This conserved lipid acyltransferase has many re-entrant segments but only one true TM helix. Most closely related to bacterial acyltransferases.. Heavily expanded in kinetoplastids for unknown reasons. 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. | yes | yes: 27 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: A0A3S5H5E4
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 4 |
GO:0006644 | phospholipid metabolic process | 4 | 4 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 4 |
GO:0006654 | phosphatidic acid biosynthetic process | 6 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0008610 | lipid biosynthetic process | 4 | 4 |
GO:0008654 | phospholipid biosynthetic process | 5 | 4 |
GO:0009058 | biosynthetic process | 2 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0019637 | organophosphate metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044249 | cellular biosynthetic process | 3 | 4 |
GO:0044255 | cellular lipid metabolic process | 3 | 4 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 4 |
GO:0046473 | phosphatidic acid metabolic process | 6 | 4 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 4 |
GO:0046486 | glycerolipid metabolic process | 4 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090407 | organophosphate biosynthetic process | 4 | 4 |
GO:1901576 | organic substance biosynthetic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 22 |
GO:0016740 | transferase activity | 2 | 22 |
GO:0016746 | acyltransferase activity | 3 | 22 |
GO:0003841 | 1-acylglycerol-3-phosphate O-acyltransferase activity | 7 | 4 |
GO:0008374 | O-acyltransferase activity | 5 | 4 |
GO:0016411 | acylglycerol O-acyltransferase activity | 6 | 4 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 4 |
GO:0042171 | lysophosphatidic acid acyltransferase activity | 6 | 4 |
GO:0071617 | lysophospholipid acyltransferase activity | 5 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.330 |
CLV_MEL_PAP_1 | 280 | 286 | PF00089 | 0.552 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.379 |
CLV_PCSK_FUR_1 | 119 | 123 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.379 |
CLV_PCSK_PC7_1 | 75 | 81 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.296 |
DOC_CYCLIN_RxL_1 | 255 | 265 | PF00134 | 0.289 |
DOC_MAPK_DCC_7 | 145 | 153 | PF00069 | 0.331 |
DOC_MAPK_DCC_7 | 191 | 199 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 145 | 153 | PF00069 | 0.309 |
DOC_MAPK_MEF2A_6 | 145 | 153 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 155 | 163 | PF00069 | 0.271 |
DOC_MAPK_MEF2A_6 | 191 | 199 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 200 | 207 | PF00149 | 0.324 |
DOC_PP1_RVXF_1 | 223 | 229 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.541 |
DOC_PP2B_LxvP_1 | 182 | 185 | PF13499 | 0.616 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 46 | 50 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 69 | 77 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.573 |
LIG_APCC_ABBA_1 | 323 | 328 | PF00400 | 0.277 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.563 |
LIG_deltaCOP1_diTrp_1 | 365 | 371 | PF00928 | 0.306 |
LIG_EH1_1 | 157 | 165 | PF00400 | 0.234 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.419 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.504 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.539 |
LIG_GBD_Chelix_1 | 135 | 143 | PF00786 | 0.433 |
LIG_LIR_Gen_1 | 129 | 139 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 247 | 257 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.291 |
LIG_LIR_LC3C_4 | 173 | 177 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 129 | 135 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.310 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.549 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.430 |
LIG_Pex14_2 | 277 | 281 | PF04695 | 0.350 |
LIG_Pex14_2 | 287 | 291 | PF04695 | 0.347 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.289 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.581 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.276 |
LIG_SH2_STAT3 | 187 | 190 | PF00017 | 0.234 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.270 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.216 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.559 |
LIG_TYR_ITIM | 139 | 144 | PF00017 | 0.419 |
LIG_WRC_WIRS_1 | 343 | 348 | PF05994 | 0.336 |
MOD_CDK_SPxK_1 | 252 | 258 | PF00069 | 0.362 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.369 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.419 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.447 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.359 |
MOD_CMANNOS | 368 | 371 | PF00535 | 0.428 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.384 |
MOD_Cter_Amidation | 2 | 5 | PF01082 | 0.433 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.409 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.328 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.250 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.426 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.448 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.429 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.417 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.427 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.368 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.308 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.404 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.455 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.425 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.439 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.321 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.411 |
MOD_PK_1 | 108 | 114 | PF00069 | 0.359 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.444 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.444 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.456 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.435 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.444 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.418 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.418 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.452 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.371 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.481 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.462 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.315 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.303 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.345 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.462 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.462 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.423 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.419 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.450 |
MOD_SUMO_for_1 | 107 | 110 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 391 | 400 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 414 | 424 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 426 | 432 | PF00179 | 0.466 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.432 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.439 |
TRG_NES_CRM1_1 | 380 | 393 | PF08389 | 0.366 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTP4 | Leptomonas seymouri | 66% | 100% |
A0A0S4JRB2 | Bodo saltans | 31% | 100% |
A0A3R7NKA0 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H7L8 | Leishmania donovani | 34% | 100% |
A0A3S7WNW6 | Leishmania donovani | 50% | 100% |
A4H419 | Leishmania braziliensis | 66% | 100% |
A4H420 | Leishmania braziliensis | 54% | 100% |
A4HHM7 | Leishmania braziliensis | 32% | 100% |
A4HSA1 | Leishmania infantum | 99% | 100% |
A4HSA2 | Leishmania infantum | 52% | 100% |
A4I4U1 | Leishmania infantum | 30% | 100% |
A4I4U2 | Leishmania infantum | 34% | 100% |
C9ZLI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AE89 | Leishmania major | 31% | 100% |
E9AE90 | Leishmania major | 33% | 100% |
E9AK86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9ALJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q9NF90 | Leishmania major | 52% | 100% |
Q9NF91 | Leishmania major | 89% | 100% |
V5C201 | Trypanosoma cruzi | 32% | 100% |