ATP metabolism, ATP synthase
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000221 | vacuolar proton-transporting V-type ATPase, V1 domain | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | 3 | 12 |
GO:0033180 | proton-transporting V-type ATPase, V1 domain | 4 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
Related structures:
AlphaFold database: A4HZD2
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015078 | proton transmembrane transporter activity | 5 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0042625 | ATPase-coupled ion transmembrane transporter activity | 3 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0044769 | ATPase activity, coupled to transmembrane movement of ions, rotational mechanism | 4 | 12 |
GO:0046961 | proton-transporting ATPase activity, rotational mechanism | 4 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.370 |
CLV_C14_Caspase3-7 | 44 | 48 | PF00656 | 0.343 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.234 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.310 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.301 |
DEG_ODPH_VHL_1 | 440 | 453 | PF01847 | 0.370 |
DEG_SCF_FBW7_1 | 374 | 381 | PF00400 | 0.358 |
DEG_SPOP_SBC_1 | 379 | 383 | PF00917 | 0.421 |
DOC_CYCLIN_RxL_1 | 13 | 23 | PF00134 | 0.448 |
DOC_CYCLIN_RxL_1 | 429 | 439 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 384 | 393 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 409 | 419 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 252 | 260 | PF00069 | 0.302 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.315 |
DOC_MAPK_NFAT4_5 | 412 | 420 | PF00069 | 0.332 |
DOC_MAPK_RevD_3 | 320 | 335 | PF00069 | 0.296 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.379 |
DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.317 |
LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.414 |
LIG_AP2alpha_1 | 145 | 149 | PF02296 | 0.370 |
LIG_BH_BH3_1 | 66 | 82 | PF00452 | 0.421 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 72 | 76 | PF00533 | 0.370 |
LIG_BRCT_BRCA1_2 | 381 | 387 | PF00533 | 0.386 |
LIG_Clathr_ClatBox_1 | 223 | 227 | PF01394 | 0.386 |
LIG_DLG_GKlike_1 | 49 | 57 | PF00625 | 0.421 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.421 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.374 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.355 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.180 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.267 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.307 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.382 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.322 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.405 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.387 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.416 |
LIG_Integrin_RGD_1 | 93 | 95 | PF01839 | 0.370 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.361 |
LIG_LRP6_Inhibitor_1 | 21 | 27 | PF00058 | 0.370 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.421 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.421 |
LIG_Pex14_1 | 222 | 226 | PF04695 | 0.287 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.421 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.456 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.358 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.390 |
LIG_SUMO_SIM_anti_2 | 10 | 16 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 229 | 235 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 216 | 221 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.358 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.448 |
LIG_TYR_ITIM | 213 | 218 | PF00017 | 0.278 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.386 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.317 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.419 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.418 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.350 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.448 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.419 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.386 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.382 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.401 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.356 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.308 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.500 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.421 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.373 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.385 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.197 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.316 |
MOD_N-GLC_1 | 140 | 145 | PF02516 | 0.442 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.333 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.313 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.343 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.301 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.525 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.313 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.418 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.409 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.350 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.386 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.421 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.421 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.421 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.413 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.448 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.389 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.319 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.427 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.317 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.414 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.356 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.441 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.302 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.375 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.376 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.287 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.448 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.317 |
MOD_SUMO_rev_2 | 268 | 274 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 79 | 87 | PF00179 | 0.234 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.317 |
TRG_NES_CRM1_1 | 10 | 23 | PF08389 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 183 | 188 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIH3 | Leptomonas seymouri | 82% | 100% |
A0A0S4JQ71 | Bodo saltans | 43% | 100% |
A0A1X0NJ38 | Trypanosomatidae | 56% | 100% |
A0A3S5H7A0 | Leishmania donovani | 100% | 100% |
A0A422NSW7 | Trypanosoma rangeli | 54% | 100% |
A4HBZ2 | Leishmania braziliensis | 87% | 100% |
D0A152 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AVB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q22494 | Caenorhabditis elegans | 28% | 100% |
Q4QC61 | Leishmania major | 98% | 100% |
Q9U5N0 | Manduca sexta | 27% | 100% |
V5B1U1 | Trypanosoma cruzi | 50% | 100% |