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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 3 |
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: E9ACI3
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 | 0.570 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.514 |
CLV_PCSK_FUR_1 | 48 | 52 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.338 |
DEG_APCC_DBOX_1 | 323 | 331 | PF00400 | 0.538 |
DEG_Kelch_Keap1_1 | 119 | 124 | PF01344 | 0.523 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 264 | 271 | PF00134 | 0.495 |
DOC_MAPK_DCC_7 | 144 | 154 | PF00069 | 0.492 |
DOC_MAPK_DCC_7 | 324 | 332 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 264 | 273 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 324 | 332 | PF00069 | 0.538 |
DOC_PP2B_LxvP_1 | 235 | 238 | PF13499 | 0.217 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.612 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.613 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.719 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.665 |
LIG_deltaCOP1_diTrp_1 | 197 | 204 | PF00928 | 0.538 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.653 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.326 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.336 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.288 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.290 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.404 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.616 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.612 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.558 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 214 | 224 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 277 | 288 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 55 | 62 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.624 |
LIG_MLH1_MIPbox_1 | 239 | 243 | PF16413 | 0.338 |
LIG_NRP_CendR_1 | 369 | 370 | PF00754 | 0.407 |
LIG_PALB2_WD40_1 | 334 | 342 | PF16756 | 0.476 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.689 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.622 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.670 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.639 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.510 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.631 |
LIG_SUMO_SIM_anti_2 | 255 | 262 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.412 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.242 |
LIG_WRC_WIRS_1 | 253 | 258 | PF05994 | 0.412 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.385 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.337 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.708 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.775 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.697 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.358 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.221 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.531 |
MOD_GlcNHglycan | 7 | 11 | PF01048 | 0.476 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.715 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.385 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.292 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.275 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.476 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.583 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.718 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.797 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.387 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.415 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.315 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.323 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.341 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.341 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.288 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.321 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.598 |
MOD_NEK2_2 | 338 | 343 | PF00069 | 0.486 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.538 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.636 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.539 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.708 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.568 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.723 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.677 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.536 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.323 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.275 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.364 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.412 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 129 | 134 | PF01217 | 0.474 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.690 |
TRG_ER_diArg_1 | 368 | 370 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.604 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAF6 | Leptomonas seymouri | 61% | 100% |
A0A3S5H538 | Leishmania donovani | 91% | 100% |
A0A3S5H540 | Leishmania donovani | 92% | 100% |
A0A451EJN9 | Leishmania donovani | 24% | 100% |
A4H3K6 | Leishmania braziliensis | 74% | 100% |
A4H3K7 | Leishmania braziliensis | 60% | 100% |
A4HRU7 | Leishmania infantum | 24% | 100% |
A4HRU8 | Leishmania infantum | 91% | 100% |
A4HRV0 | Leishmania infantum | 92% | 100% |
E9ACI2 | Leishmania major | 28% | 100% |
E9ACI5 | Leishmania major | 81% | 100% |
E9AJS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AJS2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
E9AJS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
P25613 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
V5BCC6 | Trypanosoma cruzi | 35% | 100% |