Related to animal and plant proton-coupled amino acid transporters. The family has modestly expanded in kinetoplastid parazites.
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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
GO:0005774 | vacuolar membrane | 5 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HNZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006865 | amino acid transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015849 | organic acid transport | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:1903825 | organic acid transmembrane transport | 3 | 2 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 2 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 2 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 18 | 22 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.589 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 15 | 17 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.147 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.149 |
DEG_APCC_DBOX_1 | 281 | 289 | PF00400 | 0.147 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.498 |
DEG_MDM2_SWIB_1 | 171 | 179 | PF02201 | 0.141 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.541 |
DOC_CDC14_PxL_1 | 401 | 409 | PF14671 | 0.174 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.210 |
DOC_CKS1_1 | 240 | 245 | PF01111 | 0.141 |
DOC_MAPK_FxFP_2 | 334 | 337 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 117 | 125 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 279 | 288 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 359 | 367 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.208 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.240 |
DOC_MAPK_MEF2A_6 | 360 | 369 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 426 | 433 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 441 | 450 | PF00069 | 0.456 |
DOC_MAPK_NFAT4_5 | 426 | 434 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 140 | 147 | PF00149 | 0.397 |
DOC_PP1_RVXF_1 | 242 | 249 | PF00149 | 0.186 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.160 |
DOC_PP2B_PxIxI_1 | 341 | 347 | PF00149 | 0.147 |
DOC_PP4_FxxP_1 | 334 | 337 | PF00568 | 0.307 |
DOC_PP4_FxxP_1 | 433 | 436 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.208 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.210 |
LIG_14-3-3_CanoR_1 | 59 | 65 | PF00244 | 0.515 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.226 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.289 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.174 |
LIG_Clathr_ClatBox_1 | 430 | 434 | PF01394 | 0.393 |
LIG_deltaCOP1_diTrp_1 | 173 | 180 | PF00928 | 0.282 |
LIG_EH1_1 | 91 | 99 | PF00400 | 0.296 |
LIG_eIF4E_1 | 444 | 450 | PF01652 | 0.220 |
LIG_eIF4E_1 | 92 | 98 | PF01652 | 0.262 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.373 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.226 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.213 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.286 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.248 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.194 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.240 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.196 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.712 |
LIG_GBD_Chelix_1 | 408 | 416 | PF00786 | 0.141 |
LIG_GBD_Chelix_1 | 93 | 101 | PF00786 | 0.359 |
LIG_LIR_Apic_2 | 331 | 337 | PF02991 | 0.174 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.179 |
LIG_LIR_Gen_1 | 164 | 171 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 290 | 300 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 34 | 42 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 427 | 436 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 442 | 453 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.125 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.554 |
LIG_LYPXL_yS_3 | 128 | 131 | PF13949 | 0.360 |
LIG_NRBOX | 323 | 329 | PF00104 | 0.187 |
LIG_NRBOX | 97 | 103 | PF00104 | 0.262 |
LIG_PALB2_WD40_1 | 451 | 459 | PF16756 | 0.147 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.174 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.174 |
LIG_Pex14_2 | 167 | 171 | PF04695 | 0.145 |
LIG_Pex14_2 | 291 | 295 | PF04695 | 0.147 |
LIG_Pex14_2 | 391 | 395 | PF04695 | 0.174 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.429 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.341 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.273 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.423 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 445 | 448 | PF00017 | 0.420 |
LIG_SH2_SRC | 340 | 343 | PF00017 | 0.262 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.156 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.187 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.262 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.303 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.326 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.165 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.210 |
LIG_SUMO_SIM_anti_2 | 110 | 115 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 217 | 223 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.279 |
LIG_SUMO_SIM_anti_2 | 427 | 434 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 184 | 189 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 211 | 217 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 220 | 225 | PF11976 | 0.302 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 427 | 434 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.238 |
LIG_SUMO_SIM_par_1 | 6 | 12 | PF11976 | 0.540 |
LIG_TYR_ITIM | 201 | 206 | PF00017 | 0.521 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.207 |
LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.484 |
LIG_TYR_ITIM | 459 | 464 | PF00017 | 0.392 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.147 |
