Palmitoyltransferase. Leishmaniids have +2 extra TM segments at the N-terminus while all other Kinetoplastids typically only have the 4 core ones.. Localization: ER (by homology)
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:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
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 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AVC4
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:0006897 | endocytosis | 5 | 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:0016192 | vesicle-mediated 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 | 126 | 130 | PF00656 | 0.710 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.728 |
CLV_MEL_PAP_1 | 552 | 558 | PF00089 | 0.279 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 461 | 463 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 550 | 552 | PF00675 | 0.403 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 401 | 403 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 461 | 463 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 550 | 552 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.630 |
DEG_APCC_DBOX_1 | 254 | 262 | PF00400 | 0.655 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.481 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.611 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.660 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.633 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.411 |
DOC_CYCLIN_RxL_1 | 458 | 469 | PF00134 | 0.370 |
DOC_CYCLIN_RxL_1 | 496 | 505 | PF00134 | 0.667 |
DOC_CYCLIN_yCln2_LP_2 | 423 | 429 | PF00134 | 0.348 |
DOC_MAPK_gen_1 | 311 | 320 | PF00069 | 0.665 |
DOC_MAPK_gen_1 | 550 | 558 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 307 | 314 | PF00069 | 0.673 |
DOC_MAPK_MEF2A_6 | 440 | 449 | PF00069 | 0.218 |
DOC_MAPK_MEF2A_6 | 551 | 560 | PF00069 | 0.609 |
DOC_MAPK_RevD_3 | 236 | 251 | PF00069 | 0.689 |
DOC_PP1_RVXF_1 | 36 | 43 | PF00149 | 0.521 |
DOC_PP1_RVXF_1 | 497 | 504 | PF00149 | 0.608 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.674 |
DOC_PP2B_LxvP_1 | 331 | 334 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 423 | 426 | PF13499 | 0.348 |
DOC_PP2B_PxIxI_1 | 215 | 221 | PF00149 | 0.685 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.521 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 172 | 181 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 263 | 272 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 285 | 290 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.274 |
LIG_14-3-3_CanoR_1 | 544 | 552 | PF00244 | 0.626 |
LIG_AP2alpha_1 | 503 | 507 | PF02296 | 0.594 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.685 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.500 |
LIG_CaM_NSCaTE_8 | 376 | 383 | PF13499 | 0.370 |
LIG_Clathr_ClatBox_1 | 295 | 299 | PF01394 | 0.692 |
LIG_DLG_GKlike_1 | 250 | 257 | PF00625 | 0.636 |
LIG_eIF4E_1 | 458 | 464 | PF01652 | 0.407 |
LIG_eIF4E_1 | 578 | 584 | PF01652 | 0.666 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.767 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.527 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.370 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.348 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.378 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.566 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.271 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.666 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.771 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.736 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.521 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.551 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.649 |
LIG_HP1_1 | 74 | 78 | PF01393 | 0.275 |
LIG_Integrin_RGD_1 | 225 | 227 | PF01839 | 0.528 |
LIG_LIR_Apic_2 | 111 | 115 | PF02991 | 0.711 |
LIG_LIR_Apic_2 | 490 | 494 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 454 | 464 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 53 | 60 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 72 | 83 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 563 | 568 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 580 | 584 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.262 |
LIG_LYPXL_SIV_4 | 426 | 434 | PF13949 | 0.348 |
LIG_NRBOX | 291 | 297 | PF00104 | 0.692 |
LIG_NRBOX | 77 | 83 | PF00104 | 0.370 |
LIG_Pex14_1 | 561 | 565 | PF04695 | 0.600 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.631 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.682 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.703 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.530 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.633 |
LIG_SH2_GRB2like | 458 | 461 | PF00017 | 0.407 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.407 |
LIG_SH2_PTP2 | 75 | 78 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.341 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.760 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.691 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.666 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.687 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.348 |
LIG_SH3_3 | 573 | 579 | PF00018 | 0.681 |
LIG_SUMO_SIM_par_1 | 293 | 299 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 80 | 86 | PF11976 | 0.256 |
LIG_TYR_ITIM | 386 | 391 | PF00017 | 0.370 |
LIG_TYR_ITIM | 73 | 78 | PF00017 | 0.407 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.531 |
LIG_WRC_WIRS_1 | 51 | 56 | PF05994 | 0.407 |
LIG_WRC_WIRS_1 | 565 | 570 | PF05994 | 0.525 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 84 | 89 | PF05994 | 0.407 |
LIG_WW_1 | 107 | 110 | PF00397 | 0.609 |
LIG_WW_3 | 308 | 312 | PF00397 | 0.588 |
MOD_CDC14_SPxK_1 | 410 | 413 | PF00782 | 0.407 |
MOD_CDK_SPK_2 | 167 | 172 | PF00069 | 0.593 |
MOD_CDK_SPK_2 | 188 | 193 | PF00069 | 0.633 |
MOD_CDK_SPxK_1 | 407 | 413 | PF00069 | 0.407 |
MOD_CDK_SPxxK_3 | 186 | 193 | PF00069 | 0.541 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.745 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.646 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.496 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.357 |
MOD_CK2_1 | 291 | 297 | PF00069 | 0.655 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.434 |
MOD_CMANNOS | 373 | 376 | PF00535 | 0.407 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.617 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.579 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.719 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.681 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.561 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.566 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.690 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.548 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.623 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.521 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.407 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.370 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.498 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.565 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.455 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.442 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.507 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.407 |
MOD_N-GLC_1 | 487 | 492 | PF02516 | 0.445 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.341 |
MOD_N-GLC_2 | 357 | 359 | PF02516 | 0.407 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.382 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.498 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.473 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.407 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.407 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.220 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.231 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.471 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.540 |
MOD_NEK2_2 | 470 | 475 | PF00069 | 0.370 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.659 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.562 |
MOD_PKA_1 | 250 | 256 | PF00069 | 0.538 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.636 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.463 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.274 |
MOD_PKA_2 | 543 | 549 | PF00069 | 0.410 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.735 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.506 |
MOD_Plk_1 | 466 | 472 | PF00069 | 0.407 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.470 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.664 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.590 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.407 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.389 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.239 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.487 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.677 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.722 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.522 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.578 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.407 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.440 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.523 |
TRG_DiLeu_LyEn_5 | 588 | 593 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.352 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 400 | 402 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.218 |
TRG_ER_diArg_1 | 550 | 552 | PF00400 | 0.524 |
TRG_NLS_MonoExtC_3 | 397 | 402 | PF00514 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 401 | 406 | PF00026 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 461 | 466 | PF00026 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 550 | 554 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IAF5 | Leishmania donovani | 88% | 84% |
A4HC51 | Leishmania braziliensis | 68% | 100% |
A4HZD7 | Leishmania infantum | 88% | 100% |
Q4QC55 | Leishmania major | 87% | 100% |
Q4QC56 | Leishmania major | 87% | 100% |