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. | 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: 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: 49 |
NetGPI | no | yes: 0, no: 49 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 50 |
GO:0110165 | cellular anatomical entity | 1 | 50 |
GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: A0A3S7WTL0
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 | 50 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 50 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 50 |
GO:0022857 | transmembrane transporter activity | 2 | 50 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 50 |
GO:0015205 | nucleobase transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 295 | 299 | PF00656 | 0.527 |
CLV_MEL_PAP_1 | 375 | 381 | PF00089 | 0.239 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.344 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.206 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.291 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
DOC_MAPK_DCC_7 | 404 | 413 | PF00069 | 0.290 |
DOC_MAPK_FxFP_2 | 346 | 349 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 103 | 111 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 205 | 216 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 328 | 335 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 389 | 398 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 103 | 111 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 209 | 218 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 404 | 413 | PF00069 | 0.321 |
DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.549 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.500 |
DOC_PP1_RVXF_1 | 402 | 408 | PF00149 | 0.408 |
DOC_PP2B_PxIxI_1 | 348 | 354 | PF00149 | 0.450 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.351 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.356 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.536 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.208 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 131 | 139 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 273 | 282 | PF00244 | 0.386 |
LIG_APCC_ABBA_1 | 353 | 358 | PF00400 | 0.206 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 358 | 368 | PF00928 | 0.206 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.286 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.305 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.286 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.327 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.462 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.303 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.634 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.425 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.483 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.254 |
LIG_GBD_Chelix_1 | 319 | 327 | PF00786 | 0.317 |
LIG_LIR_Apic_2 | 344 | 349 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 359 | 370 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 401 | 410 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.196 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 401 | 405 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 415 | 419 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 80 | 85 | PF02991 | 0.256 |
LIG_NRBOX | 184 | 190 | PF00104 | 0.253 |
LIG_Pex14_1 | 387 | 391 | PF04695 | 0.549 |
LIG_Pex14_2 | 147 | 151 | PF04695 | 0.438 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.414 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.260 |
LIG_SH2_CRK | 424 | 428 | PF00017 | 0.257 |
LIG_SH2_CRK | 82 | 86 | PF00017 | 0.323 |
LIG_SH2_GRB2like | 71 | 74 | PF00017 | 0.351 |
LIG_SH2_GRB2like | 81 | 84 | PF00017 | 0.272 |
LIG_SH2_NCK_1 | 82 | 86 | PF00017 | 0.375 |
LIG_SH2_PTP2 | 28 | 31 | PF00017 | 0.434 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.395 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.287 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 60 | 63 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.285 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.535 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.365 |
LIG_SUMO_SIM_anti_2 | 121 | 127 | PF11976 | 0.296 |
LIG_SUMO_SIM_anti_2 | 222 | 228 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.338 |
LIG_SUMO_SIM_anti_2 | 94 | 100 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 115 | 121 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 478 | 484 | PF11976 | 0.239 |
LIG_SUMO_SIM_par_1 | 94 | 100 | PF11976 | 0.384 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.530 |
LIG_TYR_ITSM | 78 | 85 | PF00017 | 0.260 |
LIG_UBA3_1 | 188 | 194 | PF00899 | 0.359 |
LIG_UBA3_1 | 323 | 331 | PF00899 | 0.534 |
LIG_ULM_U2AF65_1 | 328 | 333 | PF00076 | 0.393 |
LIG_WRC_WIRS_1 | 231 | 236 | PF05994 | 0.490 |
MOD_CDK_SPxxK_3 | 377 | 384 | PF00069 | 0.239 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.509 |
MOD_CK1_1 | 481 | 487 | PF00069 | 0.416 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.360 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.517 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.571 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.491 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.521 |
MOD_Cter_Amidation | 456 | 459 | PF01082 | 0.206 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.298 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.282 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.302 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.519 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.327 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.201 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.395 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.281 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.520 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.316 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.304 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.312 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.323 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.402 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.461 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.334 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.304 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.338 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.370 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.315 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.405 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.534 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.206 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.357 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.380 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.472 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.568 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.345 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.423 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.291 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.315 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.315 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.471 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.260 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.269 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.266 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.310 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.264 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.359 |
MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 450 | 460 | PF00179 | 0.406 |
TRG_DiLeu_BaEn_1 | 121 | 126 | PF01217 | 0.320 |
TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 107 | 112 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 406 | 411 | PF01217 | 0.344 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.249 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 327 | 329 | PF00400 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 34% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 29% | 98% |
A0A0N1I1J0 | Leptomonas seymouri | 27% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 23% | 98% |
A0A0N1PBQ1 | Leptomonas seymouri | 33% | 97% |
A0A0S4JBS4 | Bodo saltans | 31% | 100% |
A0A1X0NN91 | Trypanosomatidae | 35% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 33% | 100% |
A0A1X0NV38 | Trypanosomatidae | 31% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 32% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 33% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 34% | 100% |
A0A3S7XAS5 | Leishmania donovani | 31% | 98% |
A0A422MQ08 | Trypanosoma rangeli | 31% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 31% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 31% | 100% |
A0A422NR81 | Trypanosoma rangeli | 52% | 100% |
A1A4N1 | Bos taurus | 23% | 100% |
A1L272 | Danio rerio | 25% | 95% |
A4H6I0 | Leishmania braziliensis | 29% | 100% |
A4H7A5 | Leishmania braziliensis | 33% | 100% |
A4HG96 | Leishmania braziliensis | 25% | 99% |
A4HP60 | Leishmania braziliensis | 31% | 100% |
A4HUW2 | Leishmania infantum | 28% | 100% |
A4HVP9 | Leishmania infantum | 33% | 100% |
A4HWK9 | Leishmania infantum | 99% | 100% |
A4IDG6 | Leishmania infantum | 31% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 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) | 33% | 100% |
C9ZZR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
D0A6J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A6J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A6J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGM5 | Leishmania infantum | 100% | 100% |
E9AGM6 | Leishmania infantum | 99% | 100% |
E9AGM7 | Leishmania infantum | 99% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
O54698 | Rattus norvegicus | 24% | 100% |
O54699 | Rattus norvegicus | 25% | 100% |
O76343 | Leishmania donovani | 99% | 100% |
Q14542 | Homo sapiens | 25% | 100% |
Q4Q1M9 | Leishmania major | 31% | 100% |
Q4QF58 | Leishmania major | 94% | 100% |
Q4QF59 | Leishmania major | 96% | 100% |
Q4QG33 | Leishmania major | 33% | 100% |
Q61672 | Mus musculus | 25% | 100% |
Q7RTT9 | Homo sapiens | 26% | 93% |
Q8R139 | Mus musculus | 27% | 93% |
Q8VXY7 | Arabidopsis thaliana | 22% | 100% |
Q99808 | Homo sapiens | 26% | 100% |
Q9JIM1 | Mus musculus | 25% | 100% |
V5BGB1 | Trypanosoma cruzi | 33% | 100% |
V5BRM5 | Trypanosoma cruzi | 30% | 100% |
V5DSF4 | Trypanosoma cruzi | 31% | 100% |