Atomic resolution crystal structure of Kallikrein-Related Peptidase 4 complexed with a modified SFTI inhibitor FCQR(N). Determined by X-ray diffraction at 1.15 Å resolution. Released 30 Apr 2014.
Explore 4KEL in 3D Show helices and sheets RCSB PDB PDBe
4KEL contains 8 α-helices and 21 β-strands across 2 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 |
|---|---|---|---|
| β-strand | 17 | 1 | 1 |
| β-strand | 20-21 | 2 | 2 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-35 | 6 | 3 |
| β-strand | 38-48 | 10 | 3 |
| β-strand | 51-54 | 4 | 3 |
| α-helix | 56-58 | 3 | |
| β-strand | 63-67 | 5 | 3 |
| β-strand | 72 | 1 | 4 |
| β-strand | 81-85 | 5 | 3 |
| β-strand | 87-90 | 4 | 3 |
| β-strand | 104-107 | 4 | 3 |
| α-helix | 122 | 1 | |
| β-strand | 123 | 1 | 2 |
| α-helix | 124 | 1 | |
| β-strand | 135-140 | 6 | 2 |
| α-helix | 150-152 | 3 | |
| β-strand | 154 | 1 | 4 |
| β-strand | 156-162 | 7 | 2 |
| α-helix | 165-171 | 7 | |
| β-strand | 180-184 | 5 | 2 |
| β-strand | 189 | 1 | 1 |
| β-strand | 198-201 | 4 | 2 |
| β-strand | 208-217 | 10 | 2 |
| β-strand | 225-230 | 6 | 2 |
| α-helix | 231-233 | 3 | |
| α-helix | 235-243 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-4 | 3 | 2 |
| β-strand | 10-11 | 2 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Kallikrein-4 | A | protein | 223 | Homo sapiens | Q9Y5K2 (AlphaFold model) |
| Trypsin inhibitor 1 | B | protein | 14 | Helianthus annuus | Q4GWU5 (AlphaFold model) |
>4KEL_1 Kallikrein-4 (chains A) IINGEDCSPHSQPWQAALVMENELFCSGVLVHPQWVLSAAHCFQNSYTIGLGLHSLEADQ EPGSQMVEASLSVRHPEYNRPLLANDLMLIKLDESVSESDTIRSISIASQCPTAGNSCLV SGWGLLANGRMPTVLQCVNVSVVSEEVCSKLYDPLYHPSMFCAGGGQDQKDSCNGDSGGP LICNGYLQGLVSFGKAPCGQVGVPGVYTNLCKFTEWIEKTVQA
>4KEL_2 Trypsin inhibitor 1 (chains B) GFCQRSIPPICFPN
KLK4 Inhibition by Cyclic and Acyclic Peptides: Structural and Dynamical Insights into Standard-Mechanism Protease Inhibitors. Riley, B.T., Ilyichova, O., de Veer, S.J. et al. Biochemistry (2019) 58:2524-2533. DOI 10.1021/acs.biochem.9b00191 · PubMed
Other PDB entries of the same protein (UniProt Q9Y5K2 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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