| ADP | Adenosine Di-Phosphate |
|---|---|
| ADP | adenopathy; adenosine diphosphate; administrative psychiatry; approved drug product; area diastolic ... |
| AdP | adductor pollicis |
| ATP | 1) Adenosine Tri-Phosphate 2) Autoimmune Thrombocytopenic Purpura |
| ATP | adenosine triphosphate; ambient temperature and pressure; autoimmune thrombocytopenic purpura |
| AAC | ADP-ATP carrier |
|---|---|
| ADP | ATP |
| ADP | and (ATP |
| ATP(o) | ATP |
| ( ATP | ATP concentration |
| ADP | <biochemistry> ADP is used as an adenine, a ribose and a diphosphate unit. (06 May 1997) |
|---|---|
| ADP-L-glycero-D-mannoheptose-6-epimerase | <enzyme> Converts ADP-d-glycero-d-mannoheptose to ADP-l-glycero-d-mannoheptose; rfad gene product is from escherichia coli Registry number: EC 5.1.3.- Synonym: ADP-gmh-epimerase, htrm gene product, htrm protein, rfad gene product, rfad protein, lsi-6 protein (26 Jun 1999) |
| ADP ribose-histone hydrolase | <enzyme> Splits bond between ADP ribose and histone Registry number: EC 4.2.99.- Synonym: ADP-ribosyl histone splitting enzyme, ADP-ribosyl protein lyase (26 Jun 1999) |
| ADP ribosylation | Covalent attachment of an ADP-ribosyl moiety to a macromolecule; e.g., the action of diphtheria toxin. (05 Mar 2000) |
| ADP - thymidine kinase | <enzyme> Induced by herpes simplex virus infection of mouse fibroblasts Registry number: EC 2.7.1.118 Synonym: ADP-thymidine 5'-phosphotransferase (26 Jun 1999) |
| poly ADP-ribose glycohydrolase | <enzyme> Splits ribose-ribose bonds; glycohydrolase I has a higher molecular weight and is tightly bound to mammalian cell nuclei; glycohydrolase II has lower molecular weight and is found in cytosol Registry number: EC 3.2.1.- Synonym: (ADP-ribose)n glycohydrolase I, (ADP-ribose)n glycohydrolase II (26 Jun 1999) |
| NAD+ ADP-ribosyltransferase | <enzyme> An enzyme isolated from the nuclei of a variety of cells. It catalyses the incorporation of ADP-ribose groups of NAD+ into a homopolymer of repeating ADP-ribose units. Chemical name: NAD+:poly(adenosine diphosphate D-ribose)-acceptor ADP-D-ribosyltransferase Registry number: EC 2.4.2.30 (12 Dec 1998) |
| NAD(p)-arginine ADP-ribosyltransferase | <enzyme> An enzyme that catalyses the transfer of the ADP-ribose moiety from NAD to specific protein substrates with agmatine, arginine-type compounds, or guanidine as acceptors. This reaction can be catalyzed by prokaryotic and eukaryotic enzyme systems. Mono-ADP-ribosylation is a mechanism of action common to several bacterial toxins. It effects profound changes in cellular metabolism, such as activation of adenylate cyclase, regulation of protein synthesis at the level of elongation factor 2, and ion transport across biological membranes. Chemical name: NAD(+)-L-arginine ADP-D-ribosyltransferase Registry number: EC 2.4.2.31 (12 Dec 1998) |
| dinitrogenase reductase ADP-ribosyltransferase | <enzyme> Catalyses the ADP-ribosylation and concomitant inactivation of dinitrogenase reductase in rhodospirillum rubrum; encoded by drat gene of azospirillum brasilense Registry number: EC 2.4.2.- Synonym: dratransferase (26 Jun 1999) |
| anti-mitochondrial antibodies | A special serologic test that measures the level of antibodies to a particular portion of a cell (mitochondria). (27 Sep 1997) |
| bovine mitochondrial endonuclease | <enzyme> Dimer of 29kda peptide; prefers a conserved sequence in the displacement loop region of mitochondrial DNA; nicks double-stranded DNA and fragments single-stranded DNA Registry number: EC 3.1.21.- (26 Jun 1999) |
| genome, mitochondrial | The genetic information contained in the circular chromosome of the mitochondrion, a structure located outside the nucleus in the cytoplasm of the cell. The mitochondrial genome and the chromosomal (nuclear) genome together constitute the entire genome. (12 Dec 1998) |
| mitochondrial | Referring to mitochondria. (12 Dec 1998) |
| mitochondrial chromosome | The DNA component of mitochondria, the chief function of which is synthesis of adenosine triphosphate and the management of cellular energy; the chromosome contains some 16,000 base pairs arranged in a circle. The inheritance is matrilineal, and the mutation rate is unusually high; since each cell contains thousands of copies a mutant form may assume an almost continuous gradation as in a galtonian process. Most of the mutations known have their impact on the respiratory chain. (05 Mar 2000) |
| mitochondrial disease | <disease, neurology> An illnesse, frequently neurological, which can be ascribed to defects in mitochondrial function. If the defect is in the mitochondrial rather than the nuclear genome unusual patterns of inheritance can be observed. (18 Nov 1997) |
Synonyms : ADP Translocase, ATP Translocase, ATP, ADP-Carrier, ATP-ADP Translocase, Adenine Nucleotide Carrier (Mitochondrial), Mitochondrial ADP-ATP Carriers, ADP-ATP Carriers, Mitochondrial, Mitochondrial ADP ATP Carriers
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