Crystal structure of PDE4D catalytic domain in complex with arctigenin. Determined by X-ray diffraction at 1.45 Å resolution. Released 14 Apr 2021.
Explore 6LRM in 3D Show helices and sheets RCSB PDB PDBe
6LRM contains 47 α-helices and 4 β-strands across 2 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 | 87-96 | 10 | |
| α-helix | 106-112 | 7 | |
| α-helix | 117-128 | 12 | |
| α-helix | 131-135 | 5 | |
| α-helix | 139-151 | 13 | |
| α-helix | 162-176 | 15 | |
| α-helix | 179-181 | 3 | |
| α-helix | 187-199 | 13 | |
| α-helix | 209-214 | 6 | |
| α-helix | 218-223 | 6 | |
| α-helix | 228-239 | 12 | |
| α-helix | 240-242 | 3 | |
| α-helix | 254-269 | 16 | |
| α-helix | 273-275 | 3 | |
| α-helix | 276-288 | 13 | |
| β-strand | 292 | 1 | 1 |
| β-strand | 298 | 1 | 1 |
| α-helix | 299 | 1 | |
| α-helix | 303-318 | 16 | |
| α-helix | 321-323 | 3 | |
| α-helix | 326-349 | 24 | |
| α-helix | 352-355 | 4 | |
| α-helix | 365-372 | 8 | |
| α-helix | 373-377 | 5 | |
| α-helix | 378-387 | 10 | |
| α-helix | 393-409 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 89-96 | 8 | |
| α-helix | 106-112 | 7 | |
| α-helix | 117-128 | 12 | |
| α-helix | 131-135 | 5 | |
| α-helix | 139-151 | 13 | |
| α-helix | 162-176 | 15 | |
| α-helix | 179-181 | 3 | |
| α-helix | 187-199 | 13 | |
| α-helix | 209-214 | 6 | |
| α-helix | 218-223 | 6 | |
| α-helix | 228-239 | 12 | |
| α-helix | 240-242 | 3 | |
| α-helix | 254-269 | 16 | |
| α-helix | 273-275 | 3 | |
| α-helix | 276-288 | 13 | |
| β-strand | 292 | 1 | 2 |
| β-strand | 298 | 1 | 2 |
| α-helix | 303-318 | 16 | |
| α-helix | 321-323 | 3 | |
| α-helix | 326-349 | 24 | |
| α-helix | 352-355 | 4 | |
| α-helix | 365-372 | 8 | |
| α-helix | 373-377 | 5 | |
| α-helix | 378-387 | 10 | |
| α-helix | 393-408 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| cAMP-specific 3',5'-cyclic phosphodiesterase 4D | A, B | protein | 349 | Homo sapiens | Q08499 (AlphaFold model) |
>6LRM_1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D (chains A, B) MGSSHHHHHHSSGLVPRGSHMTEQEDVLAKELEDVNKWGLHVFRIAELSGNRPLTVIMHT IFQERDLLKTFKIPVDTLITYLMTLEDHYHADVAYHNNIHAADVVQSTHVLLSTPALEAV FTDLEILAAIFASAIHDVDHPGVSNQFLINTNSELALMYNDSSVLENHHLAVGFKLLQEE NCDIFQNLTKKQRQSLRKMVIDIVLATDMSKHMNLLADLKTMVETKKVTSSGVLLLDNYS DRIQVLQNMVHCADLSNPTKPLQLYRQWTDRIMEEFFRQGDRERERGMEISPMCDKHNAS VEKSQVGFIDYIVHPLWETWADLVHPDAQDILDTLEDNREWYQSTIPQS
Water and common crystallization additives (EDO) are not listed.
Identification of phosphodiesterase-4 as the therapeutic target of arctigenin in alleviating psoriatic skin inflammation. Li, H., Zhang, X., Xiang, C. et al. J Adv Res (2021) 33:241-251. DOI 10.1016/j.jare.2021.02.006 · PubMed
Other PDB entries of the same protein (UniProt Q08499 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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