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peptidyl-L-3-oxoalanine biosynthetic process from peptidyl-cysteine or peptidyl-serine

Known as: peptidyl-L-3-oxoalanine anabolism from peptidyl-cysteine or peptidyl-serine, peptidyl-L-3-oxoalanine formation from peptidyl-cysteine or peptidyl-serine, peptidyl-L-3-oxoalanine synthesis from peptidyl-cysteine or peptidyl-serine 
The modification of peptidyl-cysteine or peptidyl-serine to peptidyl-L-3-oxoalanine; characteristic of the active sites of arylsulfatases. [RESID… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Complexity generation in fungal peptidyl alkaloid biosynthesis: a two-enzyme pathway to the hexacyclic MDR export pump inhibitor ardeemin.
Ardeemins are hexacyclic peptidyl alkaloids isolated from Aspergillus fischeri as agents that block efflux of anticancer drugs by… Expand
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Review
2006
Review
2006
Calpain inhibition: a therapeutic strategy targeting multiple disease states.
  • N. Carragher
  • Current pharmaceutical design
  • 2006
    • Corpus ID: 42705976
The calpains represent a well-conserved family of calcium-dependent cysteine proteases. They consist of several ubiquitous and… Expand
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1997
1997
Discovery and biological activity of orally active peptidyl trifluoromethyl ketone inhibitors of human neutrophil elastase.
Previously we had shown that tripeptidyl trifluoromethyl ketones (TFMKs) possessing an N-terminal diarylacylsulfonamide, such as… Expand
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1994
1994
Peptidyl diazomethanes as inhibitors of cysteine and serine proteinases.
  • E. Shaw
  • Methods in enzymology
  • 1994
    • Corpus ID: 45133869
Publisher Summary This chapter highlights peptidyl diazomethanes as inhibitors of cysteine and serine proteinases. Peptidyl… Expand
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1992
1992
Human neutrophil proteinase 3: mapping of the substrate binding site using peptidyl thiobenzyl esters.
A series of peptidyl thiobenzyl esters was used to map the active site of human leukocyte proteinase 3. The steady-state kinetics… Expand
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1990
1990
Structure-activity studies of fluoroketone inhibitors of alpha-lytic protease and human leukocyte elastase.
We have synthesized a series of peptidyl fluoroketones that reversibly inhibit the serine proteases human leukocyte elastase (HLE… Expand
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1989
1989
DISSECTIO:'\ OF THE RIBOSO:\fAL PEPTIDYL TRAl'ISFERASE CEl\TER BY PHOTOAFFI:'\ITY LABELI:'\G: P- AND A-SITES ARE LOCATED AT DIFFERENT posmol'ls IX DO:\fA~ V OF 23 S RNA
Photoreactive 3-(4'-benzoylphenyl)propionyl-Phe-tRNA was bound specifically to the P-site or the A-site of the E. coli ribosome… Expand
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1986
1986
Peptidyl carbamates incorporating amino acid isosteres as novel elastase inhibitors.
The design and synthesis of 13 novel peptidyl carbamates are described. When tested for inhibitory activity toward porcine… Expand
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1986
1986
The inactivation of [Met5]-enkephalin by bestatin-sensitive aminopeptidase, captopril-sensitive peptidyl dipeptidase A and thiorphan-sensitive endopeptidase-24.11 in mouse vas deferens.
The enkephalin-hydrolyzing peptidases in mouse vas deferens were studied and compared with those in guinea pig ileum which had… Expand
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1983
1983
Human converting enzyme.
Angiotensin I converting enzyme (kininase II, peptidyl dipeptidase, ACE) was purified by reverse immunoadsorption from a membrane… Expand
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