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) | 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. | yes | yes: 18 |
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: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: A0A3Q8ICU7
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 | 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_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.793 |
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.613 |
CLV_MEL_PAP_1 | 80 | 86 | PF00089 | 0.464 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.416 |
CLV_Separin_Metazoa | 118 | 122 | PF03568 | 0.740 |
DEG_APCC_DBOX_1 | 249 | 257 | PF00400 | 0.666 |
DEG_APCC_DBOX_1 | 262 | 270 | PF00400 | 0.627 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.598 |
DEG_APCC_DBOX_1 | 500 | 508 | PF00400 | 0.654 |
DEG_Kelch_Keap1_1 | 218 | 223 | PF01344 | 0.745 |
DEG_SIAH_1 | 593 | 601 | PF03145 | 0.763 |
DOC_CKS1_1 | 475 | 480 | PF01111 | 0.715 |
DOC_CYCLIN_yCln2_LP_2 | 468 | 474 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 244 | 255 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.684 |
DOC_MAPK_MEF2A_6 | 497 | 504 | PF00069 | 0.692 |
DOC_MAPK_NFAT4_5 | 497 | 505 | PF00069 | 0.693 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.593 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.673 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.811 |
DOC_USP7_MATH_2 | 77 | 83 | PF00917 | 0.684 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 167 | 171 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.628 |
LIG_Actin_WH2_2 | 152 | 169 | PF00022 | 0.753 |
LIG_AP2alpha_1 | 492 | 496 | PF02296 | 0.672 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.749 |
LIG_APCC_ABBAyCdc20_2 | 186 | 192 | PF00400 | 0.749 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.735 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.438 |
LIG_EH1_1 | 16 | 24 | PF00400 | 0.633 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.661 |
LIG_eIF4E_1 | 333 | 339 | PF01652 | 0.461 |
LIG_eIF4E_1 | 340 | 346 | PF01652 | 0.410 |
LIG_eIF4E_1 | 41 | 47 | PF01652 | 0.552 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.717 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.786 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.667 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.707 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.666 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.376 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.754 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.735 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.709 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.657 |
LIG_GBD_Chelix_1 | 50 | 58 | PF00786 | 0.352 |
LIG_LIR_Apic_2 | 280 | 286 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.734 |
LIG_LIR_Gen_1 | 29 | 39 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 331 | 341 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 357 | 366 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 372 | 382 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.735 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 427 | 432 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.483 |
LIG_NRBOX | 405 | 411 | PF00104 | 0.718 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.471 |
LIG_PCNA_PIPBox_1 | 347 | 356 | PF02747 | 0.492 |
LIG_PCNA_yPIPBox_3 | 11 | 20 | PF02747 | 0.656 |
LIG_Pex14_1 | 358 | 362 | PF04695 | 0.328 |
LIG_Pex14_2 | 27 | 31 | PF04695 | 0.349 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.492 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.700 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.376 |
LIG_PTAP_UEV_1 | 589 | 594 | PF05743 | 0.683 |
LIG_PTB_Apo_2 | 327 | 334 | PF02174 | 0.598 |
LIG_PTB_Phospho_1 | 327 | 333 | PF10480 | 0.598 |
LIG_REV1ctd_RIR_1 | 360 | 369 | PF16727 | 0.395 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.695 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.588 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.585 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.568 |
LIG_SH2_SRC | 395 | 398 | PF00017 | 0.560 |
LIG_SH2_SRC | 429 | 432 | PF00017 | 0.779 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.162 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.743 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.162 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.362 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.754 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.620 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.756 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.758 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.514 |
LIG_SUMO_SIM_anti_2 | 254 | 259 | PF11976 | 0.670 |
LIG_SUMO_SIM_anti_2 | 48 | 54 | PF11976 | 0.330 |
LIG_SUMO_SIM_anti_2 | 566 | 573 | PF11976 | 0.742 |
LIG_SUMO_SIM_par_1 | 254 | 259 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 573 | 578 | PF11976 | 0.673 |
LIG_TRAF2_1 | 172 | 175 | PF00917 | 0.780 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.789 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.716 |
LIG_TYR_ITIM | 338 | 343 | PF00017 | 0.438 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.423 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.507 |
LIG_WRC_WIRS_1 | 89 | 94 | PF05994 | 0.471 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.685 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.809 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.376 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.720 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.763 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.734 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.641 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.498 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.415 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.712 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.692 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.549 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.598 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.700 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.729 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.486 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.348 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.521 |
MOD_GlcNHglycan | 442 | 447 | PF01048 | 0.731 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.702 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.711 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.714 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.525 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.522 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.696 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.711 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.773 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.454 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.717 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.762 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.621 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.708 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.465 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.720 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.492 |
MOD_N-GLC_2 | 289 | 291 | PF02516 | 0.492 |
MOD_N-GLC_2 | 309 | 311 | PF02516 | 0.162 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.661 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.787 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.391 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.389 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.381 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.657 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.381 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.356 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.279 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.390 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.723 |
MOD_PIKK_1 | 195 | 201 | PF00454 | 0.591 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.625 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.699 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.777 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.566 |
MOD_PKB_1 | 501 | 509 | PF00069 | 0.627 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.683 |
MOD_Plk_1 | 567 | 573 | PF00069 | 0.597 |
MOD_Plk_2-3 | 512 | 518 | PF00069 | 0.644 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.401 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.249 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.354 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.562 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.484 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.412 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.535 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.657 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.654 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.713 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.616 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.781 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.723 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.711 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_2 | 278 | 284 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.162 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.625 |
TRG_ER_diArg_1 | 556 | 559 | PF00400 | 0.683 |
TRG_NES_CRM1_1 | 232 | 246 | PF08389 | 0.681 |
TRG_NLS_MonoExtC_3 | 246 | 251 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 244 | 251 | PF00514 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7C7 | Leptomonas seymouri | 50% | 96% |
A0A3S5IRN1 | Trypanosoma rangeli | 25% | 100% |
A4H754 | Leishmania braziliensis | 74% | 100% |
A4HVJ3 | Leishmania infantum | 100% | 100% |
E9AP89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QG89 | Leishmania major | 92% | 100% |
V5AVF5 | Trypanosoma cruzi | 27% | 100% |