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: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 24 |
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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 4 |
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
Related structures:
AlphaFold database: Q4QH25
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0015851 | nucleobase transport | 5 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 20 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 20 |
GO:0015205 | nucleobase transmembrane transporter activity | 3 | 3 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 20 |
GO:0022857 | transmembrane transporter activity | 2 | 20 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.245 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.265 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.507 |
DEG_SCF_FBW7_1 | 509 | 515 | PF00400 | 0.445 |
DOC_CDC14_PxL_1 | 466 | 474 | PF14671 | 0.298 |
DOC_CKS1_1 | 509 | 514 | PF01111 | 0.503 |
DOC_CYCLIN_yClb1_LxF_4 | 56 | 62 | PF00134 | 0.293 |
DOC_MAPK_DCC_7 | 465 | 474 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 272 | 278 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 465 | 474 | PF00069 | 0.337 |
DOC_MIT_MIM_1 | 437 | 447 | PF04212 | 0.271 |
DOC_PP1_RVXF_1 | 463 | 469 | PF00149 | 0.330 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.397 |
DOC_PP2B_PxIxI_1 | 413 | 419 | PF00149 | 0.255 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.254 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.424 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.256 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.419 |
LIG_14-3-3_CanoR_1 | 375 | 383 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 443 | 448 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 158 | 176 | PF00022 | 0.309 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.277 |
LIG_BRCT_BRCA1_1 | 495 | 499 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 85 | 89 | PF00533 | 0.521 |
LIG_Clathr_ClatBox_1 | 88 | 92 | PF01394 | 0.328 |
LIG_Clathr_ClatBox_1 | 97 | 101 | PF01394 | 0.381 |
LIG_EH1_1 | 61 | 69 | PF00400 | 0.359 |
LIG_eIF4E_1 | 435 | 441 | PF01652 | 0.285 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.385 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.568 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.302 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.647 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.503 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.323 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.391 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.367 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.540 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.588 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.725 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.469 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.459 |
LIG_GBD_Chelix_1 | 165 | 173 | PF00786 | 0.359 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 178 | 189 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 202 | 211 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 424 | 435 | PF02991 | 0.328 |
LIG_LIR_LC3C_4 | 12 | 16 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 409 | 413 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.351 |
LIG_LYPXL_S_1 | 395 | 399 | PF13949 | 0.353 |
LIG_LYPXL_S_1 | 412 | 416 | PF13949 | 0.285 |
LIG_LYPXL_yS_3 | 396 | 399 | PF13949 | 0.353 |
LIG_LYPXL_yS_3 | 413 | 416 | PF13949 | 0.285 |
LIG_PALB2_WD40_1 | 422 | 430 | PF16756 | 0.245 |
LIG_Pex14_1 | 229 | 233 | PF04695 | 0.550 |
LIG_Pex14_2 | 81 | 85 | PF04695 | 0.517 |
LIG_PTB_Apo_2 | 135 | 142 | PF02174 | 0.300 |
LIG_PTB_Phospho_1 | 135 | 141 | PF10480 | 0.300 |
LIG_Rb_pABgroove_1 | 294 | 302 | PF01858 | 0.579 |
LIG_REV1ctd_RIR_1 | 302 | 311 | PF16727 | 0.611 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.295 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.293 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.307 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.359 |
LIG_SH2_NCK_1 | 507 | 511 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.271 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.465 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.262 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.405 |
LIG_Sin3_3 | 529 | 536 | PF02671 | 0.255 |
LIG_SUMO_SIM_anti_2 | 101 | 107 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 164 | 170 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 456 | 462 | PF11976 | 0.488 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.652 |
LIG_TRFH_1 | 318 | 322 | PF08558 | 0.619 |
LIG_TYR_ITIM | 189 | 194 | PF00017 | 0.359 |
LIG_TYR_ITIM | 411 | 416 | PF00017 | 0.285 |
LIG_UBA3_1 | 471 | 479 | PF00899 | 0.302 |
LIG_WRC_WIRS_1 | 403 | 408 | PF05994 | 0.300 |
LIG_WRC_WIRS_1 | 78 | 83 | PF05994 | 0.539 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.303 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.310 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.655 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.507 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.709 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.678 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.484 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.477 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.330 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.410 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.324 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.535 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.519 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.549 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.592 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.364 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.308 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.695 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.326 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.368 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.558 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.566 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.206 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.319 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.358 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.393 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.349 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.257 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.260 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.636 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.357 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.345 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.339 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.329 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.316 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.337 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.268 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.643 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.608 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.615 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.613 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.565 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.482 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.517 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.300 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.340 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.321 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.315 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.302 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.665 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.273 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.377 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.335 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.344 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.553 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.392 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.419 |
MOD_SUMO_rev_2 | 267 | 274 | PF00179 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 440 | 445 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.499 |
TRG_Pf-PMV_PEXEL_1 | 263 | 267 | PF00026 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 47% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 56% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 37% | 100% |
A0A0S4JBS4 | Bodo saltans | 31% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 37% | 100% |
A0A3S7XAS5 | Leishmania donovani | 31% | 100% |
A4H6I0 | Leishmania braziliensis | 72% | 99% |
A4H7A5 | Leishmania braziliensis | 36% | 100% |
A4HG96 | Leishmania braziliensis | 23% | 100% |
A4HP60 | Leishmania braziliensis | 32% | 100% |
A4HUW2 | Leishmania infantum | 90% | 100% |
A4HVP9 | Leishmania infantum | 37% | 100% |
A4IDG6 | Leishmania infantum | 31% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
Q4Q1M9 | Leishmania major | 32% | 93% |
Q4QG33 | Leishmania major | 34% | 91% |