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  • ¿µ¹®
    ÇѱÛ
  • fibrinolytic enzyme
    ¼¶À¯¼Ò¿ëÇØÈ¿¼Ò, ÇǺ기¿ëÇØÈ¿¼Ò
  • glycolytic enzyme
    ÇØ´çÈ¿¼Ò
  • induced enzyme
    À¯µµÈ¿¼Ò
  • inhibitory enzyme
    ¾ïÁ¦È¿¼Ò
  • inorganic enzyme
    ¹«±âÈ¿¼Ò
  • intracellular enzyme
    ¼¼Æ÷³»È¿¼Ò
  • lipoclastic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • microsomal enzyme
    ¹Ì¼¼¼Òüȿ¼Ò
  • one gene/one enzyme
    ÀÏÀ¯ÀüÀÚ/ÀÏÈ¿¼Ò¼³
  • oxidative enzyme
    »êÈ­È¿¼Ò
  • phosphorylating enzyme
    ÀλêÈ­È¿¼Ò
  • proteolytic enzyme
    ´Ü¹éÁúºÐÇØÈ¿¼Ò
  • packaging enzyme
    ²Ù¸®±âÈ¿¼Ò, Æ÷ÀåÈ¿¼Ò
  • periplasmic enzyme
    ¿øÇüÁú¸·ÁÖÀ§È¿¼Ò
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  • ¿µ¹®
    ÇѱÛ
  • enzyme-antienzyme reaction
    È¿¼ÒÇ×È¿¼Ò¹ÝÀÀ
  • extracellular enzyme
    ¼¼Æ÷¿ÜÈ¿¼Ò, ±Õü¹ÛÈ¿¼Ò
  • fibrinolytic enzyme
    ¼¶À¯¼Ò¿ëÇØÈ¿¼Ò
  • glycolytic enzyme
    ÇØ´çÈ¿¼Ò
  • induced enzyme
    À¯µµÈ¿¼Ò
  • inhibitory enzyme
    ¾ïÁ¦È¿¼Ò
  • inorganic enzyme
    ¹«±âÈ¿¼Ò
  • intracellular enzyme
    ¼¼Æ÷³»È¿¼Ò
  • lipoclastic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • lipolytic enzyme
    ÁöÁúºÐÇØÈ¿¼Ò
  • microsomal enzyme
    ¹Ì¼¼¼Òüȿ¼Ò
  • mucolytic enzyme
    Á¡¾×ºÐÇØÈ¿¼Ò
  • oxidative enzyme
    »êÈ­È¿¼Ò
  • packaging enzyme
    ²Ù¸®±âÈ¿¼Ò
  • periplasmic enzyme
    ¿øÇüÁú¸·ÁÖÀ§È¿¼Ò
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  • ¿µ¹®
    ÇѱÛ
  • regulatory enzyme
    Á¶ÀýÈ¿¼Ò(¡­ý£áÈ).
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  • ¿µ¹®
    ÇѱÛ
  • curdling enzyme
    ÀÀÀ¯È¿¼Ò(¡­ý£áÈ).
  • cytosolic enzyme
    ¼¼Æ÷ÁúÈ¿¼Ò.
  • debrancher enzyme
    ÁöÁ¦°ÅÈ¿¼Ò(ò«ð¶ËÛý£áÈ)
  • degumming enzyme
    ÇØ±³È¿¼Ò(ú°Îïý£áÈ).
  • diastatic enzyme
    ´çÈ­È¿¼Ò(ÓØûùý£áÈ).
  • digestive enzyme
    ¼ÒÈ­È¿¼Ò(á¼ûùý£áÈ).
  • enzyme
    È¿¼Ò
  • enzyme
    È¿¼Ò(ý£áÈ).
  • enzyme linked immunosorbent assay ( ELISA)
    È¿¼Ò ¸é¿ªÃøÁ¤¹ý
  • enzyme activator
    È¿¼ÒȰ¼ºÁ¦.
  • enzyme activity
    È¿¼ÒȰ¼º
  • enzyme activity
    È¿¼ÒȰ¼ºµµ
  • enzyme antibody technique
    È¿¼ÒÇ×ü¹ý.
