Shows homology to LAAT transporters found in mammals (SLC66 family).. Localization: Lysosomal (by homology)
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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005768 | endosome | 7 | 1 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031410 | cytoplasmic vesicle | 6 | 1 |
GO:0031982 | vesicle | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0097708 | intracellular vesicle | 5 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A4HF48
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006869 | lipid transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015748 | organophosphate ester transport | 5 | 1 |
GO:0015914 | phospholipid transport | 6 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0016197 | endosomal transport | 4 | 1 |
GO:0016482 | cytosolic transport | 4 | 1 |
GO:0034204 | lipid translocation | 4 | 1 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 1 |
GO:0045332 | phospholipid translocation | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097035 | regulation of membrane lipid distribution | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.292 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.485 |
CLV_PCSK_PC7_1 | 262 | 268 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.438 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.477 |
DEG_ODPH_VHL_1 | 14 | 27 | PF01847 | 0.339 |
DOC_CYCLIN_yCln2_LP_2 | 112 | 118 | PF00134 | 0.584 |
DOC_MAPK_gen_1 | 326 | 333 | PF00069 | 0.683 |
DOC_MAPK_MEF2A_6 | 5 | 14 | PF00069 | 0.408 |
DOC_MAPK_RevD_3 | 313 | 327 | PF00069 | 0.524 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.401 |
DOC_PP1_RVXF_1 | 3 | 9 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.369 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.344 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 349 | 357 | PF00244 | 0.599 |
LIG_Actin_WH2_2 | 192 | 207 | PF00022 | 0.564 |
LIG_Actin_WH2_2 | 247 | 264 | PF00022 | 0.444 |
LIG_BIR_III_2 | 170 | 174 | PF00653 | 0.621 |
LIG_Clathr_ClatBox_1 | 192 | 196 | PF01394 | 0.587 |
LIG_CSL_BTD_1 | 153 | 156 | PF09270 | 0.600 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.702 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.496 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.577 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.401 |
LIG_HP1_1 | 38 | 42 | PF01393 | 0.401 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 34 | 39 | PF02991 | 0.506 |
LIG_NBox_RRM_1 | 8 | 18 | PF00076 | 0.447 |
LIG_NRBOX | 271 | 277 | PF00104 | 0.444 |
LIG_NRBOX | 60 | 66 | PF00104 | 0.481 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.599 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.399 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.409 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.653 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 230 | 233 | PF00017 | 0.527 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.388 |
LIG_SH2_SRC | 24 | 27 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 293 | 296 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.351 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.369 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.605 |
LIG_SUMO_SIM_anti_2 | 252 | 258 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.376 |
LIG_SUMO_SIM_anti_2 | 311 | 316 | PF11976 | 0.319 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 107 | 113 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 216 | 221 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 273 | 279 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 41 | 47 | PF11976 | 0.369 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.544 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.339 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.376 |
LIG_TYR_ITIM | 318 | 323 | PF00017 | 0.522 |
MOD_CDK_SPxxK_3 | 342 | 349 | PF00069 | 0.591 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.612 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.658 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.689 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.511 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.620 |
MOD_Cter_Amidation | 129 | 132 | PF01082 | 0.413 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.530 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.525 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.571 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.565 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.516 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.396 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.412 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.487 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.627 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.702 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.695 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.657 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.487 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.512 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.684 |
MOD_LATS_1 | 263 | 269 | PF00433 | 0.490 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.291 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.306 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.337 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.401 |
MOD_PK_1 | 29 | 35 | PF00069 | 0.595 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.492 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.491 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.593 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.320 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.306 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.389 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.337 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.756 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.690 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.674 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.508 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.682 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.561 |
TRG_NES_CRM1_1 | 296 | 311 | PF08389 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVE3 | Leptomonas seymouri | 51% | 100% |
A0A0S4JM63 | Bodo saltans | 30% | 82% |
A0A3Q8IDX3 | Leishmania donovani | 71% | 97% |
A0A422N3F4 | Trypanosoma rangeli | 39% | 100% |
A4I2D2 | Leishmania infantum | 71% | 97% |
C9ZX76 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
E9AYI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q8Y8 | Leishmania major | 70% | 100% |