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: A4HP60
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 | 258 | 262 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.293 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.330 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.342 |
DOC_CDC14_PxL_1 | 415 | 423 | PF14671 | 0.427 |
DOC_CKS1_1 | 458 | 463 | PF01111 | 0.515 |
DOC_MAPK_DCC_7 | 398 | 408 | PF00069 | 0.455 |
DOC_MAPK_DCC_7 | 414 | 423 | PF00069 | 0.345 |
DOC_MAPK_DCC_7 | 426 | 434 | PF00069 | 0.295 |
DOC_MAPK_FxFP_2 | 360 | 363 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 342 | 349 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 398 | 408 | PF00069 | 0.556 |
DOC_MAPK_HePTP_8 | 108 | 120 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 211 | 220 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 401 | 408 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 426 | 434 | PF00069 | 0.309 |
DOC_MAPK_NFAT4_5 | 111 | 119 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 209 | 215 | PF00149 | 0.282 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.327 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.448 |
DOC_PP2B_PxIxI_1 | 434 | 440 | PF00149 | 0.369 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.406 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.346 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.411 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.418 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 334 | 338 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 181 | 198 | PF00022 | 0.488 |
LIG_BRCT_BRCA1_1 | 475 | 479 | PF00533 | 0.369 |
LIG_EH_1 | 233 | 237 | PF12763 | 0.503 |
LIG_eIF4E_1 | 31 | 37 | PF01652 | 0.361 |
LIG_eIF4E_1 | 436 | 442 | PF01652 | 0.366 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.522 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.605 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.354 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.486 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.375 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.307 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.464 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.412 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.220 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.533 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.523 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.522 |
LIG_IRF3_LxIS_1 | 203 | 210 | PF10401 | 0.221 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 201 | 209 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 33 | 42 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 335 | 346 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 373 | 384 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 476 | 486 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 24 | 28 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.352 |
LIG_LYPXL_S_1 | 344 | 348 | PF13949 | 0.375 |
LIG_LYPXL_yS_3 | 345 | 348 | PF13949 | 0.575 |
LIG_NRBOX | 437 | 443 | PF00104 | 0.208 |
LIG_PCNA_PIPBox_1 | 377 | 386 | PF02747 | 0.334 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.464 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.299 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.280 |
LIG_PTB_Apo_2 | 443 | 450 | PF02174 | 0.349 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.282 |
LIG_SH2_PTP2 | 436 | 439 | PF00017 | 0.428 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.333 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.308 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.431 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.340 |
LIG_SUMO_SIM_anti_2 | 391 | 397 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 221 | 227 | PF11976 | 0.295 |
LIG_TRFH_1 | 366 | 370 | PF08558 | 0.342 |
LIG_TYR_ITIM | 434 | 439 | PF00017 | 0.344 |
LIG_WRC_WIRS_1 | 22 | 27 | PF05994 | 0.498 |
LIG_WRC_WIRS_1 | 31 | 36 | PF05994 | 0.285 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.413 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.263 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.511 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.528 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.415 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.357 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.548 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.539 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.269 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.407 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.391 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.378 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.376 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.345 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.582 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.528 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.304 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.538 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.580 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.538 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.566 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.353 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.448 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.306 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.305 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.441 |
MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.306 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.538 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.351 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.354 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.282 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.254 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.545 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.514 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.379 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.334 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.348 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.418 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.469 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.663 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.393 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.534 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.569 |
MOD_Plk_1 | 467 | 473 | PF00069 | 0.496 |
MOD_Plk_1 | 488 | 494 | PF00069 | 0.451 |
MOD_Plk_2-3 | 315 | 321 | PF00069 | 0.488 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.371 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.340 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.494 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.485 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.328 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.362 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.347 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.316 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.483 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.471 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.413 |
MOD_SUMO_rev_2 | 257 | 265 | PF00179 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 411 | 416 | PF01217 | 0.378 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 33% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 69% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 31% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 27% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 33% | 99% |
A0A0S4JBS4 | Bodo saltans | 32% | 100% |
A0A1X0NN91 | Trypanosomatidae | 32% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 35% | 100% |
A0A1X0NV38 | Trypanosomatidae | 36% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 34% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 34% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WTL0 | Leishmania donovani | 31% | 100% |
A0A3S7XAS5 | Leishmania donovani | 80% | 100% |
A0A422MQ08 | Trypanosoma rangeli | 33% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 45% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 45% | 100% |
A0A422NR81 | Trypanosoma rangeli | 29% | 100% |
A1L272 | Danio rerio | 23% | 96% |
A4H6I0 | Leishmania braziliensis | 32% | 100% |
A4H7A5 | Leishmania braziliensis | 33% | 100% |
A4HG96 | Leishmania braziliensis | 25% | 100% |
A4HUW2 | Leishmania infantum | 34% | 91% |
A4HVP9 | Leishmania infantum | 34% | 100% |
A4HWK9 | Leishmania infantum | 32% | 100% |
A4IDG6 | Leishmania infantum | 80% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZY31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZZR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 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 | 31% | 100% |
E9AGM6 | Leishmania infantum | 31% | 100% |
E9AGM7 | Leishmania infantum | 31% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 91% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O76343 | Leishmania donovani | 32% | 100% |
Q4Q1M9 | Leishmania major | 79% | 100% |
Q4QF58 | Leishmania major | 31% | 100% |
Q4QF59 | Leishmania major | 31% | 100% |
Q4QG33 | Leishmania major | 33% | 98% |
Q4QH25 | Leishmania major | 32% | 100% |
V5BGB1 | Trypanosoma cruzi | 33% | 100% |
V5BRM5 | Trypanosoma cruzi | 31% | 100% |
V5DSF4 | Trypanosoma cruzi | 46% | 100% |