  • enzyme assay
    È¿¼ÒÃøÁ¤(¹ý)
  • enzyme deficiency
    È¿¼Ò°áÇÌ(Áõ)
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  • ¿µ¹®
    ÇѱÛ
  • core enzyme
    ÇÙ½ÉÈ¿¼Ò(ú·ãýý£áÈ)
  • covalent enzyme-substrate complex
    È¿¼Ò±âÁú °øÀ¯°áÇÕü(ý£áÈÐñòõÍìêóÌ¿ùêô÷) (ÔÒ) enzymesubstrate compound
  • debranching enzyme
    °¡ÁöÁ¦°Å(ð¶ËÛ) È¿¼Ò(ý£áÈ)
  • depolymerizing enzyme
    ÇØÁßÇÕ È¿¼Ò(ú°ñìùêý£áÈ)
  • desensitized enzyme
    Å»°¨ÀÛÈ¿¼Ò(÷­ÊõíÂý£áÈ)
  • digestive enzyme
    ¼ÒÈ­È¿¼Ò(á¼ûùý£áÈ)
  • dispensable enzyme
    ºñÇʼö È¿¼Ò(Þªù±âÎý£áÈ) (ÔÒ) nonessential enzyme
  • DNA-relaxing enzyme
    DNAÀÌ¿Ï È¿¼Ò(ì¬èÐý£áÈ) (ÔÒ) topoisomerase
  • DNA restriction enzyme
    DNA Á¦ÇÑ È¿¼Ò(ð¤ùÚý£áÈ) (ÔÒ) restriction enzyme
  • drug-detoxication enzyme
    ¾à¹°Çص¶ È¿¼Ò(å·Úªú°Ô¸ý£áÈ) (ÔÒ) drug-metabolizing enzyme
  • drug-metbolizing enzyme
    ¾à¹°´ë»ç È¿¼Ò(å·ÚªÓÛÞóý£áÈ)
  • early enzyme
    Á¶±â È¿¼Ò(ðÄÑ¢ý£áÈ)
  • enzyme
    È¿¼Ò(ý£áÈ)
  • enzyme I
    È¿¼Ò(ý£áÈ) I
  • enzyme II
    È¿¼Ò(ý£áÈ) II
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ACE Angiotensin Converting Enzyme
  = Kininase II
  = Dipeptidyl Carboxypepti...
EIA   1) Exercise Induced Asthma; ¿îµ¿ À¯¹ß¼º õ½Ä
  = EIB
  2) Enzyme Immu...
ELISA Enzyme-Linked Immuno-Sorbent Assay; È¿¼Ò ¸é¿ª¹ý
AAAE amino acid activating enzyme
ACE acetonitrile; acetylcholine esterase; acute cerebral encephalopathy; acute coronary event; adrenocor...
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CoQ10 Co-enzyme Q10
C-ELISA Competitive enzyme-linked immunosorbent assay
CEI Converting enzyme inhibition
CEI Converting enzyme inhibitor
DEIA DNA enzyme immuno assay
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • periplasmic enzyme
    ¿øÇüÁú¸· ÁÖÀ§ °ø°£ È¿¼Ò
  • phosphorylating enzyme
    ÀλêÈ­ È¿¼Ò
  • proteolytic enzyme
    ´Ü¹é ºÐÇØ È¿¼Ò
    ´Ü¹é ºÐÇØ¸¦ ÃËÁøÇÏ´Â È¿¼Ò.
  • Q enzyme
    Å¥ È¿¼Ò
    Æ÷µµ´ç-1-ÀλêÀÇ 1,6-C¿¡ ÀÛ¿ëÇÏ¿© À̰ÍÀ» ÁßÈ­½ÃŰ´Â È¿¼Ò.
  • rate-limiting enzyme
    ¼Óµµ Á¶Àý È¿¼Ò
  • receptor destroying enzyme
    ¼ö¿ëü ÆÄ±« È¿¼Ò
    ¼ö¿ëü¸¦ ÆÄ±«ÇÏ¿© ÀûÇ÷±¸ÀÇ ¹ÙÀÌ·¯½º ¿ëÇ÷¿¡ ´ëÇÑ °¨¼ö¼ºÀ» ÀÒ¾î¹ö¸®°Ô ÇÏ´Â È¿¼Ò.
