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1 tidase (ShPepV) as the primary Cys-Gly-3M3SH dipeptidase.
2 been shown to function as a Cys-Gly-specific dipeptidase.
3 e and brain N-acetylated alpha-linked acidic dipeptidase.
4 opeptidase, and peptidase E, an Asp-specific dipeptidase.
5 idase E (PepE) is an N-terminal Asp-specific dipeptidase.
6 d rat brain N-acetylated alpha-linked acidic dipeptidase.
7 eins gamma-glutamyl transpeptidase (GGT) and dipeptidase.
8 nterococci, is a zinc-containing d-Ala-d-Ala dipeptidase.
9 share sequence homology with other bacterial dipeptidases.
10    Here we identify two kidney disease genes Dipeptidase 1 (DPEP1) and Charged Multivesicular Body Pr
11 quire sialic acid for entry and instead uses dipeptidase 1 (DPEP1) as a receptor.
12 netic screen, resistance was correlated with dipeptidase 1 (Dpep1) variants.
13  of overexpression in CRC compared to AT was Dipeptidase 1 (DPEP1).
14 tabolic diseases and revealed connections of dipeptidase 1 with circulating digestive enzymes and wit
15 ulated the GSH metabolism regulating protein dipeptidase-1 (DPEP1) in a glucocorticoid receptor (GR)-
16 d dipeptidase-3 (MBD-3)] from membrane-bound dipeptidase-1 (MBD-1) deficient mice.
17 found that a protease, cytosolic nonspecific dipeptidase 2 (CNDP2), catalyzes their formation.
18 ein (NLDL), N-acetylated alpha-linked acidic dipeptidase 2 (NAALAD2), and prostate-specific membrane
19  membrane-bound dipeptidases [membrane-bound dipeptidase-2 (MBD-2) and membrane-bound dipeptidase-3 (
20 und dipeptidase-2 (MBD-2) and membrane-bound dipeptidase-3 (MBD-3)] from membrane-bound dipeptidase-1
21 of control, n = 3, p < .0005) and dipeptidyl dipeptidase (374 +/- 79.1% of control, n = 3, p < .005),
22 we show that inhibitors of mosquito peptidyl dipeptidase, a peptidase related to mammalian angiotensi
23 activity (intralysosome) to a region of high dipeptidase activity (cytosol).
24  transfer of dipeptides from a region of low dipeptidase activity (intralysosome) to a region of high
25                              It had very low dipeptidase activity against D-Ala-D-Ser, unlike VanX, a
26 and partially purified native AbpB displayed dipeptidase activity and degraded human type VI collagen
27 tified clinical isolates lacking D-Ala-D-Ala dipeptidase activity and unable to grow on D-Ala-D-Ala b
28  bond showed endopeptidase to be superior to dipeptidase activity for APCE.
29 observed reactivity change from the peptidyl dipeptidase activity of ACE to the carboxypeptidase acti
30 rovar Typhimurium strain contain an aspartyl dipeptidase activity that is dependent on Mn(2+).
31          The pcgL gene conferred D-Ala-D-Ala dipeptidase activity upon Escherichia coli K-12 but did
32 Furthermore, no difference in total cellular dipeptidase activity was detected between the mutant and
33  and the E181A VanX mutant has no detectable dipeptidase activity, yet maintains near-stoichiometric
34 SMA and its N-acelylated-alpha linked-acidic dipeptidase activity.
35  coelution of PM20D2 with beta-alanyl-lysine dipeptidase activity.
36 ain contained a cytosolic beta-alanyl-lysine dipeptidase activity.
37 eptide, which is subsequently cleaved by the dipeptidase Amm19 to produce a Trp-derived diaminoquinon
38  NAALADase (N-acetylated-alpha-linked-acidic dipeptidase), an enzyme responsible for the hydrolysis o
39                                  Human renal dipeptidase, an enzyme associated with glutathione metab
40 vity of the brush border enzymes, dipeptidyl dipeptidase and alkaline phosphatase, was assayed by the
41 t activation protein (FAP), an extracellular dipeptidase and clinically relevant biomarker of brain t
42  D-Ala-D-Ser has a polar effect on both D, D-dipeptidase and D,D-carboxypeptidase activities.
43                VanX and VanY have strict D,D-dipeptidase and D,D-carboxypeptidase activity, respectiv
44 tidase, rat N-acetylated alpha-linked acidic dipeptidase, and human prostate-specific membrane antige
45 netically deficient in or overexpressing the dipeptidase angiotensin-converting enzyme (ACE), we have
46 on with a vac-encoded exocytic COOH-terminal dipeptidase, angiotensin converting enzyme, to allow lib
47 ved for the product complexes of isoaspartyl dipeptidase, d-aminoacylase, and dihydroorotase from the
48 giotensin I-converting enzyme (ACE, peptidyl dipeptidase, EC 3.4.15.2) is a key enzyme in cardiovascu
49 rotein is a D-alanyl-D-alanine (D-Ala-D-Ala) dipeptidase essential for resistance to the glycopeptide
50 by binding to the accessory molecule CD26, a dipeptidase expressed on the surface of activated T cell
51                                      PepV, a dipeptidase found in culture fluids of Streptococcus gor
52     The closest homologue to the human renal dipeptidase from a fully sequenced microbe is Sco3058 fr
53 ivities is a previously characterized isoAsp dipeptidase from E. coli, the product of the iadA gene.
