Crystal structure of human O-GlcNAc Transferase in complex with UDP and a glycopeptide. Determined by X-ray diffraction at 1.7 Å resolution. Released 31 Oct 2012.
Explore 4GYW in 3D Show helices and sheets RCSB PDB PDBe
4GYW contains 86 α-helices and 48 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 315-329 | 15 | |
| α-helix | 333-346 | 14 | |
| α-helix | 351-363 | 13 | |
| α-helix | 367-380 | 14 | |
| α-helix | 385-397 | 13 | |
| α-helix | 401-414 | 14 | |
| α-helix | 419-431 | 13 | |
| α-helix | 435-448 | 14 | |
| α-helix | 453-465 | 13 | |
| α-helix | 472-488 | 17 | |
| α-helix | 499-502 | 4 | |
| α-helix | 507-526 | 20 | |
| α-helix | 530-536 | 7 | |
| β-strand | 546-552 | 7 | 1 |
| α-helix | 559-564 | 6 | |
| α-helix | 567-570 | 4 | |
| β-strand | 576-582 | 7 | 1 |
| α-helix | 590-598 | 9 | |
| β-strand | 601-604 | 4 | 1 |
| α-helix | 605-607 | 3 | |
| α-helix | 611-620 | 10 | |
| β-strand | 625-628 | 4 | 1 |
| β-strand | 633 | 1 | 2 |
| α-helix | 639-642 | 4 | |
| β-strand | 648-651 | 4 | 1 |
| β-strand | 666-669 | 4 | 1 |
| α-helix | 676-681 | 6 | |
| β-strand | 685-688 | 4 | 1 |
| α-helix | 698-701 | 4 | |
| α-helix | 703-705 | 3 | |
| β-strand | 709-711 | 3 | 3 |
| β-strand | 724-727 | 4 | 3 |
| α-helix | 731-736 | 6 | |
| β-strand | 742-744 | 3 | 3 |
| β-strand | 764-767 | 4 | 3 |
| α-helix | 771-782 | 12 | |
| β-strand | 786-789 | 4 | 3 |
| β-strand | 792-796 | 5 | 3 |
| α-helix | 800-803 | 4 | |
| α-helix | 805-809 | 5 | |
| β-strand | 817-821 | 5 | 3 |
| α-helix | 822-825 | 4 | |
| β-strand | 832-835 | 4 | 4 |
| α-helix | 840-842 | 3 | |
| α-helix | 845-857 | 13 | |
| β-strand | 861-867 | 7 | 4 |
| α-helix | 870-872 | 3 | |
| α-helix | 873-882 | 10 | |
| α-helix | 887-889 | 3 | |
| β-strand | 890-894 | 5 | 4 |
| α-helix | 898-904 | 7 | |
| α-helix | 905-907 | 3 | |
| β-strand | 910-912 | 3 | 4 |
| α-helix | 921-928 | 8 | |
| β-strand | 933-934 | 2 | 4 |
| β-strand | 935 | 1 | 5 |
| α-helix | 941-943 | 3 | |
| α-helix | 945-953 | 9 | |
| α-helix | 956-958 | 3 | |
| β-strand | 959 | 1 | 5 |
| α-helix | 963-975 | 13 | |
| α-helix | 977-993 | 17 | |
| α-helix | 999-1018 | 20 | |
| β-strand | 1026 | 1 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 23 | 1 | 2 |
| α-helix | 24-25 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 337-346 | 10 | |
| α-helix | 351-364 | 14 | |
| α-helix | 367-380 | 14 | |
| α-helix | 385-397 | 13 | |
| α-helix | 401-414 | 14 | |
| α-helix | 419-432 | 14 | |
| α-helix | 435-448 | 14 | |
| α-helix | 453-465 | 13 | |
| α-helix | 472-488 | 17 | |
| α-helix | 499-502 | 4 | |
| α-helix | 507-526 | 20 | |
| α-helix | 530-536 | 7 | |
| α-helix | 540-542 | 3 | |
| β-strand | 546-552 | 7 | 6 |
| α-helix | 559-564 | 6 | |
| α-helix | 567-570 | 4 | |
| β-strand | 576-582 | 7 | 6 |
| α-helix | 590-598 | 9 | |
| β-strand | 601-604 | 4 | 6 |
| α-helix | 605-607 | 3 | |
| α-helix | 611-621 | 11 | |
| β-strand | 625-628 | 4 | 6 |
