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. | no | 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: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 32 |
GO:0110165 | cellular anatomical entity | 1 | 32 |
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: A0A3S5H5N0
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 | 30 |
GO:0005215 | transporter activity | 1 | 32 |
GO:0005488 | binding | 1 | 30 |
GO:0005524 | ATP binding | 5 | 30 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 32 |
GO:0017076 | purine nucleotide binding | 4 | 30 |
GO:0022804 | active transmembrane transporter activity | 3 | 32 |
GO:0022857 | transmembrane transporter activity | 2 | 32 |
GO:0030554 | adenyl nucleotide binding | 5 | 30 |
GO:0032553 | ribonucleotide binding | 3 | 30 |
GO:0032555 | purine ribonucleotide binding | 4 | 30 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 30 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 30 |
GO:0036094 | small molecule binding | 2 | 30 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 32 |
GO:0043167 | ion binding | 2 | 30 |
GO:0043168 | anion binding | 3 | 30 |
GO:0097159 | organic cyclic compound binding | 2 | 30 |
GO:0097367 | carbohydrate derivative binding | 2 | 30 |
GO:0140359 | ABC-type transporter activity | 3 | 32 |
GO:0140657 | ATP-dependent activity | 1 | 32 |
GO:1901265 | nucleoside phosphate binding | 3 | 30 |
GO:1901363 | heterocyclic compound binding | 2 | 30 |
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 | 238 | 242 | PF00656 | 0.534 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.407 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.243 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.327 |
DEG_APCC_DBOX_1 | 586 | 594 | PF00400 | 0.361 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.310 |
DEG_SPOP_SBC_1 | 530 | 534 | PF00917 | 0.434 |
DOC_ANK_TNKS_1 | 420 | 427 | PF00023 | 0.233 |
DOC_CKS1_1 | 158 | 163 | PF01111 | 0.497 |
DOC_CKS1_1 | 343 | 348 | PF01111 | 0.617 |
DOC_CYCLIN_RxL_1 | 616 | 627 | PF00134 | 0.308 |
DOC_CYCLIN_yCln2_LP_2 | 158 | 164 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 140 | 148 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 194 | 203 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 215 | 224 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 386 | 392 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 613 | 621 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 215 | 224 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 372 | 381 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 647 | 656 | PF00069 | 0.368 |
DOC_MAPK_RevD_3 | 644 | 660 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 618 | 625 | PF00149 | 0.371 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.548 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.594 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.286 |
DOC_USP7_UBL2_3 | 329 | 333 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 344 | 353 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 647 | 652 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.605 |
LIG_14-3-3_CterR_2 | 659 | 663 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 112 | 128 | PF00022 | 0.507 |
LIG_Actin_WH2_2 | 632 | 649 | PF00022 | 0.344 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 443 | 447 | PF00533 | 0.310 |
LIG_Clathr_ClatBox_1 | 621 | 625 | PF01394 | 0.306 |
LIG_EH1_1 | 513 | 521 | PF00400 | 0.338 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.483 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.447 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.548 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.530 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.591 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.284 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.341 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.618 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.470 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 303 | 309 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 65 | 69 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 299 | 309 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 315 | 326 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 479 | 488 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 632 | 642 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 71 | 79 | PF02991 | 0.502 |
LIG_LIR_LC3C_4 | 537 | 540 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 19 | 23 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 479 | 483 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.502 |
LIG_Pex14_1 | 603 | 607 | PF04695 | 0.318 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.544 |
LIG_Pex14_2 | 510 | 514 | PF04695 | 0.323 |
LIG_REV1ctd_RIR_1 | 472 | 482 | PF16727 | 0.529 |
LIG_REV1ctd_RIR_1 | 641 | 651 | PF16727 | 0.436 |
LIG_RPA_C_Fungi | 352 | 364 | PF08784 | 0.423 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.316 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.401 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 582 | 585 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 402 | 406 | PF00017 | 0.188 |
LIG_SH2_STAT3 | 402 | 405 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 398 | 401 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.512 |
