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. | no | 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: A4H4G9
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 | 233 | 237 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.565 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.332 |
CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 121 | 127 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.371 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.396 |
DEG_APCC_DBOX_1 | 424 | 432 | PF00400 | 0.320 |
DEG_APCC_DBOX_1 | 581 | 589 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 610 | 618 | PF00400 | 0.255 |
DEG_SCF_TRCP1_1 | 48 | 54 | PF00400 | 0.614 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.350 |
DOC_ANK_TNKS_1 | 415 | 422 | PF00023 | 0.278 |
DOC_CKS1_1 | 153 | 158 | PF01111 | 0.541 |
DOC_CKS1_1 | 338 | 343 | PF01111 | 0.665 |
DOC_CYCLIN_RxL_1 | 611 | 622 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 153 | 159 | PF00134 | 0.597 |
DOC_MAPK_gen_1 | 135 | 143 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 210 | 219 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 381 | 387 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 608 | 616 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.623 |
DOC_MAPK_MEF2A_6 | 642 | 651 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 613 | 620 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.629 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.597 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.485 |
DOC_USP7_UBL2_3 | 324 | 328 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.397 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 339 | 348 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 381 | 385 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 436 | 445 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 574 | 578 | PF00244 | 0.291 |
LIG_14-3-3_CterR_2 | 654 | 658 | PF00244 | 0.540 |
LIG_Actin_WH2_2 | 107 | 123 | PF00022 | 0.552 |
LIG_Actin_WH2_2 | 627 | 644 | PF00022 | 0.379 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.595 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.350 |
LIG_Clathr_ClatBox_1 | 616 | 620 | PF01394 | 0.363 |
LIG_eIF4E_1 | 629 | 635 | PF01652 | 0.274 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.536 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.482 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.597 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.618 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.765 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.764 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.347 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.333 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.323 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.520 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.516 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.532 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.595 |
LIG_GBD_Chelix_1 | 407 | 415 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 298 | 304 | PF02991 | 0.495 |
LIG_LIR_Apic_2 | 59 | 64 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 270 | 278 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 576 | 585 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 626 | 637 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 66 | 74 | PF02991 | 0.546 |
LIG_LIR_LC3C_4 | 633 | 636 | PF02991 | 0.236 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 626 | 632 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.545 |
LIG_MYND_1 | 542 | 546 | PF01753 | 0.205 |
LIG_MYND_2 | 541 | 545 | PF01753 | 0.205 |
LIG_NRBOX | 636 | 642 | PF00104 | 0.205 |
LIG_Pex14_1 | 598 | 602 | PF04695 | 0.370 |
LIG_PTB_Apo_2 | 580 | 587 | PF02174 | 0.196 |
LIG_PTB_Phospho_1 | 580 | 586 | PF10480 | 0.196 |
LIG_REV1ctd_RIR_1 | 467 | 477 | PF16727 | 0.576 |
LIG_REV1ctd_RIR_1 | 636 | 646 | PF16727 | 0.484 |
LIG_RPA_C_Fungi | 347 | 359 | PF08784 | 0.460 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.351 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.445 |
LIG_SH2_CRK | 508 | 512 | PF00017 | 0.316 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 577 | 580 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 397 | 400 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.542 |
LIG_SH3_1 | 335 | 341 | PF00018 | 0.480 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.719 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.390 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 181 | 187 | PF11976 | 0.266 |
LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 576 | 582 | PF11976 | 0.255 |
LIG_SUMO_SIM_anti_2 | 633 | 638 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 224 | 230 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 313 | 320 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 383 | 388 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 510 | 516 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 645 | 650 | PF11976 | 0.325 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.363 |
LIG_TYR_ITSM | 308 | 315 | PF00017 | 0.350 |
