Structure of PDB 2f7m Chain F |
>2f7mF (length=341) Species: 9606 (Homo sapiens) [Search protein sequence] |
VYAQEKQDFVQHFSQIVRVLTEDEMGHPEIGDAIARLKEVLEYNAIGGKY NRGLTVVVAFRELVEPRKQDADSLQRAWTVGWCVELLQAFFLVADDIMDS SLTRRGQICWYQKPGVGLDAINDANLLEACIYRLLKLYCREQPYYLNLIE LFLQSSYQTEIGQTLDLLTAPQGNVDLVRFTEKRYKSIVKYKTAFYSFYL PIAAAMYMAGIDGEKEHANAKKILLEMGEFFQIQDDYLDLFGDPSVTGKI GTDIQDNKCSWLVVQCLQRATPEQYQILKENYGQKEAEKVARVKALYEEL DLPAVFLQYEEDSYSHIMALIEQYAAPLPPAVFLGLARKIY |
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PDB | 2f7m Structural basis for the exceptional in vivo efficacy of bisphosphonate drugs. |
Chain | F |
Resolution | 2.3 Å |
3D structure |
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Enzyme Commision number |
2.5.1.1: dimethylallyltranstransferase. 2.5.1.10: (2E,6E)-farnesyl diphosphate synthase. |
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Site # |
Ligand |
Ligand chain |
Binding residues on receptor (original residue number in PDB) |
Binding residues on receptor (residue number reindexed from 1) |
Binding affinity |
BS01 |
PO4 |
F |
G56 K57 Q96 R113 |
G48 K49 Q88 R105 |
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