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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
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: A4I0K2
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 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.500 |
DOC_CYCLIN_RxL_1 | 361 | 368 | PF00134 | 0.266 |
DOC_MAPK_gen_1 | 429 | 436 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.326 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 257 | 263 | PF00149 | 0.363 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.549 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.338 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 140 | 149 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.496 |
LIG_AP2alpha_2 | 76 | 78 | PF02296 | 0.480 |
LIG_APCC_ABBA_1 | 205 | 210 | PF00400 | 0.533 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.378 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.397 |
LIG_EVH1_2 | 222 | 226 | PF00568 | 0.532 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.513 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.481 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.418 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.527 |
LIG_GBD_Chelix_1 | 46 | 54 | PF00786 | 0.396 |
LIG_IBAR_NPY_1 | 247 | 249 | PF08397 | 0.498 |
LIG_LIR_Apic_2 | 224 | 229 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 76 | 81 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 83 | 87 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.411 |
LIG_MYND_1 | 395 | 399 | PF01753 | 0.456 |
LIG_MYND_1 | 87 | 91 | PF01753 | 0.524 |
LIG_PCNA_yPIPBox_3 | 364 | 378 | PF02747 | 0.322 |
LIG_RPA_C_Fungi | 30 | 42 | PF08784 | 0.364 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.574 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.411 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.575 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.383 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.411 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.575 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.513 |
LIG_SH2_SRC | 104 | 107 | PF00017 | 0.619 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 106 | 109 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.808 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.676 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.688 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.780 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.626 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.614 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.485 |
LIG_SUMO_SIM_par_1 | 45 | 52 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.412 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.353 |
LIG_UBA3_1 | 324 | 333 | PF00899 | 0.299 |
LIG_WW_1 | 222 | 225 | PF00397 | 0.667 |
LIG_WW_1 | 81 | 84 | PF00397 | 0.525 |
MOD_CDC14_SPxK_1 | 213 | 216 | PF00782 | 0.688 |
MOD_CDK_SPxK_1 | 182 | 188 | PF00069 | 0.606 |
MOD_CDK_SPxK_1 | 210 | 216 | PF00069 | 0.688 |
MOD_CDK_SPxxK_3 | 395 | 402 | PF00069 | 0.601 |
MOD_CDK_SPxxK_3 | 422 | 429 | PF00069 | 0.556 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.743 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.614 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.683 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.507 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.706 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.436 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.627 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.496 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.673 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.685 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.621 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.636 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.748 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.436 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.542 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.354 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.418 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.512 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.598 |
MOD_N-GLC_2 | 264 | 266 | PF02516 | 0.222 |
MOD_N-GLC_2 | 295 | 297 | PF02516 | 0.353 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.494 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.410 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.373 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.367 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.361 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.323 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.324 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.404 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.616 |
MOD_OFUCOSY | 385 | 392 | PF10250 | 0.501 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.436 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.390 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.723 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.645 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.436 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.377 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.436 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.523 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.746 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.751 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.539 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.781 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.700 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.589 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.611 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 361 | 366 | PF01217 | 0.299 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 259 | 262 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 394 | 397 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.526 |
TRG_NLS_MonoCore_2 | 392 | 397 | PF00514 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G9 | Leptomonas seymouri | 45% | 90% |
A0A3Q8ICN3 | Leishmania donovani | 100% | 100% |
A4HD16 | Leishmania braziliensis | 55% | 97% |
E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QB08 | Leishmania major | 82% | 100% |