An enormously expanded group of various amino acid transporters.. Localization: Cell surface (by feature)
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: 0 |
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: 24 |
NetGPI | no | yes: 0, no: 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: A4HLK3
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 3 |
GO:0006810 | transport | 3 | 3 |
GO:0006865 | amino acid transport | 5 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015849 | organic acid transport | 5 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
GO:1903825 | organic acid transmembrane transport | 3 | 3 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0005215 | transporter activity | 1 | 3 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 3 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 3 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.212 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.285 |
CLV_Separin_Metazoa | 89 | 93 | PF03568 | 0.335 |
DEG_ODPH_VHL_1 | 449 | 461 | PF01847 | 0.528 |
DEG_SCF_FBW7_1 | 127 | 134 | PF00400 | 0.319 |
DOC_ANK_TNKS_1 | 175 | 182 | PF00023 | 0.394 |
DOC_CDC14_PxL_1 | 146 | 154 | PF14671 | 0.394 |
DOC_CKS1_1 | 128 | 133 | PF01111 | 0.406 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.160 |
DOC_CYCLIN_yCln2_LP_2 | 113 | 119 | PF00134 | 0.257 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.314 |
DOC_CYCLIN_yCln2_LP_2 | 264 | 270 | PF00134 | 0.282 |
DOC_MAPK_gen_1 | 236 | 243 | PF00069 | 0.432 |
DOC_MAPK_HePTP_8 | 391 | 403 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 206 | 214 | PF00069 | 0.272 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 394 | 403 | PF00069 | 0.427 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.341 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.314 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.302 |
DOC_PP2B_LxvP_1 | 412 | 415 | PF13499 | 0.289 |
DOC_PP4_FxxP_1 | 434 | 437 | PF00568 | 0.303 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.387 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.462 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.160 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.518 |
LIG_APCC_ABBA_1 | 107 | 112 | PF00400 | 0.194 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.521 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.394 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.339 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.307 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.316 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.562 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.400 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.314 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.249 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.482 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 224 | 232 | PF00786 | 0.394 |
LIG_HCF-1_HBM_1 | 353 | 356 | PF13415 | 0.353 |
LIG_IRF3_LxIS_1 | 152 | 158 | PF10401 | 0.542 |
LIG_LIR_Apic_2 | 431 | 437 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 158 | 168 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 331 | 338 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 454 | 464 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 59 | 70 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 74 | 83 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.207 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.494 |
LIG_PCNA_PIPBox_1 | 118 | 127 | PF02747 | 0.296 |
LIG_PCNA_yPIPBox_3 | 118 | 132 | PF02747 | 0.321 |
LIG_PCNA_yPIPBox_3 | 365 | 379 | PF02747 | 0.353 |
LIG_PDZ_Class_2 | 480 | 485 | PF00595 | 0.298 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.395 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.331 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 62 | 65 | PF00017 | 0.229 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.306 |
LIG_SH2_STAT3 | 440 | 443 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.371 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.274 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.276 |
LIG_SUMO_SIM_anti_2 | 341 | 349 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 419 | 425 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 457 | 462 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 265 | 272 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 29 | 35 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 397 | 402 | PF11976 | 0.260 |
LIG_SUMO_SIM_par_1 | 416 | 422 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.605 |
LIG_SUMO_SIM_par_1 | 53 | 59 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 63 | 68 | PF11976 | 0.463 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.496 |
LIG_TYR_ITIM | 104 | 109 | PF00017 | 0.319 |
LIG_TYR_ITIM | 60 | 65 | PF00017 | 0.257 |
LIG_WRC_WIRS_1 | 135 | 140 | PF05994 | 0.238 |
LIG_WRC_WIRS_1 | 157 | 162 | PF05994 | 0.396 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.280 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.294 |
MOD_CDK_SPK_2 | 127 | 132 | PF00069 | 0.321 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.261 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.338 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.245 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.426 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.321 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.594 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.499 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.494 |
MOD_Cter_Amidation | 83 | 86 | PF01082 | 0.318 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.365 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.282 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.312 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.457 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.457 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.212 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.253 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.340 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.318 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.159 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.240 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.328 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.328 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.315 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.328 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.545 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.314 |