LIG_WRC_WIRS_1 | 445 | 450 | PF05994 | 0.437 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.486 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.486 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.486 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.307 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.339 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.471 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.435 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.448 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.343 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.543 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.483 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.211 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.345 |
MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.486 |
MOD_Cter_Amidation | 74 | 77 | PF01082 | 0.617 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.367 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.422 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.342 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.499 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.467 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.404 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.500 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.511 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.640 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.465 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.507 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.378 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.394 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.378 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.704 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.421 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.403 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.392 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.540 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.350 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.249 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.604 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.568 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.499 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.392 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.355 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.567 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.409 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.440 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.532 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.345 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.323 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.385 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.410 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.374 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.346 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.376 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.397 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.444 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.404 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.358 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.265 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.506 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.485 |
MOD_PK_1 | 211 | 217 | PF00069 | 0.429 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.489 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.431 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.357 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.510 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.517 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.742 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.477 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.401 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.350 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.420 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.457 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.443 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.486 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.492 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.338 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.429 |
MOD_Plk_2-3 | 267 | 273 | PF00069 | 0.455 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.349 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.421 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.399 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.380 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.427 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.378 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.357 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.482 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.359 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.743 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.384 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.515 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.513 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.401 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.397 |
MOD_SUMO_for_1 | 24 | 27 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 218 | 226 | PF00179 | 0.376 |
TRG_DiLeu_BaEn_2 | 296 | 302 | PF01217 | 0.205 |
TRG_DiLeu_BaEn_2 | 567 | 573 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 612 | 617 | PF01217 | 0.428 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 508 | 511 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.426 |
TRG_NES_CRM1_1 | 267 | 280 | PF08389 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 615 | 620 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSP2 | Leptomonas seymouri | 35% | 89% |
A0A0N1HZC7 | Leptomonas seymouri | 28% | 97% |
A0A0S4IJ55 | Bodo saltans | 34% | 86% |
A0A0S4IUG8 | Bodo saltans | 53% | 100% |
A0A0S4IUY5 | Bodo saltans | 29% | 100% |
A0A0S4IY23 | Bodo saltans | 35% | 100% |
A0A0S4J724 | Bodo saltans | 39% | 100% |
A0A0S4J7U2 | Bodo saltans | 35% | 94% |
A0A0S4JAS9 | Bodo saltans | 26% | 80% |
A0A0S4JBG7 | Bodo saltans | 23% | 100% |
A0A0S4JPA7 | Bodo saltans | 35% | 88% |
A0A0S4KHA3 | Bodo saltans | 34% | 100% |
A0A1X0NKI4 | Trypanosomatidae | 29% | 100% |
A0A1X0NM50 | Trypanosomatidae | 59% | 97% |
A0A1X0NTW9 | Trypanosomatidae | 36% | 99% |
A0A3Q8IA65 | Leishmania donovani | 35% | 89% |
A0A3Q8IHD8 | Leishmania donovani | 29% | 96% |
A0A3R7KEQ6 | Trypanosoma rangeli | 28% | 100% |
A0A3R7MNM8 | Trypanosoma rangeli | 56% | 99% |
A0A3S5H5N0 | Leishmania donovani | 83% | 99% |
A0A3S7WPB9 | Leishmania donovani | 81% | 100% |
A0A422N4V5 | Trypanosoma rangeli | 35% | 94% |
A4H4H6 | Leishmania braziliensis | 93% | 99% |
A4H862 | Leishmania braziliensis | 35% | 88% |
A4HPF5 | Leishmania braziliensis | 28% | 97% |
A4HSQ0 | Leishmania infantum | 81% | 100% |
A4HSQ1 | Leishmania infantum | 84% | 99% |
A4HWI7 | Leishmania infantum | 35% | 89% |
A4ID77 | Leishmania infantum | 29% | 96% |
B8ALI0 | Oryza sativa subsp. indica | 25% | 84% |
C9ZXW1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A3G8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A3K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 99% |
D3ZCM3 | Rattus norvegicus | 28% | 100% |
E9AKN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AKN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
E9AQ88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 89% |
E9AT67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 97% |
H9BZ66 | Petunia hybrida | 29% | 100% |
O80946 | Arabidopsis thaliana | 28% | 89% |
P10090 | Drosophila melanogaster | 31% | 96% |
P12428 | Drosophila melanogaster | 23% | 97% |
P45843 | Drosophila melanogaster | 28% | 99% |
P45844 | Homo sapiens | 28% | 97% |
P58428 | Rattus norvegicus | 28% | 95% |
Q05360 | Lucilia cuprina | 33% | 97% |
Q09466 | Caenorhabditis elegans | 26% | 100% |
Q11180 | Caenorhabditis elegans | 31% | 98% |
Q16928 | Anopheles albimanus | 28% | 93% |
Q17320 | Ceratitis capitata | 32% | 97% |
Q24739 | Drosophila virilis | 23% | 99% |
Q27256 | Anopheles gambiae | 31% | 95% |
Q3E9B8 | Arabidopsis thaliana | 29% | 100% |
Q4GZT4 | Bos taurus | 27% | 100% |
Q4Q1D0 | Leishmania major | 30% | 100% |
Q4QF95 | Leishmania major | 35% | 100% |
Q4QJ70 | Leishmania major | 83% | 100% |
Q4QJ71 | Leishmania major | 82% | 100% |
Q55DA0 | Dictyostelium discoideum | 28% | 100% |
Q5MB13 | Macaca mulatta | 28% | 100% |
Q64343 | Mus musculus | 27% | 99% |
Q7TMS5 | Mus musculus | 28% | 100% |
Q7XA72 | Arabidopsis thaliana | 30% | 98% |
Q80W57 | Rattus norvegicus | 27% | 100% |
Q84TH5 | Arabidopsis thaliana | 28% | 99% |
Q86HQ2 | Dictyostelium discoideum | 27% | 100% |
Q8H8V7 | Oryza sativa subsp. japonica | 25% | 84% |
Q8MIB3 | Sus scrofa | 28% | 100% |
Q8RWI9 | Arabidopsis thaliana | 29% | 95% |
Q8RXN0 | Arabidopsis thaliana | 32% | 94% |
Q8T685 | Dictyostelium discoideum | 26% | 100% |
Q8T686 | Dictyostelium discoideum | 25% | 81% |
Q8T689 | Dictyostelium discoideum | 24% | 82% |
Q91WA9 | Mus musculus | 28% | 100% |
Q93YS4 | Arabidopsis thaliana | 29% | 88% |
Q99P81 | Mus musculus | 25% | 100% |
Q99PE7 | Rattus norvegicus | 28% | 100% |
Q99PE8 | Mus musculus | 29% | 100% |
Q9C6W5 | Arabidopsis thaliana | 30% | 100% |
Q9C8J8 | Arabidopsis thaliana | 31% | 97% |
Q9C8K2 | Arabidopsis thaliana | 29% | 96% |
Q9DBM0 | Mus musculus | 28% | 98% |
Q9FLX5 | Arabidopsis thaliana | 28% | 100% |
Q9FNB5 | Arabidopsis thaliana | 30% | 91% |
Q9FT51 | Arabidopsis thaliana | 29% | 89% |
Q9H172 | Homo sapiens | 28% | 100% |
Q9H221 | Homo sapiens | 28% | 98% |
Q9H222 | Homo sapiens | 30% | 100% |
Q9LFG8 | Arabidopsis thaliana | 30% | 89% |
Q9LK50 | Arabidopsis thaliana | 29% | 96% |
Q9M2V5 | Arabidopsis thaliana | 27% | 93% |
Q9M2V6 | Arabidopsis thaliana | 28% | 99% |
Q9M2V7 | Arabidopsis thaliana | 28% | 89% |
Q9M3D6 | Arabidopsis thaliana | 27% | 91% |
Q9MAH4 | Arabidopsis thaliana | 27% | 100% |
Q9SIT6 | Arabidopsis thaliana | 26% | 100% |
Q9SW08 | Arabidopsis thaliana | 30% | 100% |
Q9SZR9 | Arabidopsis thaliana | 30% | 100% |
Q9UNQ0 | Homo sapiens | 28% | 100% |
Q9ZU35 | Arabidopsis thaliana | 30% | 91% |
Q9ZUT0 | Arabidopsis thaliana | 28% | 87% |
Q9ZUU9 | Arabidopsis thaliana | 24% | 90% |
V5BPQ0 | Trypanosoma cruzi | 37% | 94% |
V5D8T8 | Trypanosoma cruzi | 58% | 99% |
V5DGN9 | Trypanosoma cruzi | 29% | 100% |