Structure of PDB 7ulv Chain E |
>7ulvE (length=272) Species: 9606 (Homo sapiens) [Search protein sequence] |
AFGRATHAVVRALPESLGQHALRSGEEVDVARAERQHQLYVGVLGSKLGL QVVELPADESLPDCVFVEDVAVVCEETALITRPGAPSRRKEVDMMKEALE KLQLNIVEMKDENATLDGGDVLFTGREFFVGLSKRTNQRGAEILADTFKD YAVSTVPVADGLHLKSFCSMAGPNLIAIGSSESAQKALKIMQQMSDHRYD KLTVPDDIAANCIYLNIPNKGHVLLHRTPEEYPESAKVYEKLKDHMLIPV SMSELEKVDGLLTCCSVLINKK |
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PDB | 7ulv Optimization of a switchable electrophile fragment into a potent and selective covalent inhibitor of human DDAH1 |
Chain | E |
Resolution | 2.37 Å |
3D structure |
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Enzyme Commision number |
3.5.3.18: dimethylargininase. |
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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 |
NO6 |
E |
D73 F76 H173 C274 |
D63 F66 H163 C264 |
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