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PDBsum entry 1elg

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Complex (hydrolase/inhibitor) PDB id
1elg
Contents
Protein chain
240 a.a.
Ligands
BAA
Metals
_CA
Waters ×189

References listed in PDB file
Key reference
Title Nature of the inactivation of elastase by n-Peptidyl-O-Aroyl hydroxylamine as a function of ph.
Authors X.Ding, B.F.Rasmussen, H.U.Demuth, D.Ringe, A.C.Steinmetz.
Ref. Biochemistry, 1995, 34, 7749-7756. [DOI no: 10.1021/bi00023a022]
PubMed id 7779821
Note In the PDB file this reference is annotated as "TO BE PUBLISHED". The citation details given above were identified by an automated search of PubMed on title and author names, giving a perfect match.
Abstract
The mechanism of inactivation of porcine pancreatic elastase (PPE) by N-peptidyl-O-aroylhydroxylamine was studied by X-ray crystallography. The inactivator forms a stable complex with the enzyme by means of a covalent attachment to the active site Ser 203(195) O gamma. The nature of the complex is, however, different depending on the pH at which the inactivation reaction occurs. At pH 5, the complex formed is a hydroxylamine derivative of Ser 203(195) in which the O gamma of serine is the oxygen of the hydroxylamine derivative. At pH 7.5, the complex formed is a carbamate derivative at Ser 203(195) O gamma. In both types of complexes, the inactivator binds in the S' subsites of the enzyme instead of forming the usual antiparallel beta-sheet with the S subsites. The implication for the mechanism of inactivation at different pHs is discussed.
Secondary reference #1
Title Direct structural observation of an acyl-Enzyme intermediate in the hydrolysis of an ester substrate by elastase.
Authors X.Ding, B.F.Rasmussen, G.A.Petsko, D.Ringe.
Ref. Biochemistry, 1994, 33, 9285-9293. [DOI no: 10.1021/bi00197a032]
PubMed id 8049229
Full text Abstract
Secondary reference #2
Title Inhibition of proteases with enkephalin-Analogue inhibitors.
Authors H.U.Demuth, J.Silberring, F.Nyberg.
Ref. J Enzyme Inhib, 1991, 4, 289-298.
PubMed id 1669830
Abstract
Secondary reference #3
Title Competing redox and inactivation processes in the inhibition of cysteine proteinases by peptidyl o-Acylhydroxamates. 13c and 15n nmr evidence for a novel sulfenamide enzyme adduct
Authors V.J.Robinson, P.J.Coles, R.A.Smith, A.Krantz.
Ref. j am chem soc, 1991, 113, 7760.
Secondary reference #4
Title N-O bond fission as the rate-Determining step in the aqueous conversion of n-Peptiyl-O-(P-Nitrobenzoyl)hydroxylamines to p-Nitrobenzoic acid and peptidylhydroxamic acids
Authors H.-U.Demuth, G.Fischer, A.Barth, R.L.Schowen.
Ref. j org chem, 1989, 54, 5880.
Secondary reference #5
Title Crystal structure of the covalent complex formed by a peptidyl difluoro keto amide with porcine pancreatic elastase at 1.78 angstroms resolution
Authors L.H.Takahashi, R.Radhakrishnan, R.E.Rosenfield junior, E.F.Meyer junior, D.A.Trainor.
Ref. j am chem soc, 1989, 111, 3368.
PROCHECK
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