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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
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: A4HD16
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:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein 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 | 8 |
GO:0016409 | palmitoyltransferase activity | 5 | 8 |
GO:0016417 | S-acyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 8 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.285 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.527 |
DEG_ODPH_VHL_1 | 54 | 67 | PF01847 | 0.249 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.638 |
DOC_ANK_TNKS_1 | 91 | 98 | PF00023 | 0.624 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.397 |
DOC_CYCLIN_RxL_1 | 412 | 424 | PF00134 | 0.558 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.316 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.356 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.562 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.766 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.662 |
LIG_AP2alpha_2 | 334 | 336 | PF02296 | 0.226 |
LIG_AP2alpha_2 | 76 | 78 | PF02296 | 0.652 |
LIG_APCC_ABBA_1 | 194 | 199 | PF00400 | 0.717 |
LIG_BIR_III_2 | 239 | 243 | PF00653 | 0.606 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.580 |
LIG_Clathr_ClatBox_1 | 328 | 332 | PF01394 | 0.475 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.811 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.655 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.642 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.327 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.342 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.603 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.738 |
LIG_GBD_Chelix_1 | 42 | 50 | PF00786 | 0.393 |
LIG_IBAR_NPY_1 | 247 | 249 | PF08397 | 0.679 |
LIG_IRF3_LxIS_1 | 133 | 140 | PF10401 | 0.634 |
LIG_LIR_Apic_2 | 76 | 81 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 8 | 19 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.305 |
LIG_LYPXL_yS_3 | 80 | 83 | PF13949 | 0.492 |
LIG_MYND_1 | 87 | 91 | PF01753 | 0.746 |
LIG_Pex14_1 | 427 | 431 | PF04695 | 0.548 |
LIG_Rb_LxCxE_1 | 385 | 405 | PF01857 | 0.564 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.430 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.404 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.430 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.653 |
LIG_SH2_GRB2like | 245 | 248 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.501 |
LIG_SH2_SRC | 245 | 248 | PF00017 | 0.536 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.808 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.195 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.390 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.675 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.249 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.596 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.681 |
LIG_SUMO_SIM_anti_2 | 10 | 16 | PF11976 | 0.348 |
LIG_SUMO_SIM_anti_2 | 189 | 195 | PF11976 | 0.636 |
LIG_SUMO_SIM_anti_2 | 44 | 52 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 44 | 52 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.400 |
LIG_TRAF2_2 | 234 | 239 | PF00917 | 0.616 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.341 |
LIG_WW_1 | 242 | 245 | PF00397 | 0.592 |
LIG_WW_1 | 81 | 84 | PF00397 | 0.622 |
MOD_CDK_SPK_2 | 429 | 434 | PF00069 | 0.492 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.640 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.712 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.705 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.634 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.554 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.618 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.513 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.311 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.503 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.504 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.712 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.702 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.690 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.595 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.690 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.519 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.710 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.621 |
MOD_N-GLC_2 | 295 | 297 | PF02516 | 0.299 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.639 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.635 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.517 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.429 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.346 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.374 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.626 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.764 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.608 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.660 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.737 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.365 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.382 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.446 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.430 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.775 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.760 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.700 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.595 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.397 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.550 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.635 |
MOD_SUMO_rev_2 | 399 | 403 | PF00179 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 159 | 164 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.626 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G9 | Leptomonas seymouri | 40% | 90% |
A0A3Q8ICN3 | Leishmania donovani | 55% | 100% |
A4I0K2 | Leishmania infantum | 55% | 100% |
D0A6R2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 96% |
E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 53% | 100% |
Q4QB08 | Leishmania major | 52% | 98% |