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: 16 |
NetGPI | no | yes: 0, no: 16 |
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: E9B3H7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0016740 | transferase activity | 2 | 17 |
GO:0016757 | glycosyltransferase activity | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.384 |
CLV_MEL_PAP_1 | 223 | 229 | PF00089 | 0.466 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.569 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.345 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.711 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.502 |
DOC_CKS1_1 | 180 | 185 | PF01111 | 0.316 |
DOC_CYCLIN_RxL_1 | 153 | 161 | PF00134 | 0.274 |
DOC_MAPK_DCC_7 | 20 | 28 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.759 |
DOC_MAPK_HePTP_8 | 17 | 29 | PF00069 | 0.317 |
DOC_MAPK_MEF2A_6 | 20 | 29 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 335 | 343 | PF00069 | 0.474 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 584 | 588 | PF12436 | 0.374 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.426 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 400 | 409 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 539 | 543 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 553 | 558 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 88 | 95 | PF00244 | 0.523 |
LIG_BIR_III_2 | 175 | 179 | PF00653 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 262 | 268 | PF00928 | 0.334 |
LIG_deltaCOP1_diTrp_1 | 422 | 432 | PF00928 | 0.391 |
LIG_DLG_GKlike_1 | 327 | 334 | PF00625 | 0.303 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.454 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.336 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.387 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.341 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.374 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.373 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.436 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.402 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.554 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.380 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.267 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.316 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.448 |
LIG_Integrin_RGD_1 | 293 | 295 | PF01839 | 0.545 |
LIG_LIR_Apic_2 | 46 | 51 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 139 | 147 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 434 | 443 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 511 | 522 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.493 |
LIG_LYPXL_yS_3 | 338 | 341 | PF13949 | 0.400 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.318 |
LIG_Pex14_2 | 428 | 432 | PF04695 | 0.472 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.311 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 449 | 453 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.482 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 544 | 547 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.501 |
LIG_SH3_1 | 346 | 352 | PF00018 | 0.330 |
LIG_SH3_2 | 349 | 354 | PF14604 | 0.369 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.472 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.411 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.322 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.504 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.472 |
LIG_SUMO_SIM_par_1 | 177 | 182 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 36 | 41 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 394 | 399 | PF11976 | 0.323 |
LIG_SxIP_EBH_1 | 72 | 82 | PF03271 | 0.438 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.322 |
LIG_TRAF2_1 | 506 | 509 | PF00917 | 0.368 |
LIG_TRAF2_1 | 561 | 564 | PF00917 | 0.434 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.435 |
LIG_TYR_ITIM | 202 | 207 | PF00017 | 0.344 |
LIG_UBA3_1 | 180 | 189 | PF00899 | 0.354 |
LIG_UBA3_1 | 280 | 286 | PF00899 | 0.224 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.215 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.366 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.431 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.582 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.428 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.187 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.379 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.416 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.444 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.490 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.330 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.499 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.691 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.522 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.522 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.406 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.626 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.772 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.655 |
MOD_GlcNHglycan | 563 | 567 | PF01048 | 0.677 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.673 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.359 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.498 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.420 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.478 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.468 |
MOD_LATS_1 | 13 | 19 | PF00433 | 0.424 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.620 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.634 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.641 |
MOD_N-GLC_1 | 553 | 558 | PF02516 | 0.693 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.676 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.335 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.331 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.452 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.432 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.538 |
MOD_NEK2_2 | 271 | 276 | PF00069 | 0.196 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.306 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.290 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.292 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.659 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.523 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.215 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.440 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.409 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.457 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.499 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.482 |
MOD_PKB_1 | 551 | 559 | PF00069 | 0.357 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.600 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.290 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.344 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.390 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.440 |
MOD_Plk_1 | 553 | 559 | PF00069 | 0.466 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.223 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.379 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.334 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.337 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.324 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.450 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.463 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.464 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.316 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.352 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.456 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.428 |
MOD_SUMO_rev_2 | 505 | 515 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_4 | 563 | 569 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.272 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.233 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.295 |
TRG_NES_CRM1_1 | 149 | 161 | PF08389 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 560 | 564 | PF00026 | 0.751 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PES8 | Leptomonas seymouri | 26% | 100% |
A0A1X0NWK3 | Trypanosomatidae | 31% | 100% |
A0A3Q8IHI5 | Leishmania donovani | 78% | 89% |
A0A3S5H7D9 | Leishmania donovani | 28% | 100% |
A0A3S7X6F1 | Leishmania donovani | 30% | 100% |
A4HDU8 | Leishmania braziliensis | 26% | 100% |
A4HL36 | Leishmania braziliensis | 64% | 98% |
A4I143 | Leishmania infantum | 28% | 100% |
A4I8P7 | Leishmania infantum | 30% | 100% |
E9AHM5 | Leishmania infantum | 78% | 99% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q05889 | Leishmania donovani | 28% | 100% |
Q4QD44 | Leishmania major | 75% | 100% |
Q6XFB5 | Leishmania major | 31% | 100% |
Q9NC61 | Leishmania major | 27% | 100% |