3Q2Z: Human Squalene synthase

Human Squalene synthase in complex with N-[(3R,5S)-7-Chloro-5-(2,3-dimethoxyphenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetyl]-L-aspartic acid. Determined by X-ray diffraction at 2.0 Å resolution. Released 21 Dec 2011.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Homo sapiens
Chains
1
Atoms
2,806
Mol. weight
39.84 kDa
Ligands
D9A, PO4
Released
21 Dec 2011

Explore 3Q2Z in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3Q2Z 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-helix38-5114
α-helix54-596
α-helix63-8422
α-helix90-10314
α-helix119-1235
α-helix125-13410
α-helix137-15923
α-helix160-1623
α-helix165-1728
α-helix173-1775
α-helix178-18912
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-helix307-3104
α-helix318-32710
α-helix331-34717
α-helix356-36712

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Squalene synthaseAprotein340Homo sapiensP37268 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3Q2Z_1 Squalene synthase (chains A)
MDQDSLSSSLKTCYKYLNQTSRSFAAVIQALDGEMRNAVCIFYLVLRALDTLEDDMTISV
EKKVPLLHNFHSFLYQPDWRFMESKEKDRQVLEDFPTISLEFRNLAEKYQTVIADICRRM
GIGMAEFLDKHVTSEQEWDKYCHYVAGLVGIGLSRLFSASEFEDPLVGEDTERANSMGLF
LQKTNIIRDYLEDQQGGREFWPQEVWSRYVKKLGDFAKPENIDLAVQCLNELITNALHHI
PDVITYLSRLRNQSVFNFCAIPQVMAIATLAACYNNQQVFKGAVKIRKGQAVTLMMDATN
MPAVKAIIYQYMEEIYHRIPDSDPSSSKTRQIISTIRTQN

Ligands and cofactors

IDNameFormulaCopies
D9AN-{[(3R,5S)-7-chloro-5-(2,3-dimethoxyphenyl)-1-(2,2-dimethylpropyl)-2-oxo-1,2,3…C28 H33 Cl N2 O91
PO4Phosphate ionO4 P1

Primary citation

Discovery of a new 2-aminobenzhydrol template for highly potent squalene synthase inhibitors. Ichikawa, M., Yokomizo, A., Itoh, M. et al. Bioorg Med Chem (2011) 19:1930-1949. DOI 10.1016/j.bmc.2011.01.065 · 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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