Crystal structure of engineered human lipocalin 2 carrying p-boronophenylalanine at position 36. Determined by X-ray diffraction at 2.0 Å resolution. Released 11 Oct 2017.
Explore 5MHH in 3D Show helices and sheets RCSB PDB PDBe
5MHH contains 10 α-helices and 11 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 | 8-12 | 5 | |
| α-helix | 13-15 | 3 | |
| α-helix | 24-27 | 4 | |
| β-strand | 29-38 | 10 | 1 |
| α-helix | 48-49 | 2 | |
| β-strand | 50 | 1 | 2 |
| α-helix | 51 | 1 | |
| β-strand | 53-58 | 6 | 1 |
| β-strand | 64-72 | 9 | 1 |
| β-strand | 75-85 | 11 | 1 |
| β-strand | 91-94 | 4 | 1 |
| α-helix | 97-99 | 3 | |
| β-strand | 103-113 | 11 | 1 |
| β-strand | 118-127 | 10 | 1 |
| β-strand | 130-139 | 10 | 1 |
| α-helix | 146-158 | 13 | |
| α-helix | 163-165 | 3 | |
| β-strand | 166-167 | 2 | 1 |
| α-helix | 169 | 1 | |
| β-strand | 170 | 1 | 2 |
| α-helix | 171 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Neutrophil gelatinase-associated lipocalin | A | protein | 188 | Homo sapiens | P80188 (AlphaFold model) |
>5MHH_1 Neutrophil gelatinase-associated lipocalin (chains A) QDSTSDLIPAPPLSKVPLQQNFQDNQFHGKWYVVGFAGNAILREDKDPQKMFATIYELKE DKSYNVTSVLFRKKKCDYWIRTFVPGSQPGEFTLGNIKSYPGLTSYLVRVVSTNYNQHAM VFFKWVSQNREYFNITLYGRTKELTSELKENFIRFSKSLGLPENHIVFPVPIDQCIDGSA WSHPQFEK
Rational Design of an Anticalin-Type Sugar-Binding Protein Using a Genetically Encoded Boronate Side Chain. Edwardraja, S., Eichinger, A., Theobald, I. et al. ACS Synth Biol (2017) 6:2241-2247. DOI 10.1021/acssynbio.7b00199 · PubMed
Other PDB entries of the same protein (UniProt P80188 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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