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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HD15
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016409 | palmitoyltransferase activity | 5 | 11 |
GO:0016417 | S-acyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016746 | acyltransferase activity | 3 | 11 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 11 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.222 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.372 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.342 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.572 |
DOC_CDC14_PxL_1 | 43 | 51 | PF14671 | 0.218 |
DOC_MAPK_FxFP_2 | 194 | 197 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 283 | 291 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 283 | 291 | PF00069 | 0.554 |
DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.259 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.157 |
LIG_14-3-3_CanoR_1 | 10 | 19 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 106 | 115 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.480 |
LIG_Actin_WH2_2 | 36 | 52 | PF00022 | 0.420 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.312 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.170 |
LIG_deltaCOP1_diTrp_1 | 281 | 291 | PF00928 | 0.498 |
LIG_eIF4E_1 | 62 | 68 | PF01652 | 0.170 |
LIG_eIF4E_1 | 78 | 84 | PF01652 | 0.170 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.194 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.414 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.552 |
LIG_GBD_Chelix_1 | 68 | 76 | PF00786 | 0.347 |
LIG_IBAR_NPY_1 | 111 | 113 | PF08397 | 0.554 |
LIG_LIR_Apic_2 | 191 | 197 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 313 | 320 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 38 | 49 | PF02991 | 0.205 |
LIG_LIR_Gen_1 | 79 | 89 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.250 |
LIG_MLH1_MIPbox_1 | 166 | 170 | PF16413 | 0.459 |
LIG_PCNA_yPIPBox_3 | 241 | 250 | PF02747 | 0.507 |
LIG_PDZ_Class_1 | 315 | 320 | PF00595 | 0.600 |
LIG_Pex14_2 | 129 | 133 | PF04695 | 0.459 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.380 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.351 |
LIG_Pex14_2 | 196 | 200 | PF04695 | 0.242 |
LIG_Pex14_2 | 216 | 220 | PF04695 | 0.263 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.267 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.224 |
LIG_PTB_Apo_2 | 54 | 61 | PF02174 | 0.311 |
LIG_REV1ctd_RIR_1 | 197 | 204 | PF16727 | 0.173 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.181 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.325 |
LIG_SH2_CRK | 78 | 82 | PF00017 | 0.191 |
LIG_SH2_GRB2like | 78 | 81 | PF00017 | 0.260 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.247 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.260 |
LIG_SH2_STAT3 | 240 | 243 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.289 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.500 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.182 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.540 |
LIG_SUMO_SIM_anti_2 | 210 | 217 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 210 | 217 | PF11976 | 0.253 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.555 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.253 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.490 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.170 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.459 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.177 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.419 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.627 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.269 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.322 |
MOD_N-GLC_2 | 159 | 161 | PF02516 | 0.212 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.347 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.210 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.568 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.329 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.171 |
MOD_OFUCOSY | 15 | 22 | PF10250 | 0.149 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.318 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.405 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.311 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.336 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.308 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.325 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.255 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 262 | 265 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.582 |
TRG_NLS_Bipartite_1 | 253 | 267 | PF00514 | 0.571 |
TRG_NLS_MonoExtC_3 | 262 | 268 | PF00514 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I542 | Leptomonas seymouri | 25% | 100% |
A0A0N1PEH3 | Leptomonas seymouri | 69% | 100% |
A0A0S4IYT3 | Bodo saltans | 31% | 100% |
A0A0S4J1K8 | Bodo saltans | 31% | 70% |
A0A1X0NY23 | Trypanosomatidae | 45% | 100% |
A0A3Q8ICT4 | Leishmania donovani | 78% | 100% |
A0A3R7MRW9 | Trypanosoma rangeli | 30% | 99% |
A0A3S7WX91 | Leishmania donovani | 24% | 100% |
A0A422NSP1 | Trypanosoma rangeli | 25% | 97% |
A0A422NXW5 | Trypanosoma rangeli | 48% | 100% |
A2VDT6 | Bos taurus | 28% | 100% |
A4I0K1 | Leishmania infantum | 78% | 100% |
A4IBG8 | Leishmania infantum | 22% | 100% |
B1H1H3 | Danio rerio | 30% | 100% |
C9ZVD1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D0A7S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A893 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 68% |
E7F587 | Danio rerio | 26% | 99% |
E7FH11 | Danio rerio | 31% | 69% |
E9AH03 | Leishmania infantum | 24% | 100% |
E9AWG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 71% |
F1RE57 | Danio rerio | 32% | 100% |
P59267 | Mus musculus | 28% | 87% |
Q2TGK3 | Rattus norvegicus | 30% | 100% |
Q4QB09 | Leishmania major | 78% | 100% |
Q4R7E2 | Macaca fascicularis | 24% | 85% |
Q555N7 | Dictyostelium discoideum | 26% | 89% |
Q58CU4 | Bos taurus | 24% | 85% |
Q5M757 | Arabidopsis thaliana | 30% | 100% |
Q5RB84 | Pongo abelii | 27% | 100% |
Q6DHI1 | Danio rerio | 30% | 100% |
Q8IVQ6 | Homo sapiens | 27% | 100% |
Q8R173 | Mus musculus | 30% | 100% |
Q8VYP5 | Arabidopsis thaliana | 30% | 100% |
Q94C49 | Arabidopsis thaliana | 30% | 100% |
Q969W1 | Homo sapiens | 25% | 85% |
Q9C0W9 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q9D270 | Mus musculus | 27% | 100% |
Q9ESG8 | Mus musculus | 26% | 89% |
Q9JKR5 | Rattus norvegicus | 28% | 87% |
Q9NYG2 | Homo sapiens | 31% | 100% |
Q9UIJ5 | Homo sapiens | 29% | 87% |
V5BJ88 | Trypanosoma cruzi | 43% | 100% |
V5DFI9 | Trypanosoma cruzi | 32% | 100% |