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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WZK8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 21 |
GO:0016740 | transferase activity | 2 | 21 |
GO:0016757 | glycosyltransferase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 414 | 418 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.588 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 480 | 482 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 108 | 114 | PF00082 | 0.341 |
CLV_PCSK_PC7_1 | 515 | 521 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.583 |
DEG_APCC_DBOX_1 | 503 | 511 | PF00400 | 0.457 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.559 |
DOC_CDC14_PxL_1 | 231 | 239 | PF14671 | 0.274 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.412 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.428 |
DOC_CKS1_1 | 325 | 330 | PF01111 | 0.363 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 506 | 514 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 169 | 175 | PF00134 | 0.287 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 493 | 499 | PF00134 | 0.321 |
DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 330 | 336 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.312 |
DOC_MAPK_gen_1 | 80 | 88 | PF00069 | 0.671 |
DOC_MAPK_MEF2A_6 | 357 | 365 | PF00069 | 0.378 |
DOC_PP1_RVXF_1 | 110 | 117 | PF00149 | 0.432 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.471 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.348 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 112 | 117 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 203 | 207 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 245 | 255 | PF00244 | 0.383 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.547 |
LIG_BIR_III_2 | 30 | 34 | PF00653 | 0.540 |
LIG_BIR_III_2 | 73 | 77 | PF00653 | 0.537 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.404 |
LIG_Clathr_ClatBox_1 | 96 | 100 | PF01394 | 0.267 |
LIG_deltaCOP1_diTrp_1 | 379 | 389 | PF00928 | 0.412 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.409 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.427 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.326 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.585 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.463 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.591 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.410 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.502 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.585 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.380 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.447 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.372 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.786 |
LIG_LIR_Gen_1 | 115 | 124 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 228 | 239 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 349 | 353 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.393 |
LIG_MYND_1 | 436 | 440 | PF01753 | 0.385 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.322 |
LIG_REV1ctd_RIR_1 | 188 | 196 | PF16727 | 0.269 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.431 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.409 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.387 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.399 |
LIG_SH2_CRK | 454 | 458 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 350 | 354 | PF00017 | 0.399 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 461 | 464 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.426 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.472 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.552 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 201 | 208 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 356 | 362 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 520 | 525 | PF11976 | 0.479 |
LIG_TRFH_1 | 105 | 109 | PF08558 | 0.352 |
LIG_UBA3_1 | 268 | 274 | PF00899 | 0.336 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.415 |
MOD_CDK_SPK_2 | 436 | 441 | PF00069 | 0.357 |
MOD_CDK_SPxK_1 | 324 | 330 | PF00069 | 0.327 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.271 |
MOD_CDK_SPxxK_3 | 281 | 288 | PF00069 | 0.501 |
MOD_CDK_SPxxK_3 | 324 | 331 | PF00069 | 0.339 |
MOD_CDK_SPxxK_3 | 436 | 443 | PF00069 | 0.471 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.458 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.584 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.388 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.330 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.329 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.441 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.528 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.460 |
MOD_Cter_Amidation | 517 | 520 | PF01082 | 0.475 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.575 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.361 |
MOD_GlcNHglycan | 484 | 487 | PF01048 | 0.590 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.588 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.399 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.433 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.333 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.564 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.280 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.428 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.539 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.401 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.609 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.592 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.348 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.392 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.400 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.349 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.417 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.489 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.308 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.622 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.450 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.405 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.359 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.487 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.526 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.541 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.339 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.410 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.423 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.368 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.311 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.313 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.413 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.496 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.466 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.354 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.474 |
MOD_SUMO_rev_2 | 157 | 165 | PF00179 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 293 | 298 | PF01217 | 0.399 |
TRG_DiLeu_LyEn_5 | 282 | 287 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.520 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.585 |
TRG_NES_CRM1_1 | 98 | 111 | PF08389 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 519 | 523 | PF00026 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJD9 | Leptomonas seymouri | 49% | 95% |
A0A0N1PC27 | Leptomonas seymouri | 26% | 100% |
A0A0N1PES8 | Leptomonas seymouri | 30% | 100% |
A0A1X0NWM3 | Trypanosomatidae | 30% | 100% |
A0A3R7N1J7 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H7D9 | Leishmania donovani | 28% | 100% |
A0A3S7X6F1 | Leishmania donovani | 28% | 100% |
A4HDU8 | Leishmania braziliensis | 29% | 98% |
A4HER0 | Leishmania braziliensis | 78% | 100% |
A4I143 | Leishmania infantum | 29% | 100% |
A4I1Y7 | Leishmania infantum | 99% | 100% |
A4I8P7 | Leishmania infantum | 29% | 100% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 99% |
E9AY34 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9B3L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q05889 | Leishmania donovani | 28% | 100% |
Q4Q9D9 | Leishmania major | 92% | 100% |
Q4QD44 | Leishmania major | 26% | 90% |
Q6XFB5 | Leishmania major | 29% | 100% |
Q9NC61 | Leishmania major | 29% | 98% |