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: 53 |
NetGPI | no | yes: 0, no: 53 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
GO:0005886 | plasma membrane | 3 | 5 |
Related structures:
AlphaFold database: A4HVP9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0015851 | nucleobase transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 54 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 54 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 54 |
GO:0022857 | transmembrane transporter activity | 2 | 54 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 54 |
GO:0015205 | nucleobase transmembrane transporter activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.308 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.268 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.489 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.602 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.331 |
DOC_ANK_TNKS_1 | 288 | 295 | PF00023 | 0.588 |
DOC_CDC14_PxL_1 | 361 | 369 | PF14671 | 0.448 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.355 |
DOC_CYCLIN_yClb1_LxF_4 | 60 | 66 | PF00134 | 0.327 |
DOC_MAPK_gen_1 | 336 | 345 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 373 | 383 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 87 | 93 | PF00069 | 0.522 |
DOC_MAPK_HePTP_8 | 91 | 103 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 336 | 345 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 416 | 424 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.334 |
DOC_MAPK_NFAT4_5 | 94 | 102 | PF00069 | 0.425 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.323 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.328 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.247 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.555 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.558 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.380 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.374 |
DOC_USP7_UBL2_3 | 287 | 291 | PF12436 | 0.764 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.396 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 394 | 400 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 464 | 473 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 174 | 192 | PF00022 | 0.480 |
LIG_BIR_III_4 | 390 | 394 | PF00653 | 0.296 |
LIG_BRCT_BRCA1_1 | 211 | 215 | PF00533 | 0.456 |
LIG_BRCT_BRCA1_1 | 397 | 401 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.513 |
LIG_Clathr_ClatBox_1 | 101 | 105 | PF01394 | 0.370 |
LIG_EH1_1 | 356 | 364 | PF00400 | 0.417 |
LIG_eIF4E_1 | 14 | 20 | PF01652 | 0.338 |
LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.343 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.331 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.352 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.333 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.488 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.499 |
LIG_LIR_Apic_2 | 398 | 404 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 375 | 386 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 40 | 44 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.514 |
LIG_Pex14_2 | 161 | 165 | PF04695 | 0.338 |
LIG_Pex14_2 | 354 | 358 | PF04695 | 0.276 |
LIG_Pex14_2 | 424 | 428 | PF04695 | 0.351 |
LIG_PTB_Apo_2 | 445 | 452 | PF02174 | 0.326 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.476 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 145 | 149 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.394 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.421 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.379 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.336 |
LIG_SH3_1 | 429 | 435 | PF00018 | 0.171 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.285 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.398 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.500 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.310 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.338 |
LIG_SUMO_SIM_anti_2 | 360 | 366 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 380 | 385 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 360 | 366 | PF11976 | 0.377 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.503 |
LIG_TYR_ITSM | 141 | 148 | PF00017 | 0.472 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.277 |
MOD_CDK_SPxxK_3 | 80 | 87 | PF00069 | 0.391 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.317 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.384 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.516 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.532 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.304 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.326 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.552 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.312 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.308 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.280 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.509 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.779 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.453 |
MOD_N-GLC_1 | 252 | 257 | PF02516 | 0.359 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.280 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.286 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.378 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.474 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.457 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.342 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.311 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.226 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.561 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.543 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.494 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.356 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.395 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.496 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.293 |
MOD_NEK2_2 | 395 | 400 | PF00069 | 0.219 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.364 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.264 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.485 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.498 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.216 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.529 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.645 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.545 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.376 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.276 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.339 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.293 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.323 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.292 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.299 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.234 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.438 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.389 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.732 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 38% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 31% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 34% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 28% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 68% | 99% |
A0A0S4JBS4 | Bodo saltans | 33% | 100% |
A0A1X0NN91 | Trypanosomatidae | 52% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 55% | 100% |
A0A1X0NV38 | Trypanosomatidae | 36% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 37% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 99% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 55% | 100% |
A0A3S7WTL0 | Leishmania donovani | 33% | 100% |
A0A3S7XAS5 | Leishmania donovani | 33% | 100% |
A0A422MQ08 | Trypanosoma rangeli | 34% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 29% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 30% | 100% |
A0A422NR81 | Trypanosoma rangeli | 33% | 100% |
A1L272 | Danio rerio | 22% | 97% |
A4H6I0 | Leishmania braziliensis | 35% | 100% |
A4H7A5 | Leishmania braziliensis | 80% | 100% |
A4HG96 | Leishmania braziliensis | 27% | 96% |
A4HP60 | Leishmania braziliensis | 34% | 98% |
A4HUW2 | Leishmania infantum | 37% | 100% |
A4HWK9 | Leishmania infantum | 33% | 100% |
A4IDG6 | Leishmania infantum | 33% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
C9ZY31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
C9ZZR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
D0A6J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D0A6J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
D0A6J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AGM5 | Leishmania infantum | 33% | 100% |
E9AGM6 | Leishmania infantum | 33% | 100% |
E9AGM7 | Leishmania infantum | 33% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 99% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 99% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 99% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 98% |
O76343 | Leishmania donovani | 33% | 100% |
Q4Q1M9 | Leishmania major | 33% | 98% |
Q4QF58 | Leishmania major | 33% | 100% |
Q4QF59 | Leishmania major | 33% | 100% |
Q4QG33 | Leishmania major | 92% | 100% |
Q4QH25 | Leishmania major | 37% | 100% |
Q7RTT9 | Homo sapiens | 22% | 95% |
Q8R139 | Mus musculus | 22% | 95% |
V5BGB1 | Trypanosoma cruzi | 56% | 100% |
V5BRM5 | Trypanosoma cruzi | 35% | 100% |
V5DSF4 | Trypanosoma cruzi | 33% | 100% |