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: 1 |
NetGPI | no | yes: 0, no: 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACI4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006820 | monoatomic anion transport | 5 | 2 |
GO:0006835 | dicarboxylic acid transport | 7 | 2 |
GO:0006846 | acetate transport | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015711 | organic anion transport | 5 | 2 |
GO:0015718 | monocarboxylic acid transport | 7 | 2 |
GO:0015740 | C4-dicarboxylate transport | 8 | 2 |
GO:0015744 | succinate transport | 6 | 2 |
GO:0015849 | organic acid transport | 5 | 2 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0035433 | acetate transmembrane transport | 5 | 2 |
GO:0046942 | carboxylic acid transport | 6 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0071422 | succinate transmembrane transport | 5 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:1903825 | organic acid transmembrane transport | 3 | 2 |
GO:1905039 | carboxylic acid transmembrane transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0005342 | organic acid transmembrane transporter activity | 3 | 2 |
GO:0008028 | monocarboxylic acid transmembrane transporter activity | 5 | 2 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 2 |
GO:0008514 | organic anion transmembrane transporter activity | 5 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0015078 | proton transmembrane transporter activity | 5 | 2 |
GO:0015123 | acetate transmembrane transporter activity | 6 | 2 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 2 |
GO:0015293 | symporter activity | 5 | 2 |
GO:0015294 | solute:monoatomic cation symporter activity | 5 | 2 |
GO:0015295 | solute:proton symporter activity | 6 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 2 |
GO:0015355 | secondary active monocarboxylate transmembrane transporter activity | 5 | 2 |
GO:0015360 | acetate:proton symporter activity | 7 | 2 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 2 |
GO:0043893 | acetate:monoatomic cation symporter activity | 6 | 2 |
GO:0046943 | carboxylic acid transmembrane transporter activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.837 |
CLV_C14_Caspase3-7 | 76 | 80 | PF00656 | 0.795 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.633 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.656 |
DEG_Kelch_Keap1_1 | 77 | 82 | PF01344 | 0.781 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.844 |
DEG_SPOP_SBC_1 | 391 | 395 | PF00917 | 0.804 |
DOC_ANK_TNKS_1 | 324 | 331 | PF00023 | 0.842 |
DOC_CYCLIN_yCln2_LP_2 | 440 | 446 | PF00134 | 0.804 |
DOC_MAPK_DCC_7 | 102 | 112 | PF00069 | 0.650 |
DOC_MAPK_gen_1 | 339 | 346 | PF00069 | 0.810 |
DOC_MAPK_MEF2A_6 | 339 | 346 | PF00069 | 0.810 |
DOC_MAPK_MEF2A_6 | 366 | 375 | PF00069 | 0.805 |
DOC_MAPK_NFAT4_5 | 339 | 347 | PF00069 | 0.811 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.803 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.834 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.846 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.804 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 282 | 287 | PF00397 | 0.846 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.829 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 229 | 238 | PF00244 | 0.822 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 325 | 329 | PF00244 | 0.842 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 405 | 409 | PF00244 | 0.838 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.835 |
LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.850 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.814 |
LIG_Clathr_ClatBox_1 | 165 | 169 | PF01394 | 0.794 |
LIG_CtBP_PxDLS_1 | 437 | 441 | PF00389 | 0.802 |
LIG_DLG_GKlike_1 | 340 | 347 | PF00625 | 0.811 |
LIG_eIF4E_1 | 384 | 390 | PF01652 | 0.794 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.549 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.287 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.770 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.808 |
LIG_GSK3_LRP6_1 | 412 | 417 | PF00069 | 0.829 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.834 |
LIG_LIR_Gen_1 | 13 | 20 | PF02991 | 0.836 |
LIG_LIR_Gen_1 | 396 | 406 | PF02991 | 0.826 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.835 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.822 |
LIG_RPA_C_Fungi | 335 | 347 | PF08784 | 0.778 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.809 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.793 |
LIG_SH2_NCK_1 | 364 | 368 | PF00017 | 0.793 |
LIG_SH2_SRC | 49 | 52 | PF00017 | 0.809 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.809 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.808 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.796 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.809 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.785 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.824 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.800 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.775 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.784 |
LIG_SUMO_SIM_par_1 | 265 | 272 | PF11976 | 0.763 |
MOD_CDK_SPK_2 | 245 | 250 | PF00069 | 0.794 |
MOD_CDK_SPK_2 | 400 | 405 | PF00069 | 0.800 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.808 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.732 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.627 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.802 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.823 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.770 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.549 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.804 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.741 |
MOD_GlcNHglycan | 198 | 202 | PF01048 | 0.799 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.811 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.789 |
MOD_GlcNHglycan | 470 | 474 | PF01048 | 0.653 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.715 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.252 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.719 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.512 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.814 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.408 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.568 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.480 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.821 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.768 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.821 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.610 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.766 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.549 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.822 |
MOD_N-GLC_2 | 4 | 6 | PF02516 | 0.797 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.549 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.392 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.733 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.681 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.638 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.818 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.811 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.826 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.770 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.514 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.769 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.823 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.749 |
MOD_PKA_1 | 229 | 235 | PF00069 | 0.799 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.821 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.799 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.801 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.818 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.811 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.820 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.813 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.808 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.749 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.549 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.287 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.719 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.625 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.777 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.746 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.546 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.812 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.807 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.795 |
MOD_ProDKin_1 | 282 | 288 | PF00069 | 0.827 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.802 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.769 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.665 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.809 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.779 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.809 |
TRG_NLS_MonoExtC_3 | 225 | 230 | PF00514 | 0.811 |
TRG_NLS_MonoExtN_4 | 294 | 301 | PF00514 | 0.843 |