A large family of glycosyltransferases expanded in parazitic kinetoplastids (and even more in T cruzi). Localization: ER (by homology)
Glycolipid biosynthesis, GIPL galf transferase LPG1G
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:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AHM5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 15 |
GO:0016740 | transferase activity | 2 | 15 |
GO:0016757 | glycosyltransferase activity | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 231 | 237 | PF00089 | 0.472 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 542 | 544 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.518 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.545 |
DEG_APCC_DBOX_1 | 407 | 415 | PF00400 | 0.305 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.505 |
DOC_CKS1_1 | 108 | 113 | PF01111 | 0.491 |
DOC_CKS1_1 | 188 | 193 | PF01111 | 0.315 |
DOC_CKS1_1 | 376 | 381 | PF01111 | 0.328 |
DOC_MAPK_DCC_7 | 20 | 28 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.705 |
DOC_MAPK_HePTP_8 | 17 | 29 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 20 | 29 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 343 | 351 | PF00069 | 0.404 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.492 |
DOC_PP4_FxxP_1 | 467 | 470 | PF00568 | 0.438 |
DOC_SPAK_OSR1_1 | 240 | 244 | PF12202 | 0.225 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.487 |
DOC_USP7_MATH_2 | 98 | 104 | PF00917 | 0.507 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 176 | 185 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 408 | 417 | PF00244 | 0.307 |
LIG_14-3-3_CanoR_1 | 484 | 490 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.517 |
LIG_BIR_III_2 | 183 | 187 | PF00653 | 0.311 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.225 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.235 |
LIG_CSL_BTD_1 | 56 | 59 | PF09270 | 0.445 |
LIG_deltaCOP1_diTrp_1 | 270 | 276 | PF00928 | 0.304 |
LIG_deltaCOP1_diTrp_1 | 430 | 440 | PF00928 | 0.372 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.337 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.324 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.341 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.371 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.388 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.360 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.437 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.400 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.510 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.509 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.324 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.281 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.357 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.258 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.414 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.491 |
LIG_LIR_Apic_2 | 102 | 108 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 465 | 470 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 147 | 156 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 238 | 248 | PF02991 | 0.225 |
LIG_LIR_Gen_1 | 519 | 530 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.473 |
LIG_LYPXL_yS_3 | 346 | 349 | PF13949 | 0.414 |
LIG_OCRL_FandH_1 | 439 | 451 | PF00620 | 0.312 |
LIG_Pex14_2 | 198 | 202 | PF04695 | 0.316 |
LIG_Pex14_2 | 436 | 440 | PF04695 | 0.350 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.317 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 457 | 461 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 481 | 485 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 214 | 217 | PF00017 | 0.344 |
LIG_SH2_STAT3 | 552 | 555 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.433 |
LIG_SH3_1 | 354 | 360 | PF00018 | 0.342 |
LIG_SH3_2 | 357 | 362 | PF14604 | 0.335 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.476 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.405 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.298 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.511 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.476 |
LIG_SUMO_SIM_par_1 | 185 | 190 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 402 | 407 | PF11976 | 0.316 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.288 |
LIG_TRAF2_1 | 514 | 517 | PF00917 | 0.405 |
LIG_TRAF2_1 | 569 | 572 | PF00917 | 0.414 |
LIG_TYR_ITIM | 210 | 215 | PF00017 | 0.310 |
LIG_UBA3_1 | 188 | 197 | PF00899 | 0.312 |
LIG_UBA3_1 | 288 | 294 | PF00899 | 0.233 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.493 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.424 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.674 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.516 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.486 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.305 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.377 |
MOD_CK2_1 | 375 | 381 | PF00069 | 0.377 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.244 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.418 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.357 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.504 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.696 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.687 |
MOD_GlcNHglycan | 123 | 127 | PF01048 | 0.672 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.519 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.484 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.609 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.627 |
MOD_GlcNHglycan | 571 | 575 | PF01048 | 0.623 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.698 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.701 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.501 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.462 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.666 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.355 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.370 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.381 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.518 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.471 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.403 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.479 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.448 |
MOD_LATS_1 | 13 | 19 | PF00433 | 0.606 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.572 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.638 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.618 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.682 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.300 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.386 |
MOD_NEK2_1 | 525 | 530 | PF00069 | 0.424 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.379 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.443 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.473 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.243 |
MOD_NEK2_2 | 439 | 444 | PF00069 | 0.302 |
MOD_PK_1 | 3 | 9 | PF00069 | 0.659 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.435 |
MOD_PKA_2 | 490 | 496 | PF00069 | 0.372 |
MOD_PKA_2 | 558 | 564 | PF00069 | 0.414 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.513 |
MOD_PKB_1 | 50 | 58 | PF00069 | 0.470 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.350 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.387 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.446 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.364 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.451 |
MOD_Plk_2-3 | 589 | 595 | PF00069 | 0.381 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.519 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.377 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.357 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.374 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.429 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.338 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.465 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.314 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.344 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.551 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.305 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.442 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.512 |
MOD_SUMO_rev_2 | 513 | 523 | PF00179 | 0.380 |
MOD_SUMO_rev_2 | 586 | 593 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_4 | 571 | 577 | PF01217 | 0.407 |
TRG_DiLeu_BaLyEn_6 | 183 | 188 | PF01217 | 0.325 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.328 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 171 | 174 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.285 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.380 |
TRG_NES_CRM1_1 | 157 | 169 | PF08389 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 568 | 572 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHI5 | Leishmania donovani | 99% | 90% |
A0A3S5H7D9 | Leishmania donovani | 28% | 100% |
A0A3S7X6F1 | Leishmania donovani | 30% | 100% |
A4HDU8 | Leishmania braziliensis | 27% | 100% |
A4HL36 | Leishmania braziliensis | 64% | 96% |
A4I143 | Leishmania infantum | 29% | 100% |
A4I8P7 | Leishmania infantum | 30% | 100% |
E9AXX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
E9B3L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q05889 | Leishmania donovani | 28% | 100% |
Q4QD44 | Leishmania major | 84% | 100% |
Q6XFB5 | Leishmania major | 27% | 100% |
Q9NC61 | Leishmania major | 27% | 100% |