Protein pamitoylation, Palmitoyltransferase
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) | yes | yes: 3 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
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: A4HV16
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 | 10 |
GO:0016409 | palmitoyltransferase activity | 5 | 10 |
GO:0016417 | S-acyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016746 | acyltransferase activity | 3 | 10 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 10 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 10 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 511 | 515 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.357 |
CLV_PCSK_PC7_1 | 509 | 515 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.382 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.663 |
DOC_MAPK_gen_1 | 494 | 501 | PF00069 | 0.635 |
DOC_PP1_RVXF_1 | 495 | 502 | PF00149 | 0.619 |
DOC_PP4_FxxP_1 | 291 | 294 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.728 |
DOC_USP7_MATH_2 | 130 | 136 | PF00917 | 0.715 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.517 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 121 | 131 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 495 | 500 | PF00244 | 0.594 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.721 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.333 |
LIG_deltaCOP1_diTrp_1 | 246 | 253 | PF00928 | 0.679 |
LIG_eIF4E_1 | 351 | 357 | PF01652 | 0.306 |
LIG_EVH1_1 | 127 | 131 | PF00568 | 0.675 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.717 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.699 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.487 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.297 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.317 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.724 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.589 |
LIG_LIR_Gen_1 | 409 | 419 | PF02991 | 0.509 |
LIG_LIR_Gen_1 | 478 | 483 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 486 | 492 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.522 |
LIG_MLH1_MIPbox_1 | 448 | 452 | PF16413 | 0.333 |
LIG_PCNA_yPIPBox_3 | 329 | 337 | PF02747 | 0.380 |
LIG_Pex14_1 | 314 | 318 | PF04695 | 0.352 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.380 |
LIG_SH2_PTP2 | 321 | 324 | PF00017 | 0.405 |
LIG_SH2_SRC | 488 | 491 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.524 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.697 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.718 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.741 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.669 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.726 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.671 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.634 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.704 |
LIG_Sin3_3 | 340 | 347 | PF02671 | 0.317 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.311 |
LIG_SUMO_SIM_anti_2 | 352 | 358 | PF11976 | 0.377 |
LIG_SUMO_SIM_anti_2 | 461 | 466 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 106 | 112 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 93 | 98 | PF11976 | 0.668 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.719 |
LIG_TYR_ITSM | 484 | 491 | PF00017 | 0.504 |
LIG_UBA3_1 | 107 | 115 | PF00899 | 0.670 |
LIG_UBA3_1 | 354 | 360 | PF00899 | 0.425 |
LIG_WRC_WIRS_1 | 356 | 361 | PF05994 | 0.375 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.487 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.668 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.725 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.500 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.672 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.786 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.732 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.726 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.714 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.689 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.532 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.566 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.333 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.357 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.533 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.456 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.831 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.725 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.735 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.647 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.513 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.687 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.391 |
MOD_N-GLC_2 | 390 | 392 | PF02516 | 0.313 |
MOD_N-GLC_2 | 404 | 406 | PF02516 | 0.313 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.698 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.746 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.377 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.383 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.327 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.401 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.592 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.366 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.716 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.513 |
MOD_PKA_1 | 495 | 501 | PF00069 | 0.647 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.660 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.513 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.321 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.713 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.672 |
MOD_PKB_1 | 10 | 18 | PF00069 | 0.714 |
MOD_PKB_1 | 231 | 239 | PF00069 | 0.712 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.692 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.728 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.672 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.746 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.687 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.352 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.374 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.373 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.322 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.261 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.666 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.732 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.776 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.737 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.713 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.649 |
TRG_NLS_Bipartite_1 | 494 | 516 | PF00514 | 0.639 |
TRG_NLS_MonoCore_2 | 510 | 515 | PF00514 | 0.634 |
TRG_NLS_MonoExtC_3 | 494 | 500 | PF00514 | 0.549 |
TRG_NLS_MonoExtC_3 | 510 | 515 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 494 | 499 | PF00514 | 0.574 |
TRG_NLS_MonoExtN_4 | 509 | 516 | PF00514 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWJ0 | Leptomonas seymouri | 46% | 69% |
A0A3S7WRS6 | Leishmania donovani | 100% | 100% |
A4H6N2 | Leishmania braziliensis | 65% | 100% |
A4H6N3 | Leishmania braziliensis | 47% | 100% |
A4HV17 | Leishmania infantum | 53% | 100% |
E9ANQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9ANQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q4QGX2 | Leishmania major | 88% | 100% |