Related to many other eukaryotic palmitoyltransferases (e.g. mammalian ZDHHC4/9/14/24)
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 15 |
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: A4HG63
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 | 15 |
GO:0016409 | palmitoyltransferase activity | 5 | 15 |
GO:0016417 | S-acyltransferase activity | 5 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016746 | acyltransferase activity | 3 | 15 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 15 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 15 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 15 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.350 |
CLV_PCSK_FUR_1 | 171 | 175 | PF00082 | 0.210 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.404 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.591 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.658 |
DOC_CDC14_PxL_1 | 249 | 257 | PF14671 | 0.162 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.286 |
DOC_CYCLIN_RxL_1 | 46 | 58 | PF00134 | 0.575 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 327 | 336 | PF00134 | 0.443 |
DOC_MAPK_gen_1 | 205 | 214 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 46 | 54 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 77 | 84 | PF00069 | 0.612 |
DOC_MAPK_JIP1_4 | 48 | 54 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 320 | 329 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 203 | 210 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 48 | 55 | PF00149 | 0.581 |
DOC_PP1_RVXF_1 | 75 | 82 | PF00149 | 0.605 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.554 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 333 | 337 | PF12436 | 0.572 |
DOC_USP7_UBL2_3 | 46 | 50 | PF12436 | 0.698 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 208 | 213 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 65 | 73 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 135 | 153 | PF00022 | 0.436 |
LIG_CtBP_PxDLS_1 | 40 | 44 | PF00389 | 0.534 |
LIG_eIF4E_1 | 231 | 237 | PF01652 | 0.303 |
LIG_eIF4E_1 | 274 | 280 | PF01652 | 0.162 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.286 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.312 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.396 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.391 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.357 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.303 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.693 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.538 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.420 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.447 |
LIG_HP1_1 | 325 | 329 | PF01393 | 0.446 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.543 |
LIG_LYPXL_S_1 | 146 | 150 | PF13949 | 0.280 |
LIG_LYPXL_yS_3 | 147 | 150 | PF13949 | 0.485 |
LIG_MYND_1 | 41 | 45 | PF01753 | 0.597 |
LIG_NRBOX | 278 | 284 | PF00104 | 0.415 |
LIG_NRBOX | 318 | 324 | PF00104 | 0.619 |
LIG_NRBOX | 331 | 337 | PF00104 | 0.450 |
LIG_PCNA_yPIPBox_3 | 309 | 323 | PF02747 | 0.547 |
LIG_Pex14_1 | 209 | 213 | PF04695 | 0.277 |
LIG_Pex14_1 | 227 | 231 | PF04695 | 0.277 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.317 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.514 |
LIG_SH2_PTP2 | 299 | 302 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 18 | 21 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.532 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.586 |
LIG_SH3_4 | 46 | 53 | PF00018 | 0.687 |
LIG_SUMO_SIM_anti_2 | 99 | 105 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 280 | 285 | PF11976 | 0.363 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.277 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.662 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.546 |
LIG_WW_3 | 174 | 178 | PF00397 | 0.477 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 41 | 48 | PF00069 | 0.674 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.350 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.321 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.722 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.441 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.616 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.568 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.405 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.540 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.529 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.315 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.414 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.238 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.293 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.337 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.562 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.635 |
MOD_LATS_1 | 64 | 70 | PF00433 | 0.425 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.284 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.574 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.304 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.292 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.260 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.291 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.345 |
MOD_NEK2_2 | 213 | 218 | PF00069 | 0.279 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.362 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.543 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.353 |
MOD_PKA_1 | 309 | 315 | PF00069 | 0.475 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.502 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.363 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.466 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.598 |
MOD_Plk_2-3 | 346 | 352 | PF00069 | 0.547 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.636 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.212 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.401 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.529 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.324 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.693 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.705 |
TRG_DiLeu_BaLyEn_6 | 331 | 336 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.311 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 171 | 174 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 275 | 285 | PF08389 | 0.162 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P729 | Leptomonas seymouri | 30% | 100% |
A0A0N1HZ19 | Leptomonas seymouri | 59% | 100% |
A0A0S4IT15 | Bodo saltans | 41% | 100% |
A0A0S4IXZ6 | Bodo saltans | 29% | 100% |
A0A0S4JCH4 | Bodo saltans | 25% | 97% |
A0A0S4JRL4 | Bodo saltans | 40% | 99% |
A0A1X0NX08 | Trypanosomatidae | 41% | 100% |
A0A3Q8ICY2 | Leishmania donovani | 71% | 100% |
A0A3Q8IIC8 | Leishmania donovani | 27% | 93% |
A0A3R7N519 | Trypanosoma rangeli | 38% | 100% |
A4HCH5 | Leishmania braziliensis | 24% | 89% |
A4HMS9 | Leishmania braziliensis | 30% | 100% |
A4I395 | Leishmania infantum | 71% | 100% |
A4IBG8 | Leishmania infantum | 27% | 93% |
B3DN87 | Arabidopsis thaliana | 27% | 100% |
D0A7S1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AF82 | Leishmania major | 27% | 100% |
E9AZI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9B6D8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
O74384 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O80685 | Arabidopsis thaliana | 27% | 87% |
Q06551 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 99% |
Q0WQK2 | Arabidopsis thaliana | 25% | 81% |
Q4Q8P8 | Leishmania major | 72% | 99% |
Q5PNZ1 | Arabidopsis thaliana | 27% | 86% |
Q6FSS4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 29% | 100% |
Q9FLM3 | Arabidopsis thaliana | 26% | 87% |
Q9NXF8 | Homo sapiens | 24% | 100% |
V5BC02 | Trypanosoma cruzi | 40% | 100% |