A complex and fast-evolving family of glycosyltransferases. Their structural innovations and expansion is in accordance with a role in interactions with the environment. Despite the short hydrophobic segment, the N-terminal signal-like stretch is likely to be a signal-anchor as wil all Golgi-resident glycosyltransferases, not a secretory signal. Localization: Golgi (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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4I6W5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016757 | glycosyltransferase activity | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.416 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.392 |
CLV_PCSK_PC7_1 | 499 | 505 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.532 |
CLV_Separin_Metazoa | 486 | 490 | PF03568 | 0.228 |
DOC_ANK_TNKS_1 | 452 | 459 | PF00023 | 0.228 |
DOC_MAPK_gen_1 | 180 | 189 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 317 | 324 | PF00069 | 0.236 |
DOC_MAPK_gen_1 | 340 | 347 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 204 | 213 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 303 | 310 | PF00149 | 0.272 |
DOC_PP2B_PxIxI_1 | 386 | 392 | PF00149 | 0.186 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.282 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.326 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.219 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.336 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.296 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.228 |
LIG_14-3-3_CanoR_1 | 106 | 114 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 143 | 147 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 294 | 303 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 350 | 357 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 59 | 68 | PF00244 | 0.376 |
LIG_deltaCOP1_diTrp_1 | 236 | 245 | PF00928 | 0.253 |
LIG_deltaCOP1_diTrp_1 | 438 | 445 | PF00928 | 0.228 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.405 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.415 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.219 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.436 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.286 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.241 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.333 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.219 |
LIG_LIR_Apic_2 | 109 | 114 | PF02991 | 0.273 |
LIG_LIR_Apic_2 | 409 | 414 | PF02991 | 0.221 |
LIG_LIR_Apic_2 | 418 | 423 | PF02991 | 0.223 |
LIG_LIR_Apic_2 | 437 | 442 | PF02991 | 0.468 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 163 | 172 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 243 | 249 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.442 |
LIG_LYPXL_yS_3 | 386 | 389 | PF13949 | 0.258 |
LIG_PCNA_yPIPBox_3 | 50 | 62 | PF02747 | 0.381 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.237 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.292 |
LIG_PTAP_UEV_1 | 332 | 337 | PF05743 | 0.308 |
LIG_REV1ctd_RIR_1 | 174 | 184 | PF16727 | 0.368 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.353 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 405 | 408 | PF00017 | 0.228 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 405 | 409 | PF00017 | 0.228 |
LIG_SH2_NCK_1 | 65 | 69 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 125 | 128 | PF00017 | 0.243 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.310 |
LIG_SH2_SRC | 405 | 408 | PF00017 | 0.228 |
LIG_SH2_SRC | 470 | 473 | PF00017 | 0.228 |
LIG_SH2_STAT3 | 276 | 279 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.228 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.359 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.285 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.228 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.228 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.441 |
LIG_SUMO_SIM_par_1 | 343 | 349 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.228 |
LIG_SUMO_SIM_par_1 | 432 | 438 | PF11976 | 0.228 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.344 |
LIG_TYR_ITIM | 156 | 161 | PF00017 | 0.335 |
LIG_TYR_ITSM | 61 | 68 | PF00017 | 0.414 |
LIG_WRC_WIRS_1 | 309 | 314 | PF05994 | 0.350 |
MOD_CDC14_SPxK_1 | 255 | 258 | PF00782 | 0.326 |
MOD_CDK_SPxK_1 | 252 | 258 | PF00069 | 0.306 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.365 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.278 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.311 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.278 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.317 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.228 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.375 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.489 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.270 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.478 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.228 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.219 |
MOD_CMANNOS | 22 | 25 | PF00535 | 0.384 |
MOD_Cter_Amidation | 501 | 504 | PF01082 | 0.228 |
MOD_GlcNHglycan | 110 | 114 | PF01048 | 0.289 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.383 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.335 |
MOD_GlcNHglycan | 395 | 399 | PF01048 | 0.228 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.452 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.406 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.386 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.357 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.546 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.228 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.229 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.464 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.430 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.272 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.277 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.286 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.310 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.381 |
MOD_NEK2_2 | 9 | 14 | PF00069 | 0.371 |
MOD_OFUCOSY | 285 | 291 | PF10250 | 0.327 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.278 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.341 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.362 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.334 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.298 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.282 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.306 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.228 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.309 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.396 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.427 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.274 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.330 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.315 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.318 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.451 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.380 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.306 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.440 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.228 |
MOD_SUMO_for_1 | 312 | 315 | PF00179 | 0.254 |
TRG_DiLeu_BaEn_1 | 341 | 346 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 249 | 251 | PF00400 | 0.241 |
TRG_ER_diArg_1 | 499 | 501 | PF00400 | 0.228 |
TRG_ER_diArg_1 | 503 | 506 | PF00400 | 0.216 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.388 |
TRG_NLS_MonoExtC_3 | 201 | 207 | PF00514 | 0.392 |
TRG_NLS_MonoExtN_4 | 199 | 206 | PF00514 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.311 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JMU2 | Bodo saltans | 33% | 74% |
E9B1Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |