Design and synthesis of novel, conformationally restricted HMG-COA reductase inhibitors. Determined by X-ray diffraction at 2.0 Å resolution. Released 17 Jul 2007.
Explore 2Q6C in 3D Show helices and sheets RCSB PDB PDBe
2Q6C contains 80 α-helices and 80 β-strands across 4 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 |
|---|---|---|---|
| α-helix | 445-452 | 8 | |
| α-helix | 464-472 | 9 | |
| α-helix | 478-480 | 3 | |
| α-helix | 481-484 | 4 | |
| α-helix | 488-502 | 15 | |
| α-helix | 519-521 | 3 | |
| β-strand | 523 | 1 | 1 |
| β-strand | 527 | 1 | 1 |
| β-strand | 530-546 | 17 | 2 |
| β-strand | 549-556 | 8 | 2 |
| α-helix | 562-575 | 14 | |
| β-strand | 579 | 1 | 2 |
| β-strand | 580-587 | 8 | 3 |
| β-strand | 588-590 | 3 | 4 |
| β-strand | 593-595 | 3 | 5 |
| α-helix | 599-610 | 12 | |
| α-helix | 612-623 | 12 | |
| β-strand | 631 | 1 | 4 |
| β-strand | 635-639 | 5 | 5 |
| β-strand | 642-646 | 5 | 5 |
| β-strand | 647-649 | 3 | 4 |
| β-strand | 651 | 1 | 6 |
| β-strand | 653 | 1 | 6 |
| β-strand | 654 | 1 | 7 |
| α-helix | 657-674 | 18 | |
| β-strand | 679-682 | 4 | 5 |
| α-helix | 695-700 | 6 | |
| β-strand | 703-712 | 10 | 3 |
| α-helix | 714-719 | 6 | |
| α-helix | 725-731 | 7 | |
| α-helix | 732-737 | 6 | |
| α-helix | 738-742 | 5 | |
| β-strand | 748-749 | 2 | 3 |
| α-helix | 753-763 | 11 | |
| α-helix | 768-770 | 3 | |
| α-helix | 771-774 | 4 | |
| β-strand | 777-784 | 8 | 3 |
| β-strand | 790-800 | 11 | 3 |
| β-strand | 805 | 1 | 7 |
| α-helix | 807-810 | 4 | |
| α-helix | 812-821 | 10 | |
| α-helix | 833-859 | 27 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 445-453 | 9 | |
| α-helix | 464-472 | 9 | |
| α-helix | 478-481 | 4 | |
| α-helix | 488-502 | 15 | |
| β-strand | 523 | 1 | 8 |
| β-strand | 527 | 1 | 8 |
| β-strand | 530-546 | 17 | 2 |
| β-strand | 549-556 | 8 | 2 |
| α-helix | 562-575 | 14 | |
| β-strand | 579 | 1 | 2 |
| β-strand | 580-587 | 8 | 9 |
| β-strand | 588-590 | 3 | 10 |
| β-strand | 593-595 | 3 | 11 |
| α-helix | 599-610 | 12 | |
| α-helix | 612-623 | 12 | |
| β-strand | 631 | 1 | 10 |
| β-strand | 635-639 | 5 | 11 |
| β-strand | 642-646 | 5 | 11 |
| β-strand | 647-649 | 3 | 10 |
| β-strand | 651 | 1 | 12 |
| β-strand | 653 | 1 | 12 |
| β-strand | 654 | 1 | 13 |
| α-helix | 657-674 | 18 | |
| β-strand | 679-682 | 4 | 11 |
| α-helix | 695-700 | 6 | |
| β-strand | 703-712 | 10 | 9 |
| α-helix | 714-719 | 6 | |
| α-helix | 725-731 | 7 | |
| α-helix | 732-737 | 6 | |
| α-helix | 738-742 | 5 | |
| β-strand | 748-749 | 2 | 9 |
| α-helix | 753-763 | 11 | |
| α-helix | 768-770 | 3 | |
| α-helix | 771-774 | 4 | |
| β-strand | 777-784 | 8 | 9 |
| β-strand | 790-800 | 11 | 9 |
| β-strand | 805 | 1 | 13 |
| α-helix | 807-810 | 4 | |
| α-helix | 812-821 | 10 | |
| α-helix | 833-859 | 27 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 446-453 | 8 | |
| α-helix | 464-472 | 9 | |
| α-helix | 488-500 | 13 | |
| α-helix | 506-511 | 6 | |
| α-helix | 519-521 | 3 | |
| β-strand | 523 | 1 | 14 |
| β-strand | 527 | 1 | 14 |
| β-strand | 530-546 | 17 | 15 |
| β-strand | 549-556 | 8 | 15 |
| α-helix | 562-575 | 14 | |
| β-strand | 579-587 | 9 | 15 |
| β-strand | 588-590 | 3 | 16 |
| β-strand | 593-595 | 3 | 17 |
| α-helix | 599-610 | 12 | |
