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: 8 |
Forrest at al. (procyclic) | no | yes: 8 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 51 |
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: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 59 |
NetGPI | no | yes: 0, no: 59 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 48 |
GO:0110165 | cellular anatomical entity | 1 | 48 |
Related structures:
AlphaFold database: A4I2V2
Term | Name | Level | Count |
---|---|---|---|
GO:0003333 | amino acid transmembrane transport | 5 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006865 | amino acid transport | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015849 | organic acid transport | 5 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0055085 | transmembrane transport | 2 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:1903825 | organic acid transmembrane transport | 3 | 11 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0005215 | transporter activity | 1 | 11 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 11 |
GO:0015171 | amino acid transmembrane transporter activity | 5 | 11 |
GO:0015179 | L-amino acid transmembrane transporter activity | 6 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.355 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.359 |
CLV_PCSK_PC7_1 | 507 | 513 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.323 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.520 |
DOC_MAPK_gen_1 | 426 | 433 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 511 | 521 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 340 | 347 | PF00069 | 0.223 |
DOC_MAPK_MEF2A_6 | 426 | 433 | PF00069 | 0.569 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.602 |
DOC_PP1_RVXF_1 | 505 | 511 | PF00149 | 0.556 |
DOC_PP1_RVXF_1 | 562 | 569 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.359 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.325 |
DOC_USP7_MATH_2 | 216 | 222 | PF00917 | 0.477 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.222 |
LIG_14-3-3_CanoR_1 | 223 | 228 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 564 | 569 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 580 | 584 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.575 |
LIG_BRCT_BRCA1_1 | 272 | 276 | PF00533 | 0.300 |
LIG_CtBP_PxDLS_1 | 544 | 548 | PF00389 | 0.579 |
LIG_DLG_GKlike_1 | 136 | 143 | PF00625 | 0.422 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.303 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.388 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.586 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.550 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.657 |
LIG_Integrin_isoDGR_2 | 251 | 253 | PF01839 | 0.416 |
LIG_IRF3_LxIS_1 | 299 | 306 | PF10401 | 0.420 |
LIG_LIR_Gen_1 | 122 | 130 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 273 | 284 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 559 | 566 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 559 | 563 | PF02991 | 0.559 |
LIG_NRBOX | 63 | 69 | PF00104 | 0.516 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.406 |
LIG_SH2_GRB2like | 336 | 339 | PF00017 | 0.214 |
LIG_SH2_PTP2 | 349 | 352 | PF00017 | 0.345 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 322 | 325 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.581 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.358 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.592 |
LIG_SUMO_SIM_anti_2 | 107 | 114 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.239 |
LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 42 | 51 | PF11976 | 0.577 |
LIG_SUMO_SIM_par_1 | 542 | 550 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 91 | 99 | PF11976 | 0.278 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.481 |
LIG_TYR_ITIM | 334 | 339 | PF00017 | 0.255 |
LIG_TYR_ITIM | 347 | 352 | PF00017 | 0.348 |
LIG_UBA3_1 | 210 | 217 | PF00899 | 0.425 |
LIG_Vh1_VBS_1 | 105 | 123 | PF01044 | 0.272 |
LIG_WRC_WIRS_1 | 188 | 193 | PF05994 | 0.245 |
LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.561 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.462 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.270 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.250 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.317 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.554 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.531 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.529 |
MOD_CMANNOS | 503 | 506 | PF00535 | 0.359 |
MOD_Cter_Amidation | 133 | 136 | PF01082 | 0.221 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.532 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.314 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.350 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.369 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.320 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.228 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.355 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.260 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.471 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.622 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.603 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.544 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.250 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.640 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.301 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.319 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.330 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.245 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.382 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.674 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.565 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.570 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.238 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.653 |
MOD_PK_1 | 223 | 229 | PF00069 | 0.455 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.638 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.221 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.537 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.571 |
MOD_PKB_1 | 57 | 65 | PF00069 | 0.549 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.387 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.422 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.321 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.407 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.425 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.323 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.571 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.542 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.481 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.595 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.545 |
TRG_DiLeu_BaEn_1 | 486 | 491 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.605 |
TRG_ER_diArg_1 | 135 | 137 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 425 | 427 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 58 | 61 | PF00400 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID74 | Leishmania donovani | 36% | 100% |
A0A3Q8IDG8 | Leishmania donovani | 99% | 100% |
A0A3Q8IG00 | Leishmania donovani | 35% | 100% |
A0A3Q8IHG8 | Leishmania donovani | 41% | 100% |
A0A3Q8IJX8 | Leishmania donovani | 38% | 100% |
A0A3Q8ILE0 | Leishmania donovani | 38% | 100% |
A0A3S5H6T4 | Leishmania donovani | 41% | 100% |
A0A3S7WQ39 | Leishmania donovani | 39% | 100% |
A0A3S7X443 | Leishmania donovani | 42% | 100% |
A0A3S7X458 | Leishmania donovani | 42% | 100% |
A0A3S7X4A1 | Leishmania donovani | 38% | 100% |
A0A3S7XA86 | Leishmania donovani | 24% | 100% |
A0A3S7XCE3 | Leishmania donovani | 25% | 100% |
A4HC75 | Leishmania braziliensis | 38% | 100% |
A4HFT5 | Leishmania braziliensis | 78% | 100% |
A4HJ06 | Leishmania braziliensis | 37% | 100% |
A4HJ07 | Leishmania braziliensis | 41% | 100% |
A4HJ09 | Leishmania braziliensis | 39% | 100% |
A4HJ63 | Leishmania braziliensis | 40% | 100% |
A4HNJ6 | Leishmania braziliensis | 26% | 100% |
A4HNJ7 | Leishmania braziliensis | 26% | 100% |
A4HTE2 | Leishmania infantum | 39% | 100% |
A4HZQ0 | Leishmania infantum | 38% | 100% |
A4I6I1 | Leishmania infantum | 39% | 100% |
A4I6J8 | Leishmania infantum | 36% | 100% |
A4I6J9 | Leishmania infantum | 42% | 100% |
A4I6L3 | Leishmania infantum | 35% | 100% |
A4I6L4 | Leishmania infantum | 39% | 100% |
A4IC53 | Leishmania infantum | 24% | 100% |
A4IC66 | Leishmania infantum | 27% | 100% |
A4ICC3 | Leishmania infantum | 25% | 100% |
E8NHF9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9AD44 | Leishmania major | 41% | 100% |
E9AD45 | Leishmania major | 37% | 100% |
E9ADD7 | Leishmania major | 92% | 100% |
E9AG08 | Leishmania major | 26% | 100% |
E9AG09 | Leishmania major | 27% | 100% |
E9AHD7 | Leishmania infantum | 41% | 100% |
E9AHD9 | Leishmania infantum | 36% | 100% |
E9AHL2 | Leishmania infantum | 35% | 100% |
E9ALD5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AUB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AVK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9AYW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AYW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AZ62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B1I4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9B1K8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9B1N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B1N9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9B761 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9B762 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q072 | Leishmania major | 25% | 100% |
Q4Q6K6 | Leishmania major | 33% | 100% |
Q4Q6M8 | Leishmania major | 37% | 100% |
Q4Q6M9 | Leishmania major | 41% | 100% |
Q4Q6N0 | Leishmania major | 41% | 100% |
Q4QBX3 | Leishmania major | 37% | 100% |