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: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A4HG96
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 13 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 13 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 13 |
GO:0022857 | transmembrane transporter activity | 2 | 13 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.507 |
CLV_MEL_PAP_1 | 213 | 219 | PF00089 | 0.181 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.159 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.188 |
DEG_SCF_FBW7_2 | 259 | 266 | PF00400 | 0.359 |
DOC_CKS1_1 | 430 | 435 | PF01111 | 0.181 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.406 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.288 |
DOC_MAPK_DCC_7 | 418 | 428 | PF00069 | 0.182 |
DOC_MAPK_gen_1 | 328 | 335 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 122 | 129 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.338 |
DOC_MAPK_MEF2A_6 | 328 | 337 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 409 | 417 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 475 | 484 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 62 | 71 | PF00069 | 0.311 |
DOC_PP2B_LxvP_1 | 108 | 111 | PF13499 | 0.306 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.237 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.304 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.159 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.385 |
LIG_14-3-3_CanoR_1 | 122 | 126 | PF00244 | 0.181 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 229 | 236 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 469 | 477 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 95 | 105 | PF00244 | 0.338 |
LIG_Actin_WH2_2 | 200 | 218 | PF00022 | 0.181 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.372 |
LIG_CORNRBOX | 175 | 183 | PF00104 | 0.181 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.370 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.326 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.243 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.248 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.104 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.193 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.240 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.365 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.297 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.345 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.215 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.211 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.395 |
LIG_GBD_Chelix_1 | 326 | 334 | PF00786 | 0.276 |
LIG_GBD_Chelix_1 | 495 | 503 | PF00786 | 0.349 |
LIG_LIR_Gen_1 | 144 | 154 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 340 | 349 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.180 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.205 |
LIG_LIR_Nem_3 | 491 | 495 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.344 |
LIG_PDZ_Class_2 | 500 | 505 | PF00595 | 0.475 |
LIG_Pex14_2 | 401 | 405 | PF04695 | 0.410 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.361 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 44 | 48 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.217 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.345 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.345 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 494 | 500 | PF11976 | 0.252 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 179 | 186 | PF11976 | 0.159 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 497 | 502 | PF11976 | 0.345 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.408 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.496 |
LIG_TRAF2_1 | 263 | 266 | PF00917 | 0.359 |
LIG_TYR_ITIM | 92 | 97 | PF00017 | 0.387 |
LIG_UBA3_1 | 149 | 156 | PF00899 | 0.359 |
LIG_Vh1_VBS_1 | 323 | 341 | PF01044 | 0.359 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.227 |
MOD_CDK_SPK_2 | 429 | 434 | PF00069 | 0.181 |
MOD_CDK_SPxK_1 | 364 | 370 | PF00069 | 0.159 |
MOD_CDK_SPxxK_3 | 215 | 222 | PF00069 | 0.476 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.210 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.476 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.205 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.130 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.275 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.403 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.455 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.438 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.104 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.246 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.232 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.369 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.274 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.474 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.383 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.262 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.230 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.304 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.494 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.343 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.353 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.265 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.307 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.209 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.342 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.285 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.180 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.251 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.292 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.213 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.301 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.390 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.490 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.420 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.445 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.240 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.496 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.237 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.371 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.463 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.359 |
MOD_NEK2_2 | 319 | 324 | PF00069 | 0.533 |
MOD_OFUCOSY | 225 | 232 | PF10250 | 0.159 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.511 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.533 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.159 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.461 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.476 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.159 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.461 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.408 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.389 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.238 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.313 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.419 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.369 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.318 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.263 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.247 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.476 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.401 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.338 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.472 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.159 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.345 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.380 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.181 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.167 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 26% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 24% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 23% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 56% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 25% | 100% |
A0A0S4JBS4 | Bodo saltans | 28% | 100% |
A0A1X0NN91 | Trypanosomatidae | 24% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 25% | 100% |
A0A1X0NV38 | Trypanosomatidae | 24% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 27% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 27% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WTL0 | Leishmania donovani | 25% | 100% |
A0A3S7XAS5 | Leishmania donovani | 26% | 100% |
A0A422MQ08 | Trypanosoma rangeli | 26% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 25% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 26% | 100% |
A0A422NR81 | Trypanosoma rangeli | 25% | 100% |
A1A4N1 | Bos taurus | 22% | 100% |
A1L272 | Danio rerio | 21% | 97% |
A4H6I0 | Leishmania braziliensis | 22% | 98% |
A4H7A5 | Leishmania braziliensis | 25% | 97% |
A4HP60 | Leishmania braziliensis | 25% | 100% |
A4HUW2 | Leishmania infantum | 24% | 92% |
A4HVP9 | Leishmania infantum | 27% | 100% |
A4HWK9 | Leishmania infantum | 25% | 100% |
A4IDG6 | Leishmania infantum | 26% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZY31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZZR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A6J2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A6J4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A6J6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9AGM5 | Leishmania infantum | 25% | 100% |
E9AGM6 | Leishmania infantum | 25% | 100% |
E9AGM7 | Leishmania infantum | 25% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 92% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
O54698 | Rattus norvegicus | 25% | 100% |
O54699 | Rattus norvegicus | 27% | 100% |
O76343 | Leishmania donovani | 25% | 100% |
Q14542 | Homo sapiens | 26% | 100% |
Q4Q1M9 | Leishmania major | 26% | 98% |
Q4QF58 | Leishmania major | 24% | 96% |
Q4QF59 | Leishmania major | 23% | 100% |
Q4QG33 | Leishmania major | 26% | 95% |
Q4QH25 | Leishmania major | 23% | 100% |
Q61672 | Mus musculus | 26% | 100% |
Q7RTT9 | Homo sapiens | 22% | 95% |
Q80WK7 | Rattus norvegicus | 23% | 100% |
Q8R139 | Mus musculus | 22% | 96% |
Q99P65 | Mus musculus | 23% | 100% |
Q9BZD2 | Homo sapiens | 24% | 100% |
V5BGB1 | Trypanosoma cruzi | 27% | 100% |
V5BRM5 | Trypanosoma cruzi | 24% | 100% |
V5DSF4 | Trypanosoma cruzi | 26% | 100% |