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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
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 |
Related structures:
AlphaFold database: E9AWG3
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:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein 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 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 14 |
GO:0016409 | palmitoyltransferase activity | 5 | 14 |
GO:0016417 | S-acyltransferase activity | 5 | 14 |
GO:0016740 | transferase activity | 2 | 14 |
GO:0016746 | acyltransferase activity | 3 | 14 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 14 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 14 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 14 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.691 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.352 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.302 |
DOC_CYCLIN_RxL_1 | 414 | 427 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 35 | 43 | PF00069 | 0.202 |
DOC_MAPK_gen_1 | 431 | 438 | PF00069 | 0.590 |
DOC_MAPK_HePTP_8 | 33 | 45 | PF00069 | 0.202 |
DOC_MAPK_MEF2A_6 | 302 | 311 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 36 | 45 | PF00069 | 0.298 |
DOC_PP1_RVXF_1 | 259 | 265 | PF00149 | 0.459 |
DOC_PP1_RVXF_1 | 339 | 345 | PF00149 | 0.295 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.631 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.598 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 128 | 138 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 417 | 423 | PF00244 | 0.551 |
LIG_AP2alpha_2 | 76 | 78 | PF02296 | 0.547 |
LIG_APCC_ABBA_1 | 150 | 155 | PF00400 | 0.627 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.537 |
LIG_CtBP_PxDLS_1 | 86 | 92 | PF00389 | 0.553 |
LIG_EVH1_1 | 241 | 245 | PF00568 | 0.613 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.658 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.432 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.530 |
LIG_GBD_Chelix_1 | 11 | 19 | PF00786 | 0.206 |
LIG_GBD_Chelix_1 | 46 | 54 | PF00786 | 0.379 |
LIG_IBAR_NPY_1 | 249 | 251 | PF08397 | 0.669 |
LIG_Integrin_isoDGR_2 | 259 | 261 | PF01839 | 0.202 |
LIG_IRF3_LxIS_1 | 350 | 357 | PF10401 | 0.206 |
LIG_LIR_Apic_2 | 76 | 81 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.544 |
LIG_MYND_1 | 87 | 91 | PF01753 | 0.610 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.380 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.664 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.362 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.529 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 314 | 318 | PF00017 | 0.376 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.301 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.531 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.373 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.855 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.661 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.647 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.243 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.615 |
LIG_SUMO_SIM_par_1 | 17 | 24 | PF11976 | 0.206 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.339 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.361 |
LIG_WW_1 | 81 | 84 | PF00397 | 0.575 |
LIG_WW_3 | 160 | 164 | PF00397 | 0.632 |
MOD_CDC14_SPxK_1 | 160 | 163 | PF00782 | 0.628 |
MOD_CDK_SPxK_1 | 157 | 163 | PF00069 | 0.635 |
MOD_CDK_SPxxK_3 | 121 | 128 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 397 | 404 | PF00069 | 0.565 |
MOD_CDK_SPxxK_3 | 424 | 431 | PF00069 | 0.549 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.713 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.609 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.510 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.558 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.498 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.433 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.421 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.703 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.715 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.719 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.802 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.344 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.621 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.340 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.557 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.436 |
MOD_N-GLC_2 | 297 | 299 | PF02516 | 0.311 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.642 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.378 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.406 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.320 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.328 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.347 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.255 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.658 |
MOD_PIKK_1 | 360 | 366 | PF00454 | 0.286 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.694 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.648 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.308 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.450 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.517 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.304 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.766 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.689 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.707 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.717 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.703 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.610 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.585 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.302 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.506 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.593 |
TRG_NLS_MonoExtN_4 | 125 | 132 | PF00514 | 0.643 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G9 | Leptomonas seymouri | 42% | 91% |
A0A3Q8ICN3 | Leishmania donovani | 77% | 100% |
A0A3Q8ICT4 | Leishmania donovani | 30% | 100% |
A0A3S7WXW1 | Leishmania donovani | 28% | 100% |
A4HD15 | Leishmania braziliensis | 29% | 100% |
A4HD16 | Leishmania braziliensis | 53% | 97% |
A4I0K1 | Leishmania infantum | 30% | 100% |
A4I0K2 | Leishmania infantum | 77% | 100% |
A4I0K3 | Leishmania infantum | 28% | 100% |
E9AWG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4QB08 | Leishmania major | 75% | 100% |
Q4QB09 | Leishmania major | 28% | 100% |