4HIQ: V122I Mutant Transthyretin

The Structure of V122I Mutant Transthyretin in Complex with AG10. Determined by X-ray diffraction at 1.18 Å resolution. Released 5 Jun 2013.

Method
X-ray diffraction
Resolution
1.18 Å
Organism
Homo sapiens
Chains
2
Atoms
2,203
Mol. weight
28.17 kDa
Ligands
16V
Released
5 Jun 2013

Explore 4HIQ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4HIQ contains 2 α-helices and 22 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.

Chain A: 1 helix, 12 β-strands

ElementResiduesLengthSheet
β-strand12-1871
β-strand23-2421
β-strand29-3572
β-strand41-4882
β-strand54-5521
β-strand67-7372
α-helix75-817
β-strand8813
β-strand91-9772
β-strand9914
β-strand10114
β-strand104-11291
β-strand115-12391
Chain B: 1 helix, 10 β-strands
ElementResiduesLengthSheet
β-strand12-1871
β-strand23-2421
β-strand29-3573
β-strand41-4883
β-strand54-5521
β-strand67-7373
α-helix75-817
β-strand88-9032
β-strand91-9773
β-strand104-11181
β-strand115-12391

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
TransthyretinA, Bprotein127Homo sapiensP02766 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4HIQ_1 Transthyretin (chains A, B)
GPTGTGESKCPLMVKVLDAVRGSPAINVAVHVFRKAADDTWEPFASGKTSESGELHGLTT
EEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDSGPRRYTIAALLSPYSYSTTA
VITNPKE

Ligands and cofactors

IDNameFormulaCopies
16V3-[3-(3,5-dimethyl-1H-pyrazol-4-yl)propoxy]-4-fluorobenzoic acidC15 H17 F N2 O32

Primary citation

AG10 inhibits amyloidogenesis and cellular toxicity of the familial amyloid cardiomyopathy-associated V122I transthyretin. Penchala, S.C., Connelly, S., Wang, Y. et al. Proc Natl Acad Sci U S A (2013) 110:9992-9997. DOI 10.1073/pnas.1300761110 · PubMed

Other PDB entries of the same protein (UniProt P02766 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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