Related to other eukaryotic ZDHHC palmitoyltransferases, especially animal ZDHHC2.
| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005783 | endoplasmic reticulum | 5 | 2 |
| GO:0005794 | Golgi apparatus | 5 | 2 |
| GO:0016020 | membrane | 2 | 12 |
| GO:0043226 | organelle | 2 | 2 |
| GO:0043227 | membrane-bounded organelle | 3 | 2 |
| GO:0043229 | intracellular organelle | 3 | 2 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4QB09
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006497 | protein lipidation | 5 | 2 |
| GO:0006605 | protein targeting | 5 | 2 |
| GO:0006612 | protein targeting to membrane | 5 | 2 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
| GO:0006810 | transport | 3 | 2 |
| GO:0006886 | intracellular protein transport | 4 | 2 |
| GO:0006897 | endocytosis | 5 | 2 |
| GO:0008104 | protein localization | 4 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0009987 | cellular process | 1 | 2 |
| GO:0015031 | protein transport | 4 | 2 |
| GO:0016192 | vesicle-mediated transport | 4 | 2 |
| GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
| GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
| GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
| GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
| GO:0018345 | protein palmitoylation | 6 | 2 |
| GO:0019538 | protein metabolic process | 3 | 2 |
| GO:0033036 | macromolecule localization | 2 | 2 |
| GO:0036211 | protein modification process | 4 | 2 |
| GO:0043170 | macromolecule metabolic process | 3 | 2 |
| GO:0043412 | macromolecule modification | 4 | 2 |
| GO:0043543 | protein acylation | 5 | 2 |
| GO:0044238 | primary metabolic process | 2 | 2 |
| GO:0045184 | establishment of protein localization | 3 | 2 |
| GO:0046907 | intracellular transport | 3 | 2 |
| GO:0051179 | localization | 1 | 2 |
| GO:0051234 | establishment of localization | 2 | 2 |
| GO:0051641 | cellular localization | 2 | 2 |
| GO:0051649 | establishment of localization in cell | 3 | 2 |
| GO:0051668 | localization within membrane | 3 | 2 |
| GO:0070727 | cellular macromolecule localization | 3 | 2 |
| GO:0071702 | organic substance transport | 4 | 2 |
| GO:0071704 | organic substance metabolic process | 2 | 2 |
| GO:0071705 | nitrogen compound transport | 4 | 2 |
| GO:0072657 | protein localization to membrane | 4 | 2 |
| GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0016409 | palmitoyltransferase activity | 5 | 12 |
| GO:0016417 | S-acyltransferase activity | 5 | 12 |
| GO:0016740 | transferase activity | 2 | 12 |
| GO:0016746 | acyltransferase activity | 3 | 12 |
| GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
| GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 12 |
| GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 12 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.557 |
| CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.442 |
| CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.360 |
| CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.451 |
| CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.371 |
| CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.360 |
| CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.451 |
| CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.407 |
| CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.284 |
| CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.259 |
| CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.203 |
| CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.325 |
| DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.584 |
| DOC_MAPK_FxFP_2 | 194 | 197 | PF00069 | 0.274 |
| DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.274 |
| DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.592 |
| DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.573 |
| DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.591 |
| LIG_14-3-3_CanoR_1 | 10 | 17 | PF00244 | 0.583 |
| LIG_14-3-3_CanoR_1 | 106 | 115 | PF00244 | 0.557 |
| LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.484 |
| LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.487 |
| LIG_Actin_WH2_2 | 36 | 52 | PF00022 | 0.437 |
| LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.474 |
| LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.335 |
| LIG_BRCT_BRCA1_1 | 217 | 221 | PF00533 | 0.314 |
| LIG_deltaCOP1_diTrp_1 | 282 | 292 | PF00928 | 0.517 |
| LIG_EH1_1 | 64 | 72 | PF00400 | 0.380 |
| LIG_FHA_2 | 201 | 207 | PF00498 | 0.167 |
| LIG_GBD_Chelix_1 | 68 | 76 | PF00786 | 0.390 |
| LIG_IBAR_NPY_1 | 111 | 113 | PF08397 | 0.587 |
| LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.348 |
| LIG_LIR_Apic_2 | 314 | 320 | PF02991 | 0.585 |
| LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.576 |
| LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.536 |
| LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.474 |
| LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.122 |
| LIG_LIR_Gen_1 | 218 | 229 | PF02991 | 0.314 |
| LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.573 |
| LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.621 |
| LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.505 |
| LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.122 |
| LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.314 |
| LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.524 |
| LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.255 |
| LIG_MLH1_MIPbox_1 | 166 | 170 | PF16413 | 0.474 |
| LIG_PCNA_yPIPBox_3 | 242 | 251 | PF02747 | 0.532 |
| LIG_PDZ_Class_1 | 316 | 321 | PF00595 | 0.718 |
| LIG_Pex14_2 | 129 | 133 | PF04695 | 0.474 |
| LIG_Pex14_2 | 169 | 173 | PF04695 | 0.397 |
| LIG_Pex14_2 | 190 | 194 | PF04695 | 0.359 |
| LIG_Pex14_2 | 196 | 200 | PF04695 | 0.270 |
| LIG_Pex14_2 | 232 | 236 | PF04695 | 0.290 |
| LIG_PTB_Apo_2 | 54 | 61 | PF02174 | 0.328 |
| LIG_SH2_CRK | 286 | 290 | PF00017 | 0.503 |
| LIG_SH2_CRK | 65 | 69 | PF00017 | 0.354 |
| LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.270 |
| LIG_SH2_SRC | 176 | 179 | PF00017 | 0.326 |
| LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.557 |
| LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.518 |
| LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.432 |
| LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.290 |
| LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.299 |
| LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.310 |
| LIG_SH3_3 | 288 | 294 | PF00018 | 0.499 |
| LIG_SH3_3 | 90 | 96 | PF00018 | 0.523 |
| LIG_SUMO_SIM_anti_2 | 212 | 218 | PF11976 | 0.292 |
| LIG_SUMO_SIM_par_1 | 212 | 218 | PF11976 | 0.264 |
| LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.459 |
| LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.296 |
| LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.474 |
| MOD_CK1_1 | 188 | 194 | PF00069 | 0.285 |
| MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.353 |
| MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.357 |
| MOD_GSK3_1 | 184 | 191 | PF00069 | 0.311 |
| MOD_GSK3_1 | 215 | 222 | PF00069 | 0.318 |
| MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.488 |
| MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.243 |
| MOD_NEK2_1 | 199 | 204 | PF00069 | 0.273 |
| MOD_NEK2_1 | 234 | 239 | PF00069 | 0.419 |
| MOD_NEK2_1 | 250 | 255 | PF00069 | 0.567 |
| MOD_PKB_1 | 10 | 18 | PF00069 | 0.513 |
| MOD_PKB_1 | 123 | 131 | PF00069 | 0.438 |
| MOD_Plk_1 | 200 | 206 | PF00069 | 0.234 |
| MOD_Plk_1 | 56 | 62 | PF00069 | 0.313 |
| MOD_Plk_4 | 185 | 191 | PF00069 | 0.358 |
| MOD_Plk_4 | 209 | 215 | PF00069 | 0.295 |
| MOD_Plk_4 | 220 | 226 | PF00069 | 0.342 |
| MOD_Plk_4 | 56 | 62 | PF00069 | 0.291 |
| TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.561 |
| TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.518 |
| TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.310 |
| TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.540 |
| TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.299 |
| TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.357 |
| TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.529 |
| TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.560 |
| TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.252 |
| TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.627 |
| TRG_NLS_Bipartite_1 | 254 | 268 | PF00514 | 0.570 |
| TRG_NLS_MonoExtC_3 | 263 | 269 | PF00514 | 0.556 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I542 | Leptomonas seymouri | 24% | 100% |
| A0A0N1PEH3 | Leptomonas seymouri | 75% | 100% |
| A0A0S4IYT3 | Bodo saltans | 30% | 100% |
| A0A0S4J1K8 | Bodo saltans | 30% | 70% |
| A0A0S4JCH4 | Bodo saltans | 25% | 87% |
| A0A0S4KLP7 | Bodo saltans | 29% | 79% |
| A0A1X0NUX2 | Trypanosomatidae | 25% | 87% |
| A0A1X0NVK1 | Trypanosomatidae | 23% | 100% |
| A0A1X0NY23 | Trypanosomatidae | 46% | 100% |
| A0A3Q8ICT4 | Leishmania donovani | 94% | 100% |
| A0A3R7MRW9 | Trypanosoma rangeli | 32% | 100% |
| A0A422NXW5 | Trypanosoma rangeli | 47% | 100% |
| A2VDT6 | Bos taurus | 26% | 100% |
| A4H7G8 | Leishmania braziliensis | 23% | 100% |
| A4HD15 | Leishmania braziliensis | 78% | 100% |
| A4I0K1 | Leishmania infantum | 94% | 100% |
| B1H1H3 | Danio rerio | 27% | 100% |
| C9ZVD1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
| E9AVW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 81% |
| E9AWG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
| E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 71% |
| O60069 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 90% |
| P59267 | Mus musculus | 31% | 88% |
| Q2TGK3 | Rattus norvegicus | 26% | 100% |
| Q4R7E2 | Macaca fascicularis | 24% | 85% |
| Q4WC37 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 75% |
| Q555N7 | Dictyostelium discoideum | 25% | 90% |
| Q58CU4 | Bos taurus | 23% | 85% |
| Q5M757 | Arabidopsis thaliana | 27% | 100% |
| Q5PNZ1 | Arabidopsis thaliana | 23% | 78% |
| Q5REH2 | Pongo abelii | 27% | 78% |
| Q8R173 | Mus musculus | 27% | 100% |
| Q8VYP5 | Arabidopsis thaliana | 23% | 100% |
| Q94C49 | Arabidopsis thaliana | 26% | 100% |
| Q969W1 | Homo sapiens | 24% | 85% |
| Q9D270 | Mus musculus | 27% | 100% |
| Q9ESG8 | Mus musculus | 26% | 89% |
| Q9H6R6 | Homo sapiens | 27% | 78% |
| Q9JKR5 | Rattus norvegicus | 28% | 88% |
| Q9NYG2 | Homo sapiens | 27% | 100% |
| Q9UIJ5 | Homo sapiens | 31% | 87% |
| V5B7I7 | Trypanosoma cruzi | 27% | 100% |
| V5BJ88 | Trypanosoma cruzi | 44% | 100% |
| V5DFI9 | Trypanosoma cruzi | 30% | 100% |