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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005886 | plasma membrane | 3 | 3 |
Related structures:
AlphaFold database: E9AJS2
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_NRD_NRD_1 | 144 | 146 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.451 |
CLV_PCSK_FUR_1 | 49 | 53 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.377 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.577 |
DOC_MAPK_DCC_7 | 145 | 155 | PF00069 | 0.530 |
DOC_MAPK_DCC_7 | 325 | 333 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 265 | 274 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 325 | 333 | PF00069 | 0.577 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.807 |
LIG_14-3-3_CanoR_1 | 49 | 59 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 99 | 104 | PF00244 | 0.726 |
LIG_Actin_RPEL_3 | 318 | 337 | PF02755 | 0.486 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.698 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.636 |
LIG_deltaCOP1_diTrp_1 | 198 | 205 | PF00928 | 0.516 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.677 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.346 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.344 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.405 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.359 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.583 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.658 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.617 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.245 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 256 | 264 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 56 | 63 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.609 |
LIG_LYPXL_S_1 | 14 | 18 | PF13949 | 0.419 |
LIG_LYPXL_yS_3 | 15 | 18 | PF13949 | 0.617 |
LIG_MLH1_MIPbox_1 | 240 | 244 | PF16413 | 0.316 |
LIG_Pex14_1 | 339 | 343 | PF04695 | 0.510 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.647 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.689 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.697 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 276 | 281 | PF11976 | 0.369 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.369 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.524 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.605 |
MOD_CDK_SPK_2 | 361 | 366 | PF00069 | 0.604 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.605 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.204 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.771 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.585 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.676 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.527 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.455 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.446 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.250 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.309 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.374 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.610 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.703 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.478 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.457 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.429 |
MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.528 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.332 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.337 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.323 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.340 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.378 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.386 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.516 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.624 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.643 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.615 |
MOD_PKA_1 | 359 | 365 | PF00069 | 0.605 |
MOD_PKA_1 | 82 | 88 | PF00069 | 0.681 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.606 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.706 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.630 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.698 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.275 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.491 |
MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.562 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.613 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.340 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.329 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.310 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.321 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.373 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.605 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.650 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 48 | 51 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAF6 | Leptomonas seymouri | 59% | 100% |
A0A3S5H538 | Leishmania donovani | 80% | 100% |
A0A3S5H540 | Leishmania donovani | 89% | 100% |
A0A451EJN9 | Leishmania donovani | 25% | 100% |
A4H3K6 | Leishmania braziliensis | 75% | 100% |
A4H3K7 | Leishmania braziliensis | 67% | 100% |
A4HRU8 | Leishmania infantum | 80% | 100% |
A4HRV0 | Leishmania infantum | 89% | 100% |
E9ACI2 | Leishmania major | 28% | 100% |
E9ACI3 | Leishmania major | 78% | 100% |
E9ACI5 | Leishmania major | 78% | 100% |
E9AJS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AJS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5BCC6 | Trypanosoma cruzi | 35% | 100% |