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: 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. | no | 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 |
Related structures:
AlphaFold database: A4H9G4
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 | 192 | 194 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.369 |
CLV_PCSK_FUR_1 | 284 | 288 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.353 |
CLV_PCSK_PC1ET2_1 | 372 | 374 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.371 |
DOC_CDC14_PxL_1 | 39 | 47 | PF14671 | 0.386 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.436 |
DOC_MAPK_DCC_7 | 72 | 81 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 193 | 201 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 313 | 322 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 24 | 30 | PF00149 | 0.525 |
DOC_PP2B_LxvP_1 | 360 | 363 | PF13499 | 0.472 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.386 |
DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.436 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.351 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.408 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.246 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.370 |
LIG_14-3-3_CanoR_1 | 120 | 128 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 165 | 174 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 332 | 350 | PF00022 | 0.351 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.351 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.418 |
LIG_deltaCOP1_diTrp_1 | 238 | 244 | PF00928 | 0.351 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.516 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.472 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.344 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.698 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.472 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.457 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.513 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.385 |
LIG_HP1_1 | 401 | 405 | PF01393 | 0.424 |
LIG_LIR_Apic_2 | 248 | 252 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 399 | 410 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 4 | 11 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 226 | 231 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.712 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.168 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.314 |
LIG_LYPXL_S_1 | 377 | 381 | PF13949 | 0.367 |
LIG_LYPXL_yS_3 | 378 | 381 | PF13949 | 0.367 |
LIG_LYPXL_yS_3 | 400 | 403 | PF13949 | 0.461 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.436 |
LIG_Pex14_1 | 239 | 243 | PF04695 | 0.351 |
LIG_SH2_PTP2 | 249 | 252 | PF00017 | 0.472 |
LIG_SH2_PTP2 | 402 | 405 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.498 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.386 |
LIG_TRFH_1 | 349 | 353 | PF08558 | 0.351 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.661 |
LIG_WRC_WIRS_1 | 123 | 128 | PF05994 | 0.472 |
LIG_WW_3 | 351 | 355 | PF00397 | 0.351 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.517 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.386 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.434 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.331 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.368 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.356 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.351 |
MOD_GlcNHglycan | 113 | 118 | PF01048 | 0.453 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.435 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.246 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.436 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.504 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.397 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.299 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.436 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.429 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.365 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.455 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.192 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.365 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.435 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.362 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.366 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.351 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.558 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.462 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.498 |
MOD_NEK2_2 | 197 | 202 | PF00069 | 0.386 |
MOD_NEK2_2 | 401 | 406 | PF00069 | 0.415 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.408 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.410 |
MOD_PK_1 | 118 | 124 | PF00069 | 0.370 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.382 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.367 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.248 |
MOD_Plk_2-3 | 297 | 303 | PF00069 | 0.240 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.745 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.292 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.381 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.401 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.269 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.361 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.537 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.351 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.370 |
MOD_SUMO_rev_2 | 146 | 155 | PF00179 | 0.472 |
MOD_SUMO_rev_2 | 277 | 282 | PF00179 | 0.367 |
MOD_SUMO_rev_2 | 297 | 307 | PF00179 | 0.168 |
MOD_SUMO_rev_2 | 312 | 318 | PF00179 | 0.424 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.694 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.436 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.472 |
TRG_NES_CRM1_1 | 32 | 46 | PF08389 | 0.382 |
TRG_NES_CRM1_1 | 380 | 392 | PF08389 | 0.659 |
TRG_NLS_Bipartite_1 | 273 | 289 | PF00514 | 0.351 |
TRG_NLS_MonoCore_2 | 283 | 288 | PF00514 | 0.367 |
TRG_NLS_MonoExtN_4 | 284 | 289 | PF00514 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 202 | 206 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2N6 | Leptomonas seymouri | 85% | 100% |
A0A0S4IV71 | Bodo saltans | 54% | 98% |
A0A1X0P723 | Trypanosomatidae | 69% | 100% |
A0A3S5IRA4 | Trypanosoma rangeli | 64% | 100% |
A0A3S7WV19 | Leishmania donovani | 88% | 100% |
A4HXT1 | Leishmania infantum | 88% | 100% |
D0A063 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9ARJ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P21282 | Bos taurus | 31% | 100% |
P21283 | Homo sapiens | 31% | 100% |
P31412 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P54648 | Dictyostelium discoideum | 28% | 100% |
Q4QDY6 | Leishmania major | 85% | 100% |
Q4R5H9 | Macaca fascicularis | 31% | 100% |
Q5FVI6 | Rattus norvegicus | 31% | 100% |
Q5RDQ7 | Pongo abelii | 31% | 100% |
Q5XH14 | Xenopus laevis | 31% | 100% |
Q5XIY6 | Danio rerio | 32% | 100% |
Q612A4 | Caenorhabditis briggsae | 28% | 100% |
Q6P4Y9 | Xenopus tropicalis | 31% | 100% |
Q7T385 | Danio rerio | 30% | 100% |
Q9HDW6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9NDR5 | Ascidia sydneiensis samea | 31% | 100% |
Q9SCB9 | Hordeum vulgare | 30% | 100% |
Q9SDS7 | Arabidopsis thaliana | 30% | 100% |
Q9U5N1 | Manduca sexta | 29% | 100% |
Q9XXU9 | Caenorhabditis elegans | 28% | 100% |
Q9Z1G3 | Mus musculus | 31% | 100% |
V5B6H3 | Trypanosoma cruzi | 67% | 100% |