3WEG: Human squalene synthase

Crystal structure of the human squalene synthase in complex with farnesyl thiopyrophosphate and magnesium ion. Determined by X-ray diffraction at 1.75 Å resolution. Released 12 Feb 2014.

Method
X-ray diffraction
Resolution
1.75 Å
Organism
Homo sapiens
Chains
1
Atoms
3,036
Mol. weight
40.32 kDa
Ligands
MG, FPS
Released
12 Feb 2014

Explore 3WEG in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3WEG contains 24 α-helices and 0 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.

Chain A: 24 helices, 0 β-strands

ElementResiduesLengthSheet
α-helix38-5013
α-helix55-595
α-helix65-8420
α-helix90-10314
α-helix120-1234
α-helix125-13410
α-helix137-15620
α-helix157-1593
α-helix165-1728
α-helix173-1775
α-helix178-19013
α-helix195-1995
α-helix201-21818
α-helix220-2256
α-helix233-2364
α-helix243-2475
α-helix249-2513
α-helix252-26716
α-helix270-2789
α-helix283-30321
α-helix307-3115
α-helix318-32710
α-helix331-34616
α-helix356-36813

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Squalene synthaseAprotein343Homo sapiensP37268 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3WEG_1 Squalene synthase (chains A)
GSHMDQDSLSSSLKTCYKYLNQTSRSFAAVIQALDGEMRNAVCIFYLVLRALDTLEDDMT
ISVEKKVPLLHNFHSFLYQPDWRFMESKEKDRQVLEDFPTISLEFRNLAEKYQTVIADIC
RRMGIGMAEFLDKHVTSEQEWDKYCHYVAGLVGIGLSRLFSASEFEDPLVGEDTERANSM
GLFLQKTNIIRDYLEDQQGGREFWPQEVWSRYVKKLGDFAKPENIDLAVQCLNELITNAL
HHIPDVITYLSRLRNQSVFNFCAIPQVMAIATLAACYNNQQVFKGAVKIRKGQAVTLMMD
ATNMPAVKAIIYQYMEEIYHRIPDSDPSSSKTRQIISTIRTQN

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg3
FPSS-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] trihydrogen thiodiphosphateC15 H28 O6 P2 S2

Primary citation

Structural insights into the catalytic mechanism of human squalene synthase. Liu, C.I., Jeng, W.Y., Chang, W.J. et al. Acta Crystallogr D Biol Crystallogr (2014) 70:231-241. DOI 10.1107/S1399004713026230 · PubMed

Other PDB entries of the same protein (UniProt P37268 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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