ATP metabolism, ATP synthase subunit epsilon
| 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. | yes | yes: 5 |
| 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: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 2 |
| NetGPI | no | yes: 0, no: 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000275 | mitochondrial proton-transporting ATP synthase complex, catalytic sector F(1) | 4 | 3 |
| GO:0016020 | membrane | 2 | 2 |
| GO:0032991 | protein-containing complex | 1 | 3 |
| GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | 3 | 3 |
| GO:0045261 | proton-transporting ATP synthase complex, catalytic core F(1) | 4 | 3 |
| GO:0098796 | membrane protein complex | 2 | 3 |
| GO:0098798 | mitochondrial protein-containing complex | 2 | 3 |
| GO:0098800 | inner mitochondrial membrane protein complex | 3 | 3 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pescher et al. (upgregulation) | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4ICS2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 3 |
| GO:0005215 | transporter activity | 1 | 3 |
| GO:0005216 | monoatomic ion channel activity | 4 | 3 |
| GO:0005261 | monoatomic cation channel activity | 5 | 3 |
| GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 3 |
| GO:0015078 | proton transmembrane transporter activity | 5 | 3 |
| GO:0015252 | proton channel activity | 6 | 3 |
| GO:0015267 | channel activity | 4 | 3 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 3 |
| GO:0016874 | ligase activity | 2 | 3 |
| GO:0022803 | passive transmembrane transporter activity | 3 | 3 |
| GO:0022857 | transmembrane transporter activity | 2 | 3 |
| GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 3 |
| GO:0046933 | proton-transporting ATP synthase activity, rotational mechanism | 3 | 3 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 114 | 120 | PF00089 | 0.710 |
| CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.658 |
| CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.504 |
| CLV_PCSK_FUR_1 | 145 | 149 | PF00082 | 0.725 |
| CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.726 |
| CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.658 |
| CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.519 |
| CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.726 |
| CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.660 |
| DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.484 |
| DEG_APCC_DBOX_1 | 194 | 202 | PF00400 | 0.373 |
| DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.661 |
| DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.509 |
| DOC_CKS1_1 | 140 | 145 | PF01111 | 0.415 |
| DOC_CYCLIN_yCln2_LP_2 | 122 | 128 | PF00134 | 0.506 |
| DOC_MAPK_DCC_7 | 43 | 52 | PF00069 | 0.482 |
| DOC_MAPK_gen_1 | 195 | 201 | PF00069 | 0.469 |
| DOC_MAPK_HePTP_8 | 118 | 130 | PF00069 | 0.506 |
| DOC_MAPK_HePTP_8 | 40 | 52 | PF00069 | 0.484 |
| DOC_MAPK_JIP1_4 | 5 | 11 | PF00069 | 0.544 |
| DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.507 |
| DOC_MAPK_MEF2A_6 | 43 | 52 | PF00069 | 0.482 |
| DOC_PP1_RVXF_1 | 169 | 176 | PF00149 | 0.445 |
| DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.501 |
| DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.357 |
| DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.499 |
| DOC_PP4_FxxP_1 | 236 | 239 | PF00568 | 0.421 |
| DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.495 |
| DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.357 |
| DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.517 |
| DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.439 |
| DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.509 |
| DOC_USP7_UBL2_3 | 228 | 232 | PF12436 | 0.439 |
| DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.453 |
| DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.424 |
| DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.483 |
| DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.360 |
| DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.480 |
| DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.510 |
| LIG_14-3-3_CanoR_1 | 117 | 125 | PF00244 | 0.422 |
| LIG_14-3-3_CanoR_1 | 145 | 155 | PF00244 | 0.522 |
| LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.381 |
| LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.466 |
| LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.322 |
| LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.425 |
| LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.485 |
| LIG_FHA_1 | 147 | 153 | PF00498 | 0.524 |
| LIG_FHA_1 | 216 | 222 | PF00498 | 0.404 |
| LIG_FHA_2 | 130 | 136 | PF00498 | 0.512 |
| LIG_LIR_Apic_2 | 234 | 239 | PF02991 | 0.426 |
| LIG_LIR_Apic_2 | 65 | 69 | PF02991 | 0.499 |
| LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.476 |
| LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.469 |
| LIG_LIR_Nem_3 | 209 | 213 | PF02991 | 0.320 |
| LIG_Pex14_2 | 168 | 172 | PF04695 | 0.454 |
| LIG_Pex14_2 | 49 | 53 | PF04695 | 0.485 |
| LIG_SH2_CRK | 164 | 168 | PF00017 | 0.462 |
| LIG_SH2_CRK | 45 | 49 | PF00017 | 0.480 |
| LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.405 |
| LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.523 |
| LIG_SH2_SRC | 213 | 216 | PF00017 | 0.405 |
| LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.535 |
| LIG_SH2_STAT3 | 107 | 110 | PF00017 | 0.504 |
| LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.512 |
| LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.317 |
| LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.437 |
| LIG_SH3_2 | 140 | 145 | PF14604 | 0.415 |
| LIG_SH3_3 | 10 | 16 | PF00018 | 0.424 |
| LIG_SH3_3 | 134 | 140 | PF00018 | 0.519 |
| LIG_SH3_3 | 74 | 80 | PF00018 | 0.468 |
| LIG_SH3_3 | 98 | 104 | PF00018 | 0.517 |
| LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.544 |
| LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.505 |
| LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.448 |
| LIG_TYR_ITIM | 211 | 216 | PF00017 | 0.405 |
| LIG_UBA3_1 | 52 | 56 | PF00899 | 0.498 |
| LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.424 |
| LIG_WW_1 | 124 | 127 | PF00397 | 0.508 |
| LIG_WW_3 | 142 | 146 | PF00397 | 0.418 |
| MOD_CDK_SPK_2 | 112 | 117 | PF00069 | 0.363 |
| MOD_CDK_SPxK_1 | 139 | 145 | PF00069 | 0.417 |
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.424 |
| MOD_CK1_1 | 120 | 126 | PF00069 | 0.504 |
| MOD_CK1_1 | 139 | 145 | PF00069 | 0.327 |
| MOD_CK1_1 | 160 | 166 | PF00069 | 0.474 |
| MOD_CK1_1 | 234 | 240 | PF00069 | 0.430 |
| MOD_CK1_1 | 84 | 90 | PF00069 | 0.515 |
| MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.550 |
| MOD_GSK3_1 | 112 | 119 | PF00069 | 0.510 |
| MOD_GSK3_1 | 129 | 136 | PF00069 | 0.341 |
| MOD_GSK3_1 | 7 | 14 | PF00069 | 0.424 |
| MOD_GSK3_1 | 80 | 87 | PF00069 | 0.447 |
| MOD_LATS_1 | 176 | 182 | PF00433 | 0.456 |
| MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.604 |
| MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.588 |
| MOD_NEK2_1 | 194 | 199 | PF00069 | 0.473 |
| MOD_NEK2_1 | 7 | 12 | PF00069 | 0.424 |
| MOD_NEK2_2 | 151 | 156 | PF00069 | 0.483 |
| MOD_PK_1 | 178 | 184 | PF00069 | 0.469 |
| MOD_PKA_1 | 178 | 184 | PF00069 | 0.469 |
| MOD_PKA_2 | 116 | 122 | PF00069 | 0.432 |
| MOD_PKA_2 | 158 | 164 | PF00069 | 0.486 |
| MOD_PKA_2 | 178 | 184 | PF00069 | 0.269 |
| MOD_PKA_2 | 185 | 191 | PF00069 | 0.417 |
| MOD_PKA_2 | 194 | 200 | PF00069 | 0.311 |
| MOD_PKA_2 | 234 | 240 | PF00069 | 0.430 |
| MOD_PKA_2 | 93 | 99 | PF00069 | 0.442 |
| MOD_Plk_4 | 133 | 139 | PF00069 | 0.519 |
| MOD_Plk_4 | 178 | 184 | PF00069 | 0.459 |
| MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.452 |
| MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.424 |
| MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.484 |
| MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.360 |
| MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.478 |
| MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.509 |
| MOD_SUMO_rev_2 | 248 | 258 | PF00179 | 0.456 |
| TRG_DiLeu_BaLyEn_6 | 3 | 8 | PF01217 | 0.710 |
| TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.512 |
| TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.464 |
| TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.405 |
| TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.433 |
| TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.357 |
| TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.459 |
| TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.364 |
| TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.307 |
| TRG_NES_CRM1_1 | 206 | 219 | PF08389 | 0.406 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3S7XAE3 | Leishmania donovani | 99% | 100% |