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Ligands
Code Name Style Show Link
FM0 (3r)-3-(fluoromethyl)-3-hydroxy-5-{[(S)-hydroxy(phosphonooxy)phosphoryl]oxy}pentanoic acid
AGS Phosphothiophosphoric acid-adenylate ester
Non-standard Residues
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Glycosylation
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Code : 4DPU   PDBj   RCSB PDB   PDBe
Header : LYASE/LYASE INHIBITOR
Title : Crystal structure of Staphylococcus epidermidis S192A mevalonate diphosphate decarboxylase complexed with inhibitor 6-FMVAPP and ATPgS
Release Data : 2012-07-11
Compound :
mol_id molecule chains
1 Mevalonate diphosphate decarboxylase A,B
ec: 4.1.1.33
mutation: S192A
Source :
mol_id organism_scientific expression_system
1 Staphylococcus epidermidis  (taxid:1282) Escherichia coli  (taxid:469008)
gene: mvaD
expression_system_strain: BL21(DE3)
expression_system_vector_type: plasmid
expression_system_plasmid: pT7HMT
Authors : Barta, M.L., McWhorter, W.J., Geisbrecht, B.V.
Keywords : GHMP Kinase Family, LYASE-LYASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.900 Å )
Citation :

Structural basis for nucleotide binding and reaction catalysis in mevalonate diphosphate decarboxylase.

Barta, M.L.,McWhorter, W.J.,Miziorko, H.M.  et al.
(2012)  Biochemistry  51 : 5611 - 5621

PubMed: 22734632
DOI: 10.1021/bi300591x

Chain : A, B
UniProt : Q9FD73 (Q9FD73_STAEP)
Reaction : -