Crystal structure of kallikrein-related peptidase 4. Determined by X-ray diffraction at 2.32 Å resolution. Released 30 Apr 2014.
Explore 4KGA in 3D Show helices and sheets RCSB PDB PDBe
4KGA contains 19 α-helices and 34 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 | 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 | |
| α-helix | 128-129 | 2 | |
| β-strand | 135-140 | 6 | 2 |
| β-strand | 156-162 | 7 | 2 |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 2 |
| β-strand | 189 | 1 | 1 |
| β-strand | 198-201 | 4 | 2 |
| β-strand | 208-215 | 8 | 2 |
| α-helix | 225 | 1 | |
| β-strand | 226-230 | 5 | 2 |
| α-helix | 231-233 | 3 | |
| α-helix | 235-243 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 17 | 1 | 4 |
| β-strand | 20-21 | 2 | 5 |
| α-helix | 22-23 | 2 | |
| β-strand | 30-35 | 6 | 6 |
| β-strand | 38-48 | 10 | 6 |
| β-strand | 51-54 | 4 | 6 |
| α-helix | 56-58 | 3 | |
| β-strand | 63-66 | 4 | 6 |
| β-strand | 82-85 | 4 | 6 |
| β-strand | 87-90 | 4 | 6 |
| β-strand | 104-107 | 4 | 6 |
| α-helix | 122 | 1 | |
| β-strand | 123 | 1 | 5 |
| α-helix | 124 | 1 | |
| α-helix | 128-129 | 2 | |
| β-strand | 135-140 | 6 | 5 |
| β-strand | 156-162 | 7 | 5 |
| α-helix | 165-171 | 7 | |
| β-strand | 180-183 | 4 | 5 |
| β-strand | 189 | 1 | 4 |
| β-strand | 198-201 | 4 | 5 |
| β-strand | 208-215 | 8 | 5 |
| α-helix | 217 | 1 | |
| α-helix | 225 | 1 | |
| β-strand | 226-230 | 5 | 5 |
| α-helix | 231-233 | 3 | |
| α-helix | 235-243 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Kallikrein-4 | A, B | protein | 223 | Homo sapiens | Q9Y5K2 (AlphaFold model) |
>4KGA_1 Kallikrein-4 (chains A, B) IINGEDCSPHSQPWQAALVMENELFCSGVLVHPQWVLSAAHCFQNSYTIGLGLHSLEADQ EPGSQMVEASLSVRHPEYNRPLLANDLMLIKLDESVSESDTIRSISIASQCPTAGNSCLV SGWGLLANGRMPTVLQCVNVSVVSEEVCSKLYDPLYHPSMFCAGGGQDQKDSCNGDSGGP LICNGYLQGLVSFGKAPCGQVGVPGVYTNLCKFTEWIEKTVQA
| ID | Name | Formula | Copies |
|---|---|---|---|
| NI | Nickel (II) ion | Ni | 4 |
Water and common crystallization additives (EDO) are not listed.
Direct and indirect mechanisms of KLK4 inhibition revealed by structure and dynamics. Riley, B.T., Ilyichova, O., Costa, M.G.S. et al. Sci Rep (2016) 6:35385-35385. DOI 10.1038/srep35385 · 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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