Crystal structure of chimeric beta-lactamase cTEM-19m at 1.1 angstrom resolution. Determined by X-ray diffraction at 1.1 Å resolution. Released 11 Nov 2015.
Explore 4R4S in 3D Show helices and sheets RCSB PDB PDBe
4R4S contains 13 α-helices and 9 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 27-40 | 14 | |
| β-strand | 43-50 | 8 | 1 |
| β-strand | 56-60 | 5 | 1 |
| β-strand | 66-67 | 2 | 2 |
| α-helix | 69-71 | 3 | |
| α-helix | 72-85 | 14 | |
| β-strand | 94-95 | 2 | 3 |
| α-helix | 99-101 | 3 | |
| α-helix | 109-111 | 3 | |
| β-strand | 117-118 | 2 | 3 |
| α-helix | 119-128 | 10 | |
| α-helix | 132-142 | 11 | |
| α-helix | 145-154 | 10 | |
| α-helix | 168-170 | 3 | |
| β-strand | 180-181 | 2 | 2 |
| α-helix | 183-194 | 12 | |
| α-helix | 201-212 | 12 | |
| α-helix | 225-226 | 2 | |
| β-strand | 230-237 | 8 | 1 |
| β-strand | 244-251 | 8 | 1 |
| β-strand | 259-266 | 8 | 1 |
| α-helix | 272-288 | 17 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Beta-lactamase TEM,Beta-lactamase PSE-4 | A | protein | 263 | Escherichia coli, Pseudomonas aeruginosa | P16897 (AlphaFold model), P62593 (AlphaFold model) |
>4R4S_1 Beta-lactamase TEM,Beta-lactamase PSE-4 (chains A) HPETLVKVKDAEDQLGARVGYIELDLNSGKILESFRPEERFPLTSTFKVLLCGAVLSRVD AGQEQLGRRIHYSQNDLVEYSPVTEKHLTDGMTVRELCSAAITMSDNTAANLLLTTIGGP KELTDFLRQIGDKETRLDRIEPDLNEGKLGDLRDTTTPKAIASTLRKLLTGELLTLASRQ QLIDWMEADKVAGPLLRSALPAGWFIADKSGAGERGSRGIIAALGPDGKPSRIVVIYTTG SQATMDERNRQIAEIGASLIKHW
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 4 |
Water and common crystallization additives (CL) are not listed.
The Structural Dynamics of Engineered beta-Lactamases Vary Broadly on Three Timescales yet Sustain Native Function. Gobeil, S.M.C., Ebert, M.C.C.J.C., Park, J. et al. Sci Rep (2019) 9:6656-6656. DOI 10.1038/s41598-019-42866-8 · PubMed
Other PDB entries of the same protein (UniProt P16897 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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