LIG_SH3_1 | 340 | 346 | PF00018 | 0.441 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.349 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.682 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.221 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.294 |
LIG_SUMO_SIM_anti_2 | 638 | 643 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 648 | 653 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 21 | 27 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 318 | 325 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.323 |
LIG_TYR_ITIM | 496 | 501 | PF00017 | 0.324 |
LIG_TYR_ITSM | 313 | 320 | PF00017 | 0.310 |
LIG_WRC_WIRS_1 | 450 | 455 | PF05994 | 0.393 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.438 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.438 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.451 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.471 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.186 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.474 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.427 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.346 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.687 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.245 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.297 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.502 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.688 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.295 |
MOD_Cter_Amidation | 128 | 131 | PF01082 | 0.438 |
MOD_Cter_Amidation | 657 | 660 | PF01082 | 0.455 |
MOD_Cter_Amidation | 79 | 82 | PF01082 | 0.536 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.323 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.299 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.370 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.293 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.450 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.427 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.501 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.735 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.375 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.307 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.352 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.409 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.395 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.360 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.332 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.494 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.639 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.302 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.220 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.444 |
MOD_LATS_1 | 33 | 39 | PF00433 | 0.535 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.317 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.342 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.297 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.467 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.367 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.396 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.492 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.281 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.338 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.305 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.283 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.622 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.318 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.302 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.580 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.332 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.342 |
MOD_NEK2_1 | 635 | 640 | PF00069 | 0.356 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.330 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.415 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.358 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.443 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.437 |
MOD_PK_1 | 216 | 222 | PF00069 | 0.386 |
MOD_PK_1 | 647 | 653 | PF00069 | 0.269 |
MOD_PKA_1 | 172 | 178 | PF00069 | 0.386 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.299 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.517 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.347 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.302 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.350 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.757 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.442 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.491 |