| β-strand | 633 | 1 | 7 |
| α-helix | 639-642 | 4 | |
| β-strand | 648-651 | 4 | 6 |
| β-strand | 666-669 | 4 | 6 |
| α-helix | 676-681 | 6 | |
| β-strand | 685-688 | 4 | 6 |
| α-helix | 698-701 | 4 | |
| α-helix | 703-705 | 3 | |
| β-strand | 709-711 | 3 | 8 |
| β-strand | 724-727 | 4 | 8 |
| α-helix | 731-736 | 6 | |
| α-helix | 741 | 1 | |
| β-strand | 742-744 | 3 | 8 |
| β-strand | 764-767 | 4 | 8 |
| α-helix | 771-782 | 12 | |
| β-strand | 786-789 | 4 | 8 |
| β-strand | 792-796 | 5 | 8 |
| α-helix | 800-803 | 4 | |
| α-helix | 805-808 | 4 | |
| β-strand | 817-821 | 5 | 8 |
| α-helix | 822-825 | 4 | |
| β-strand | 832-835 | 4 | 9 |
| α-helix | 840-842 | 3 | |
| α-helix | 845-857 | 13 | |
| β-strand | 861-867 | 7 | 9 |
| α-helix | 870-872 | 3 | |
| α-helix | 873-882 | 10 | |
| α-helix | 887-889 | 3 | |
| β-strand | 890-894 | 5 | 9 |
| α-helix | 898-904 | 7 | |
| α-helix | 905-907 | 3 | |
| β-strand | 910-912 | 3 | 9 |
| α-helix | 921-928 | 8 | |
| β-strand | 933-934 | 2 | 9 |
| β-strand | 935 | 1 | 10 |
| α-helix | 941-943 | 3 | |
| α-helix | 945-953 | 9 | |
| α-helix | 956-958 | 3 | |
| β-strand | 959 | 1 | 10 |
| α-helix | 963-975 | 13 | |
| α-helix | 977-993 | 17 | |
| α-helix | 999-1018 | 20 | |
| α-helix | 1021-1023 | 3 | |
| β-strand | 1026 | 1 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit | A, C | protein | 723 | Homo sapiens | O15294 (AlphaFold model) |
| Casein kinase II subunit alpha | B, D | protein | 14 | Homo sapiens | P68400 (AlphaFold model) |
>4GYW_1 UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit (chains A, C) GPGSCPTHADSLNNLANIKREQGNIEEAVRLYRKALEVFPEFAAAHSNLASVLQQQGKLQ EALMHYKEAIRISPTFADAYSNMGNTLKEMQDVQGALQCYTRAIQINPAFADAHSNLASI HKDSGNIPEAIASYRTALKLKPDFPDAYCNLAHCLQIVCDWTDYDERMKKLVSIVADQLE KNRLPSVHPHHSMLYPLSHGFRKAIAERHGNLCLDKINVLHKPPYEHPKDLKLSDGRLRV GYVSSDFGNHPTSHLMQSIPGMHNPDKFEVFCYALSPDDGTNFRVKVMAEANHFIDLSQI PCNGKAADRIHQDGIHILVNMNGYTKGARNELFALRPAPIQAMWLGYPGTSGALFMDYII TDQETSPAEVAEQYSEKLAYMPHTFFIGDHANMFPHLKKKAVIDFKSNGHIYDNRIVLNG IDLKAFLDSLPDVKIVKMKCPDGGDNADSSNTALNMPVIPMNTIAEAVIEMINRGQIQIT INGFSISNGLATTQINNKAATGEEVPRTIIVTTRSQYGLPEDAIVYCNFNQLYKIDPSTL QMWANILKRVPNSVLWLLRFPAVGEPNIQQYAQNMGLPQNRIIFSPVAPKEEHVRRGQLA DVCLDTPLCNGHTTGMDVLWAGTPMVTMPGETLASRVAASQLTCLGCLELIAKNRQEYED IAVKLGTDLEYLKKVRGKVWKQRISSPLFNTKQYTMELERLYLQMWEHYAAGNKPDHMIK PVE
>4GYW_2 Casein kinase II subunit alpha (chains B, D) YPGGSTPVSSANMM
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
| UDP | Uridine-5'-diphosphate | C9 H14 N2 O12 P2 | 2 |
Water and common crystallization additives (SO4) are not listed.
Structural snapshots of the reaction coordinate for O-GlcNAc transferase. Lazarus, M.B., Jiang, J., Gloster, T.M. et al. Nat Chem Biol (2012) 8:966-968. DOI 10.1038/nchembio.1109 · PubMed
Other PDB entries of the same protein (UniProt O15294 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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