Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. 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: 60 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 46 |
NetGPI | no | yes: 0, no: 46 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 47 |
GO:0110165 | cellular anatomical entity | 1 | 47 |
GO:0000139 | Golgi membrane | 5 | 11 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
Related structures:
AlphaFold database: A4HNK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 47 |
GO:0006807 | nitrogen compound metabolic process | 2 | 47 |
GO:0008152 | metabolic process | 1 | 47 |
GO:0019538 | protein metabolic process | 3 | 47 |
GO:0036211 | protein modification process | 4 | 47 |
GO:0043170 | macromolecule metabolic process | 3 | 47 |
GO:0043412 | macromolecule modification | 4 | 47 |
GO:0043413 | macromolecule glycosylation | 3 | 47 |
GO:0044238 | primary metabolic process | 2 | 47 |
GO:0070085 | glycosylation | 2 | 47 |
GO:0071704 | organic substance metabolic process | 2 | 47 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 47 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 47 |
GO:0016740 | transferase activity | 2 | 47 |
GO:0016757 | glycosyltransferase activity | 3 | 47 |
GO:0016758 | hexosyltransferase activity | 4 | 47 |
GO:0008194 | UDP-glycosyltransferase activity | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.354 |
CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.602 |
CLV_PCSK_FUR_1 | 573 | 577 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 575 | 579 | PF00082 | 0.359 |
DEG_SCF_FBW7_1 | 228 | 235 | PF00400 | 0.606 |
DOC_ANK_TNKS_1 | 158 | 165 | PF00023 | 0.350 |
DOC_CDC14_PxL_1 | 304 | 312 | PF14671 | 0.257 |
DOC_CKS1_1 | 229 | 234 | PF01111 | 0.612 |
DOC_CYCLIN_yCln2_LP_2 | 226 | 232 | PF00134 | 0.621 |
DOC_CYCLIN_yCln2_LP_2 | 25 | 31 | PF00134 | 0.394 |
DOC_MAPK_MEF2A_6 | 256 | 263 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 312 | 321 | PF00069 | 0.315 |
DOC_MAPK_NFAT4_5 | 256 | 264 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 290 | 297 | PF00149 | 0.494 |
DOC_PP1_RVXF_1 | 471 | 477 | PF00149 | 0.361 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.366 |
DOC_PP2B_PxIxI_1 | 197 | 203 | PF00149 | 0.305 |
DOC_PP4_FxxP_1 | 483 | 486 | PF00568 | 0.295 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.509 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.383 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 130 | 136 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 329 | 336 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 338 | 343 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 556 | 560 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 314 | 331 | PF00022 | 0.319 |
LIG_Actin_WH2_2 | 485 | 503 | PF00022 | 0.263 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.538 |
LIG_EH_1 | 395 | 399 | PF12763 | 0.394 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.425 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.443 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.413 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.557 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.499 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.396 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.504 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.573 |
LIG_LIR_Apic_2 | 278 | 284 | PF02991 | 0.579 |
LIG_LIR_Apic_2 | 335 | 339 | PF02991 | 0.362 |
LIG_LIR_Apic_2 | 481 | 486 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 258 | 264 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 315 | 325 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 420 | 428 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 475 | 483 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 101 | 105 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 475 | 479 | PF02991 | 0.519 |
LIG_NRBOX | 404 | 410 | PF00104 | 0.395 |
LIG_Pex14_1 | 369 | 373 | PF04695 | 0.325 |
LIG_RPA_C_Fungi | 455 | 467 | PF08784 | 0.317 |
LIG_SH2_NCK_1 | 152 | 156 | PF00017 | 0.491 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.475 |
LIG_SH2_STAT3 | 330 | 333 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 559 | 562 | PF00017 | 0.449 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.347 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.614 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.420 |
LIG_SH3_3 | 483 | 489 | PF00018 | 0.349 |
LIG_SUMO_SIM_anti_2 | 401 | 407 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 420 | 426 | PF11976 | 0.281 |
LIG_SUMO_SIM_par_1 | 544 | 549 | PF11976 | 0.320 |
LIG_TRAF2_1 | 6 | 9 | PF00917 | 0.538 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.545 |
LIG_TYR_ITIM | 371 | 376 | PF00017 | 0.294 |
MOD_CDK_SPK_2 | 132 | 137 | PF00069 | 0.461 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.652 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.475 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.390 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.353 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.303 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.496 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.498 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.607 |