LIG_WRC_WIRS_1 | 388 | 393 | PF05994 | 0.187 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.141 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.244 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.423 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.531 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.556 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.520 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.348 |
MOD_Cter_Amidation | 13 | 16 | PF01082 | 0.340 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.379 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.293 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.171 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.426 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.174 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.635 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.327 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.606 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.359 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.505 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.341 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.147 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.462 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.254 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.240 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.616 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.373 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.237 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.289 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.413 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.406 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.262 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.166 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.530 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.177 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.174 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.147 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.265 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.393 |
MOD_PKA_1 | 15 | 21 | PF00069 | 0.542 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.688 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.141 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.293 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.314 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.158 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.360 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.590 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.341 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.570 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.347 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.236 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.276 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.254 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.296 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.304 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.742 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.227 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.179 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.285 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.175 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.411 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.282 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.343 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.208 |
MOD_SUMO_rev_2 | 354 | 362 | PF00179 | 0.423 |
TRG_DiLeu_BaEn_1 | 427 | 432 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.141 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.661 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.474 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6H0 | Leptomonas seymouri | 31% | 100% |
A0A0N0P8T9 | Leptomonas seymouri | 21% | 94% |
A0A0N1PCP5 | Leptomonas seymouri | 29% | 99% |
A0A0S4ISI1 | Bodo saltans | 22% | 78% |
A0A1X0NHS6 | Trypanosomatidae | 31% | 98% |
A0A1X0NNX9 | Trypanosomatidae | 22% | 100% |
A0A1X0NZK6 | Trypanosomatidae | 34% | 97% |
A0A1X0P7Z8 | Trypanosomatidae | 50% | 75% |
A0A381MBS1 | Leishmania infantum | 30% | 96% |
A0A3Q8IB21 | Leishmania donovani | 30% | 96% |
A0A3R7RFB5 | Trypanosoma rangeli | 21% | 93% |
A0A3S5H6G5 | Leishmania donovani | 30% | 96% |
A0A422MZQ8 | Trypanosoma rangeli | 52% | 79% |
A4H662 | Leishmania braziliensis | 34% | 100% |
A4HNQ0 | Leishmania braziliensis | 23% | 97% |
A4HUI4 | Leishmania infantum | 29% | 96% |
A4I887 | Leishmania infantum | 21% | 97% |
C9ZW15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 96% |
D0A2X2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 81% |
E9AN82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 96% |
F4ILY9 | Arabidopsis thaliana | 24% | 100% |
F4KBM7 | Arabidopsis thaliana | 22% | 100% |
P36062 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 68% |
Q10074 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 71% |
Q495M3 | Homo sapiens | 23% | 97% |
Q495N2 | Homo sapiens | 26% | 100% |
Q4KL91 | Xenopus laevis | 22% | 90% |
Q4QHE2 | Leishmania major | 31% | 100% |
Q4QHE4 | Leishmania major | 31% | 100% |
Q4V5R4 | Drosophila melanogaster | 23% | 100% |
Q4V8B1 | Rattus norvegicus | 24% | 98% |
Q6YBV0 | Homo sapiens | 26% | 93% |
Q7Z2H8 | Homo sapiens | 24% | 99% |
Q811P0 | Mus musculus | 24% | 98% |
Q8BHK3 | Mus musculus | 25% | 98% |
Q8CH36 | Mus musculus | 25% | 94% |
Q8K415 | Rattus norvegicus | 26% | 98% |
Q8K4D3 | Mus musculus | 24% | 99% |
Q924A5 | Rattus norvegicus | 24% | 99% |
Q9FKY3 | Arabidopsis thaliana | 26% | 100% |
Q9M8L9 | Arabidopsis thaliana | 23% | 96% |
Q9SVG0 | Arabidopsis thaliana | 26% | 100% |
Q9W056 | Drosophila melanogaster | 24% | 100% |
V5BHF0 | Trypanosoma cruzi | 30% | 99% |
V5BJY7 | Trypanosoma cruzi | 53% | 79% |