5MHH: Neutrophil gelatinase-associated lipocalin

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.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Homo sapiens
Chains
1
Atoms
1,557
Mol. weight
22.16 kDa
Released
11 Oct 2017

Explore 5MHH in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain A: 10 helices, 11 β-strands

ElementResiduesLengthSheet
α-helix8-125
α-helix13-153
α-helix24-274
β-strand29-38101
α-helix48-492
β-strand5012
α-helix511
β-strand53-5861
β-strand64-7291
β-strand75-85111
β-strand91-9441
α-helix97-993
β-strand103-113111
β-strand118-127101
β-strand130-139101
α-helix146-15813
α-helix163-1653
β-strand166-16721
α-helix1691
β-strand17012
α-helix1711

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Neutrophil gelatinase-associated lipocalinAprotein188Homo sapiensP80188 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5MHH_1 Neutrophil gelatinase-associated lipocalin (chains A)
QDSTSDLIPAPPLSKVPLQQNFQDNQFHGKWYVVGFAGNAILREDKDPQKMFATIYELKE
DKSYNVTSVLFRKKKCDYWIRTFVPGSQPGEFTLGNIKSYPGLTSYLVRVVSTNYNQHAM
VFFKWVSQNREYFNITLYGRTKELTSELKENFIRFSKSLGLPENHIVFPVPIDQCIDGSA
WSHPQFEK

Primary citation

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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