DCN1 bound to 8. Determined by X-ray diffraction at 2.1 Å resolution. Released 2 Jun 2021.
Explore 6XOM in 3D Show helices and sheets RCSB PDB PDBe
6XOM contains 22 α-helices and 11 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 | 3-10 | 8 | |
| β-strand | 14-15 | 2 | 1 |
| β-strand | 16 | 1 | 2 |
| β-strand | 17-19 | 3 | 1 |
| β-strand | 25-28 | 4 | 1 |
| β-strand | 31-34 | 4 | 1 |
| α-helix | 39-50 | 12 | |
| β-strand | 57 | 1 | 2 |
| α-helix | 60-79 | 20 | |
| α-helix | 85-90 | 6 | |
| α-helix | 93-112 | 20 | |
| α-helix | 115-122 | 8 | |
| α-helix | 126-133 | 8 | |
| α-helix | 138-141 | 4 | |
| α-helix | 143-155 | 13 | |
| α-helix | 159-1072 | 17 | |
| β-strand | 1073-1074 | 2 | 3 |
| β-strand | 1077-1081 | 5 | 3 |
| α-helix | 1083-1092 | 10 | |
| α-helix | 1100-1108 | 9 | |
| β-strand | 1117-1118 | 2 | 3 |
| α-helix | 1119-1128 | 10 | |
| α-helix | 1134-1147 | 14 | |
| α-helix | 1151-1165 | 15 | |
| α-helix | 1167 | 1 | |
| β-strand | 1173 | 1 | 4 |
| α-helix | 1175-1185 | 11 | |
| α-helix | 1193-1199 | 7 | |
| α-helix | 1200-1204 | 5 | |
| β-strand | 1208 | 1 | 4 |
| α-helix | 1210-1222 | 13 | |
| α-helix | 1238-1247 | 10 | |
| α-helix | 1248-1250 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Lysozyme, DCN1-like protein 1 chimera | A | protein | 386 | Enterobacteria phage T4, Homo sapiens | D9IEF7, Q96GG9 (AlphaFold model) |
>6XOM_1 Lysozyme, DCN1-like protein 1 chimera (chains A) MHHHHHHSSGVDLGTENLYFQSNAMNIFEMLRIDEGLRLKIYKDTEGYYTIGIGHLLTKS PSLNAAKSELDKAIGRNTNGVITKDEAEKLFNQDVDAAVRGILRNAKLKPVYDSLDAVRR AALINMVFQMGETGVAGFTNSLRMLQQKRWAEAAVNLAKSRWYNQTPNRTKRVITTFATG TWDAYKNLRKKLEQLYNRYKDPQDENKIGIDGIQQFCDDLALDPASISVLIIAWKFRAAT QCEFSKQEFMDGMTELGCDSIEKLKAQIPKMEQELKEPGRFKDFYQFTFNFAKNPGQKGL DLEMAIAYWNLVLNGRFKFLDLWNKFLLEHHKRSIPKDTWNLLLDFSTMIADDMSNYDEE GAWPVLIDDFVEFARPQIAGTKSTTV
| ID | Name | Formula | Copies |
|---|---|---|---|
| H8V | (2R)-N-[(2S)-2-cyclohexyl-2-({N-propanoyl-3-[6-(propan-2-yl)-1,3-benzothiazol-2… | C33 H51 N5 O4 S | 1 |
Water and common crystallization additives (EDO) are not listed.
Selective inhibition of cullin 3 neddylation through covalent targeting DCN1 protects mice from acetaminophen-induced liver toxicity. Zhou, H., Lu, J., Chinnaswamy, K. et al. Nat Commun (2021) 12:2621-2621. DOI 10.1038/s41467-021-22924-4 · PubMed
Other PDB entries of the same protein (UniProt D9IEF7), best resolution first:
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