MOD_PKB_1 | 170 | 178 | PF00069 | 0.386 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.727 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.410 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.309 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.281 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.370 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.354 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.372 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.332 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.608 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.397 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.342 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.319 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.432 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.316 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.771 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.336 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.466 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.492 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.360 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 121 | 128 | PF00179 | 0.399 |
MOD_SUMO_rev_2 | 223 | 231 | PF00179 | 0.346 |
TRG_DiLeu_BaEn_2 | 572 | 578 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 617 | 622 | PF01217 | 0.381 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.229 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.545 |
TRG_NES_CRM1_1 | 272 | 285 | PF08389 | 0.386 |
TRG_NLS_MonoExtC_3 | 332 | 337 | PF00514 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 620 | 625 | PF00026 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 36% | 90% |
A0A0S4IJ55 | Bodo saltans | 36% | 87% |
A0A0S4IQG2 | Bodo saltans | 35% | 100% |
A0A0S4IRK2 | Bodo saltans | 26% | 67% |
A0A0S4IUG8 | Bodo saltans | 55% | 100% |
A0A0S4IUY5 | Bodo saltans | 28% | 100% |
A0A0S4IY23 | Bodo saltans | 37% | 100% |
A0A0S4J724 | Bodo saltans | 37% | 100% |
A0A0S4J7U2 | Bodo saltans | 37% | 95% |
A0A0S4JAS9 | Bodo saltans | 24% | 81% |
A0A0S4JBG7 | Bodo saltans | 22% | 100% |
A0A0S4JPA7 | Bodo saltans | 35% | 89% |
A0A0S4KMF6 | Bodo saltans | 22% | 82% |
A0A1X0NKI4 | Trypanosomatidae | 28% | 100% |
A0A1X0NM50 | Trypanosomatidae | 56% | 98% |
A0A1X0NTW9 | Trypanosomatidae | 36% | 100% |
A0A3Q8IA65 | Leishmania donovani | 36% | 100% |
A0A3Q8IHD8 | Leishmania donovani | 28% | 100% |
A0A3R7KEQ6 | Trypanosoma rangeli | 28% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 58% | 100% |
A0A3S7WPB9 | Leishmania donovani | 95% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 35% | 95% |
A4H4G9 | Leishmania braziliensis | 83% | 100% |
A4H4H6 | Leishmania braziliensis | 84% | 100% |
A4H862 | Leishmania braziliensis | 36% | 100% |
A4HPF5 | Leishmania braziliensis | 29% | 100% |
A4HSQ0 | Leishmania infantum | 95% | 100% |
A4HSQ1 | Leishmania infantum | 99% | 100% |
A4HWI7 | Leishmania infantum | 36% | 100% |
A4ID77 | Leishmania infantum | 28% | 100% |
B8ALI0 | Oryza sativa subsp. indica | 28% | 84% |
B9G5Y5 | Oryza sativa subsp. japonica | 29% | 66% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 99% |
D3ZCM3 | Rattus norvegicus | 29% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
H9BZ66 | Petunia hybrida | 29% | 100% |
O80946 | Arabidopsis thaliana | 28% | 90% |
P10090 | Drosophila melanogaster | 32% | 97% |
P45843 | Drosophila melanogaster | 29% | 100% |
P45844 | Homo sapiens | 28% | 98% |
P58428 | Rattus norvegicus | 28% | 96% |
Q05360 | Lucilia cuprina | 32% | 98% |
Q09466 | Caenorhabditis elegans | 25% | 100% |
Q11180 | Caenorhabditis elegans | 30% | 99% |
Q16928 | Anopheles albimanus | 28% | 94% |
Q17320 | Ceratitis capitata | 31% | 98% |
Q27256 | Anopheles gambiae | 31% | 95% |
Q3E9B8 | Arabidopsis thaliana | 28% | 100% |
Q4GZT4 | Bos taurus | 28% | 100% |
Q4Q1D0 | Leishmania major | 29% | 100% |
Q4QF95 | Leishmania major | 36% | 100% |
Q4QJ70 | Leishmania major | 94% | 100% |
Q4QJ71 | Leishmania major | 93% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 27% | 100% |
Q64343 | Mus musculus | 27% | 100% |
Q7TMS5 | Mus musculus | 28% | 100% |
Q7XA72 | Arabidopsis thaliana | 29% | 99% |
Q80W57 | Rattus norvegicus | 27% | 100% |
Q84TH5 | Arabidopsis thaliana | 28% | 100% |
Q86HQ2 | Dictyostelium discoideum | 27% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 28% | 84% |
Q8MIB3 | Sus scrofa | 29% | 100% |
Q8RWI9 | Arabidopsis thaliana | 29% | 96% |
Q8RXN0 | Arabidopsis thaliana | 31% | 94% |
Q8T685 | Dictyostelium discoideum | 25% | 100% |
Q8T686 | Dictyostelium discoideum | 26% | 81% |
Q91WA9 | Mus musculus | 28% | 100% |
Q93YS4 | Arabidopsis thaliana | 28% | 88% |
Q99P81 | Mus musculus | 25% | 100% |
Q99PE7 | Rattus norvegicus | 27% | 100% |
Q99PE8 | Mus musculus | 28% | 100% |
Q9C6W5 | Arabidopsis thaliana | 28% | 100% |
Q9C8J8 | Arabidopsis thaliana | 31% | 98% |
Q9C8K2 | Arabidopsis thaliana | 29% | 97% |
Q9DBM0 | Mus musculus | 28% | 99% |
Q9FLX5 | Arabidopsis thaliana | 29% | 100% |
Q9FNB5 | Arabidopsis thaliana | 30% | 91% |
Q9FT51 | Arabidopsis thaliana | 28% | 90% |
Q9H172 | Homo sapiens | 28% | 100% |
Q9H221 | Homo sapiens | 28% | 99% |
Q9H222 | Homo sapiens | 29% | 100% |
Q9LFG8 | Arabidopsis thaliana | 30% | 90% |
Q9LK50 | Arabidopsis thaliana | 29% | 97% |
Q9M2V5 | Arabidopsis thaliana | 28% | 94% |
Q9M2V6 | Arabidopsis thaliana | 28% | 100% |
Q9M2V7 | Arabidopsis thaliana | 29% | 90% |
Q9M3D6 | Arabidopsis thaliana | 27% | 91% |
Q9MAH4 | Arabidopsis thaliana | 27% | 100% |
Q9SIT6 | Arabidopsis thaliana | 28% | 100% |
Q9SW08 | Arabidopsis thaliana | 29% | 100% |
Q9SZR9 | Arabidopsis thaliana | 28% | 100% |
Q9UNQ0 | Homo sapiens | 28% | 100% |
Q9ZU35 | Arabidopsis thaliana | 29% | 91% |
Q9ZUT0 | Arabidopsis thaliana | 29% | 88% |
Q9ZUU9 | Arabidopsis thaliana | 25% | 91% |
V5BPQ0 | Trypanosoma cruzi | 35% | 95% |
V5D8T8 | Trypanosoma cruzi | 59% | 100% |
V5DGN9 | Trypanosoma cruzi | 28% | 100% |