Acidocalcisome, vacuolar ATP synthase subunit c
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: 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. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
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 |
GO:0000221 | vacuolar proton-transporting V-type ATPase, V1 domain | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
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: A0A3S7WV19
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
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 | 8 |
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_NRD_NRD_1 | 19 | 21 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.271 |
CLV_PCSK_FUR_1 | 284 | 288 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.220 |
CLV_PCSK_PC1ET2_1 | 372 | 374 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.367 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.417 |
DOC_CDC14_PxL_1 | 39 | 47 | PF14671 | 0.253 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.312 |
DOC_MAPK_DCC_7 | 72 | 81 | PF00069 | 0.233 |
DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.218 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.218 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.219 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.233 |
DOC_PP1_RVXF_1 | 10 | 16 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 360 | 363 | PF13499 | 0.361 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.253 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.361 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.249 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.280 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.253 |
LIG_14-3-3_CanoR_1 | 120 | 128 | PF00244 | 0.228 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.386 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.218 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.218 |
LIG_deltaCOP1_diTrp_1 | 238 | 244 | PF00928 | 0.218 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.362 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.234 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.593 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.361 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.339 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.279 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.460 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.255 |
LIG_HP1_1 | 401 | 405 | PF01393 | 0.294 |
LIG_LIR_Apic_2 | 248 | 252 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.221 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.234 |
LIG_LIR_Gen_1 | 399 | 410 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.233 |
LIG_LYPXL_S_1 | 377 | 381 | PF13949 | 0.233 |
LIG_LYPXL_yS_3 | 378 | 381 | PF13949 | 0.233 |
LIG_LYPXL_yS_3 | 400 | 403 | PF13949 | 0.331 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.312 |
LIG_Pex14_1 | 239 | 243 | PF04695 | 0.258 |
LIG_Pex14_2 | 71 | 75 | PF04695 | 0.246 |
LIG_PTB_Apo_2 | 209 | 216 | PF02174 | 0.185 |
LIG_PTB_Phospho_1 | 209 | 215 | PF10480 | 0.185 |
LIG_SH2_PTP2 | 249 | 252 | PF00017 | 0.361 |
LIG_SH2_PTP2 | 402 | 405 | PF00017 | 0.263 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.217 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.361 |
LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.368 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.258 |
LIG_SUMO_SIM_par_1 | 26 | 32 | PF11976 | 0.381 |
LIG_TRFH_1 | 349 | 353 | PF08558 | 0.218 |
LIG_WRC_WIRS_1 | 123 | 128 | PF05994 | 0.361 |
LIG_WW_3 | 351 | 355 | PF00397 | 0.218 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.253 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.308 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.396 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.234 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.381 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.239 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.254 |
MOD_GlcNHglycan | 113 | 118 | PF01048 | 0.361 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.302 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.377 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.312 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.264 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.174 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.312 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.385 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.330 |
MOD_LATS_1 | 19 | 25 | PF00433 | 0.392 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.231 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.337 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.105 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.268 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.355 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.310 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.235 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.234 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.413 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.459 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.363 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.321 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.253 |
MOD_NEK2_2 | 401 | 406 | PF00069 | 0.285 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.220 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.304 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.236 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.309 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.233 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.553 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.300 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.163 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.218 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.382 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.242 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.438 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.218 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.253 |
MOD_SUMO_rev_2 | 146 | 155 | PF00179 | 0.361 |
MOD_SUMO_rev_2 | 277 | 282 | PF00179 | 0.233 |
MOD_SUMO_rev_2 | 312 | 318 | PF00179 | 0.296 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.218 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.230 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.385 |
TRG_NES_CRM1_1 | 222 | 236 | PF08389 | 0.211 |
TRG_NES_CRM1_1 | 32 | 46 | PF08389 | 0.222 |
TRG_NES_CRM1_1 | 380 | 392 | PF08389 | 0.270 |
TRG_NLS_Bipartite_1 | 273 | 289 | PF00514 | 0.218 |
TRG_NLS_MonoCore_2 | 283 | 288 | PF00514 | 0.233 |
TRG_NLS_MonoExtN_4 | 284 | 289 | PF00514 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.361 |
TRG_Pf-PMV_PEXEL_1 | 305 | 309 | PF00026 | 0.296 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2N6 | Leptomonas seymouri | 87% | 100% |
A0A0S4IV71 | Bodo saltans | 54% | 98% |
A0A1X0P723 | Trypanosomatidae | 70% | 100% |
A0A3S5IRA4 | Trypanosoma rangeli | 64% | 100% |
A4H9G4 | Leishmania braziliensis | 88% | 100% |
A4HXT1 | Leishmania infantum | 100% | 100% |
D0A063 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9ARJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
P21282 | Bos taurus | 30% | 100% |
P21283 | Homo sapiens | 30% | 100% |
P31412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P54648 | Dictyostelium discoideum | 28% | 100% |
Q4QDY6 | Leishmania major | 95% | 100% |
Q4R5H9 | Macaca fascicularis | 30% | 100% |
Q5FVI6 | Rattus norvegicus | 30% | 100% |
Q5RDQ7 | Pongo abelii | 30% | 100% |
Q5XH14 | Xenopus laevis | 31% | 100% |
Q5XIY6 | Danio rerio | 31% | 100% |
Q612A4 | Caenorhabditis briggsae | 27% | 100% |
Q6AYE4 | Rattus norvegicus | 26% | 97% |
Q6P4Y9 | Xenopus tropicalis | 31% | 100% |
Q7T385 | Danio rerio | 29% | 100% |
Q8NEY4 | Homo sapiens | 26% | 96% |
Q99L60 | Mus musculus | 26% | 96% |
Q9HDW6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9NDR5 | Ascidia sydneiensis samea | 31% | 100% |
Q9SCB9 | Hordeum vulgare | 27% | 100% |
Q9SDS7 | Arabidopsis thaliana | 29% | 100% |
Q9U5N1 | Manduca sexta | 28% | 100% |
Q9XXU9 | Caenorhabditis elegans | 27% | 100% |
Q9Z1G3 | Mus musculus | 30% | 100% |
V5B6H3 | Trypanosoma cruzi | 68% | 100% |