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:0005774 | vacuolar membrane | 5 | 3 |
GO:0016020 | membrane | 2 | 19 |
GO:0031090 | organelle membrane | 3 | 3 |
GO:0098588 | bounding membrane of organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: Q4QHE4
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: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_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.728 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.241 |
DEG_APCC_KENBOX_2 | 80 | 84 | PF00400 | 0.620 |
DOC_MAPK_FxFP_2 | 356 | 359 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 196 | 205 | PF00069 | 0.306 |
DOC_MAPK_gen_1 | 376 | 385 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 462 | 472 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 133 | 142 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 347 | 356 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 386 | 393 | PF00069 | 0.263 |
DOC_MAPK_MEF2A_6 | 463 | 472 | PF00069 | 0.480 |
DOC_MAPK_NFAT4_5 | 386 | 394 | PF00069 | 0.340 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.346 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.299 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.392 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.322 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 3 | 13 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 443 | 447 | PF00244 | 0.534 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.749 |
LIG_BRCT_BRCA1_1 | 181 | 185 | PF00533 | 0.363 |
LIG_EH1_1 | 113 | 121 | PF00400 | 0.316 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.397 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.354 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.484 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.254 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.246 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.347 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.325 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.331 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.706 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.335 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.753 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.761 |
LIG_GBD_Chelix_1 | 115 | 123 | PF00786 | 0.388 |
LIG_GBD_Chelix_1 | 311 | 319 | PF00786 | 0.434 |
LIG_LIR_Apic_2 | 100 | 106 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 233 | 244 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 30 | 38 | PF02991 | 0.724 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.747 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 198 | 203 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.758 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 379 | 383 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.357 |
LIG_PALB2_WD40_1 | 265 | 273 | PF16756 | 0.311 |
LIG_PDZ_Class_2 | 483 | 488 | PF00595 | 0.483 |
LIG_Pex14_1 | 313 | 317 | PF04695 | 0.364 |
LIG_Pex14_1 | 449 | 453 | PF04695 | 0.582 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.367 |
LIG_PTB_Apo_2 | 350 | 357 | PF02174 | 0.377 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.483 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.384 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 482 | 486 | PF00017 | 0.321 |
LIG_SH2_STAT3 | 358 | 361 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.754 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.524 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 217 | 224 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 281 | 287 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 221 | 227 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 303 | 308 | PF11976 | 0.403 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.346 |
LIG_TYR_ITIM | 234 | 239 | PF00017 | 0.412 |
LIG_TYR_ITSM | 146 | 153 | PF00017 | 0.529 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.346 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.506 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.323 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.740 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.693 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.335 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.753 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.728 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.737 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.358 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.512 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.296 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.545 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.357 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.322 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.507 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.315 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.251 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.443 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.378 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.354 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.273 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.343 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.210 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.306 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.311 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.338 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.403 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.282 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.216 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.340 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.498 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.440 |
MOD_NEK2_2 | 342 | 347 | PF00069 | 0.314 |
MOD_NEK2_2 | 457 | 462 | PF00069 | 0.625 |
MOD_OFUCOSY | 210 | 215 | PF10250 | 0.378 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.714 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.510 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.343 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.332 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.518 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.730 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.527 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.340 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.479 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.473 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.315 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.315 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.332 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.395 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.310 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.746 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.270 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.477 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.249 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.274 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.187 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.322 |
MOD_SUMO_rev_2 | 50 | 59 | PF00179 | 0.778 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.193 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.754 |
TRG_NLS_Bipartite_1 | 450 | 466 | PF00514 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6H0 | Leptomonas seymouri | 71% | 100% |
A0A0N0P8T9 | Leptomonas seymouri | 21% | 98% |
A0A0N1PCP5 | Leptomonas seymouri | 70% | 100% |
A0A1X0NHS6 | Trypanosomatidae | 46% | 100% |
A0A1X0NRL3 | Trypanosomatidae | 23% | 100% |
A0A1X0NYI3 | Trypanosomatidae | 22% | 98% |
A0A1X0NZK6 | Trypanosomatidae | 49% | 100% |
A0A1X0P7Z8 | Trypanosomatidae | 32% | 78% |
A0A381MBS1 | Leishmania infantum | 93% | 100% |
A0A3Q8IB21 | Leishmania donovani | 94% | 100% |
A0A3Q8IFZ0 | Leishmania donovani | 22% | 95% |
A0A3S5H6G5 | Leishmania donovani | 94% | 100% |
A0A3S5H6T4 | Leishmania donovani | 23% | 96% |
A0A3S5ISG3 | Trypanosoma rangeli | 24% | 99% |
A0A3S7WQ39 | Leishmania donovani | 21% | 100% |
A0A422MW74 | Trypanosoma rangeli | 21% | 95% |
A0A422MZQ8 | Trypanosoma rangeli | 35% | 82% |
A4H565 | Leishmania braziliensis | 21% | 99% |
A4H662 | Leishmania braziliensis | 78% | 100% |
A4HNZ6 | Leishmania braziliensis | 31% | 100% |
A4HTE2 | Leishmania infantum | 21% | 99% |
A4HUI4 | Leishmania infantum | 94% | 100% |
A4I6K0 | Leishmania infantum | 22% | 95% |
C9ZW15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D0A2X2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 85% |
E9AN82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 98% |
F4ILY9 | Arabidopsis thaliana | 24% | 100% |
P36062 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 71% |
Q10074 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 74% |
Q495M3 | Homo sapiens | 20% | 100% |
Q495N2 | Homo sapiens | 21% | 100% |
Q4KL91 | Xenopus laevis | 21% | 93% |
Q4Q6M8 | Leishmania major | 23% | 95% |
Q4QHE2 | Leishmania major | 100% | 100% |
Q4QIH0 | Leishmania major | 23% | 99% |
Q4V8B1 | Rattus norvegicus | 22% | 100% |
Q6YBV0 | Homo sapiens | 21% | 97% |
Q7Z2H8 | Homo sapiens | 21% | 100% |
Q811P0 | Mus musculus | 22% | 100% |
Q8BHK3 | Mus musculus | 21% | 100% |
Q8CH36 | Mus musculus | 22% | 98% |
Q8K415 | Rattus norvegicus | 21% | 100% |
Q8K4D3 | Mus musculus | 23% | 100% |
Q924A5 | Rattus norvegicus | 22% | 100% |
Q9SS86 | Arabidopsis thaliana | 20% | 100% |
Q9SVG0 | Arabidopsis thaliana | 24% | 100% |
Q9VT04 | Drosophila melanogaster | 20% | 100% |
Q9W056 | Drosophila melanogaster | 24% | 100% |
V5BHF0 | Trypanosoma cruzi | 44% | 100% |
V5BJY7 | Trypanosoma cruzi | 34% | 82% |