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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9B1Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016757 | glycosyltransferase activity | 3 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 628 | 630 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 324 | 330 | PF00082 | 0.369 |
CLV_PCSK_PC7_1 | 624 | 630 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.333 |
CLV_Separin_Metazoa | 611 | 615 | PF03568 | 0.424 |
DOC_ANK_TNKS_1 | 577 | 584 | PF00023 | 0.477 |
DOC_CDC14_PxL_1 | 508 | 516 | PF14671 | 0.283 |
DOC_CYCLIN_RxL_1 | 467 | 477 | PF00134 | 0.264 |
DOC_MAPK_FxFP_2 | 536 | 539 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 305 | 314 | PF00069 | 0.534 |
DOC_MAPK_gen_1 | 442 | 449 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 465 | 472 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.711 |
DOC_MAPK_MEF2A_6 | 329 | 338 | PF00069 | 0.623 |
DOC_PP1_RVXF_1 | 428 | 435 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.464 |
DOC_PP4_FxxP_1 | 323 | 326 | PF00568 | 0.558 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.340 |
DOC_PP4_FxxP_1 | 577 | 580 | PF00568 | 0.382 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 602 | 606 | PF00917 | 0.351 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 176 | 182 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 268 | 272 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 419 | 428 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.678 |
LIG_BIR_III_4 | 100 | 104 | PF00653 | 0.630 |
LIG_BIR_III_4 | 454 | 458 | PF00653 | 0.347 |
LIG_CtBP_PxDLS_1 | 461 | 465 | PF00389 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 361 | 370 | PF00928 | 0.381 |
LIG_deltaCOP1_diTrp_1 | 563 | 570 | PF00928 | 0.444 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.547 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.486 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.359 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.716 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.750 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.564 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.426 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.621 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.340 |
LIG_LIR_Apic_2 | 24 | 30 | PF02991 | 0.753 |
LIG_LIR_Apic_2 | 534 | 539 | PF02991 | 0.341 |
LIG_LIR_Apic_2 | 543 | 548 | PF02991 | 0.342 |
LIG_LIR_Apic_2 | 562 | 567 | PF02991 | 0.340 |
LIG_LIR_Apic_2 | 574 | 580 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 188 | 196 | PF02991 | 0.637 |
LIG_LIR_Gen_1 | 368 | 374 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 79 | 87 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 368 | 373 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 510 | 514 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.644 |
LIG_LYPXL_yS_3 | 511 | 514 | PF13949 | 0.476 |
LIG_Pex14_2 | 433 | 437 | PF04695 | 0.468 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.566 |
LIG_PTAP_UEV_1 | 457 | 462 | PF05743 | 0.542 |
LIG_REV1ctd_RIR_1 | 299 | 309 | PF16727 | 0.677 |
LIG_REV1ctd_RIR_1 | 320 | 325 | PF16727 | 0.296 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.688 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.708 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.670 |
LIG_SH2_GRB2like | 530 | 533 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.649 |
LIG_SH2_NCK_1 | 396 | 400 | PF00017 | 0.614 |
LIG_SH2_NCK_1 | 530 | 534 | PF00017 | 0.499 |
LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.707 |
LIG_SH2_NCK_1 | 99 | 103 | PF00017 | 0.670 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.555 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.499 |
LIG_SH2_SRC | 595 | 598 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 401 | 404 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.564 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.697 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.420 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.754 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.433 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.394 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 513 | 518 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.399 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.530 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.676 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.713 |
LIG_TYR_ITSM | 186 | 193 | PF00017 | 0.586 |
LIG_WRC_WIRS_1 | 434 | 439 | PF05994 | 0.474 |
MOD_CDC14_SPxK_1 | 380 | 383 | PF00782 | 0.541 |
MOD_CDK_SPK_2 | 28 | 33 | PF00069 | 0.511 |
MOD_CDK_SPxK_1 | 377 | 383 | PF00069 | 0.521 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.550 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.754 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.588 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.670 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.415 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.570 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.493 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.705 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.393 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.764 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.396 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.534 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.503 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.171 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.365 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.614 |
MOD_CMANNOS | 147 | 150 | PF00535 | 0.607 |
MOD_Cter_Amidation | 626 | 629 | PF01082 | 0.384 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.695 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.733 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.629 |
MOD_GlcNHglycan | 22 | 26 | PF01048 | 0.679 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.670 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.576 |
MOD_GlcNHglycan | 520 | 524 | PF01048 | 0.377 |
MOD_GlcNHglycan | 563 | 567 | PF01048 | 0.291 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.711 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.742 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.633 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.587 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.526 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.486 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.338 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.694 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.610 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.303 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.416 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.473 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.560 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.696 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.621 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.573 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.457 |
MOD_NEK2_2 | 297 | 302 | PF00069 | 0.664 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.514 |
MOD_PKA_1 | 66 | 72 | PF00069 | 0.707 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.668 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.736 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.572 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.570 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.284 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.499 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.645 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.568 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.484 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.585 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.635 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.660 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.461 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.418 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.318 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.573 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.503 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.521 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.593 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.469 |
MOD_SUMO_for_1 | 437 | 440 | PF00179 | 0.375 |
TRG_DiLeu_BaEn_1 | 466 | 471 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.708 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.663 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 478 | 480 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 628 | 631 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.662 |
TRG_NLS_MonoExtC_3 | 326 | 332 | PF00514 | 0.603 |
TRG_NLS_MonoExtN_4 | 324 | 331 | PF00514 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 636 | 640 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JMU2 | Bodo saltans | 34% | 91% |
A0A1X0NJI2 | Trypanosomatidae | 38% | 74% |
A0A3R7RH60 | Trypanosoma rangeli | 39% | 77% |
A0A3S7X4M2 | Leishmania donovani | 91% | 68% |
A0A3S7X4P3 | Leishmania donovani | 91% | 68% |
A4HJG8 | Leishmania braziliensis | 78% | 100% |
A4I6W5 | Leishmania infantum | 90% | 100% |
A4I6X8 | Leishmania infantum | 91% | 77% |
E9B1Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B1Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 75% |
Q4Q674 | Leishmania major | 89% | 100% |
Q4Q675 | Leishmania major | 89% | 100% |
V5BEQ4 | Trypanosoma cruzi | 38% | 77% |