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: A4HBZ2
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_NRD_NRD_1 | 178 | 180 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.256 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.301 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.241 |
DEG_APCC_KENBOX_2 | 187 | 191 | PF00400 | 0.161 |
DEG_SCF_FBW7_1 | 374 | 381 | PF00400 | 0.298 |
DEG_SPOP_SBC_1 | 379 | 383 | PF00917 | 0.384 |
DOC_CYCLIN_RxL_1 | 13 | 24 | PF00134 | 0.304 |
DOC_CYCLIN_RxL_1 | 429 | 439 | PF00134 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 438 | 444 | PF00134 | 0.161 |
DOC_MAPK_gen_1 | 178 | 187 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 249 | 258 | PF00069 | 0.241 |
DOC_MAPK_gen_1 | 384 | 393 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 409 | 419 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 252 | 260 | PF00069 | 0.254 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 49 | 57 | PF00069 | 0.252 |
DOC_MAPK_RevD_3 | 320 | 335 | PF00069 | 0.234 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 438 | 441 | PF13499 | 0.173 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.370 |
DOC_USP7_UBL2_3 | 272 | 276 | PF12436 | 0.304 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.254 |
LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.397 |
LIG_BH_BH3_1 | 66 | 82 | PF00452 | 0.384 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.163 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.273 |
LIG_BRCT_BRCA1_2 | 305 | 311 | PF00533 | 0.161 |
LIG_BRCT_BRCA1_2 | 381 | 387 | PF00533 | 0.333 |
LIG_Clathr_ClatBox_1 | 223 | 227 | PF01394 | 0.333 |
LIG_DLG_GKlike_1 | 49 | 57 | PF00625 | 0.384 |
LIG_eIF4E_1 | 228 | 234 | PF01652 | 0.384 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.317 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.316 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.240 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.203 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.333 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.277 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.366 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.276 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.338 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.161 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.118 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.375 |
LIG_LIR_Gen_1 | 142 | 152 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 181 | 185 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 360 | 365 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.118 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.384 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.384 |
LIG_Pex14_1 | 222 | 226 | PF04695 | 0.239 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.384 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.249 |
LIG_REV1ctd_RIR_1 | 184 | 191 | PF16727 | 0.188 |
LIG_SH2_GRB2like | 273 | 276 | PF00017 | 0.298 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.161 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.239 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.161 |
LIG_Sin3_3 | 105 | 112 | PF02671 | 0.353 |
LIG_SUMO_SIM_anti_2 | 10 | 16 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 229 | 235 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 216 | 221 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 413 | 420 | PF11976 | 0.161 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.304 |
LIG_UBA3_1 | 401 | 406 | PF00899 | 0.268 |
LIG_WRC_WIRS_1 | 191 | 196 | PF05994 | 0.161 |
LIG_WRC_WIRS_1 | 223 | 228 | PF05994 | 0.333 |
LIG_WRC_WIRS_1 | 359 | 364 | PF05994 | 0.254 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.435 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.173 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.287 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.304 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.384 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.168 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.118 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.333 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.341 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.379 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.375 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.297 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.175 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.254 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.482 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.384 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.321 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.337 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.188 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.257 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.243 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.247 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.268 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.275 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.297 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.174 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.239 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.507 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.254 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.237 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.390 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.347 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.333 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.384 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.384 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.384 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.304 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.329 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.245 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.251 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.408 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.273 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.372 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.350 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.328 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.376 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.169 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.256 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.328 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.333 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.250 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.268 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.304 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.254 |
MOD_SUMO_for_1 | 391 | 394 | PF00179 | 0.161 |
MOD_SUMO_rev_2 | 268 | 274 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_1 | 227 | 232 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.333 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.303 |
TRG_NES_CRM1_1 | 10 | 23 | PF08389 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IIH3 | Leptomonas seymouri | 83% | 100% |
A0A0S4JQ71 | Bodo saltans | 43% | 100% |
A0A1X0NJ38 | Trypanosomatidae | 56% | 100% |
A0A3S5H7A0 | Leishmania donovani | 87% | 100% |
A0A422NSW7 | Trypanosoma rangeli | 53% | 100% |
A4HZD2 | Leishmania infantum | 87% | 100% |
D0A152 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AVB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O14265 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q4QC61 | Leishmania major | 87% | 100% |
Q9U5N0 | Manduca sexta | 27% | 100% |
Q9V3J1 | Drosophila melanogaster | 31% | 100% |
V5B1U1 | Trypanosoma cruzi | 50% | 100% |