |
MOD_SUMO_rev_2 | 200 | 207 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 35 | 43 | PF00179 | 0.795 |
MOD_SUMO_rev_2 | 356 | 364 | PF00179 | 0.679 |
MOD_SUMO_rev_2 | 726 | 734 | PF00179 | 0.692 |
TRG_DiLeu_BaEn_2 | 116 | 122 | PF01217 | 0.559 |
TRG_DiLeu_BaEn_2 | 444 | 450 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_4 | 356 | 362 | PF01217 | 0.681 |
TRG_DiLeu_BaLyEn_6 | 532 | 537 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 604 | 607 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.639 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 170 | 172 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 639 | 642 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 651 | 654 | PF00400 | 0.655 |
TRG_NES_CRM1_1 | 313 | 328 | PF08389 | 0.678 |
TRG_NLS_Bipartite_1 | 641 | 656 | PF00514 | 0.545 |
TRG_NLS_MonoExtN_4 | 649 | 656 | PF00514 | 0.725 |
TRG_NLS_MonoExtN_4 | 735 | 741 | PF00514 | 0.709 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 82% | 100% |
A0A0N1HZC7 | Leptomonas seymouri | 28% | 100% |
A0A0S4IJ55 | Bodo saltans | 58% | 97% |
A0A0S4IQG2 | Bodo saltans | 54% | 100% |
A0A0S4IRK2 | Bodo saltans | 24% | 75% |
A0A0S4IUG8 | Bodo saltans | 36% | 100% |
A0A0S4IUY5 | Bodo saltans | 31% | 100% |
A0A0S4IY23 | Bodo saltans | 57% | 100% |
A0A0S4J7U2 | Bodo saltans | 56% | 100% |
A0A0S4JAS9 | Bodo saltans | 24% | 91% |
A0A0S4JBG7 | Bodo saltans | 22% | 100% |
A0A0S4JPA7 | Bodo saltans | 52% | 99% |
A0A0S4KMF6 | Bodo saltans | 22% | 92% |
A0A1X0NKI4 | Trypanosomatidae | 30% | 100% |
A0A1X0NM50 | Trypanosomatidae | 35% | 100% |
A0A1X0NTW9 | Trypanosomatidae | 73% | 100% |
A0A1X0P4K0 | Trypanosomatidae | 21% | 100% |
A0A3Q8IHD8 | Leishmania donovani | 27% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 31% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 36% | 100% |
A0A3S5H5N0 | Leishmania donovani | 36% | 100% |
A0A3S7WPB9 | Leishmania donovani | 34% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 74% | 100% |
A4H4G9 | Leishmania braziliensis | 35% | 99% |
A4H4H6 | Leishmania braziliensis | 35% | 100% |
A4H862 | Leishmania braziliensis | 86% | 100% |
A4HPF5 | Leishmania braziliensis | 27% | 100% |
A4HSQ0 | Leishmania infantum | 34% | 100% |
A4HSQ1 | Leishmania infantum | 36% | 100% |
A4HWI7 | Leishmania infantum | 100% | 100% |
A4ID77 | Leishmania infantum | 27% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 27% | 94% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D3ZCM3 | Rattus norvegicus | 28% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
H9BZ66 | Petunia hybrida | 31% | 100% |
O80946 | Arabidopsis thaliana | 28% | 100% |
P10090 | Drosophila melanogaster | 34% | 100% |
P12428 | Drosophila melanogaster | 23% | 100% |
P45843 | Drosophila melanogaster | 27% | 100% |
P45844 | Homo sapiens | 31% | 100% |
P58428 | Rattus norvegicus | 26% | 100% |
Q05360 | Lucilia cuprina | 33% | 100% |
Q09466 | Caenorhabditis elegans | 28% | 100% |
Q11180 | Caenorhabditis elegans | 30% | 100% |
Q16928 | Anopheles albimanus | 34% | 100% |
Q17320 | Ceratitis capitata | 31% | 100% |
Q27256 | Anopheles gambiae | 33% | 100% |
Q3E9B8 | Arabidopsis thaliana | 26% | 100% |
Q4GZT4 | Bos taurus | 29% | 100% |
Q4Q1D0 | Leishmania major | 27% | 100% |
Q4QF95 | Leishmania major | 97% | 100% |
Q4QJ70 | Leishmania major | 36% | 100% |
Q4QJ71 | Leishmania major | 36% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 30% | 100% |
Q64343 | Mus musculus | 30% | 100% |
Q7TMS5 | Mus musculus | 30% | 100% |
Q7XA72 | Arabidopsis thaliana | 29% | 100% |
Q80W57 | Rattus norvegicus | 30% | 100% |
Q84TH5 | Arabidopsis thaliana | 29% | 100% |
Q86HQ2 | Dictyostelium discoideum | 30% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 27% | 94% |
Q8MIB3 | Sus scrofa | 30% | 100% |
Q8RWI9 | Arabidopsis thaliana | 30% | 100% |
Q8RXN0 | Arabidopsis thaliana | 30% | 100% |
Q8T685 | Dictyostelium discoideum | 29% | 100% |
Q8T686 | Dictyostelium discoideum | 27% | 91% |
Q8T689 | Dictyostelium discoideum | 27% | 93% |
Q91WA9 | Mus musculus | 28% | 100% |
Q93YS4 | Arabidopsis thaliana | 30% | 99% |
Q99P81 | Mus musculus | 29% | 100% |
Q99PE7 | Rattus norvegicus | 28% | 100% |
Q99PE8 | Mus musculus | 28% | 100% |
Q9C6W5 | Arabidopsis thaliana | 28% | 100% |
Q9C8J8 | Arabidopsis thaliana | 29% | 100% |
Q9C8K2 | Arabidopsis thaliana | 29% | 100% |
Q9DBM0 | Mus musculus | 27% | 100% |
Q9FLX5 | Arabidopsis thaliana | 29% | 100% |
Q9FNB5 | Arabidopsis thaliana | 29% | 100% |
Q9FT51 | Arabidopsis thaliana | 28% | 100% |
Q9H172 | Homo sapiens | 28% | 100% |
Q9H221 | Homo sapiens | 26% | 100% |
Q9H222 | Homo sapiens | 27% | 100% |
Q9LFG8 | Arabidopsis thaliana | 28% | 100% |
Q9LK50 | Arabidopsis thaliana | 30% | 100% |
Q9M2V5 | Arabidopsis thaliana | 26% | 100% |
Q9M2V6 | Arabidopsis thaliana | 27% | 100% |
Q9M2V7 | Arabidopsis thaliana | 28% | 100% |
Q9M3D6 | Arabidopsis thaliana | 27% | 100% |
Q9MAH4 | Arabidopsis thaliana | 25% | 100% |
Q9SIT6 | Arabidopsis thaliana | 26% | 100% |
Q9SJK6 | Arabidopsis thaliana | 28% | 68% |
Q9SW08 | Arabidopsis thaliana | 29% | 100% |
Q9SZR9 | Arabidopsis thaliana | 30% | 100% |
Q9UNQ0 | Homo sapiens | 30% | 100% |
Q9ZU35 | Arabidopsis thaliana | 29% | 100% |
Q9ZUT0 | Arabidopsis thaliana | 27% | 98% |
Q9ZUU9 | Arabidopsis thaliana | 26% | 100% |
V5BCE1 | Trypanosoma cruzi | 28% | 73% |
V5BPQ0 | Trypanosoma cruzi | 72% | 100% |
V5D8T8 | Trypanosoma cruzi | 36% | 100% |
V5DGN9 | Trypanosoma cruzi | 29% | 100% |