A large family of glycosyltransferases expanded in parazitic kinetoplastids (and even more in T cruzi). 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: 38 |
NetGPI | no | yes: 0, no: 38 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9B3L0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 39 |
GO:0016740 | transferase activity | 2 | 39 |
GO:0016757 | glycosyltransferase activity | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.514 |
CLV_PCSK_PC7_1 | 221 | 227 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.628 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.547 |
DEG_APCC_DBOX_1 | 375 | 383 | PF00400 | 0.426 |
DEG_SCF_FBW7_1 | 232 | 239 | PF00400 | 0.257 |
DOC_MAPK_DCC_7 | 166 | 176 | PF00069 | 0.226 |
DOC_MAPK_gen_1 | 16 | 22 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.192 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.370 |
DOC_PP1_RVXF_1 | 15 | 22 | PF00149 | 0.547 |
DOC_PP2B_PxIxI_1 | 171 | 177 | PF00149 | 0.345 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.369 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.467 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.361 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 249 | 254 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.558 |
LIG_Actin_WH2_2 | 118 | 135 | PF00022 | 0.382 |
LIG_APCC_Cbox_2 | 189 | 195 | PF00515 | 0.202 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.196 |
LIG_BRCT_BRCA1_1 | 319 | 323 | PF00533 | 0.253 |
LIG_deltaCOP1_diTrp_1 | 300 | 306 | PF00928 | 0.399 |
LIG_deltaCOP1_diTrp_1 | 369 | 374 | PF00928 | 0.378 |
LIG_deltaCOP1_diTrp_1 | 96 | 103 | PF00928 | 0.374 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.407 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.330 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.338 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.407 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.430 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.355 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.406 |
LIG_IRF3_LxIS_1 | 236 | 241 | PF10401 | 0.236 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.349 |
LIG_Pex14_2 | 173 | 177 | PF04695 | 0.331 |
LIG_Pex14_2 | 323 | 327 | PF04695 | 0.420 |
LIG_REV1ctd_RIR_1 | 324 | 333 | PF16727 | 0.254 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.357 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.308 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.236 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.330 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.362 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.211 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.393 |
LIG_SH2_STAT3 | 115 | 118 | PF00017 | 0.382 |
LIG_SH2_STAT3 | 145 | 148 | PF00017 | 0.256 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.304 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.195 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.378 |
LIG_SH3_5 | 363 | 367 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 280 | 286 | PF11976 | 0.379 |
LIG_SUMO_SIM_anti_2 | 30 | 35 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 32 | 38 | PF11976 | 0.203 |
LIG_SUMO_SIM_par_1 | 408 | 414 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 91 | 96 | PF11976 | 0.270 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.235 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.384 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.260 |
LIG_TYR_ITIM | 248 | 253 | PF00017 | 0.209 |
MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.644 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.659 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.506 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.291 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.274 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.465 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.501 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.650 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.599 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.417 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.352 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.341 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.464 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.417 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.579 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.266 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.295 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.272 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.404 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.408 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.407 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.406 |
MOD_NEK2_2 | 224 | 229 | PF00069 | 0.420 |
MOD_PK_1 | 416 | 422 | PF00069 | 0.456 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.360 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.429 |
MOD_PKB_1 | 247 | 255 | PF00069 | 0.253 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.393 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.308 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.406 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.229 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.675 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.408 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.362 |
MOD_SUMO_rev_2 | 366 | 373 | PF00179 | 0.374 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.230 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.272 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 72 | 74 | PF00400 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 207 | 211 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 73 | 78 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P269 | Leptomonas seymouri | 29% | 100% |
A0A0N1PC27 | Leptomonas seymouri | 65% | 99% |
A0A0N1PES8 | Leptomonas seymouri | 30% | 100% |
A0A1X0NWK3 | Trypanosomatidae | 35% | 100% |
A0A1X0NWM3 | Trypanosomatidae | 35% | 100% |
A0A3Q8IHI5 | Leishmania donovani | 29% | 67% |
A0A3R7N1J7 | Trypanosoma rangeli | 35% | 100% |
A0A3S5H7D9 | Leishmania donovani | 30% | 100% |
A0A3S7WZK8 | Leishmania donovani | 30% | 83% |
A0A3S7X6F1 | Leishmania donovani | 93% | 97% |
A4HDU8 | Leishmania braziliensis | 29% | 100% |
A4HER0 | Leishmania braziliensis | 28% | 66% |
A4HL36 | Leishmania braziliensis | 33% | 77% |
A4I143 | Leishmania infantum | 30% | 100% |
A4I1Y7 | Leishmania infantum | 30% | 83% |
A4I8P7 | Leishmania infantum | 93% | 97% |
E9AHM5 | Leishmania infantum | 29% | 75% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AY34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B3H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 76% |
Q05889 | Leishmania donovani | 30% | 100% |
Q4Q9D9 | Leishmania major | 29% | 100% |
Q4QD44 | Leishmania major | 28% | 74% |
Q6XFB5 | Leishmania major | 92% | 100% |
Q9NC61 | Leishmania major | 29% | 100% |
V5AJV9 | Trypanosoma cruzi | 37% | 100% |
V5AJW5 | Trypanosoma cruzi | 36% | 100% |
V5AM55 | Trypanosoma cruzi | 38% | 100% |
V5AR28 | Trypanosoma cruzi | 38% | 100% |
V5ASN8 | Trypanosoma cruzi | 36% | 100% |
V5AUJ2 | Trypanosoma cruzi | 37% | 100% |
V5B2H2 | Trypanosoma cruzi | 37% | 100% |
V5B4V1 | Trypanosoma cruzi | 35% | 100% |
V5B8H6 | Trypanosoma cruzi | 36% | 100% |
V5BB47 | Trypanosoma cruzi | 37% | 100% |
V5BRK8 | Trypanosoma cruzi | 37% | 100% |
V5BXG8 | Trypanosoma cruzi | 36% | 100% |
V5DD11 | Trypanosoma cruzi | 35% | 100% |