Siderocalin-mediated recognition and cellular uptake of actinides. Determined by X-ray diffraction at 2.04 Å resolution. Released 5 Aug 2015.
Explore 4ZHH in 3D Show helices and sheets RCSB PDB PDBe
4ZHH contains 60 α-helices and 68 β-strands across 6 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 |
|---|---|---|---|
| α-helix | 8-12 | 5 | |
| α-helix | 13-15 | 3 | |
| 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 |
| α-helix | 63 | 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 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7 | 1 | 1 |
| α-helix | 8-12 | 5 | |
| α-helix | 13-15 | 3 | |
| β-strand | 29-38 | 10 | 3 |
| α-helix | 48-49 | 2 | |
| β-strand | 50 | 1 | 4 |
| α-helix | 51 | 1 | |
| β-strand | 53-58 | 6 | 3 |
| β-strand | 64-72 | 9 | 3 |
| β-strand | 75-85 | 11 | 3 |
| β-strand | 91-94 | 4 | 3 |
| α-helix | 97-99 | 3 | |
| β-strand | 103-113 | 11 | 3 |
| β-strand | 118-127 | 10 | 3 |
| β-strand | 130-139 | 10 | 3 |
| α-helix | 146-158 | 13 | |
| α-helix | 163-165 | 3 | |
| β-strand | 166-167 | 2 | 3 |
| α-helix | 169 | 1 | |
| β-strand | 170 | 1 | 4 |
| α-helix | 171 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7 | 1 | 5 |
| α-helix | 8-12 | 5 | |
| α-helix | 13-15 | 3 | |
| α-helix | 24-27 | 4 | |
| β-strand | 29-38 | 10 | 6 |
| α-helix | 48-49 | 2 | |
| β-strand | 50 | 1 | 7 |
| α-helix | 51 | 1 | |
| β-strand | 53-58 | 6 | 6 |
| α-helix | 63 | 1 | |
| β-strand | 64-72 | 9 | 6 |
| β-strand | 75-85 | 11 | 6 |
| β-strand | 91-94 | 4 | 6 |
| α-helix | 97-99 | 3 | |
| β-strand | 103-113 | 11 | 6 |
| β-strand | 118-127 | 10 | 6 |
| β-strand | 130-139 | 10 | 6 |
| α-helix | 146-158 | 13 | |
| α-helix | 163-165 | 3 | |
| β-strand | 166-167 | 2 | 6 |
| α-helix | 169 | 1 | |
| β-strand | 170 | 1 | 7 |
| α-helix | 171 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 8-12 | 5 | |
| α-helix | 13-15 | 3 | |
| α-helix | 24-27 | 4 | |
| β-strand | 29-38 | 10 | 9 |
| α-helix | 48-49 | 2 | |
| β-strand | 50 | 1 | 10 |
| α-helix | 51 | 1 | |
| β-strand | 53-58 | 6 | 9 |
| β-strand | 64-72 | 9 | 9 |
| β-strand | 75-85 | 11 | 9 |
| β-strand | 91-94 | 4 | 9 |
| α-helix | 97-99 | 3 | |
| β-strand | 103-113 | 11 | 9 |
| β-strand | 118-127 | 10 | 9 |
| β-strand | 130-139 | 10 | 9 |
| α-helix | 146-158 | 13 | |
| α-helix | 163-165 | 3 | |
| β-strand | 166-167 | 2 | 9 |
| α-helix | 169 | 1 | |
| β-strand | 170 | 1 | 10 |
| α-helix | 171 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Neutrophil gelatinase-associated lipocalin | A, B, C, D, E, F | protein | 180 | Homo sapiens | P80188 (AlphaFold model) |
>4ZHH_1 Neutrophil gelatinase-associated lipocalin (chains A, B, C, D, E, F) GSQDSTSDLIPAPPLSKVPLQQNFQDNQFQGKWYVVGLAGNAILREDKDPQKMYATIYEL KEDKSYNVTSVLFRKKKCDYWIRTFVPGSQPGEFTLGNIKSYPGLTSYLVRVVSTNYNQH AMVFFKKVSQNREYFKITLYGRTKELTSELKENFIRFSKSLGLPENHIVFPVPIDQCIDG
| ID | Name | Formula | Copies |
|---|---|---|---|
| 4OL | N,N'-butane-1,4-diylbis[1-hydroxy-N-(3-{[(1-hydroxy-6-oxo-1,6-dihydropyridin-2-… | C34 H38 N8 O12 | 6 |
| SM | Samarium (III) ion | Sm | 6 |
Water and common crystallization additives (SO4, CL, GOL) are not listed.
Siderocalin-mediated recognition, sensitization, and cellular uptake of actinides. Allred, B.E., Rupert, P.B., Gauny, S.S. et al. Proc Natl Acad Sci U S A (2015) 112:10342-10347. DOI 10.1073/pnas.1508902112 · 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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