An expanded family of eukaryotic equlibrative nuceloside transporters.
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 4 |
| Forrest at al. (procyclic) | no | yes: 4 |
| 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: 10 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 47 |
| NetGPI | no | yes: 0, no: 47 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 48 |
| GO:0110165 | cellular anatomical entity | 1 | 48 |
| GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: E9AQB5
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 1 |
| GO:0015851 | nucleobase transport | 5 | 1 |
| GO:0051179 | localization | 1 | 1 |
| GO:0051234 | establishment of localization | 2 | 1 |
| GO:0071702 | organic substance transport | 4 | 1 |
| GO:0071705 | nitrogen compound transport | 4 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 48 |
| GO:0005337 | nucleoside transmembrane transporter activity | 4 | 48 |
| GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 48 |
| GO:0022857 | transmembrane transporter activity | 2 | 48 |
| GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 48 |
| GO:0015205 | nucleobase transmembrane transporter activity | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.606 |
| CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.570 |
| CLV_MEL_PAP_1 | 375 | 381 | PF00089 | 0.277 |
| CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.336 |
| CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.387 |
| CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.315 |
| CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.253 |
| CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.253 |
| CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.484 |
| CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.595 |
| CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.353 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.685 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 79 | 88 | PF00134 | 0.406 |
| DOC_MAPK_DCC_7 | 404 | 413 | PF00069 | 0.326 |
| DOC_MAPK_FxFP_2 | 346 | 349 | PF00069 | 0.376 |
| DOC_MAPK_gen_1 | 108 | 117 | PF00069 | 0.494 |
| DOC_MAPK_gen_1 | 205 | 216 | PF00069 | 0.354 |
| DOC_MAPK_gen_1 | 389 | 398 | PF00069 | 0.544 |
| DOC_MAPK_HePTP_8 | 107 | 119 | PF00069 | 0.514 |
| DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.345 |
| DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.409 |
| DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.396 |
| DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.454 |
| DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.352 |
| DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.595 |
| DOC_PP1_RVXF_1 | 402 | 408 | PF00149 | 0.470 |
| DOC_PP2B_PxIxI_1 | 348 | 354 | PF00149 | 0.493 |
| DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.392 |
| DOC_PP4_FxxP_1 | 385 | 388 | PF00568 | 0.599 |
| DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.396 |
| DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.551 |
| DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.600 |
| DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.255 |
| DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.506 |
| DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.522 |
| DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.402 |
| LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.508 |
| LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.431 |
| LIG_APCC_ABBA_1 | 353 | 358 | PF00400 | 0.248 |
| LIG_BIR_III_2 | 66 | 70 | PF00653 | 0.293 |
| LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.395 |
| LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.500 |
| LIG_deltaCOP1_diTrp_1 | 358 | 368 | PF00928 | 0.248 |
| LIG_FHA_1 | 184 | 190 | PF00498 | 0.339 |
| LIG_FHA_1 | 342 | 348 | PF00498 | 0.325 |
| LIG_FHA_1 | 362 | 368 | PF00498 | 0.370 |
| LIG_FHA_1 | 482 | 488 | PF00498 | 0.493 |
| LIG_FHA_2 | 1 | 7 | PF00498 | 0.681 |
| LIG_FHA_2 | 311 | 317 | PF00498 | 0.523 |
| LIG_FHA_2 | 484 | 490 | PF00498 | 0.298 |
| LIG_GBD_Chelix_1 | 319 | 327 | PF00786 | 0.359 |
| LIG_IRF3_LxIS_1 | 185 | 192 | PF10401 | 0.436 |
| LIG_LIR_Apic_2 | 344 | 349 | PF02991 | 0.354 |
| LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.598 |
| LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.438 |
| LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.486 |
| LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.576 |
| LIG_LIR_Gen_1 | 359 | 370 | PF02991 | 0.347 |
| LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.336 |
| LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.407 |
| LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.319 |
| LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.432 |
| LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.313 |
| LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.290 |
| LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.370 |
| LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.495 |
| LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.540 |
| LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.319 |
| LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.363 |
| LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.372 |
| LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.345 |
| LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.331 |
| LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.340 |
| LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.305 |
| LIG_NRBOX | 184 | 190 | PF00104 | 0.289 |
| LIG_Pex14_1 | 387 | 391 | PF04695 | 0.595 |
| LIG_Pex14_2 | 147 | 151 | PF04695 | 0.483 |
| LIG_Pex14_2 | 167 | 171 | PF04695 | 0.472 |
| LIG_SH2_CRK | 416 | 420 | PF00017 | 0.307 |
| LIG_SH2_CRK | 424 | 428 | PF00017 | 0.303 |
| LIG_SH2_CRK | 82 | 86 | PF00017 | 0.355 |
| LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.306 |
| LIG_SH2_NCK_1 | 82 | 86 | PF00017 | 0.410 |
| LIG_SH2_PTP2 | 28 | 31 | PF00017 | 0.478 |
| LIG_SH2_SRC | 28 | 31 | PF00017 | 0.433 |
| LIG_SH2_SRC | 418 | 421 | PF00017 | 0.326 |
| LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.626 |
| LIG_SH2_STAT3 | 60 | 63 | PF00017 | 0.428 |
| LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.525 |
| LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.344 |
| LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.308 |
| LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.351 |
| LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.304 |
| LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.332 |
| LIG_SH3_3 | 306 | 312 | PF00018 | 0.581 |
| LIG_SH3_3 | 442 | 448 | PF00018 | 0.414 |
| LIG_SUMO_SIM_anti_2 | 121 | 127 | PF11976 | 0.328 |
| LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.372 |
| LIG_SUMO_SIM_anti_2 | 94 | 100 | PF11976 | 0.507 |
| LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.334 |
| LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.485 |
| LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.277 |
| LIG_SUMO_SIM_par_1 | 94 | 100 | PF11976 | 0.421 |
| LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.573 |
| LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.187 |
| LIG_TYR_ITSM | 78 | 85 | PF00017 | 0.295 |
| LIG_UBA3_1 | 188 | 194 | PF00899 | 0.394 |
| LIG_UBA3_1 | 323 | 331 | PF00899 | 0.578 |
| LIG_WRC_WIRS_1 | 220 | 225 | PF05994 | 0.383 |
| LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.530 |
| MOD_CDK_SPxxK_3 | 377 | 384 | PF00069 | 0.277 |
| MOD_CK1_1 | 169 | 175 | PF00069 | 0.553 |
| MOD_CK1_1 | 322 | 328 | PF00069 | 0.556 |
| MOD_CK1_1 | 481 | 487 | PF00069 | 0.457 |
| MOD_CK2_1 | 151 | 157 | PF00069 | 0.395 |
| MOD_CK2_1 | 20 | 26 | PF00069 | 0.557 |
| MOD_CK2_1 | 310 | 316 | PF00069 | 0.530 |
| MOD_CK2_1 | 483 | 489 | PF00069 | 0.557 |
| MOD_Cter_Amidation | 456 | 459 | PF01082 | 0.252 |
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.341 |
| MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.400 |
| MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.565 |
| MOD_GSK3_1 | 151 | 158 | PF00069 | 0.246 |
| MOD_GSK3_1 | 166 | 173 | PF00069 | 0.435 |
| MOD_GSK3_1 | 179 | 186 | PF00069 | 0.315 |
| MOD_GSK3_1 | 318 | 325 | PF00069 | 0.566 |
| MOD_GSK3_1 | 356 | 363 | PF00069 | 0.342 |
| MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.224 |
| MOD_NEK2_1 | 151 | 156 | PF00069 | 0.360 |
| MOD_NEK2_1 | 171 | 176 | PF00069 | 0.504 |
| MOD_NEK2_1 | 189 | 194 | PF00069 | 0.330 |
| MOD_NEK2_1 | 318 | 323 | PF00069 | 0.508 |
| MOD_NEK2_1 | 341 | 346 | PF00069 | 0.365 |
| MOD_NEK2_1 | 412 | 417 | PF00069 | 0.388 |
| MOD_NEK2_1 | 432 | 437 | PF00069 | 0.418 |
| MOD_NEK2_1 | 466 | 471 | PF00069 | 0.348 |
| MOD_NEK2_1 | 483 | 488 | PF00069 | 0.436 |
| MOD_PIKK_1 | 481 | 487 | PF00454 | 0.572 |
| MOD_PKA_1 | 205 | 211 | PF00069 | 0.248 |
| MOD_PKA_2 | 130 | 136 | PF00069 | 0.409 |
| MOD_PKA_2 | 272 | 278 | PF00069 | 0.431 |
| MOD_Plk_1 | 156 | 162 | PF00069 | 0.511 |