MOD_N-GLC_2 | 201 | 203 | PF02516 | 0.353 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.318 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.313 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.494 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.328 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.326 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.276 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.452 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.320 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.353 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.312 |
MOD_NEK2_2 | 479 | 484 | PF00069 | 0.272 |
MOD_NEK2_2 | 53 | 58 | PF00069 | 0.320 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.490 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.482 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.518 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.551 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.500 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.278 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.211 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.464 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.344 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.324 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.523 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.263 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.313 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.470 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.271 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.393 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.312 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.160 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_3 | 342 | 348 | PF01217 | 0.353 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.273 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.239 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.521 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P613 | Leptomonas seymouri | 39% | 100% |
A0A0N1I3F8 | Leptomonas seymouri | 26% | 91% |
A0A0N1I3H4 | Leptomonas seymouri | 25% | 88% |
A0A0N1IAJ0 | Leptomonas seymouri | 28% | 100% |
A0A0N1IJ81 | Leptomonas seymouri | 75% | 100% |
A0A0N1PA98 | Leptomonas seymouri | 20% | 79% |
A0A0S4IV32 | Bodo saltans | 31% | 99% |
A0A0S4JHM8 | Bodo saltans | 23% | 100% |
A0A0S4JQ87 | Bodo saltans | 26% | 100% |
A0A1X0NNX9 | Trypanosomatidae | 27% | 100% |
A0A1X0P1N2 | Trypanosomatidae | 47% | 100% |
A0A1X0P4S1 | Trypanosomatidae | 39% | 100% |
A0A3Q8ID74 | Leishmania donovani | 24% | 91% |
A0A3Q8IHH7 | Leishmania donovani | 85% | 99% |
A0A3R7MQD8 | Trypanosoma rangeli | 26% | 100% |
A0A3R7MWF1 | Trypanosoma rangeli | 49% | 100% |
A0A3S7X4L2 | Leishmania donovani | 20% | 80% |
A0A3S7X4N4 | Leishmania donovani | 20% | 80% |
A0A3S7XA86 | Leishmania donovani | 38% | 100% |
A0A3S7XCE3 | Leishmania donovani | 26% | 100% |
A0A422MW74 | Trypanosoma rangeli | 24% | 95% |
A0A422N5W8 | Trypanosoma rangeli | 38% | 100% |
A1YG32 | Pan paniscus | 26% | 96% |
A4HFT5 | Leishmania braziliensis | 26% | 100% |
A4HJ35 | Leishmania braziliensis | 26% | 100% |
A4HJF8 | Leishmania braziliensis | 21% | 100% |
A4HJF9 | Leishmania braziliensis | 21% | 100% |
A4HJG1 | Leishmania braziliensis | 21% | 100% |
A4HJG3 | Leishmania braziliensis | 21% | 100% |
A4HJG5 | Leishmania braziliensis | 21% | 100% |
A4HNJ6 | Leishmania braziliensis | 37% | 100% |
A4HNJ7 | Leishmania braziliensis | 43% | 100% |
A4I6J8 | Leishmania infantum | 24% | 91% |
A4I914 | Leishmania infantum | 85% | 99% |
A4IC53 | Leishmania infantum | 38% | 100% |
A4IC66 | Leishmania infantum | 39% | 100% |
A4ICC3 | Leishmania infantum | 26% | 100% |
D0A4B3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 86% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AD45 | Leishmania major | 24% | 91% |
E9ADD7 | Leishmania major | 26% | 100% |
E9AG08 | Leishmania major | 38% | 87% |
E9AG09 | Leishmania major | 38% | 87% |
E9AHD9 | Leishmania infantum | 24% | 91% |
E9AHL2 | Leishmania infantum | 21% | 100% |
E9AUB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B3X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B762 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
F4KBM7 | Arabidopsis thaliana | 23% | 100% |
G3UVW3 | Mus musculus | 25% | 100% |
P38176 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 100% |
P40074 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P40501 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 99% |
Q28HE5 | Xenopus tropicalis | 26% | 100% |
Q4Q072 | Leishmania major | 27% | 100% |
Q4Q445 | Leishmania major | 84% | 100% |
Q4Q6N1 | Leishmania major | 23% | 91% |
Q503G8 | Danio rerio | 25% | 100% |
Q5E9S9 | Bos taurus | 23% | 100% |
Q5F468 | Gallus gallus | 24% | 97% |
Q5R9F5 | Pongo abelii | 24% | 100% |
Q5XH90 | Xenopus tropicalis | 23% | 98% |
Q6DEL1 | Danio rerio | 23% | 100% |
Q6DFE7 | Xenopus laevis | 22% | 100% |
Q6JWR2 | Rattus norvegicus | 23% | 100% |
Q6WWW3 | Rattus norvegicus | 27% | 100% |
Q8BWH0 | Mus musculus | 24% | 100% |
Q8R1S9 | Mus musculus | 23% | 89% |
Q8WUX1 | Homo sapiens | 23% | 100% |
Q96QD8 | Homo sapiens | 26% | 96% |
Q99624 | Homo sapiens | 24% | 96% |
Q9DCP2 | Mus musculus | 25% | 96% |
Q9EQ25 | Rattus norvegicus | 22% | 89% |
Q9JHE5 | Rattus norvegicus | 25% | 96% |
Q9JHZ9 | Rattus norvegicus | 25% | 96% |
Q9LI61 | Arabidopsis thaliana | 21% | 100% |
Q9LYM2 | Arabidopsis thaliana | 23% | 100% |
Q9M8L9 | Arabidopsis thaliana | 22% | 99% |
Q9NVC3 | Homo sapiens | 24% | 100% |
V5AXD0 | Trypanosoma cruzi | 48% | 100% |
V5BQ72 | Trypanosoma cruzi | 22% | 87% |