Most closely related to Prokaryotic SatP transporters. Especially expanded in the Leptomonas lineage
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
GO:0005886 | plasma membrane | 3 | 3 |
Related structures:
AlphaFold database: A0A3S5H538
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0006811 | monoatomic ion transport | 4 | 3 |
GO:0006820 | monoatomic anion transport | 5 | 3 |
GO:0006835 | dicarboxylic acid transport | 7 | 3 |
GO:0006846 | acetate transport | 6 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0015711 | organic anion transport | 5 | 3 |
GO:0015718 | monocarboxylic acid transport | 7 | 3 |
GO:0015740 | C4-dicarboxylate transport | 8 | 3 |
GO:0015744 | succinate transport | 6 | 3 |
GO:0015849 | organic acid transport | 5 | 3 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
GO:0035433 | acetate transmembrane transport | 5 | 3 |
GO:0046942 | carboxylic acid transport | 6 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0071422 | succinate transmembrane transport | 5 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0098656 | monoatomic anion transmembrane 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:0008028 | monocarboxylic acid transmembrane transporter activity | 5 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 3 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 3 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
GO:0015078 | proton transmembrane transporter activity | 5 | 3 |
GO:0015123 | acetate transmembrane transporter activity | 6 | 3 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 3 |
GO:0015293 | symporter activity | 5 | 3 |
GO:0015294 | solute:monoatomic cation symporter activity | 5 | 3 |
GO:0015295 | solute:proton symporter activity | 6 | 3 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
GO:0015355 | secondary active monocarboxylate transmembrane transporter activity | 5 | 3 |
GO:0015360 | acetate:proton symporter activity | 7 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 3 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 3 |
GO:0022857 | transmembrane transporter activity | 2 | 3 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
GO:0043893 | acetate:monoatomic cation symporter activity | 6 | 3 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.646 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.463 |
CLV_PCSK_FUR_1 | 48 | 52 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.444 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.575 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 264 | 271 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 144 | 154 | PF00069 | 0.528 |
DOC_MAPK_DCC_7 | 324 | 332 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 324 | 332 | PF00069 | 0.575 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.348 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.833 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 31 | 39 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.636 |
LIG_Actin_RPEL_3 | 317 | 336 | PF02755 | 0.487 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.321 |
LIG_deltaCOP1_diTrp_1 | 197 | 204 | PF00928 | 0.517 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.694 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.344 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.346 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.312 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.360 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.583 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.642 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.661 |
LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 55 | 62 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.601 |
LIG_MLH1_MIPbox_1 | 239 | 243 | PF16413 | 0.317 |
LIG_NRP_CendR_1 | 369 | 370 | PF00754 | 0.412 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.642 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.704 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.644 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.484 |
LIG_SUMO_SIM_anti_2 | 255 | 262 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.369 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.369 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.710 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.264 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.712 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.776 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.681 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.353 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.529 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.403 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.694 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.281 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.266 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.396 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.585 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.700 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.815 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.765 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.364 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.480 |
MOD_N-GLC_2 | 70 | 72 | PF02516 | 0.418 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.353 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.353 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.342 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.339 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.342 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.365 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.518 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.555 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.683 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.590 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.717 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.703 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.514 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.627 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.353 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.304 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.316 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.373 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.621 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAF6 | Leptomonas seymouri | 60% | 100% |
A0A3S5H540 | Leishmania donovani | 91% | 100% |
A4H3K6 | Leishmania braziliensis | 70% | 100% |
A4H3K7 | Leishmania braziliensis | 63% | 100% |
A4HRU8 | Leishmania infantum | 99% | 100% |
A4HRV0 | Leishmania infantum | 90% | 100% |
E9ACI2 | Leishmania major | 27% | 100% |
E9ACI3 | Leishmania major | 91% | 100% |
E9ACI5 | Leishmania major | 82% | 100% |
E9AJS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AJS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AJS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BCC6 | Trypanosoma cruzi | 35% | 100% |