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: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 32 |
NetGPI | no | yes: 0, no: 32 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 33 |
GO:0110165 | cellular anatomical entity | 1 | 33 |
GO:0005886 | plasma membrane | 3 | 4 |
Related structures:
AlphaFold database: A4H6I0
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 | 33 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 33 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 33 |
GO:0022857 | transmembrane transporter activity | 2 | 33 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 33 |
GO:0015205 | nucleobase transmembrane transporter activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 179 | 183 | PF00656 | 0.184 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.815 |
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.300 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.281 |
CLV_PCSK_FUR_1 | 237 | 241 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.472 |
CLV_Separin_Metazoa | 278 | 282 | PF03568 | 0.598 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.556 |
DEG_SCF_FBW7_1 | 512 | 518 | PF00400 | 0.428 |
DOC_CDC14_PxL_1 | 469 | 477 | PF14671 | 0.368 |
DOC_CKS1_1 | 512 | 517 | PF01111 | 0.475 |
DOC_CYCLIN_yClb1_LxF_4 | 59 | 65 | PF00134 | 0.325 |
DOC_MAPK_DCC_7 | 468 | 477 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 396 | 403 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 468 | 477 | PF00069 | 0.387 |
DOC_MIT_MIM_1 | 440 | 450 | PF04212 | 0.249 |
DOC_PP1_RVXF_1 | 466 | 472 | PF00149 | 0.422 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.353 |
DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.420 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.455 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.228 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 305 | 313 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 87 | 91 | PF00244 | 0.517 |
LIG_Actin_WH2_2 | 161 | 179 | PF00022 | 0.429 |
LIG_BRCT_BRCA1_1 | 368 | 372 | PF00533 | 0.559 |
LIG_BRCT_BRCA1_1 | 498 | 502 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_2 | 53 | 59 | PF00533 | 0.244 |
LIG_Clathr_ClatBox_1 | 91 | 95 | PF01394 | 0.375 |
LIG_CSL_BTD_1 | 454 | 457 | PF09270 | 0.420 |
LIG_EH1_1 | 64 | 72 | PF00400 | 0.404 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.371 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.531 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.631 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.369 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.607 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.668 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.508 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.345 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.359 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.410 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.484 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.175 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.381 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.704 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.826 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.541 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.511 |
LIG_GBD_Chelix_1 | 168 | 176 | PF00786 | 0.404 |
LIG_IBAR_NPY_1 | 215 | 217 | PF08397 | 0.518 |
LIG_LIR_Gen_1 | 142 | 152 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 427 | 437 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.359 |
LIG_LIR_LC3C_4 | 15 | 19 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 449 | 454 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.315 |
LIG_LYPXL_S_1 | 398 | 402 | PF13949 | 0.370 |
LIG_LYPXL_yS_3 | 399 | 402 | PF13949 | 0.448 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.292 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.264 |
LIG_PALB2_WD40_1 | 425 | 433 | PF16756 | 0.228 |
LIG_Pex14_1 | 232 | 236 | PF04695 | 0.601 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.528 |
LIG_PTB_Apo_2 | 138 | 145 | PF02174 | 0.345 |
LIG_PTB_Phospho_1 | 138 | 144 | PF10480 | 0.345 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.325 |
LIG_SH2_CRK | 217 | 221 | PF00017 | 0.502 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.334 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.462 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 65 | 69 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.341 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.497 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.613 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.327 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.488 |
LIG_SH3_5 | 360 | 364 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 104 | 110 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 66 | 72 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 151 | 156 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 200 | 205 | PF11976 | 0.350 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 97 | 104 | PF11976 | 0.221 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.404 |
LIG_UBA3_1 | 171 | 177 | PF00899 | 0.448 |
LIG_UBA3_1 | 474 | 482 | PF00899 | 0.289 |
LIG_WRC_WIRS_1 | 406 | 411 | PF05994 | 0.345 |
LIG_WRC_WIRS_1 | 61 | 66 | PF05994 | 0.364 |
LIG_WRC_WIRS_1 | 81 | 86 | PF05994 | 0.480 |
LIG_WW_3 | 455 | 459 | PF00397 | 0.438 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.314 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.489 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.379 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.695 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.694 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.742 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.637 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.485 |
MOD_DYRK1A_RPxSP_1 | 319 | 323 | PF00069 | 0.612 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.368 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.400 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.292 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.490 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.511 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.591 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.570 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.576 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.306 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.597 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.601 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.827 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.403 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.310 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.330 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.405 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.686 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.315 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.502 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.323 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.265 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.270 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.631 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.725 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.370 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.332 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.332 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.433 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.366 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.378 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.345 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.272 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.621 |
MOD_PK_1 | 238 | 244 | PF00069 | 0.552 |
MOD_PKA_1 | 238 | 244 | PF00069 | 0.736 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.527 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.564 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.624 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.497 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.403 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.345 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.639 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.332 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.336 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.332 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.323 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.317 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.306 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.315 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.360 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.363 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.323 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.430 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.617 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.633 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.373 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.422 |
MOD_SUMO_for_1 | 353 | 356 | PF00179 | 0.661 |
MOD_SUMO_rev_2 | 253 | 262 | PF00179 | 0.633 |
TRG_DiLeu_BaLyEn_6 | 443 | 448 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 47% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 29% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 58% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 25% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 36% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 35% | 100% |
A0A3S7WTL0 | Leishmania donovani | 29% | 100% |
A0A3S7XAS5 | Leishmania donovani | 31% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 28% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 29% | 100% |
A4H7A5 | Leishmania braziliensis | 35% | 100% |
A4HG96 | Leishmania braziliensis | 22% | 100% |
A4HP60 | Leishmania braziliensis | 32% | 100% |
A4HUW2 | Leishmania infantum | 75% | 100% |
A4HVP9 | Leishmania infantum | 35% | 100% |
A4HWK9 | Leishmania infantum | 29% | 100% |
A4IDG6 | Leishmania infantum | 31% | 100% |
C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AGM5 | Leishmania infantum | 29% | 100% |
E9AGM6 | Leishmania infantum | 29% | 100% |
E9AGM7 | Leishmania infantum | 29% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 91% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 91% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
O76343 | Leishmania donovani | 29% | 100% |
Q4Q1M9 | Leishmania major | 31% | 93% |
Q4QF58 | Leishmania major | 28% | 91% |
Q4QG33 | Leishmania major | 34% | 91% |
Q4QH25 | Leishmania major | 72% | 100% |