Catalytic Domain of Human Phenylalanine Hydroxylase Fe(II) in Complex with Tetrahydrobiopterin. Determined by X-ray diffraction at 1.5 Å resolution. Released 22 May 2002.
Explore 1J8U in 3D Show helices and sheets RCSB PDB PDBe
1J8U contains 20 α-helices and 12 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 |
|---|---|---|---|
| β-strand | 124 | 1 | 1 |
| α-helix | 125-133 | 9 | |
| α-helix | 140-142 | 3 | |
| α-helix | 152-167 | 16 | |
| α-helix | 173-176 | 4 | |
| α-helix | 181-201 | 21 | |
| β-strand | 202 | 1 | 2 |
| α-helix | 204-217 | 14 | |
| β-strand | 220 | 1 | 3 |
| β-strand | 223 | 1 | 3 |
| α-helix | 224-226 | 3 | |
| α-helix | 227-238 | 12 | |
| β-strand | 241-244 | 4 | 4 |
| α-helix | 248-250 | 3 | |
| α-helix | 251-259 | 9 | |
| β-strand | 262-265 | 4 | 4 |
| α-helix | 283-284 | 2 | |
| α-helix | 285-290 | 6 | |
| α-helix | 291-294 | 4 | |
| α-helix | 297-310 | 14 | |
| α-helix | 315-325 | 11 | |
| α-helix | 326-330 | 5 | |
| β-strand | 333-336 | 4 | 2 |
| β-strand | 339-342 | 4 | 2 |
| α-helix | 345-348 | 4 | |
| α-helix | 351-357 | 7 | |
| β-strand | 363-366 | 4 | 2 |
| α-helix | 369-372 | 4 | |
| β-strand | 385-389 | 5 | 2 |
| α-helix | 392-403 | 12 | |
| β-strand | 412-415 | 4 | 1 |
| β-strand | 420-423 | 4 | 1 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Phenylalanine-4-hydroxylase | A | protein | 325 | Homo sapiens | P00439 (AlphaFold model) |
>1J8U_1 PHENYLALANINE-4-HYDROXYLASE (chains A) GATVHELSRDKKKDTVPWFPRTIQELDRFANQILSYGAELDADHPGFKDPVYRARRKQFA DIAYNYRHGQPIPRVEYMEEEKKTWGTVFKTLKSLYKTHACYEYNHIFPLLEKYCGFHED NIPQLEDVSQFLQTCTGFRLRPVAGLLSSRDFLGGLAFRVFHCTQYIRHGSKPMYTPEPD ICHELLGHVPLFSDRSFAQFSQEIGLASLGAPDEYIEKLATIYWFTVEFGLCKQGDSIKA YGAGLLSSFGELQYCLSEKPKLLPLELEKTAIQNYTVTEFQPLYYVAESFNDAKEKVRNF AATIPRPFSVRYDPYTQRIEVLDNT
High resolution crystal structures of the catalytic domain of human phenylalanine hydroxylase in its catalytically active Fe(II) form and binary complex with tetrahydrobiopterin. Andersen, O.A., Flatmark, T., Hough, E. J Mol Biol (2001) 314:279-291. DOI 10.1006/jmbi.2001.5061 · PubMed
Other PDB entries of the same protein (UniProt P00439 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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