Kinetic analysis of the inhibition of phenylalanine ammonia-lyase by 2-aminoindan-2-phosphonic acid and other phenylalanine analogues

scientific article published in February 2003

Kinetic analysis of the inhibition of phenylalanine ammonia-lyase by 2-aminoindan-2-phosphonic acid and other phenylalanine analogues is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/S0031-9422(02)00561-7
P698PubMed publication ID12620354

P2093author name stringNikolaus Amrhein
Jerzy Zoń
Christoph Appert
P2860cites workCrystal structure of histidine ammonia-lyase revealing a novel polypeptide modification as the catalytic electrophileQ27618058
The mechanism of action of phenylalanine ammonia-lyase: the role of prosthetic dehydroalanineQ33979841
Structural and catalytic properties of the four phenylalanine ammonia-lyase isoenzymes from parsley (Petroselinum crispum Nym.).Q34323317
Maize phenylalanine ammonia-lyase has tyrosine ammonia-lyase activityQ34414390
Interference of ʟ-α-Aminooxy-β-Phenylpropionic Acid with Phenylalanine Metabolism in BuckwheatQ39911565
A linear equation that describes the steady-state kinetics of enzymes and subcellular particles interacting with tightly bound inhibitorsQ42924868
Inhibitors of phenylalanine ammonia-lyase: 1-aminobenzylphosphonic acids substituted in the benzene ringQ43832153
An active site homology model of phenylalanine ammonia-lyase from Petroselinum crispum.Q44033135
17 The kinetics of reversible tight-binding inhibitionQ52779426
Tight-binding inhibitors--III. A new approach for the determination of competition between tight-binding inhibitors and substrates--inhibition of adenosine deaminase by coformycin.Q52837001
Tight-binding inhibitors-I. Kinetic behaviorQ67364914
Phenylalanine ammonia-lyase: Mirror-image packing of d- and l-phenylalanine and d- and l-transition state analogs into the active siteQ70996769
Spectroscopic Evidence for a 4-Methylidene Imidazol-5-one in Histidine and Phenylalanine Ammonia-Lyases We thank Prof. G. E. Schulz and Dipl.-Chem. M. Baedeker (University of Freiburg) for providing us with the new PAL expression system and Dr. M. SQ74166169
Inhibition of anthocyanin formation in seedlings and flowers by the enantiomers of α-aminooxy-β-phenylpropionic acid and their N-benzyloxycarbonyl derivativesQ87063662
P433issue3
P304page(s)415-422
P577publication date2003-02-01
P1433published inPhytochemistryQ1884753
P1476titleKinetic analysis of the inhibition of phenylalanine ammonia-lyase by 2-aminoindan-2-phosphonic acid and other phenylalanine analogues
P478volume62

Reverse relations

cites work (P2860)
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