Phospholipid biosynthesis, acyl transferase lysophosphatidylglycerol acyl transferase
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 3, no: 7 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4I4V5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0008374 | O-acyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016746 | acyltransferase activity | 3 | 11 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
GO:0005488 | binding | 1 | 2 |
GO:0005509 | calcium ion binding | 5 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.522 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.500 |
DEG_APCC_KENBOX_2 | 239 | 243 | PF00400 | 0.333 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.669 |
DOC_CKS1_1 | 122 | 127 | PF01111 | 0.493 |
DOC_MAPK_gen_1 | 239 | 245 | PF00069 | 0.305 |
DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.613 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.498 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 181 | 189 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 253 | 260 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 347 | 355 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 98 | 103 | PF00244 | 0.580 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.253 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.357 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.321 |
LIG_BRCT_BRCA1_1 | 56 | 60 | PF00533 | 0.395 |
LIG_CaM_NSCaTE_8 | 35 | 42 | PF13499 | 0.451 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.285 |
LIG_deltaCOP1_diTrp_1 | 223 | 233 | PF00928 | 0.451 |
LIG_eIF4E_1 | 355 | 361 | PF01652 | 0.379 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.677 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.416 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.306 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.395 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.271 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.350 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.538 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.550 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.550 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.287 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.335 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.385 |
LIG_LIR_Apic_2 | 121 | 125 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 168 | 173 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.315 |
LIG_MLH1_MIPbox_1 | 243 | 247 | PF16413 | 0.329 |
LIG_NRP_CendR_1 | 412 | 415 | PF00754 | 0.608 |
LIG_PCNA_yPIPBox_3 | 375 | 389 | PF02747 | 0.319 |
LIG_Pex14_1 | 174 | 178 | PF04695 | 0.345 |
LIG_Pex14_1 | 68 | 72 | PF04695 | 0.294 |
LIG_Pex14_2 | 144 | 148 | PF04695 | 0.347 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.349 |
LIG_Pex14_2 | 327 | 331 | PF04695 | 0.277 |
LIG_PTAP_UEV_1 | 281 | 286 | PF05743 | 0.329 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.530 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.334 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 122 | 126 | PF00017 | 0.596 |
LIG_SH2_SRC | 106 | 109 | PF00017 | 0.558 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.370 |
LIG_SH2_SRC | 355 | 358 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 197 | 200 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.631 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.338 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.264 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.316 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.642 |
LIG_TRAF2_1 | 366 | 369 | PF00917 | 0.361 |
LIG_TYR_ITIM | 34 | 39 | PF00017 | 0.373 |
LIG_TYR_ITIM | 353 | 358 | PF00017 | 0.354 |
LIG_WRC_WIRS_1 | 233 | 238 | PF05994 | 0.253 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.309 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.267 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.299 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.563 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.253 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.327 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.330 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.402 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.434 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.356 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.695 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.326 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.533 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.522 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.294 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.121 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.311 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.370 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.306 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.313 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.325 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.305 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.321 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.326 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.333 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.292 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.343 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.249 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.253 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.186 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.305 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.324 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.362 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.661 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.498 |
MOD_SUMO_rev_2 | 209 | 214 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 368 | 376 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 394 | 404 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.663 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.342 |
TRG_ER_diLys_1 | 412 | 415 | PF00400 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C8 | Leptomonas seymouri | 61% | 99% |
A0A0S4IPK1 | Bodo saltans | 45% | 86% |
A0A1X0P927 | Trypanosomatidae | 48% | 88% |
A0A3R7NZP9 | Trypanosoma rangeli | 49% | 91% |
A0A3S7X2X4 | Leishmania donovani | 100% | 100% |
A4HHP0 | Leishmania braziliensis | 82% | 100% |
C9ZL05 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 89% |
E9AEA3 | Leishmania major | 94% | 100% |
E9ALI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q8BYI6 | Mus musculus | 31% | 76% |
Q8S8S2 | Arabidopsis thaliana | 29% | 77% |