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: 10 |
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. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000275 | mitochondrial proton-transporting ATP synthase complex, catalytic sector F(1) | 4 | 4 |
GO:0032991 | protein-containing complex | 1 | 4 |
GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | 3 | 4 |
GO:0045261 | proton-transporting ATP synthase complex, catalytic core F(1) | 4 | 4 |
GO:0098796 | membrane protein complex | 2 | 4 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 4 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 4 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7XAE3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005215 | transporter activity | 1 | 4 |
GO:0005216 | monoatomic ion channel activity | 4 | 4 |
GO:0005261 | monoatomic cation channel activity | 5 | 4 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 4 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 4 |
GO:0015078 | proton transmembrane transporter activity | 5 | 4 |
GO:0015252 | proton channel activity | 6 | 4 |
GO:0015267 | channel activity | 4 | 4 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 4 |
GO:0016874 | ligase activity | 2 | 4 |
GO:0022803 | passive transmembrane transporter activity | 3 | 4 |
GO:0022857 | transmembrane transporter activity | 2 | 4 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 4 |
GO:0046933 | proton-transporting ATP synthase activity, rotational mechanism | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 115 | 121 | PF00089 | 0.721 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.760 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.540 |
CLV_PCSK_FUR_1 | 146 | 150 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.760 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 148 | 150 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.756 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 195 | 203 | PF00400 | 0.454 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 123 | 129 | PF00134 | 0.524 |
DOC_MAPK_DCC_7 | 44 | 53 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 196 | 202 | PF00069 | 0.549 |
DOC_MAPK_HePTP_8 | 119 | 131 | PF00069 | 0.522 |
DOC_MAPK_HePTP_8 | 41 | 53 | PF00069 | 0.502 |
DOC_MAPK_JIP1_4 | 6 | 12 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 122 | 131 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.483 |
DOC_PP2B_LxvP_1 | 123 | 126 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.512 |
DOC_PP4_FxxP_1 | 237 | 240 | PF00568 | 0.495 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.529 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.512 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 118 | 126 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 146 | 156 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 157 | 165 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 196 | 200 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.499 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.503 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.617 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.482 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.533 |
LIG_GSK3_LRP6_1 | 141 | 146 | PF00069 | 0.480 |
LIG_LIR_Apic_2 | 235 | 240 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 66 | 70 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.478 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.474 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.506 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.560 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.502 |
LIG_SH2_GRB2like | 214 | 217 | PF00017 | 0.478 |
LIG_SH2_GRB2like | 89 | 92 | PF00017 | 0.520 |
LIG_SH2_SRC | 214 | 217 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 108 | 111 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.514 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.399 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.598 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.498 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.522 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.542 |
LIG_TRAF2_1 | 107 | 110 | PF00917 | 0.510 |
LIG_TRAF2_1 | 252 | 255 | PF00917 | 0.403 |
LIG_TYR_ITIM | 212 | 217 | PF00017 | 0.477 |
LIG_UBA3_1 | 53 | 57 | PF00899 | 0.461 |
LIG_WRC_WIRS_1 | 9 | 14 | PF05994 | 0.399 |
LIG_WW_1 | 125 | 128 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 141 | 146 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.479 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.521 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.399 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.569 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.545 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.406 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.514 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.606 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.593 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.420 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.399 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.480 |
MOD_LATS_1 | 177 | 183 | PF00433 | 0.483 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.678 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.658 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.542 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.477 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.357 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.488 |
MOD_NEK2_2 | 152 | 157 | PF00069 | 0.539 |
MOD_PK_1 | 179 | 185 | PF00069 | 0.490 |
MOD_PKA_1 | 179 | 185 | PF00069 | 0.490 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.522 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.564 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.390 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.464 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.371 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.505 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.520 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.539 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.564 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.613 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.399 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.419 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.560 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.514 |
MOD_SUMO_rev_2 | 249 | 259 | PF00179 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 4 | 9 | PF01217 | 0.711 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.310 |
TRG_ER_diArg_1 | 169 | 172 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.337 |
TRG_NES_CRM1_1 | 207 | 220 | PF08389 | 0.479 |