Crystal Structure of Human Renin Complexed with Inhibitor. Determined by X-ray diffraction at 1.9 Å resolution. Released 14 Nov 2006.
Explore 2IKO in 3D Show helices and sheets RCSB PDB PDBe
2IKO contains 30 α-helices and 68 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 | 1 | 1 | 1 |
| β-strand | 3-7 | 5 | 2 |
| β-strand | 8-10 | 3 | 3 |
| β-strand | 14-16 | 3 | 3 |
| β-strand | 17-21 | 5 | 4 |
| β-strand | 26-33 | 8 | 4 |
| β-strand | 39-42 | 4 | 4 |
| β-strand | 43 | 1 | 5 |
| α-helix | 51-54 | 4 | |
| β-strand | 59 | 1 | 5 |
| α-helix | 61-63 | 3 | |
| β-strand | 68-78 | 11 | 4 |
| β-strand | 81-94 | 14 | 4 |
| β-strand | 97-108 | 12 | 4 |
| α-helix | 111-114 | 4 | |
| β-strand | 121-124 | 4 | 4 |
| α-helix | 128-130 | 3 | |
| α-helix | 132-134 | 3 | |
| α-helix | 135-137 | 3 | |
| α-helix | 138-143 | 6 | |
| β-strand | 148 | 1 | 1 |
| β-strand | 152-157 | 6 | 2 |
| α-helix | 158-160 | 3 | |
| β-strand | 169-173 | 5 | 2 |
| α-helix | 178-180 | 3 | |
| β-strand | 181-189 | 9 | 2 |
| β-strand | 190 | 1 | 6 |
| β-strand | 197-200 | 4 | 6 |
| β-strand | 202-205 | 4 | 7 |
| β-strand | 211 | 1 | 7 |
| β-strand | 216-220 | 5 | 6 |
| β-strand | 227-229 | 3 | 6 |
| α-helix | 231-241 | 11 | |
| α-helix | 243 | 1 | |
| β-strand | 244-245 | 2 | 8 |
| β-strand | 250-253 | 4 | 8 |
| α-helix | 254-259 | 6 | |
| α-helix | 260-262 | 3 | |
| β-strand | 263-267 | 5 | 7 |
| β-strand | 270-274 | 5 | 7 |
| α-helix | 276-279 | 4 | |
| β-strand | 280 | 1 | 9 |
| β-strand | 290-292 | 3 | 8 |
| β-strand | 293 | 1 | 9 |
| β-strand | 295-297 | 3 | 6 |
| α-helix | 300-301 | 2 | |
| β-strand | 308-310 | 3 | 6 |
| α-helix | 312-315 | 4 | |
| β-strand | 318-323 | 6 | 2 |
| β-strand | 328-334 | 7 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 1 | 1 | 10 |
| β-strand | 3-7 | 5 | 11 |
| β-strand | 8-10 | 3 | 12 |
| β-strand | 14-16 | 3 | 12 |
| β-strand | 17-21 | 5 | 13 |
| β-strand | 26-33 | 8 | 13 |
| β-strand | 39-42 | 4 | 13 |
| β-strand | 43 | 1 | 14 |
| α-helix | 51-53 | 3 | |
| β-strand | 59 | 1 | 14 |
| α-helix | 61-63 | 3 | |
| β-strand | 68-75 | 8 | 13 |
| β-strand | 84-94 | 11 | 13 |
| β-strand | 97-108 | 12 | 13 |
| β-strand | 121-124 | 4 | 13 |
| α-helix | 128-130 | 3 | |
| α-helix | 132-134 | 3 | |
| α-helix | 135-137 | 3 | |
| α-helix | 138-143 | 6 | |
| β-strand | 148 | 1 | 10 |
| β-strand | 152-157 | 6 | 11 |
| α-helix | 158-160 | 3 | |
| β-strand | 169-173 | 5 | 11 |
| α-helix | 178-180 | 3 | |
| β-strand | 182-189 | 8 | 11 |
| β-strand | 190 | 1 | 15 |
| β-strand | 197-200 | 4 | 15 |
| β-strand | 202-205 | 4 | 16 |
| β-strand | 211 | 1 | 16 |
| β-strand | 216-220 | 5 | 15 |
| β-strand | 227-229 | 3 | 15 |
| α-helix | 231-241 | 11 | |
| β-strand | 244-245 | 2 | 17 |
| β-strand | 250-253 | 4 | 17 |
| α-helix | 254-259 | 6 | |
| α-helix | 261-262 | 2 | |
| β-strand | 263-267 | 5 | 16 |
| β-strand | 270-274 | 5 | 16 |
| α-helix | 276-279 | 4 | |
| β-strand | 280 | 1 | 18 |
| β-strand | 290-292 | 3 | 17 |
| β-strand | 293 | 1 | 18 |
| β-strand | 295-297 | 3 | 15 |
| α-helix | 300-301 | 2 | |
| β-strand | 308-310 | 3 | 15 |
| α-helix | 312-317 | 6 | |
| β-strand | 318-323 | 6 | 11 |
| β-strand | 328-333 | 6 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Renin | A, B | protein | 340 | Homo sapiens | P00797 (AlphaFold model) |
>2IKO_1 Renin (chains A, B) LTLGNTTSSVILTNYMDTQYYGEIGIGTPPQTFKVVFDTGSSNVWVPSSKCSRLYTACVY HKLFDASDSSSYKHNGTELTLRYSTGTVSGFLSQDIITVGGITVTQMFGEVTEMPALPFM LAEFDGVVGMGFIEQAIGRVTPIFDNIISQGVLKEDVFSFYYNRDSENSQSLGGQIVLGG SDPQHYEGNFHYINLIKTGVWQIQMKGVSVGSSTLLCEDGCLALVDTGASYISGSTSSIE KLMEALGAKKRLFDYVVKCNEGPTLPDISFHLGGKEYTLTSADYVFQESYSSKKLCTLAI HAMDIPPPTGPTWALGATFIRKFYTEFDRRNNRIGFALAR
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7IG | 5-{4-[(3,5-difluorobenzyl)amino]phenyl}-6-ethylpyrimidine-2,4-diamine | C19 H19 F2 N5 | 1 |
Binding thermodynamics of substituted diaminopyrimidine renin inhibitors. Sarver, R.W., Peevers, J., Cody, W.L. et al. Anal Biochem (2007) 360:30-40. DOI 10.1016/j.ab.2006.10.017 · 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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