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1 ure of an N-truncated rabbit skeletal muscle AMP deaminase.
2 t is highly conserved in other adenosine and AMP deaminases.
3 een suggested that an acquired deficiency of AMP deaminase 1 (AMPD1) may be responsible for muscle we
4 ctivation of anaplerotic reactions driven by AMP deaminase 3 (Ampd3) and catabolism of branched-chain
5                                    Mammalian AMP deaminase 3 (AMPD3) enzymes reportedly bind to intra
6       A rapid increase of transcript for the AMP deaminase 3 gene (AMPD3) and its enzymatic activity
7 ing enzymes cytosolic 5'-nucleotidase 1A and AMP-deaminase 3, which suppress AMPK activity.
8                   We found a 47% increase in AMP deaminase activity in the AA-deficient zebrafish, co
9   We found that metformin inhibited purified AMP deaminase activity.
10 n of the synthetase under conditions of high AMP deaminase activity.
11                       The second exon of the AMP deaminase (AMPD) 1 gene is alternatively spliced in
12                                              AMP deaminase (AMPD) converts AMP to IMP and is a divers
13  document that another AMP-dependent enzyme, AMP deaminase (AMPD) is activated in the liver of diabet
14                                              AMP deaminase (AMPD) is essential for plant life, but th
15 arliest expressed plant genes and encodes an AMP deaminase (AMPD), which is also an identified herbic
16 min might increase AMP through inhibition of AMP deaminase (AMPD).
17                              A highly potent AMP deaminase (AMPDA) inhibitor series was discovered by
18                                              AMP deaminase (AMPDA) inhibitors increase the levels of
19 d coformycin aglycon analogues with improved AMP deaminase (AMPDA) inhibitory potency are described.
20  by activating the activities of the enzymes AMP deaminase and xanthine oxidase.
21  been identified as inhibition of the enzyme AMP deaminase (EC 3.5.4.6) following phosphorylation at
22                              Strains lacking AMP deaminase form short, thick stalks and glassy sori w
23        Synadenol (14) was also deaminated by AMP deaminase from aspergillus sp.
24 n of the ribosome protein gene RPS5a and the AMP deaminase gene FAC1, both of which are essential for
25                                Helix pomatia AMP deaminase (HPAMPD), an enzyme enriched in the foot m
26                                              AMP deaminase inhibitor decreased IMP levels and signifi
27 t was duplicated by a structurally unrelated AMP deaminase inhibitor.
28 ata: 1) confirm that available literature on AMP deaminase is likely derived from N-truncated enzymes
29               Moreover, Acd1, an ortholog of AMP deaminase, is dispensable for growth but essential f
30                                  Erythrocyte AMP deaminase [isoform E (AMPD3)] is activated in respon
31                                              AMP deaminase isoforms purified from endogenous sources
32 n to be a potent, tight binding inhibitor of AMP deaminase isolated from pea seedlings.
33            It is proposed that inhibition of AMP deaminase leads to the death of the plant through pe
34 osine metabolism (for adenosine receptor and AMP deaminase), or catecholamine receptors.
35 egradation pathway through the activation of AMP deaminase resulting in uric acid production and the
36 hat disruption of the gene amdA that encodes AMP deaminase results in a significantly increased propo
37 ically up-regulated (lipin, metallothionein, AMP deaminase, RNA helicase-related protein, TG interact
38 a cell-autonomous consequence of the loss of AMP deaminase since mutant cells developed together with
39 able to its being a more potent inhibitor of AMP deaminase than is DCF.
40 ed a decrease in the extractable activity of AMP deaminase that correlates with a strong, noncovalent
41 his finding, we investigated the activity of AMP deaminase, the enzyme that irreversibly deaminates A