New Classes of Potent and Bioavailable Human Renin Inhibitors. Determined by X-ray diffraction at 1.5 Å resolution. Released 2 Mar 2010.
Explore 3K1W in 3D Show helices and sheets RCSB PDB PDBe
3K1W contains 30 α-helices and 67 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 | 6 | 1 | 1 |
| β-strand | 8-12 | 5 | 2 |
| β-strand | 13-15 | 3 | 3 |
| β-strand | 19-21 | 3 | 3 |
| β-strand | 22-26 | 5 | 4 |
| β-strand | 31-38 | 8 | 4 |
| β-strand | 44-47 | 4 | 4 |
| β-strand | 48 | 1 | 5 |
| α-helix | 56-59 | 4 | |
| β-strand | 64 | 1 | 5 |
| α-helix | 66-68 | 3 | |
| β-strand | 73-83 | 11 | 4 |
| β-strand | 86-99 | 14 | 4 |
| β-strand | 102-113 | 12 | 4 |
| α-helix | 116-119 | 4 | |
| β-strand | 126-129 | 4 | 4 |
| α-helix | 133-135 | 3 | |
| α-helix | 137-139 | 3 | |
| α-helix | 140-142 | 3 | |
| α-helix | 143-150 | 8 | |
| β-strand | 153 | 1 | 1 |
| β-strand | 157-162 | 6 | 2 |
| β-strand | 174-178 | 5 | 2 |
| α-helix | 183-185 | 3 | |
| β-strand | 186-194 | 9 | 2 |
| β-strand | 202-205 | 4 | 6 |
| β-strand | 208-210 | 3 | 7 |
| β-strand | 213-216 | 4 | 7 |
| β-strand | 221-225 | 5 | 6 |
| β-strand | 232-234 | 3 | 6 |
| α-helix | 236-246 | 11 | |
| β-strand | 249-250 | 2 | 8 |
| β-strand | 255-258 | 4 | 8 |
| α-helix | 259-264 | 6 | |
| α-helix | 265-267 | 3 | |
| β-strand | 268-272 | 5 | 7 |
| β-strand | 275-279 | 5 | 7 |
| α-helix | 281-284 | 4 | |
| β-strand | 285 | 1 | 9 |
| β-strand | 295-297 | 3 | 8 |
| β-strand | 298 | 1 | 9 |
| β-strand | 300-302 | 3 | 6 |
| α-helix | 305-306 | 2 | |
| β-strand | 313-315 | 3 | 6 |
| α-helix | 317-320 | 4 | |
| β-strand | 323-328 | 6 | 2 |
| β-strand | 333-339 | 7 | 2 |
| α-helix | 340 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8-12 | 5 | 10 |
| β-strand | 13-15 | 3 | 11 |
| β-strand | 19-21 | 3 | 11 |
| β-strand | 22-26 | 5 | 12 |
| β-strand | 31-38 | 8 | 12 |
| β-strand | 44-47 | 4 | 12 |
| β-strand | 48 | 1 | 13 |
| α-helix | 56-59 | 4 | |
| β-strand | 64 | 1 | 13 |
| α-helix | 66-68 | 3 | |
| β-strand | 73-83 | 11 | 12 |
| β-strand | 86-99 | 14 | 12 |
| β-strand | 102-113 | 12 | 12 |
| α-helix | 116-119 | 4 | |
| β-strand | 126-129 | 4 | 12 |
| α-helix | 133-135 | 3 | |
| α-helix | 137-139 | 3 | |
| α-helix | 140-142 | 3 | |
| α-helix | 143-150 | 8 | |
| β-strand | 157-162 | 6 | 10 |
| α-helix | 163-165 | 3 | |
| β-strand | 174-178 | 5 | 10 |
| α-helix | 183-185 | 3 | |
| β-strand | 186 | 1 | 14 |
| β-strand | 191-194 | 4 | 10 |
| β-strand | 195 | 1 | 15 |
| β-strand | 202-205 | 4 | 15 |
| β-strand | 207-210 | 4 | 16 |
| β-strand | 213-216 | 4 | 16 |
| β-strand | 221-225 | 5 | 15 |
| β-strand | 232-234 | 3 | 15 |
| α-helix | 236-246 | 11 | |
| β-strand | 249-250 | 2 | 17 |
| β-strand | 255-258 | 4 | 17 |
| α-helix | 262-264 | 3 | |
| α-helix | 266-267 | 2 | |
| β-strand | 268-272 | 5 | 16 |
| β-strand | 275-279 | 5 | 16 |
| α-helix | 281-284 | 4 | |
| β-strand | 285 | 1 | 18 |
| β-strand | 295-297 | 3 | 17 |
| β-strand | 298 | 1 | 18 |
| β-strand | 300-302 | 3 | 15 |
| α-helix | 305-306 | 2 | |
| β-strand | 313-315 | 3 | 15 |
| α-helix | 317-322 | 6 | |
| β-strand | 323-328 | 6 | 10 |
| β-strand | 333-338 | 6 | 10 |
| β-strand | 339 | 1 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Renin | A, B | protein | 341 | Homo sapiens | P00797 (AlphaFold model) |
>3K1W_1 Renin (chains A, B) LTLGNTTSSVILTNYMDTQYYGEIGIGTPPQTFKVVFDTGSSNVWVPSSKCSRLYTACVY HKLFDASDSSSYKHNGTELTLRYSTGTVSGFLSQDIITVGGITVTQMFGEVTEMPALPFM LAEFDGVVGMGFIEQAIGRVTPIFDNIISQGVLKEDVFSFYYNRDSENSQSLGGQIVLGG SDPQHYEGNFHYINLIKTGVWQIQMKGVSVGSSTLLCEDGCLALVDTGASYISGSTSSIE KLMEALGAKKRLFDYVVKCNEGPTLPDISFHLGGKEYTLTSADYVFQESYSSKKLCTLAI HAMDIPPPTGPTWALGATFIRKFYTEFDRRNNRIGFALARH
| ID | Name | Formula | Copies |
|---|---|---|---|
| HSQ | 2-acetylamino-2-deoxy-alpha-L-idopyranose | C8 H15 N O6 | 1 |
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 1 |
| BFX | 4-{4-[3-(2-bromo-5-fluorophenoxy)propyl]phenyl}-N-(2-chlorobenzyl)-N-cyclopropy… | C31 H31 Br Cl F N2 O2 | 2 |
Water and common crystallization additives (CL, FMT) are not listed.
New classes of potent and bioavailable human renin inhibitors. Remen, L., Bezencon, O., Richard-Bildstein, S. et al. Bioorg Med Chem Lett (2009) 19:6762-6765. DOI 10.1016/j.bmcl.2009.09.104 · PubMed
Other PDB entries of the same protein (UniProt P00797 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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