GPI anchor biosynthesis, GPI-GlcNAc transferase complex, PIG-H component
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000506 | glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) complex | 3 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0098796 | membrane protein complex | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 7 |
GO:1902494 | catalytic complex | 2 | 7 |
GO:1990234 | transferase complex | 3 | 7 |
Related structures:
AlphaFold database: A4HTG6
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 7 |
GO:0006505 | GPI anchor metabolic process | 6 | 7 |
GO:0006506 | GPI anchor biosynthetic process | 6 | 7 |
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006643 | membrane lipid metabolic process | 4 | 7 |
GO:0006644 | phospholipid metabolic process | 4 | 7 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 7 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 7 |
GO:0006664 | glycolipid metabolic process | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0008610 | lipid biosynthetic process | 4 | 7 |
GO:0008654 | phospholipid biosynthetic process | 5 | 7 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0009247 | glycolipid biosynthetic process | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 7 |
GO:0046467 | membrane lipid biosynthetic process | 4 | 7 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 7 |
GO:0046486 | glycerolipid metabolic process | 4 | 7 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
GO:1903509 | liposaccharide metabolic process | 4 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.620 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.345 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.373 |
DEG_APCC_DBOX_1 | 431 | 439 | PF00400 | 0.504 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.454 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.688 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.657 |
DOC_CYCLIN_RxL_1 | 41 | 52 | PF00134 | 0.628 |
DOC_MAPK_gen_1 | 379 | 386 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 379 | 388 | PF00069 | 0.469 |
DOC_MAPK_RevD_3 | 331 | 346 | PF00069 | 0.303 |
DOC_PP1_RVXF_1 | 201 | 207 | PF00149 | 0.641 |
DOC_PP1_RVXF_1 | 309 | 316 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 415 | 422 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 153 | 156 | PF13499 | 0.680 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.659 |
DOC_USP7_MATH_2 | 446 | 452 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.792 |
LIG_14-3-3_CanoR_1 | 183 | 187 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 231 | 235 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 458 | 466 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.606 |
LIG_Actin_WH2_2 | 418 | 434 | PF00022 | 0.515 |
LIG_AP_GAE_1 | 474 | 480 | PF02883 | 0.682 |
LIG_APCC_ABBAyCdc20_2 | 439 | 445 | PF00400 | 0.536 |
LIG_EH1_1 | 381 | 389 | PF00400 | 0.516 |
LIG_eIF4E_1 | 355 | 361 | PF01652 | 0.541 |
LIG_EVH1_1 | 7 | 11 | PF00568 | 0.611 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.501 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.671 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.318 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.432 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.299 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.313 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.359 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.660 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.538 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.688 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.620 |
LIG_GBD_Chelix_1 | 343 | 351 | PF00786 | 0.412 |
LIG_Integrin_isoDGR_2 | 181 | 183 | PF01839 | 0.425 |
LIG_LIR_Gen_1 | 247 | 256 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 339 | 347 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.469 |
LIG_MYND_1 | 57 | 61 | PF01753 | 0.670 |
LIG_MYND_3 | 251 | 255 | PF01753 | 0.341 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.369 |
LIG_Pex14_1 | 202 | 206 | PF04695 | 0.641 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.516 |
LIG_REV1ctd_RIR_1 | 396 | 402 | PF16727 | 0.469 |
LIG_RPA_C_Fungi | 37 | 49 | PF08784 | 0.533 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 117 | 121 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.477 |
LIG_SH3_1 | 5 | 11 | PF00018 | 0.505 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.735 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.304 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.369 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.564 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.533 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.650 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.747 |
LIG_SUMO_SIM_anti_2 | 328 | 335 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 357 | 363 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 213 | 219 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 225 | 230 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 332 | 340 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 95 | 101 | PF11976 | 0.424 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.510 |
LIG_WRC_WIRS_1 | 338 | 343 | PF05994 | 0.270 |
MOD_CDK_SPxxK_3 | 176 | 183 | PF00069 | 0.598 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.559 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.611 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.531 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.483 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.597 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.552 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.465 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.537 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.642 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.450 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.620 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.597 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.551 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.304 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.502 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.567 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.612 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.638 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.615 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.573 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.751 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.532 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.660 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.760 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.580 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.377 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.369 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.469 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.536 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.582 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.609 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.574 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.683 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.559 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.695 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.542 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.675 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.525 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.535 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.601 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.652 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.580 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.494 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.583 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.272 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.314 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.304 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.304 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.304 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.525 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.514 |
MOD_PKA_1 | 345 | 351 | PF00069 | 0.471 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.588 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.501 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.471 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.530 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.508 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.572 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.331 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.597 |
MOD_Plk_2-3 | 448 | 454 | PF00069 | 0.502 |
MOD_Plk_2-3 | 470 | 476 | PF00069 | 0.477 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.574 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.565 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.404 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.369 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.443 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.689 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.623 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.556 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.606 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.292 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.590 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.533 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.753 |
MOD_SUMO_rev_2 | 408 | 415 | PF00179 | 0.369 |
TRG_DiLeu_BaEn_4 | 447 | 453 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.304 |
TRG_NES_CRM1_1 | 385 | 396 | PF08389 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I406 | Leptomonas seymouri | 52% | 100% |
A0A3S5H631 | Leishmania donovani | 99% | 96% |
A4H582 | Leishmania braziliensis | 68% | 100% |
E9AM94 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4QIF4 | Leishmania major | 90% | 100% |