A large family of glycosyltransferases expanded in parazitic kinetoplastids (and even more in T cruzi). Localization: ER (by homology)
Glycolipid biosynthesis, Beta galactofuranosyl transferase LPG1
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: 37 |
NetGPI | no | yes: 0, no: 37 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4I143
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 38 |
GO:0016740 | transferase activity | 2 | 38 |
GO:0016757 | glycosyltransferase activity | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 15 | 21 | PF00089 | 0.177 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.534 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.527 |
CLV_PCSK_PC7_1 | 361 | 367 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.355 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.493 |
DOC_CYCLIN_RxL_1 | 117 | 124 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.251 |
DOC_MAPK_DCC_7 | 79 | 89 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 10 | 19 | PF00069 | 0.636 |
DOC_MAPK_gen_1 | 417 | 426 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.344 |
DOC_PP1_RVXF_1 | 317 | 324 | PF00149 | 0.319 |
DOC_PP1_RVXF_1 | 423 | 430 | PF00149 | 0.260 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.364 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.530 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.286 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 228 | 235 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 69 | 73 | PF00244 | 0.402 |
LIG_Actin_WH2_2 | 203 | 220 | PF00022 | 0.274 |
LIG_APCC_ABBA_1 | 374 | 379 | PF00400 | 0.268 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.744 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.389 |
LIG_eIF4E_1 | 133 | 139 | PF01652 | 0.356 |
LIG_eIF4E_1 | 22 | 28 | PF01652 | 0.226 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.345 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.352 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.378 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.227 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.419 |
LIG_FXI_DFP_1 | 426 | 430 | PF00024 | 0.432 |
LIG_HCF-1_HBM_1 | 298 | 301 | PF13415 | 0.381 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 418 | 422 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.341 |
LIG_NRBOX | 20 | 26 | PF00104 | 0.373 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.232 |
LIG_PTB_Apo_2 | 110 | 117 | PF02174 | 0.353 |
LIG_PTB_Apo_2 | 219 | 226 | PF02174 | 0.240 |
LIG_PTB_Apo_2 | 339 | 346 | PF02174 | 0.282 |
LIG_PTB_Phospho_1 | 339 | 345 | PF10480 | 0.280 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.438 |
LIG_SH2_PTP2 | 30 | 33 | PF00017 | 0.223 |
LIG_SH2_PTP2 | 82 | 85 | PF00017 | 0.217 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.238 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.213 |
LIG_SH2_STAP1 | 422 | 426 | PF00017 | 0.256 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.203 |
LIG_SH2_STAT3 | 345 | 348 | PF00017 | 0.397 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.235 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.371 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.419 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.381 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.421 |
LIG_TRFH_1 | 82 | 86 | PF08558 | 0.453 |
LIG_TYR_ITIM | 80 | 85 | PF00017 | 0.247 |
LIG_ULM_U2AF65_1 | 365 | 370 | PF00076 | 0.372 |
LIG_WRC_WIRS_1 | 271 | 276 | PF05994 | 0.385 |
LIG_WRPW_2 | 419 | 422 | PF00400 | 0.278 |
LIG_WW_3 | 2 | 6 | PF00397 | 0.382 |
MOD_CDK_SPK_2 | 46 | 51 | PF00069 | 0.321 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.227 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.303 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.356 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.407 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.564 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.443 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.560 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.428 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.203 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.379 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.500 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.313 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.266 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.481 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.494 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.369 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.548 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.426 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.500 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.456 |
MOD_PIKK_1 | 227 | 233 | PF00454 | 0.470 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.489 |
MOD_PKA_1 | 402 | 408 | PF00069 | 0.448 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.386 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.498 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.502 |
MOD_PKB_1 | 40 | 48 | PF00069 | 0.343 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.443 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.320 |
MOD_Plk_2-3 | 68 | 74 | PF00069 | 0.319 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.480 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.431 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.356 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.350 |
MOD_SUMO_rev_2 | 90 | 97 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_2 | 315 | 321 | PF01217 | 0.258 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 364 | 366 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 120 | 124 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 204 | 208 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 404 | 408 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P269 | Leptomonas seymouri | 52% | 100% |
A0A0N1IJD9 | Leptomonas seymouri | 26% | 76% |
A0A0N1PC27 | Leptomonas seymouri | 30% | 96% |
A0A0N1PES8 | Leptomonas seymouri | 58% | 98% |
A0A1X0NWK3 | Trypanosomatidae | 33% | 100% |
A0A1X0NWM3 | Trypanosomatidae | 34% | 100% |
A0A3R7N1J7 | Trypanosoma rangeli | 32% | 100% |
A0A3S5H7D9 | Leishmania donovani | 100% | 100% |
A0A3S7WZK8 | Leishmania donovani | 29% | 81% |
A0A3S7X6F1 | Leishmania donovani | 31% | 94% |
A4HDU8 | Leishmania braziliensis | 73% | 100% |
A4HL36 | Leishmania braziliensis | 29% | 75% |
A4I1Y7 | Leishmania infantum | 29% | 81% |
A4I8P7 | Leishmania infantum | 31% | 94% |
E9AHM5 | Leishmania infantum | 29% | 73% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AY34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B3H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q05889 | Leishmania donovani | 99% | 100% |
Q4Q9D9 | Leishmania major | 28% | 100% |
Q4QD44 | Leishmania major | 27% | 72% |
Q6XFB5 | Leishmania major | 32% | 100% |
Q9NC61 | Leishmania major | 85% | 100% |
V5AJV9 | Trypanosoma cruzi | 32% | 100% |
V5AJW5 | Trypanosoma cruzi | 33% | 100% |
V5AM55 | Trypanosoma cruzi | 32% | 100% |
V5AR28 | Trypanosoma cruzi | 33% | 100% |
V5ASN8 | Trypanosoma cruzi | 33% | 100% |
V5AUJ2 | Trypanosoma cruzi | 32% | 100% |
V5B2H2 | Trypanosoma cruzi | 34% | 100% |
V5B4V1 | Trypanosoma cruzi | 32% | 100% |
V5B8H6 | Trypanosoma cruzi | 32% | 100% |
V5BB47 | Trypanosoma cruzi | 32% | 100% |
V5BRK8 | Trypanosoma cruzi | 33% | 100% |
V5BXG8 | Trypanosoma cruzi | 33% | 100% |
V5DD11 | Trypanosoma cruzi | 32% | 100% |