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: 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. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | 3 | 2 |
GO:0045261 | proton-transporting ATP synthase complex, catalytic core F(1) | 4 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
Related structures:
AlphaFold database: E8NHD0
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 3 |
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:0005488 | binding | 1 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 3 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 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:0015399 | primary active transmembrane transporter activity | 4 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 3 |
GO:0022803 | passive transmembrane transporter activity | 3 | 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:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0042625 | ATPase-coupled ion transmembrane transporter activity | 3 | 3 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0044769 | ATPase activity, coupled to transmembrane movement of ions, rotational mechanism | 4 | 3 |
GO:0046933 | proton-transporting ATP synthase activity, rotational mechanism | 3 | 3 |
GO:0046961 | proton-transporting ATPase activity, rotational mechanism | 4 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.243 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.382 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.174 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.384 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.400 |
DOC_CYCLIN_yClb1_LxF_4 | 48 | 54 | PF00134 | 0.215 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.295 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.387 |
DOC_USP7_MATH_2 | 149 | 155 | PF00917 | 0.215 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.295 |
LIG_14-3-3_CanoR_1 | 211 | 216 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.174 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.215 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.236 |
LIG_APCC_ABBA_1 | 50 | 55 | PF00400 | 0.215 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.276 |
LIG_Clathr_ClatBox_1 | 51 | 55 | PF01394 | 0.215 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.253 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.265 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.215 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.203 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.215 |
LIG_GBD_Chelix_1 | 169 | 177 | PF00786 | 0.272 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.173 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.228 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.282 |
LIG_LYPXL_S_1 | 143 | 147 | PF13949 | 0.215 |
LIG_LYPXL_yS_3 | 144 | 147 | PF13949 | 0.215 |
LIG_PCNA_yPIPBox_3 | 59 | 71 | PF02747 | 0.215 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 167 | 171 | PF00017 | 0.274 |
LIG_SH2_NCK_1 | 248 | 252 | PF00017 | 0.285 |
LIG_SH2_PTP2 | 230 | 233 | PF00017 | 0.309 |
LIG_SH2_SRC | 110 | 113 | PF00017 | 0.215 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.230 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.339 |
LIG_SUMO_SIM_anti_2 | 185 | 191 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 160 | 165 | PF11976 | 0.423 |
LIG_WRC_WIRS_1 | 237 | 242 | PF05994 | 0.265 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.215 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.195 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.215 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.282 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.203 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.215 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.483 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.259 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.174 |
MOD_GlcNHglycan | 66 | 70 | PF01048 | 0.215 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.270 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.376 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.229 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.579 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.323 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.282 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.273 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.215 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.274 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.215 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.215 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.274 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.215 |
MOD_Plk_1 | 65 | 71 | PF00069 | 0.215 |
MOD_Plk_2-3 | 129 | 135 | PF00069 | 0.215 |
MOD_Plk_2-3 | 193 | 199 | PF00069 | 0.334 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.363 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.375 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 193 | 202 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 7 | 15 | PF00179 | 0.290 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.215 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.254 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.174 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.616 |
TRG_NES_CRM1_1 | 182 | 194 | PF08389 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.270 |