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: A4H662
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_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.246 |
DEG_APCC_KENBOX_2 | 75 | 79 | PF00400 | 0.616 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.576 |
DEG_SCF_FBW7_1 | 449 | 455 | PF00400 | 0.594 |
DOC_CKS1_1 | 449 | 454 | PF01111 | 0.600 |
DOC_MAPK_FxFP_2 | 351 | 354 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 290 | 298 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 369 | 378 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.501 |
DOC_MAPK_HePTP_8 | 368 | 380 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 291 | 300 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 371 | 380 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 381 | 388 | PF00069 | 0.271 |
DOC_MAPK_NFAT4_5 | 373 | 381 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 340 | 346 | PF00149 | 0.347 |
DOC_PP4_FxxP_1 | 351 | 354 | PF00568 | 0.347 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.307 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.321 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.645 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 371 | 376 | PF00244 | 0.406 |
LIG_BRCT_BRCA1_1 | 176 | 180 | PF00533 | 0.419 |
LIG_EH1_1 | 108 | 116 | PF00400 | 0.320 |
LIG_EH1_1 | 463 | 471 | PF00400 | 0.236 |
LIG_eIF4E_1 | 195 | 201 | PF01652 | 0.237 |
LIG_eIF4E_1 | 464 | 470 | PF01652 | 0.235 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.402 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.342 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.483 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.322 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.713 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.264 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.241 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.354 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.326 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.339 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.687 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.337 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.743 |
LIG_GBD_Chelix_1 | 378 | 386 | PF00786 | 0.170 |
LIG_Integrin_RGD_1 | 139 | 141 | PF01839 | 0.157 |
LIG_LIR_Apic_2 | 95 | 101 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 143 | 152 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 307 | 317 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.737 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 455 | 459 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.738 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.364 |
LIG_LYPXL_yS_3 | 11 | 14 | PF13949 | 0.562 |
LIG_PALB2_WD40_1 | 260 | 268 | PF16756 | 0.315 |
LIG_PDZ_Class_3 | 478 | 483 | PF00595 | 0.416 |
LIG_Pex14_1 | 308 | 312 | PF04695 | 0.370 |
LIG_Pex14_1 | 444 | 448 | PF04695 | 0.581 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.488 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.390 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 477 | 481 | PF00017 | 0.399 |
LIG_SH2_PTP2 | 195 | 198 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 462 | 465 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.386 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.740 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.529 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.611 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.653 |
LIG_SUMO_SIM_anti_2 | 127 | 132 | PF11976 | 0.356 |
LIG_SUMO_SIM_anti_2 | 199 | 204 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 212 | 219 | PF11976 | 0.487 |
LIG_SUMO_SIM_anti_2 | 276 | 282 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 299 | 304 | PF11976 | 0.313 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 216 | 222 | PF11976 | 0.496 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.353 |
LIG_TYR_ITIM | 229 | 234 | PF00017 | 0.414 |
LIG_TYR_ITSM | 141 | 148 | PF00017 | 0.532 |
LIG_UBA3_1 | 128 | 134 | PF00899 | 0.170 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.353 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.214 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.327 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.338 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.722 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.741 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.716 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.457 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.325 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.392 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.365 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.510 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.441 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.405 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.296 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.210 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.353 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.324 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.320 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.256 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.469 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.519 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.421 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.278 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.376 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.201 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.343 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.278 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.269 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.349 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.507 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.295 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.213 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.347 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.442 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.306 |
MOD_NEK2_2 | 452 | 457 | PF00069 | 0.628 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.514 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.350 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.335 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.583 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.347 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.484 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.176 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.712 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.478 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.604 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.525 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.302 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.315 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.320 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.734 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.397 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.374 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.277 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.482 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.343 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.257 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.279 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.192 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.317 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.326 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.697 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.598 |
MOD_SUMO_for_1 | 330 | 333 | PF00179 | 0.157 |
TRG_DiLeu_BaLyEn_6 | 378 | 383 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.724 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.740 |
TRG_NLS_Bipartite_1 | 445 | 461 | PF00514 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5D2 | Leptomonas seymouri | 22% | 100% |
A0A0N0P6H0 | Leptomonas seymouri | 73% | 100% |
A0A0N1PCP5 | Leptomonas seymouri | 71% | 100% |
A0A1X0NHS6 | Trypanosomatidae | 45% | 100% |
A0A1X0NRL3 | Trypanosomatidae | 23% | 100% |
A0A1X0NYI3 | Trypanosomatidae | 22% | 97% |
A0A1X0NZK6 | Trypanosomatidae | 52% | 100% |
A0A1X0P7Z8 | Trypanosomatidae | 30% | 77% |
A0A381MBS1 | Leishmania infantum | 79% | 99% |
A0A3Q8IB21 | Leishmania donovani | 79% | 99% |
A0A3Q8IFZ0 | Leishmania donovani | 21% | 95% |
A0A3S5H6G5 | Leishmania donovani | 80% | 99% |
A0A3S5H6T4 | Leishmania donovani | 23% | 95% |
A0A422MZQ8 | Trypanosoma rangeli | 35% | 82% |
A4HJ07 | Leishmania braziliensis | 22% | 97% |
A4HJ09 | Leishmania braziliensis | 22% | 100% |
A4HNZ6 | Leishmania braziliensis | 34% | 100% |
A4HUI4 | Leishmania infantum | 78% | 99% |
C9ZW15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 99% |
D0A2X2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 84% |
E9AN82 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
F4ILY9 | Arabidopsis thaliana | 23% | 100% |
P36062 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 70% |
P50944 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 21% | 68% |
Q10074 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 74% |
Q495M3 | Homo sapiens | 22% | 100% |
Q495N2 | Homo sapiens | 22% | 100% |
Q4KL91 | Xenopus laevis | 23% | 93% |
Q4QHE2 | Leishmania major | 78% | 100% |
Q4QHE4 | Leishmania major | 78% | 100% |
Q4V8B1 | Rattus norvegicus | 22% | 100% |
Q6YBV0 | Homo sapiens | 21% | 96% |
Q7Z2H8 | Homo sapiens | 22% | 100% |
Q811P0 | Mus musculus | 22% | 100% |
Q8BHK3 | Mus musculus | 23% | 100% |
Q8CH36 | Mus musculus | 21% | 97% |
Q8K415 | Rattus norvegicus | 22% | 100% |
Q8K4D3 | Mus musculus | 22% | 100% |
Q924A5 | Rattus norvegicus | 22% | 100% |
Q9FKY3 | Arabidopsis thaliana | 24% | 100% |
Q9SS86 | Arabidopsis thaliana | 22% | 100% |
Q9SVG0 | Arabidopsis thaliana | 22% | 100% |
Q9VT04 | Drosophila melanogaster | 21% | 100% |
Q9W056 | Drosophila melanogaster | 24% | 100% |
V5BHF0 | Trypanosoma cruzi | 42% | 100% |
V5BJY7 | Trypanosoma cruzi | 33% | 81% |