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. | yes | 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:0005886 | plasma membrane | 3 | 6 |
GO:0016020 | membrane | 2 | 54 |
GO:0110165 | cellular anatomical entity | 1 | 54 |
Related structures:
AlphaFold database: Q4Q1M9
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 | 259 | 263 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.360 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.360 |
DOC_CKS1_1 | 459 | 464 | PF01111 | 0.533 |
DOC_MAPK_DCC_7 | 415 | 424 | PF00069 | 0.363 |
DOC_MAPK_DCC_7 | 427 | 435 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 343 | 350 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 399 | 409 | PF00069 | 0.573 |
DOC_MAPK_HePTP_8 | 108 | 120 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 104 | 112 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 211 | 220 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 393 | 400 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 402 | 409 | PF00069 | 0.533 |
DOC_MAPK_MEF2A_6 | 415 | 424 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 427 | 435 | PF00069 | 0.326 |
DOC_MAPK_NFAT4_5 | 111 | 119 | PF00069 | 0.466 |
DOC_PP1_RVXF_1 | 209 | 215 | PF00149 | 0.299 |
DOC_PP2B_LxvP_1 | 116 | 119 | PF13499 | 0.344 |
DOC_PP2B_PxIxI_1 | 435 | 441 | PF00149 | 0.386 |
DOC_PP4_FxxP_1 | 368 | 371 | PF00568 | 0.364 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 335 | 339 | PF00244 | 0.594 |
LIG_Actin_WH2_2 | 387 | 404 | PF00022 | 0.431 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.422 |
LIG_CORNRBOX | 187 | 195 | PF00104 | 0.452 |
LIG_EH_1 | 233 | 237 | PF12763 | 0.520 |
LIG_eIF4E_1 | 31 | 37 | PF01652 | 0.379 |
LIG_eIF4E_1 | 437 | 443 | PF01652 | 0.384 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.548 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.624 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.569 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.372 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.504 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.355 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.393 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.324 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.482 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.237 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.554 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.540 |
LIG_IRF3_LxIS_1 | 203 | 210 | PF10401 | 0.238 |
LIG_LIR_Gen_1 | 201 | 209 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 30 | 39 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 434 | 445 | PF02991 | 0.419 |
LIG_LIR_LC3C_4 | 122 | 125 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.372 |
LIG_LYPXL_S_1 | 345 | 349 | PF13949 | 0.392 |
LIG_LYPXL_yS_3 | 346 | 349 | PF13949 | 0.592 |
LIG_PCNA_PIPBox_1 | 378 | 387 | PF02747 | 0.351 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.526 |
LIG_Pex14_2 | 353 | 357 | PF04695 | 0.317 |
LIG_Pex14_2 | 363 | 367 | PF04695 | 0.297 |
LIG_PTB_Apo_2 | 444 | 451 | PF02174 | 0.366 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.299 |
LIG_SH2_PTP2 | 437 | 440 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 88 | 91 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.355 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.523 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.326 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 122 | 128 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 182 | 189 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 316 | 322 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 378 | 383 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 406 | 412 | PF11976 | 0.547 |
LIG_TRFH_1 | 367 | 371 | PF08558 | 0.359 |
LIG_TYR_ITIM | 435 | 440 | PF00017 | 0.361 |
LIG_UBA3_1 | 397 | 406 | PF00899 | 0.538 |
LIG_WRC_WIRS_1 | 31 | 36 | PF05994 | 0.303 |
LIG_WRC_WIRS_1 | 410 | 415 | PF05994 | 0.270 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.478 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.432 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.272 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.546 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.431 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.313 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.375 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.569 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.557 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.462 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.409 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.545 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.408 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.394 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.362 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.597 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.312 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.561 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.396 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.399 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.371 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.466 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.410 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.327 |
MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.458 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.554 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.384 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.358 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.326 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.271 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.563 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.531 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.395 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.352 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.365 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.436 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.501 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.675 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.433 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.415 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.570 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.514 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.468 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.428 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.359 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.363 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.507 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.331 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.380 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.364 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.336 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.511 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.500 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.434 |
MOD_SUMO_rev_2 | 256 | 266 | PF00179 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 417 | 422 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 32% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 68% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 30% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 26% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 33% | 99% |
A0A0S4JBS4 | Bodo saltans | 32% | 100% |
A0A1X0NN91 | Trypanosomatidae | 33% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 35% | 100% |
A0A1X0NV38 | Trypanosomatidae | 34% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 32% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 33% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WTL0 | Leishmania donovani | 31% | 100% |
A0A3S7XAS5 | Leishmania donovani | 95% | 100% |
A0A422MQ08 | Trypanosoma rangeli | 33% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 45% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 46% | 100% |
A0A422NR81 | Trypanosoma rangeli | 30% | 100% |
A1L272 | Danio rerio | 24% | 96% |
A4H6I0 | Leishmania braziliensis | 31% | 90% |
A4H7A5 | Leishmania braziliensis | 34% | 100% |
A4HG96 | Leishmania braziliensis | 26% | 99% |
A4HP60 | Leishmania braziliensis | 79% | 100% |
A4HUW2 | Leishmania infantum | 33% | 91% |
A4HVP9 | Leishmania infantum | 33% | 100% |
A4HWK9 | Leishmania infantum | 31% | 100% |
A4IDG6 | Leishmania infantum | 95% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 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) | 41% | 100% |
D0A6J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A6J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
D0A6J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AGM5 | Leishmania infantum | 31% | 100% |
E9AGM6 | Leishmania infantum | 31% | 100% |
E9AGM7 | Leishmania infantum | 31% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 91% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
O76343 | Leishmania donovani | 32% | 100% |
Q4QF58 | Leishmania major | 32% | 100% |
Q4QF59 | Leishmania major | 32% | 76% |
Q4QG33 | Leishmania major | 31% | 100% |
Q4QH25 | Leishmania major | 32% | 91% |
Q7RTT9 | Homo sapiens | 23% | 94% |
V5BGB1 | Trypanosoma cruzi | 35% | 100% |
V5BRM5 | Trypanosoma cruzi | 33% | 100% |
V5DSF4 | Trypanosoma cruzi | 47% | 100% |