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Xaa-Pro dipeptidyl-peptidase activity

OBSOLETE. Catalysis of the hydrolysis of the terminal bond of Xaa-Pro-Xaa motifs to release unblocked, N-terminal dipeptides from substrates… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2009
0119932009

Related topics

Related topics

1 relation
Xaa-Pro dipeptidyl-peptidase

Related mentions per year

Related mentions per year

1993-2009
19901995200020052010
Xaa-Pro dipeptidyl-peptidase activity
Xaa-Pro dipeptidyl-peptidase

Papers overview

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2009
2009
High-resolution structures of collagen-like peptides [(Pro-Pro-Gly)4-Xaa-Yaa-Gly-(Pro-Pro-Gly)4]: implications for triple-helix hydration and Hyp(X) puckering.
Structures of (Pro-Pro-Gly)4-Xaa-Yaa-Gly-(Pro-Pro-Gly)4 (ppg9-XYG) where (Xaa, Yaa)=(Pro, Hyp), (Hyp, Pro) or (Hyp, Hyp) were… (More)
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2006
2006
Old molecules for new receptors: Trp(Nps) dipeptide derivatives as vanilloid TRPV1 channel blockers.
The transient receptor potential vanilloid member 1 (TRPV1), an integrator of multiple pain-producing stimuli, is regarded… (More)
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2005
2005
Recombinant human cathepsin X is a carboxymonopeptidase only: a comparison with cathepsins B and L.
The S1 and S2 subsite specificity of recombinant human cathepsins X was studied using fluorescence resonance energy transfer… (More)
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2003
2003
Tandem ligation of multipartite peptides with cell-permeable activity.
To prepare multipartite peptides with several functional cargoes including a cell-permeable sequence or transportant for… (More)
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Highly Cited
2002
Highly Cited
2002
New biarsenical ligands and tetracysteine motifs for protein labeling in vitro and in vivo: synthesis and biological applications.
We recently introduced a method (Griffin, B. A.; Adams, S. R.; Tsien, R. Y. Science 1998, 281, 269-272 and Griffin, B. A.; Adams… (More)
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2000
2000
14-3-3 proteins are required for the inhibition of Ras by exoenzyme S.
14-3-3 proteins play a regulatory role and participate in both signal transduction and checkpoint control pathways. 14-3-3… (More)
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2000
2000
Thioxo amino acid pyrrolidides and thiazolidides: new inhibitors of proline specific peptidases.
Aminopeptidase P (APP), dipeptidyl peptidase II (DP II), dipeptidyl peptidase IV (DP IV) and prolyl oligopeptidase (POP) are… (More)
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1999
1999
Decisive structural determinants for the interaction of proline derivatives with the intestinal H+/peptide symporter.
To elucidate the decisive structural factors relevant for dipeptide-carrier interaction, the affinity of short amide and imide… (More)
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1994
1994
Phosphorylation of synthetic fragments of inhibitor-2 of protein phosphatase-1 by casein kinase-1 and -2. Evidence that phosphorylated residues are not strictly required for efficient targeting by…
The major phosphorylation site for both casein kinase-2 (CK2) and casein kinase-1 (CK1) in protein phosphatase-1 (PP-1) inhibitor… (More)
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1993
1993
Purification and characterization of a scorpion defensin, a 4kDa antibacterial peptide presenting structural similarities with insect defensins and scorpion toxins.
Insect defensins are a group of inducible small-sized antibacterial peptides with three intramolecular disulfide bridges. NMR… (More)
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