Discovery of novel, orally efficacious Liver X Receptor (LXR) beta agonists. Determined by X-ray diffraction at 2.61 Å resolution. Released 29 Jun 2016.
Explore 5I4V in 3D Show helices and sheets RCSB PDB PDBe
5I4V contains 57 α-helices and 10 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 | 222-244 | 23 | |
| α-helix | 246-248 | 3 | |
| α-helix | 250-253 | 4 | |
| α-helix | 257-258 | 2 | |
| α-helix | 262-288 | 27 | |
| α-helix | 292-294 | 3 | |
| α-helix | 297-318 | 22 | |
| β-strand | 320-321 | 2 | 1 |
| β-strand | 326-329 | 4 | 1 |
| β-strand | 333-336 | 4 | 1 |
| α-helix | 337-342 | 6 | |
| α-helix | 347-363 | 17 | |
| α-helix | 367-378 | 12 | |
| α-helix | 389-410 | 22 | |
| α-helix | 417-444 | 28 | |
| α-helix | 447-450 | 4 | |
| α-helix | 451-457 | 7 | |
| α-helix | 470-476 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 301-310 | 10 | |
| α-helix | 336-356 | 21 | |
| α-helix | 365-387 | 23 | |
| α-helix | 388-390 | 3 | |
| β-strand | 394-396 | 3 | 2 |
| β-strand | 402-404 | 3 | 2 |
| α-helix | 405-410 | 6 | |
| α-helix | 414-420 | 7 | |
| α-helix | 421-425 | 5 | |
| α-helix | 426-431 | 6 | |
| α-helix | 435-446 | 12 | |
| α-helix | 457-478 | 22 | |
| α-helix | 485-490 | 6 | |
| α-helix | 492-511 | 20 | |
| α-helix | 520-526 | 7 | |
| α-helix | 537-541 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 222-244 | 23 | |
| α-helix | 246-248 | 3 | |
| α-helix | 250-253 | 4 | |
| α-helix | 262-288 | 27 | |
| α-helix | 292-294 | 3 | |
| α-helix | 297-318 | 22 | |
| β-strand | 320-321 | 2 | 3 |
| β-strand | 326-329 | 4 | 3 |
| β-strand | 333-336 | 4 | 3 |
| α-helix | 337-342 | 6 | |
| α-helix | 347-363 | 17 | |
| α-helix | 367-378 | 12 | |
| α-helix | 389-410 | 22 | |
| α-helix | 417-444 | 28 | |
| α-helix | 447-450 | 4 | |
| α-helix | 451-457 | 7 | |
| α-helix | 470-476 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 301-310 | 10 | |
| α-helix | 336-356 | 21 | |
| α-helix | 365-387 | 23 | |
| α-helix | 388-390 | 3 | |
| β-strand | 394-396 | 3 | 4 |
| β-strand | 402-404 | 3 | 4 |
| α-helix | 405-410 | 6 | |
| α-helix | 414-420 | 7 | |
| α-helix | 421-425 | 5 | |
| α-helix | 426-430 | 5 | |
| α-helix | 435-446 | 12 | |
| α-helix | 457-478 | 22 | |
| α-helix | 485-490 | 6 | |
| α-helix | 492-511 | 20 | |
| α-helix | 520-526 | 7 | |
| α-helix | 536-541 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Oxysterols receptor LXR-beta,Nuclear receptor coactivator 2 | A, E | protein | 270 | Homo sapiens | P55055 (AlphaFold model), Q15596 (AlphaFold model) |
| Retinoic acid receptor RXR-beta,Nuclear receptor coactivator 2 | B, F | protein | 255 | Homo sapiens | P28702 (AlphaFold model), Q15596 (AlphaFold model) |
>5I4V_1 Oxysterols receptor LXR-beta,Nuclear receptor coactivator 2 (chains A, E) GSHMGEGVQLTAAQELMIQQLVAAQLQCNKRSFSDQPKVTPWPLGADPASGSASQQRFAH FTELAIISVQEIVDFAKQVPGFLQLGREDQIALLKASTIEIMLLETARRYNHETECITFL KDFTYSKDDFHRAGLQVEFINPIFEFSRAMRRLGLDDAEYALLIAINIFSADRPNVQEPG RVEALQQPYVEALLSYTRIKRPQDQLRFPRMLMKLVSLRTLSSVHSEQVFALRLQDKKLP PLLSEIWDVHEGSGSGSHKILHRLLQDSSS
>5I4V_2 Retinoic acid receptor RXR-beta,Nuclear receptor coactivator 2 (chains B, F) MGAPEEMPVDRILEAELAVEQKSDQGVEGPGGTGGSGSSPNDPVTNICQAADKQLFTLVE WAKRIPHFSSLPLDDQVILLRAGWNELLIASFSHRSIDVRDGILLATGLHVHRNSAHSAG VGAIFDRVLTELVSKMRDMRMDKTELGCLRAIILFNPDAKGLSNPSEVEVLREKVYASLE TYCKQKYPEQQGRFAKLLLRLPALRSIGLKCLEHLFFFKLIGDTPIDTFLMEMLEAGSGS GSHKILHRLLQDSSS
| ID | Name | Formula | Copies |
|---|---|---|---|
| 67S | {2-[(2R)-4-[4-(hydroxymethyl)-3-(methylsulfonyl)phenyl]-2-(propan-2-yl)piperazi… | C21 H27 F3 N4 O4 S | 2 |
Discovery of a Novel, Orally Efficacious Liver X Receptor (LXR) beta Agonist. Zheng, Y., Zhuang, L., Fan, K.Y. et al. J Med Chem (2016) 59:3264-3271. DOI 10.1021/acs.jmedchem.5b02029 · PubMed
Other PDB entries of the same protein (UniProt P55055 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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