| MOD_Plk_1 | 301 | 307 | PF00069 | 0.620 |
| MOD_Plk_4 | 143 | 149 | PF00069 | 0.307 |
| MOD_Plk_4 | 151 | 157 | PF00069 | 0.383 |
| MOD_Plk_4 | 171 | 177 | PF00069 | 0.516 |
| MOD_Plk_4 | 184 | 190 | PF00069 | 0.343 |
| MOD_Plk_4 | 219 | 225 | PF00069 | 0.367 |
| MOD_Plk_4 | 319 | 325 | PF00069 | 0.479 |
| MOD_Plk_4 | 36 | 42 | PF00069 | 0.348 |
| MOD_Plk_4 | 461 | 467 | PF00069 | 0.514 |
| MOD_Plk_4 | 475 | 481 | PF00069 | 0.295 |
| MOD_Plk_4 | 53 | 59 | PF00069 | 0.304 |
| MOD_Plk_4 | 77 | 83 | PF00069 | 0.304 |
| MOD_Plk_4 | 87 | 93 | PF00069 | 0.342 |
| MOD_Plk_4 | 94 | 100 | PF00069 | 0.297 |
| MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.506 |
| MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.522 |
| MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.402 |
| MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.453 |
| MOD_SUMO_rev_2 | 450 | 460 | PF00179 | 0.448 |
| TRG_DiLeu_BaEn_1 | 121 | 126 | PF01217 | 0.353 |
| TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.277 |
| TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.381 |
| TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.504 |
| TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.302 |
| TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.310 |
| TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.363 |
| TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.340 |
| TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.320 |
| TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.304 |
| TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.500 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P486 | Leptomonas seymouri | 31% | 100% |
| A0A0N0P6Z5 | Leptomonas seymouri | 29% | 98% |
| A0A0N1I8E8 | Leptomonas seymouri | 24% | 98% |
| A0A0N1PBQ1 | Leptomonas seymouri | 32% | 97% |
| A0A0S4JBS4 | Bodo saltans | 30% | 100% |
| A0A1X0NN91 | Trypanosomatidae | 34% | 100% |
| A0A1X0NPL0 | Trypanosomatidae | 34% | 100% |
| A0A1X0NV38 | Trypanosomatidae | 29% | 100% |
| A0A1X0NWJ5 | Trypanosomatidae | 30% | 100% |
| A0A3Q8ICX7 | Leishmania donovani | 31% | 98% |
| A0A3R7NQR3 | Trypanosoma rangeli | 35% | 100% |
| A0A3S7WTL0 | Leishmania donovani | 90% | 100% |
| A0A3S7XAS5 | Leishmania donovani | 31% | 98% |
| A0A422MQ08 | Trypanosoma rangeli | 29% | 100% |
| A0A422N8M2 | Trypanosoma rangeli | 31% | 100% |
| A0A422NHH9 | Trypanosoma rangeli | 30% | 100% |
| A0A422NR81 | Trypanosoma rangeli | 49% | 100% |
| A1A4N1 | Bos taurus | 21% | 100% |
| A1L272 | Danio rerio | 24% | 95% |
| A4H6I0 | Leishmania braziliensis | 28% | 89% |
| A4H7A5 | Leishmania braziliensis | 33% | 100% |
| A4HG96 | Leishmania braziliensis | 25% | 98% |
| A4HP60 | Leishmania braziliensis | 30% | 100% |
| A4HVP9 | Leishmania infantum | 32% | 98% |
| A4HWK9 | Leishmania infantum | 90% | 100% |
| A4IDG6 | Leishmania infantum | 31% | 98% |
| C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
| C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
| C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
| C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
| C9ZY31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
| C9ZZR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
| D0A6J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| D0A6J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| D0A6J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
| E9AGM5 | Leishmania infantum | 90% | 100% |
| E9AGM6 | Leishmania infantum | 89% | 100% |
| E9AGM7 | Leishmania infantum | 89% | 100% |
| E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
| E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
| E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 98% |
| O54698 | Rattus norvegicus | 24% | 100% |
| O54699 | Rattus norvegicus | 25% | 100% |
| O76343 | Leishmania donovani | 90% | 100% |
| Q14542 | Homo sapiens | 26% | 100% |
| Q4Q1M9 | Leishmania major | 31% | 100% |
| Q4QF58 | Leishmania major | 88% | 100% |
| Q4QF59 | Leishmania major | 88% | 100% |
| Q4QG33 | Leishmania major | 32% | 100% |
| Q61672 | Mus musculus | 25% | 100% |
| Q7RTT9 | Homo sapiens | 23% | 93% |
| Q80WK7 | Rattus norvegicus | 22% | 100% |
| Q8R139 | Mus musculus | 26% | 93% |
| Q8VXY7 | Arabidopsis thaliana | 22% | 100% |
| Q99808 | Homo sapiens | 27% | 100% |
| Q9JIM1 | Mus musculus | 25% | 100% |
| V5BGB1 | Trypanosoma cruzi | 33% | 100% |
| V5BRM5 | Trypanosoma cruzi | 30% | 100% |
| V5DSF4 | Trypanosoma cruzi | 31% | 100% |