Crystal structure of the orphan nuclear receptor RORgamma ligand-binding domain in complex with 4alpha-caboxyl, 4beta-methyl-zymosterol (4ACD8). Determined by X-ray diffraction at 3.54 Å resolution. Released 11 Feb 2015.
Explore 4S14 in 3D Show helices and sheets RCSB PDB PDBe
4S14 contains 18 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 | 267-283 | 17 | |
| α-helix | 289-294 | 6 | |
| α-helix | 295-297 | 3 | |
| β-strand | 299 | 1 | 1 |
| α-helix | 300-301 | 2 | |
| α-helix | 302-309 | 8 | |
| α-helix | 313-337 | 25 | |
| α-helix | 346-364 | 19 | |
| α-helix | 365-367 | 3 | |
| β-strand | 369-370 | 2 | 1 |
| β-strand | 375-378 | 4 | 1 |
| β-strand | 381-383 | 3 | 1 |
| α-helix | 385-391 | 7 | |
| α-helix | 394-409 | 16 | |
| α-helix | 414-425 | 12 | |
| α-helix | 436-456 | 21 | |
| α-helix | 462-465 | 4 | |
| α-helix | 467-468 | 2 | |
| α-helix | 469-489 | 21 | |
| α-helix | 491-496 | 6 | |
| α-helix | 500-506 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 499-504 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Nuclear receptor ROR-gamma | A | protein | 259 | Homo sapiens | P51449 (AlphaFold model) |
| Nuclear receptor-interacting protein 1 | C | protein | 12 | Homo sapiens | P48552 (AlphaFold model) |
>4S14_1 Nuclear receptor ROR-gamma (chains A) GSAPYASLTEIEHLVQSVCKSYRETCQLRLEDLLRQRSNIFSREEVTGYQRKSMWEMWER CAHHLTEAIQYVVEFAKRLSGFMELCQNDQIVLLKAGAMEVVLVRMCRAYNADNRTVFFE GKYGGMELFRALGCSELISSIFDFSHSLSALHFSEDEIALYTALVLINAHRPGLQEKRKV EQLQYNLELAFHHHLCKTHRQSILAKLPPKGKLRSLCSQHVERLQIFQHLHPIVVQAAFP PLYKELFSTETESPVGLSK
>4S14_2 Nuclear receptor-interacting protein 1 (chains C) TLLQLLLGHKNE
| ID | Name | Formula | Copies |
|---|---|---|---|
| 4D8 | (3beta,4alpha,5beta,14beta)-3-hydroxy-4-methylcholesta-8,24-diene-4-carboxylic… | C29 H46 O3 | 1 |
Identification of Natural ROR gamma Ligands that Regulate the Development of Lymphoid Cells. Santori, F.R., Huang, P., van de Pavert, S.A. et al. Cell Metab (2015) 21:286-297. DOI 10.1016/j.cmet.2015.01.004 · PubMed
Other PDB entries of the same protein (UniProt P51449 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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