Human Transthyretin (TTR) complexed with 2-((3,5-dichloro-4-hydroxyphenyl)amino)benzoic acid. Determined by X-ray diffraction at 1.2 Å resolution. Released 17 Nov 2010.
Explore 3M1O in 3D Show helices and sheets RCSB PDB PDBe
3M1O contains 2 α-helices and 20 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 |
|---|---|---|---|
| β-strand | 12-18 | 7 | 1 |
| β-strand | 23-24 | 2 | 1 |
| β-strand | 29-35 | 7 | 2 |
| β-strand | 41-48 | 8 | 2 |
| β-strand | 54-55 | 2 | 1 |
| β-strand | 67-73 | 7 | 2 |
| α-helix | 75-81 | 7 | |
| β-strand | 88-97 | 10 | 2 |
| β-strand | 99 | 1 | 3 |
| β-strand | 101 | 1 | 3 |
| β-strand | 104-112 | 9 | 1 |
| β-strand | 115-123 | 9 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-18 | 7 | 1 |
| β-strand | 23-24 | 2 | 1 |
| β-strand | 29-35 | 7 | 2 |
| β-strand | 41-48 | 8 | 2 |
| β-strand | 54-55 | 2 | 1 |
| β-strand | 67-73 | 7 | 2 |
| α-helix | 75-81 | 7 | |
| β-strand | 88-97 | 10 | 2 |
| β-strand | 105-112 | 8 | 1 |
| β-strand | 115-122 | 8 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Transthyretin | A, B | protein | 127 | Homo sapiens | P02766 (AlphaFold model) |
>3M1O_1 Transthyretin (chains A, B) GPTGTGESKCPLMVKVLDAVRGSPAINVAVHVFRKAADDTWEPFASGKTSESGELHGLTT EEEFVEGIYKVEIDTKSYWKALGISPFHEHAEVVFTANDSGPRRYTIAALLSPYSYSTTA VVTNPKE
| ID | Name | Formula | Copies |
|---|---|---|---|
| CJZ | 2-[(3,5-dichloro-4-hydroxyphenyl)amino]benzoic acid | C13 H9 Cl2 N O3 | 2 |
Trapping of palindromic ligands within native transthyretin prevents amyloid formation. Kolstoe, S.E., Mangione, P.P., Bellotti, V. et al. Proc Natl Acad Sci U S A (2010) 107:20483-20488. DOI 10.1073/pnas.1008255107 · PubMed
Other PDB entries of the same protein (UniProt P02766 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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