Related to other Eukaryotic ZDHHC-type palmitoyltransferases (e.g animal ZDHHC20).
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
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: E9B3K1
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 | 9 |
GO:0016409 | palmitoyltransferase activity | 5 | 9 |
GO:0016417 | S-acyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 9 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.383 |
DEG_APCC_KENBOX_2 | 296 | 300 | PF00400 | 0.275 |
DOC_CKS1_1 | 400 | 405 | PF01111 | 0.605 |
DOC_MAPK_gen_1 | 128 | 137 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.643 |
DOC_MAPK_MEF2A_6 | 265 | 272 | PF00069 | 0.484 |
DOC_PP4_FxxP_1 | 140 | 143 | PF00568 | 0.702 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.732 |
DOC_PP4_FxxP_1 | 45 | 48 | PF00568 | 0.416 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.511 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.395 |
LIG_14-3-3_CanoR_1 | 128 | 137 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 168 | 173 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 305 | 314 | PF00244 | 0.185 |
LIG_14-3-3_CanoR_1 | 363 | 368 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 369 | 379 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 413 | 418 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 502 | 510 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 513 | 519 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.526 |
LIG_APCC_ABBA_1 | 435 | 440 | PF00400 | 0.636 |
LIG_BIR_III_2 | 406 | 410 | PF00653 | 0.692 |
LIG_BRCT_BRCA1_1 | 349 | 353 | PF00533 | 0.437 |
LIG_Clathr_ClatBox_1 | 102 | 106 | PF01394 | 0.474 |
LIG_EH1_1 | 109 | 117 | PF00400 | 0.474 |
LIG_eIF4E_1 | 264 | 270 | PF01652 | 0.484 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.474 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.369 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.351 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.289 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.392 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.624 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.432 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.692 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 138 | 143 | PF02991 | 0.700 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.736 |
LIG_LIR_Apic_2 | 229 | 233 | PF02991 | 0.555 |
LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.447 |
LIG_LIR_Apic_2 | 43 | 48 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 493 | 499 | PF02991 | 0.779 |
LIG_LIR_Gen_1 | 6 | 17 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 71 | 82 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.663 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.779 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.356 |
LIG_NRBOX | 267 | 273 | PF00104 | 0.425 |
LIG_Pex14_1 | 478 | 482 | PF04695 | 0.463 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.388 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.580 |
LIG_REV1ctd_RIR_1 | 477 | 483 | PF16727 | 0.600 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.579 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.669 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.555 |
LIG_SH2_CRK | 30 | 34 | PF00017 | 0.394 |
LIG_SH2_GRB2like | 220 | 223 | PF00017 | 0.492 |
LIG_SH2_GRB2like | 380 | 383 | PF00017 | 0.650 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.669 |
LIG_SH2_SRC | 248 | 251 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.362 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 460 | 464 | PF00017 | 0.719 |
LIG_SH2_STAT3 | 488 | 491 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.721 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.507 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.295 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.704 |
LIG_SUMO_SIM_anti_2 | 10 | 16 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 10 | 16 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 268 | 274 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.354 |
LIG_TYR_ITIM | 271 | 276 | PF00017 | 0.337 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.686 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.726 |
LIG_WW_3 | 231 | 235 | PF00397 | 0.555 |
LIG_WW_3 | 318 | 322 | PF00397 | 0.377 |
MOD_CDK_SPK_2 | 399 | 404 | PF00069 | 0.712 |
MOD_CDK_SPxxK_3 | 314 | 321 | PF00069 | 0.355 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.760 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.671 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.427 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.744 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.696 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.560 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.699 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.525 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.524 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.456 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.681 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.745 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.464 |
MOD_DYRK1A_RPxSP_1 | 146 | 150 | PF00069 | 0.764 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.421 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.525 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.575 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.420 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.423 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.360 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.509 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.491 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.665 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.558 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.702 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.668 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.661 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.663 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.437 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.337 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.337 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.770 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.680 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.512 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.526 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.492 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.284 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.691 |
MOD_N-GLC_2 | 222 | 224 | PF02516 | 0.355 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.150 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.646 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.362 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.555 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.351 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.226 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.345 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.298 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.674 |
MOD_NEK2_2 | 504 | 509 | PF00069 | 0.748 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.681 |
MOD_PKA_1 | 306 | 312 | PF00069 | 0.185 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.681 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.267 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.771 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.543 |
MOD_PKB_1 | 305 | 313 | PF00069 | 0.185 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.484 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.654 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.660 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.377 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.337 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.391 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.337 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.337 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.345 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.290 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.519 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.716 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.371 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.768 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.355 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.775 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.387 |
TRG_DiLeu_BaEn_1 | 548 | 553 | PF01217 | 0.689 |
TRG_DiLeu_BaEn_4 | 548 | 554 | PF01217 | 0.689 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.718 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 518 | 521 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 125 | 128 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.766 |
TRG_ER_diArg_1 | 469 | 472 | PF00400 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 432 | 436 | PF00026 | 0.400 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U1 | Leptomonas seymouri | 61% | 98% |
A0A1X0P0I7 | Trypanosomatidae | 34% | 100% |
A0A3R7KZF6 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X6D2 | Leishmania donovani | 92% | 100% |
A4I8P0 | Leishmania infantum | 92% | 100% |
D0A4L6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q4K0 | Leishmania major | 91% | 100% |