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:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 7 |
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 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4QB08
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 |
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 | 123 | 127 | PF00656 | 0.444 |
CLV_C14_Caspase3-7 | 154 | 158 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.545 |
CLV_PCSK_FUR_1 | 407 | 411 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.603 |
DOC_CDC14_PxL_1 | 83 | 91 | PF14671 | 0.350 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.279 |
DOC_MAPK_gen_1 | 429 | 436 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 257 | 263 | PF00149 | 0.295 |
DOC_PP1_RVXF_1 | 337 | 343 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.503 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 67 | 70 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.441 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.320 |
LIG_14-3-3_CanoR_1 | 131 | 136 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.407 |
LIG_AP2alpha_2 | 76 | 78 | PF02296 | 0.384 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.306 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.315 |
LIG_EVH1_2 | 222 | 226 | PF00568 | 0.466 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.486 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.473 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.558 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.292 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.474 |
LIG_IBAR_NPY_1 | 247 | 249 | PF08397 | 0.402 |
LIG_LIR_Apic_2 | 76 | 81 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.338 |
LIG_MYND_1 | 395 | 399 | PF01753 | 0.389 |
LIG_PCNA_yPIPBox_3 | 368 | 378 | PF02747 | 0.267 |
LIG_Pex14_2 | 99 | 103 | PF04695 | 0.407 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.352 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.435 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.312 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.386 |
LIG_SH2_NCK_1 | 249 | 253 | PF00017 | 0.288 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 84 | 88 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.200 |
LIG_SH2_STAT5 | 6 | 9 | PF00017 | 0.279 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.568 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.267 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.356 |
LIG_SUMO_SIM_anti_2 | 169 | 175 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.325 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.352 |
LIG_WW_1 | 222 | 225 | PF00397 | 0.464 |
LIG_WW_1 | 81 | 84 | PF00397 | 0.337 |
MOD_CDC14_SPxK_1 | 213 | 216 | PF00782 | 0.478 |
MOD_CDK_SPxK_1 | 210 | 216 | PF00069 | 0.483 |
MOD_CDK_SPxxK_3 | 395 | 402 | PF00069 | 0.409 |
MOD_CDK_SPxxK_3 | 422 | 429 | PF00069 | 0.385 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.535 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.481 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.381 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.740 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.547 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.697 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.488 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.543 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.542 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.340 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.368 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.314 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.293 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.474 |
MOD_N-GLC_2 | 295 | 297 | PF02516 | 0.501 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.419 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.334 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.354 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.359 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.328 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.340 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.506 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.444 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.457 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.443 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.428 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.295 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.369 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.524 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.573 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.513 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.566 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.469 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.398 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.437 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.279 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 259 | 262 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 394 | 397 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 407 | 410 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 428 | 430 | PF00400 | 0.367 |
TRG_NES_CRM1_1 | 334 | 349 | PF08389 | 0.421 |
TRG_NLS_MonoCore_2 | 392 | 397 | PF00514 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6G9 | Leptomonas seymouri | 43% | 90% |
A0A3Q8ICN3 | Leishmania donovani | 82% | 100% |
A4HD16 | Leishmania braziliensis | 52% | 100% |
A4I0K2 | Leishmania infantum | 82% | 100% |
E9AWG3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |