Crystal structure of human O-GlcNAc transferase bound to a peptide from HCF-1 pro-repeat 2 (11-26) and inhibitor 4a. Determined by X-ray diffraction at 2.75 Å resolution. Released 17 Oct 2018.
Explore 6MA1 in 3D Show helices and sheets RCSB PDB PDBe
6MA1 contains 42 α-helices and 21 β-strands across 1 chain. 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 | 314-329 | 16 | |
| 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 | 419-432 | 14 | |
| α-helix | 435-448 | 14 | |
| α-helix | 453-465 | 13 | |
| α-helix | 472-488 | 17 | |
| α-helix | 497-500 | 4 | |
| α-helix | 507-526 | 20 | |
| α-helix | 530-536 | 7 | |
| β-strand | 546-552 | 7 | 1 |
| α-helix | 561-564 | 4 | |
| 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 |
| α-helix | 639-642 | 4 | |
| β-strand | 648-652 | 5 | 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 | 2 |
| β-strand | 724-727 | 4 | 2 |
| α-helix | 731-736 | 6 | |
| β-strand | 742-744 | 3 | 2 |
| β-strand | 764-767 | 4 | 2 |
| α-helix | 771-782 | 12 | |
| β-strand | 786-789 | 4 | 2 |
| β-strand | 792-796 | 5 | 2 |
| α-helix | 797-799 | 3 | |
| α-helix | 800-803 | 4 | |
| α-helix | 805-808 | 4 | |
| β-strand | 817-821 | 5 | 2 |
| α-helix | 822-825 | 4 | |
| β-strand | 832-836 | 5 | 3 |
| α-helix | 840-842 | 3 | |
| α-helix | 845-857 | 13 | |
| β-strand | 861-866 | 6 | 3 |
| α-helix | 872-882 | 11 | |
| α-helix | 887-889 | 3 | |
| β-strand | 890-893 | 4 | 3 |
| α-helix | 898-903 | 6 | |
| α-helix | 904-907 | 4 | |
| β-strand | 910-912 | 3 | 3 |
| α-helix | 920-928 | 9 | |
| β-strand | 933-934 | 2 | 3 |
| β-strand | 935 | 1 | 4 |
| α-helix | 945-953 | 9 | |
| α-helix | 956-958 | 3 | |
| β-strand | 959 | 1 | 4 |
| α-helix | 963-975 | 13 | |
| α-helix | 977-993 | 17 | |
| α-helix | 995-997 | 3 | |
| α-helix | 999-1019 | 21 | |
| α-helix | 1021-1023 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit | A | protein | 723 | Homo sapiens | O15294 (AlphaFold model) |
| Host Cell Factor 1 peptide | B | protein | 16 | Homo sapiens | P51610 (AlphaFold model) |
>6MA1_1 UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit (chains A) GPGSCPTHADSLNNLANIKREQGNIEEAVRLYRKALEVFPEFAAAHSNLASVLQQQGKLQ EALMHYKEAIRISPTFADAYSNMGNTLKEMQDVQGALQCYTRAIQINPAFADAHSNLASI HKDSGNIPEAIASYRTALKLKPDFPDAYCNLAHCLQIVCDWTDYDERMKKLVSIVADQLE KNRLPSVHPHHSMLYPLSHGFRKAIAERHGNLCLDKINVLHKPPYEHPKDLKLSDGRLRV GYVSSDFGNHPTSHLMQSIPGMHNPDKFEVFCYALSPDDGTNFRVKVMAEANHFIDLSQI PCNGKAADRIHQDGIHILVNMNGYTKGARNELFALRPAPIQAMWLGYPGTSGALFMDYII TDQETSPAEVAEQYSEKLAYMPHTFFIGDHANMFPHLKKKAVIDFKSNGHIYDNRIVLNG IDLKAFLDSLPDVKIVKMKCPDGGDNADSSNTALNMPVIPMNTIAEAVIEMINRGQIQIT INGFSISNGLATTQINNKAATGEEVPRTIIVTTRSQYGLPEDAIVYCNFNQLYKIDPSTL QMWANILKRVPNSVLWLLRFPAVGEPNIQQYAQNMGLPQNRIIFSPVAPKEEHVRRGQLA DVCLDTPLCNGHTTGMDVLWAGTPMVTMPGETLASRVAASQLTCLGCLELIAKNRQEYED IAVKLGTDLEYLKKVRGKVWKQRISSPLFNTKQYTMELERLYLQMWEHYAAGNKPDHMIK PVE
>6MA1_2 Host Cell Factor 1 peptide (chains B) THETGTTNTATTATSN
| ID | Name | Formula | Copies |
|---|---|---|---|
| JA4 | N-[(2R)-2-{[(7-chloro-2-oxo-1,2-dihydroquinolin-6-yl)sulfonyl]amino}-2-(2-metho… | C25 H22 Cl N3 O7 S2 | 1 |
Structure-Based Evolution of Low Nanomolar O-GlcNAc Transferase Inhibitors. Martin, S.E.S., Tan, Z.W., Itkonen, H.M. et al. J Am Chem Soc (2018) 140:13542-13545. DOI 10.1021/jacs.8b07328 · 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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