| α-helix | 612-623 | 12 | |
| β-strand | 630-631 | 2 | 16 |
| β-strand | 635-639 | 5 | 17 |
| β-strand | 642-646 | 5 | 17 |
| β-strand | 647-650 | 4 | 16 |
| β-strand | 654 | 1 | 18 |
| α-helix | 657-674 | 18 | |
| β-strand | 679-682 | 4 | 17 |
| α-helix | 695-700 | 6 | |
| β-strand | 703-712 | 10 | 15 |
| α-helix | 714-719 | 6 | |
| α-helix | 725-731 | 7 | |
| α-helix | 732-737 | 6 | |
| α-helix | 738-742 | 5 | |
| β-strand | 748-749 | 2 | 15 |
| α-helix | 753-763 | 11 | |
| α-helix | 768-770 | 3 | |
| α-helix | 771-774 | 4 | |
| β-strand | 777-784 | 8 | 15 |
| β-strand | 790-800 | 11 | 15 |
| β-strand | 805 | 1 | 18 |
| α-helix | 807-810 | 4 | |
| α-helix | 812-820 | 9 | |
| α-helix | 833-859 | 27 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 464-472 | 9 | |
| α-helix | 481-484 | 4 | |
| α-helix | 488-500 | 13 | |
| α-helix | 506-509 | 4 | |
| α-helix | 519-521 | 3 | |
| β-strand | 523 | 1 | 19 |
| β-strand | 527 | 1 | 19 |
| β-strand | 530-546 | 17 | 15 |
| β-strand | 549-556 | 8 | 15 |
| α-helix | 562-575 | 14 | |
| β-strand | 579-587 | 9 | 15 |
| β-strand | 588-590 | 3 | 20 |
| β-strand | 593-595 | 3 | 21 |
| α-helix | 599-610 | 12 | |
| α-helix | 612-623 | 12 | |
| β-strand | 630-631 | 2 | 20 |
| β-strand | 635-639 | 5 | 21 |
| β-strand | 642-646 | 5 | 21 |
| β-strand | 647-650 | 4 | 20 |
| β-strand | 651 | 1 | 22 |
| β-strand | 653 | 1 | 22 |
| β-strand | 654 | 1 | 23 |
| α-helix | 657-674 | 18 | |
| β-strand | 679-682 | 4 | 21 |
| α-helix | 695-700 | 6 | |
| β-strand | 703-712 | 10 | 15 |
| α-helix | 714-719 | 6 | |
| α-helix | 725-731 | 7 | |
| α-helix | 732-737 | 6 | |
| α-helix | 738-742 | 5 | |
| β-strand | 748-749 | 2 | 15 |
| α-helix | 753-763 | 11 | |
| α-helix | 768-770 | 3 | |
| α-helix | 771-774 | 4 | |
| β-strand | 777-784 | 8 | 15 |
| β-strand | 790-800 | 11 | 15 |
| β-strand | 805 | 1 | 23 |
| α-helix | 807-810 | 4 | |
| α-helix | 812-821 | 10 | |
| α-helix | 833-859 | 27 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| 3-hydroxy-3-methylglutaryl-coenzyme A reductase | A, B, C, D | protein | 441 | Homo sapiens | P04035 (AlphaFold model) |
>2Q6C_1 3-hydroxy-3-methylglutaryl-coenzyme A reductase (chains A, B, C, D) HHHHHHEPRPNEECLQILGNAEKGAKFLSDAEIIQLVNAKHIPAYKLETLIETHERGVSI RRQLLSKKLSEPSSLQYLPYRDYNYSLVMGACCENVIGYMPIPVGVAGPLCLDEKEFQVP MATTEGCLVASTNRGCRAIGLGGGASSRVLADGMTRGPVVRLPRACDSAEVKAWLETSEG FAVIKEAFDSTSRFARLQKLHTSIAGRNLYIRFQSRSGDAMGMNMISKGTEKALSKLHEY FPEMQILAVSGNYCTDKKPAAINWIEGRGKSVVCEAVIPAKVVREVLKTTTEAMIEVNIN KNLVGSAMAGSIGGYNAHAANIVTAIYIACGQDAAQNVGSSNCITLMEASGPTNEDLYIS CTMPSIEIGTVGGGTNLLPQQACLQMLGVQGACKDNPGENARQLARIVCGTVMAGELSLM AALAAGHLVKSHMIHNRSKIN
| ID | Name | Formula | Copies |
|---|---|---|---|
| HR1 | (3R,5R)-7-[1-(4-fluorophenyl)-3-isopropyl-4-oxo-5-phenyl-4,5-dihydro-3H-pyrrolo… | C33 H33 F N2 O5 | 4 |
Water and common crystallization additives (SO4) are not listed.
Design and synthesis of novel, conformationally restricted HMG-CoA reductase inhibitors. Pfefferkorn, J.A., Choi, C., Song, Y. et al. Bioorg Med Chem Lett (2007) 17:4531-4537. DOI 10.1016/j.bmcl.2007.05.097 · PubMed
Other PDB entries of the same protein (UniProt P04035 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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