MOD_Cter_Amidation | 449 | 452 | PF01082 | 0.348 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.631 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.519 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.339 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.629 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.375 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.435 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.438 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.357 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.538 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.404 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.315 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.421 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.451 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.571 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.489 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.349 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.437 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.425 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.291 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.497 |
MOD_NEK2_2 | 413 | 418 | PF00069 | 0.325 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.441 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.522 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.321 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.382 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.498 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.505 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.470 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.433 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.302 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.302 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.291 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.352 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.583 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.545 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.318 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.332 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.450 |
MOD_Plk_2-3 | 129 | 135 | PF00069 | 0.502 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.401 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.503 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.376 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.348 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.522 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.414 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.335 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.345 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.489 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.503 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.604 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.469 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.556 |
MOD_SUMO_rev_2 | 499 | 509 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 7 | 13 | PF00179 | 0.517 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.286 |
TRG_DiLeu_BaEn_1 | 505 | 510 | PF01217 | 0.359 |
TRG_DiLeu_LyEn_5 | 505 | 510 | PF01217 | 0.356 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.264 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 459 | 462 | PF00400 | 0.362 |
TRG_NLS_MonoExtN_4 | 573 | 579 | PF00514 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 407 | 411 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.390 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IGN9 | Leishmania donovani | 73% | 72% |
A0A3S5H4Y6 | Leishmania donovani | 41% | 73% |
A0A3S7WWA6 | Leishmania donovani | 73% | 72% |
A0A451EJD9 | Leishmania donovani | 64% | 72% |
A0A451EJF4 | Leishmania donovani | 41% | 72% |
A0A451EJF6 | Leishmania donovani | 41% | 90% |
A0A451EJF8 | Leishmania donovani | 38% | 76% |
A0A451EJF9 | Leishmania donovani | 41% | 68% |
A4H3A9 | Leishmania braziliensis | 42% | 100% |
A4H3B4 | Leishmania braziliensis | 41% | 100% |
A4H3B5 | Leishmania braziliensis | 41% | 100% |
A4H3B6 | Leishmania braziliensis | 41% | 100% |
A4H3B8 | Leishmania braziliensis | 41% | 100% |
A4H3B9 | Leishmania braziliensis | 38% | 66% |
A4H4W8 | Leishmania braziliensis | 95% | 100% |
A4HJ20 | Leishmania braziliensis | 41% | 100% |
A4HNK6 | Leishmania braziliensis | 97% | 74% |
A4HRL9 | Leishmania infantum | 41% | 72% |
A4HRM0 | Leishmania infantum | 39% | 80% |
A4HRM1 | Leishmania infantum | 41% | 90% |
A4HRS1 | Leishmania infantum | 41% | 68% |
A4HRS5 | Leishmania infantum | 38% | 76% |
A4HZM0 | Leishmania infantum | 64% | 72% |
A4I7C7 | Leishmania infantum | 64% | 72% |
A4IAQ2 | Leishmania infantum | 60% | 72% |
E9AC91 | Leishmania major | 40% | 100% |
E9AC92 | Leishmania major | 40% | 100% |
E9AC95 | Leishmania major | 38% | 100% |
E9AC96 | Leishmania major | 41% | 100% |
E9AEH8 | Leishmania major | 65% | 100% |
E9AHA6 | Leishmania infantum | 64% | 72% |
E9AIP8 | Leishmania braziliensis | 95% | 100% |
E9AJI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 72% |
E9AJI4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 74% |
E9AJI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 76% |
E9ALD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 79% |
E9ASB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 72% |
E9AXX8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 72% |
E9B2C0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 72% |
Q4Q5T6 | Leishmania major | 65% | 100% |
Q4QCL8 | Leishmania major | 71% | 100% |
Q4QIG9 | Leishmania major | 71% | 100% |
Q7YXU9 | Leishmania major | 71% | 100% |
Q7YXV1 | Leishmania major | 71% | 100% |
Q7YXV2 | Leishmania major | 71% | 100% |