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: 37 |
NetGPI | no | yes: 0, no: 37 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: A0A3S7X6F1
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_NRD_NRD_1 | 16 | 18 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.656 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.420 |
DEG_APCC_DBOX_1 | 376 | 384 | PF00400 | 0.444 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.572 |
DEG_SCF_FBW7_1 | 233 | 240 | PF00400 | 0.256 |
DOC_CYCLIN_RxL_1 | 14 | 24 | PF00134 | 0.368 |
DOC_MAPK_DCC_7 | 167 | 177 | PF00069 | 0.223 |
DOC_MAPK_gen_1 | 16 | 22 | PF00069 | 0.217 |
DOC_MAPK_MEF2A_6 | 406 | 413 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 15 | 22 | PF00149 | 0.209 |
DOC_PP2B_PxIxI_1 | 172 | 178 | PF00149 | 0.339 |
DOC_PP4_FxxP_1 | 393 | 396 | PF00568 | 0.360 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.474 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.352 |
LIG_14-3-3_CanoR_1 | 226 | 230 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 250 | 255 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 74 | 82 | PF00244 | 0.420 |
LIG_Actin_WH2_2 | 119 | 136 | PF00022 | 0.377 |
LIG_APCC_Cbox_2 | 190 | 196 | PF00515 | 0.198 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.246 |
LIG_deltaCOP1_diTrp_1 | 301 | 307 | PF00928 | 0.397 |
LIG_deltaCOP1_diTrp_1 | 370 | 375 | PF00928 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 97 | 104 | PF00928 | 0.368 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.402 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.324 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.331 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.433 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.363 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.409 |
LIG_IRF3_LxIS_1 | 237 | 242 | PF10401 | 0.235 |
LIG_LIR_Apic_2 | 392 | 396 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.224 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.343 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.326 |
LIG_Pex14_2 | 324 | 328 | PF04695 | 0.235 |
LIG_PTB_Apo_2 | 308 | 315 | PF02174 | 0.209 |
LIG_REV1ctd_RIR_1 | 325 | 334 | PF16727 | 0.256 |
LIG_SH2_NCK_1 | 349 | 353 | PF00017 | 0.232 |
LIG_SH2_NCK_1 | 37 | 41 | PF00017 | 0.347 |
LIG_SH2_PTP2 | 192 | 195 | PF00017 | 0.201 |
LIG_SH2_SRC | 114 | 117 | PF00017 | 0.357 |
LIG_SH2_SRC | 192 | 195 | PF00017 | 0.208 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.249 |
LIG_SH2_STAP1 | 197 | 201 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.256 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 116 | 119 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 146 | 149 | PF00017 | 0.254 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.222 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.299 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.533 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.376 |
LIG_SH3_5 | 364 | 368 | PF00018 | 0.381 |
LIG_SUMO_SIM_anti_2 | 281 | 287 | PF11976 | 0.375 |
LIG_SUMO_SIM_anti_2 | 30 | 35 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 124 | 131 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 32 | 39 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 409 | 415 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 92 | 97 | PF11976 | 0.268 |
LIG_TRAF2_1 | 122 | 125 | PF00917 | 0.233 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.380 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.258 |
LIG_TYR_ITIM | 195 | 200 | PF00017 | 0.213 |
LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.251 |
MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.651 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.666 |
MOD_CDK_SPxxK_3 | 10 | 17 | PF00069 | 0.516 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.317 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.268 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.271 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.312 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.487 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.587 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.553 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.415 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.403 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.347 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.354 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.492 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.439 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.519 |
MOD_N-GLC_1 | 427 | 432 | PF02516 | 0.570 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.298 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.349 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.260 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.286 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.264 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.446 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.408 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.510 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.403 |
MOD_NEK2_2 | 225 | 230 | PF00069 | 0.416 |
MOD_PK_1 | 417 | 423 | PF00069 | 0.481 |
MOD_PKA_1 | 315 | 321 | PF00069 | 0.215 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.353 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.428 |
MOD_PKB_1 | 248 | 256 | PF00069 | 0.250 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.387 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.283 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.269 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.218 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.400 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.225 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.683 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.404 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.338 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.355 |
MOD_SUMO_rev_2 | 367 | 374 | PF00179 | 0.379 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.227 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 114 | 117 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.320 |
TRG_Pf-PMV_PEXEL_1 | 141 | 145 | PF00026 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.616 |
TRG_Pf-PMV_PEXEL_1 | 74 | 79 | PF00026 | 0.529 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P269 | Leptomonas seymouri | 29% | 100% |
A0A0N1PC27 | Leptomonas seymouri | 65% | 100% |
A0A0N1PES8 | Leptomonas seymouri | 31% | 100% |
A0A1X0NWK3 | Trypanosomatidae | 36% | 100% |
A0A1X0NWM3 | Trypanosomatidae | 36% | 100% |
A0A3Q8IHI5 | Leishmania donovani | 30% | 70% |
A0A3R7N1J7 | Trypanosoma rangeli | 35% | 100% |
A0A3S5H7D9 | Leishmania donovani | 32% | 100% |
A0A3S7WZK8 | Leishmania donovani | 28% | 100% |
A4HDU8 | Leishmania braziliensis | 31% | 100% |
A4HER0 | Leishmania braziliensis | 28% | 69% |
A4HL36 | Leishmania braziliensis | 33% | 80% |
A4I143 | Leishmania infantum | 31% | 100% |
A4I1Y7 | Leishmania infantum | 29% | 100% |
A4I8P7 | Leishmania infantum | 100% | 100% |
E9AHM5 | Leishmania infantum | 30% | 77% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AY34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B3H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 78% |
E9B3L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q05889 | Leishmania donovani | 31% | 100% |
Q4Q9D9 | Leishmania major | 28% | 100% |
Q6XFB5 | Leishmania major | 94% | 100% |
Q9NC61 | Leishmania major | 29% | 100% |
V5AJV9 | Trypanosoma cruzi | 38% | 100% |
V5AJW5 | Trypanosoma cruzi | 37% | 100% |
V5AM55 | Trypanosoma cruzi | 39% | 100% |
V5AR28 | Trypanosoma cruzi | 38% | 100% |
V5ASN8 | Trypanosoma cruzi | 36% | 100% |
V5AUJ2 | Trypanosoma cruzi | 38% | 100% |
V5B2H2 | Trypanosoma cruzi | 38% | 100% |
V5B4V1 | Trypanosoma cruzi | 37% | 100% |
V5B8H6 | Trypanosoma cruzi | 37% | 100% |
V5BB47 | Trypanosoma cruzi | 38% | 100% |
V5BRK8 | Trypanosoma cruzi | 38% | 100% |
V5BXG8 | Trypanosoma cruzi | 36% | 100% |
V5DD11 | Trypanosoma cruzi | 38% | 100% |