54                                  Isoaspartyl dipeptidase from Escherichia coli functions in protein d
55           Homology was found with a putative dipeptidase from Streptococcus pyogenes and nonspecific
56  from Streptococcus pyogenes and nonspecific dipeptidases from Lactobacillus helveticus and Lactococc
57 ht end of Tn5382 and downstream of the vanXB dipeptidase gene exhibit significant homology to genes e
58                               The Salmonella dipeptidase gene, designated pcgL, appears to have been
59 ndent receptors, two OmpA family proteins, a dipeptidase, GlpQ, two alkaline phosphatases, 3-phytase,
60                                  Isoaspartyl dipeptidase (IAD) is a member of the amidohydrolase supe
61 ated enzymes with this activity, isoaspartyl dipeptidase (IadA) and isoaspartyl aminopeptidase (IaaA)
62 gonist, NS5, to prolidase (PEPD), a cellular dipeptidase implicated in primary immune deficiencies in
63 iotensin-converting enzyme (ACE), a peptidyl dipeptidase implicated in regulation of blood pressure a
64 w report the identification of a D-Ala-D-Ala dipeptidase in the gram-negative species Salmonella ente
65  mutant of gene all3922 encoding isoaspartyl dipeptidase in the model heterocyst-forming cyanobacteri
66 alysis confirms the placement of isoaspartyl dipeptidase into the urease-related amidohydrolase super
67  specific cell types showed that isoaspartyl dipeptidase is present at significantly lower levels in
68 share the metallopeptidase function of renal dipeptidase, it still has the corresponding peptide-bind
69 ked HBC-3 cells into wild-type or dipeptidyl dipeptidase IV (DPPIV) knockout blastocysts.
70                           Using a dipeptidyl dipeptidase IV genetic marker system to follow the fate
71             N-acetylated alpha-linked acidic dipeptidase-like protein (NAALADase L), encoded by the N
72 2 or PSMA), N-acetylated alpha-linked acidic dipeptidase-like protein (NLDL), N-acetylated alpha-link
73                               Membrane-bound dipeptidase (MBD) participates in the degradation of glu
74 e developed mice deficient in membrane-bound dipeptidase (MBD, EC 3.4.13.19), the enzyme believed to
75                                     Membrane dipeptidase (MDP) is a zinc metalloenzyme located in the
76 hed the identity of the receptor as membrane dipeptidase (MDP), a cell-surface zinc metalloprotease i
77 oding previously unidentified membrane-bound dipeptidases [membrane-bound dipeptidase-2 (MBD-2) and m
78 zing enzyme N-acetylated alpha-linked acidic dipeptidase (NAAG peptidase activity) or glutamate carbo
79 nhibition of xPSM N-acetyl-alpha-linked acid dipeptidase (NAALADase) enzymatic activity.
80 rain enzyme N-acetylated alpha-linked acidic dipeptidase (NAALADase) has been shown to remove sequent
81             N-acetylated alpha-linked acidic dipeptidase (NAALADase) hydrolyzes acidic peptides, such
82 en known as N-acetylated alpha-linked acidic dipeptidase (NAALADase), and is identical to the prostat
83 ropeptidase N-acetylated alpha-linked acidic dipeptidase (NAALADase).
84 ties of the N-acetylated alpha-linked acidic dipeptidase (NAALADase).
85             Prolidase, also known as Xaa-Pro dipeptidase or peptidase D (PEPD), is a ubiquitously exp
86 ic space of Salmonella, suggesting that this dipeptidase participates in peptidoglycan metabolism.
87           Previously, the gene for a general dipeptidase (pepDA) was isolated from a gene bank of Lac
88 structure of Salmonella typhimurium aspartyl dipeptidase, peptidase E, was solved crystallographicall
89 des of the X-proline type are cleaved by the dipeptidase prolidase.
90        The effects of the compounds on X-Pro dipeptidase (prolidase) and leucyl aminopeptidase are al
91                                      Proline dipeptidase (prolidase) was purified from cell extracts
92                       Quiescent cell proline dipeptidase (QPP) is an intracellular serine protease th
93 ovel serine protease, quiescent cell proline dipeptidase (QPP), with substrate specificity similar to
94 e that we have termed quiescent cell proline dipeptidase (QPP).
95        We propose that PvdM belongs to a new dipeptidase-related protein subfamily with inactivated Z
96  known about the role of PvdM, a human renal dipeptidase-related protein that is predicted to be peri
97  protein with sequence similarity to VanX, a dipeptidase required for resistance to vancomycin.
98 ted both alkaline phosphatase and dipeptidyl dipeptidase specific activity by 116 +/- 5.4% and 256 +/
99  enterica harbours a periplasmic D-Ala-D-Ala dipeptidase (termed PcgL), which confers the ability to
100  VanX is a zinc-dependent D-alanyl-D-alanine dipeptidase that is a critical component in a system tha
101 eptidase IV (DP-IV) is a cell surface serine dipeptidase that is involved in the regulation of the in
102        Biosynthesis of MCTR3 was mediated by dipeptidases that cleaved the cysteinyl-glycinyl bond of
103 ases beta-aspartyl-arginine) and isoaspartyl dipeptidase (that produces aspartate and arginine).
104 ovel serine protease, quiescent cell proline dipeptidase, that we have recently isolated and cloned.
105 -containing D-alanyl-D-alanine (D-Ala-D-Ala) dipeptidase VanX has been detected in both Gram-positive
106 ptidase and N-acetylated alpha-linked acidic dipeptidase, while immunoblots using monoclonal antibody
107 y X-ray crystallography and reveals a Zn(2+)-dipeptidase with a unique overall fold and a well-define
108 have shown that it is indeed an Asp-specific dipeptidase with properties very similar to those of ser
109  proteins currently annotated as nonspecific dipeptidases within the amidohydrolase superfamily.

 
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