Membrane-bound O-acyltransferase involved in the remodeling of glycosylphosphatidylinositol (GPI) anchors. Related to fungal GUP1 proteins.
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A4HA83
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.625 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.378 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.596 |
DOC_ANK_TNKS_1 | 161 | 168 | PF00023 | 0.331 |
DOC_CDC14_PxL_1 | 81 | 89 | PF14671 | 0.572 |
DOC_CYCLIN_RxL_1 | 90 | 100 | PF00134 | 0.559 |
DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 256 | 265 | PF00069 | 0.648 |
DOC_PP1_RVXF_1 | 91 | 98 | PF00149 | 0.725 |
DOC_PP2B_LxvP_1 | 153 | 156 | PF13499 | 0.316 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.726 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.314 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.209 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.616 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 178 | 186 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 23 | 31 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 64 | 72 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.611 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_BRCT_BRCA1_1 | 59 | 63 | PF00533 | 0.572 |
LIG_deltaCOP1_diTrp_1 | 173 | 179 | PF00928 | 0.457 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.407 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.297 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.210 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.258 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.438 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.667 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.654 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.377 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.390 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 285 | 293 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 285 | 290 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.627 |
LIG_LYPXL_S_1 | 111 | 115 | PF13949 | 0.332 |
LIG_LYPXL_yS_3 | 112 | 115 | PF13949 | 0.533 |
LIG_NRBOX | 149 | 155 | PF00104 | 0.323 |
LIG_Pex14_1 | 350 | 354 | PF04695 | 0.522 |
LIG_PTB_Apo_2 | 106 | 113 | PF02174 | 0.539 |
LIG_PTB_Phospho_1 | 106 | 112 | PF10480 | 0.541 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.657 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.493 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.651 |
LIG_SH2_NCK_1 | 163 | 167 | PF00017 | 0.329 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.331 |
LIG_SH2_STAT3 | 349 | 352 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.581 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.451 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.604 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.645 |
LIG_Sin3_3 | 66 | 73 | PF02671 | 0.572 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.271 |
LIG_WRC_WIRS_1 | 94 | 99 | PF05994 | 0.554 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.625 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.732 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.680 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.657 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.618 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.566 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.611 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.190 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.385 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.409 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.339 |
MOD_GlcNHglycan | 249 | 253 | PF01048 | 0.384 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.437 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.689 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.660 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.500 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.603 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.656 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.699 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.641 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.469 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.654 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.665 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.592 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.282 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.604 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.631 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.461 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.377 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.361 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.209 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.631 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.318 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.664 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.605 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.310 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.550 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.562 |
MOD_PKB_1 | 91 | 99 | PF00069 | 0.558 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.216 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.590 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.660 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.313 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.247 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.239 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.440 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.384 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.613 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.612 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.517 |
TRG_DiLeu_BaEn_1 | 361 | 366 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_2 | 187 | 193 | PF01217 | 0.209 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 90 | 95 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.314 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2M9 | Leptomonas seymouri | 43% | 98% |
A0A0N1P9T2 | Leptomonas seymouri | 39% | 100% |
A0A0N1PDM7 | Leptomonas seymouri | 32% | 91% |
A4HA77 | Leishmania braziliensis | 50% | 66% |