  • splitting enzyme
    ºÐÇÒ È¿¼Ò
  • Z-enzyme
    ÁîÀÌ È¿¼Ò
    º£Å¸-¾Æ¹Ð¶óÁ¦¿Í Çù·ÂÇÏ¿© ¾Æ¹Ð·ÎÁ¦ÀÇ ¿ÏÀü ºÐÇØ¸¦ ÀÏÀ¸Å²´Ù.
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pantoate-activating enzyme pantothenate synthetase
marker enzyme <enzyme> An enzyme that is used to identify a specific cell type, cell organelle, or cell component.
(05 Mar 2000)
reducing enzyme <enzyme> An enzyme that catalyses a reduction; since all enzymes catalyze reactions in either direction, any reductase can, under the proper conditions, behave as an oxidase and vice versa, hence the term oxidoreductase. For individual reductase's, see the specific names.
Synonym: reducing enzyme.
(05 Mar 2000)
regulatory enzyme <biochemistry> An enzyme that regulatescertain functions due to its ability to undergoa change in its catalytic activity through modification of its structure.
(09 Oct 1997)
relaxing enzyme <biochemistry> Any of several enzymes, such ashelicase, that unwind DNA prior to its replication.
(09 Oct 1997)
R enzyme <enzyme> An enzyme with action similar to that of isoamylase; it cleaves 1,6-alpha-glucosidic linkages in pullalan, amylopectin, and glycogen, and in alpha-and beta-amylase limit-dextrins of amylopectin and glycogen.
Compare: isoamylase.
Synonym: limit dextrinase, pullulanase, R enzyme.
(05 Mar 2000)
repair enzyme <enzyme, molecular biology> An enzyme that can catalyze the repair of damaged DNA; e.g., DNA ligase.
(05 Mar 2000)
repressible enzyme <biochemistry> In bacteria, an enzyme whose creation is inhibited when its reaction product is plentiful.
(09 Oct 1997)
respiratory enzyme One of those enzyme's in tissues that is a part of an oxidation-reduction system accomplishing the conversion of substrates to CO2 and H2O and the transfer of the electrons removed to O2.
(05 Mar 2000)
respiratory enzyme complexes <biochemistry> The enzymes that make up the respiratory chain: NADH Q reductase, succinate Q reductase, cytochrome reductase, cytochrome C and cytochrome oxidase.
(18 Nov 1997)
glycogen debranching enzyme system 1,4-alpha-d-glucan-1,4-alpha-d-glucan 4-alpha-d-glucosyltransferase/dextrin 6 alpha-d-glucanohydrolase. An enzyme system having both 4-alpha-glucanotransferase (ec 2.4.1.25) and amylo-1,6-glucosidase (ec 3.2.1.33) activities. As a transferase it transfers a segment of a 1,4-alpha-d-glucan to a new 4-position in an acceptor, which may be glucose or another 1,4-alpha-d-glucan. As a glucosidase it catalyses the endohydrolysis of 1,6-alpha-d-glucoside linkages at points of branching in chains of 1,4-linked alpha-d-glucose residues. Amylo-1,6-glucosidase activity is deficient in glycogen storage disease type III.
(12 Dec 1998)
restriction enzyme <enzyme, molecular biology> Class of bacterial enzymes that cut DNA at specific sites. In bacteria their function is to destroy foreign DNA, such as that of bacteriophages (host DNA is specifically modified at these sites).
Type I restriction endonucleases occur as a complex with the methylase and a polypeptide that binds to the recognition site on DNA. They are often not very specific and cut at a remote site.
Type II restriction endonucleases are the classic experimental tools. They have very specific recognition and cutting sites. The recognition sites are short, 4-8 nucleotides and are usually palindromic sequences. Because both strands have the same sequence running in opposite directions the enzymes make double stranded breaks, which, if the site of cleavage is off centre, generates fragments with short single stranded tails, these can hybridise to the tails of other fragments and are called sticky ends.
They are generally named according to the bacterium from which they were isolated (first letter of genus name and the first two letters of the specific name). The bacterial strain is identified next and multiple enzymes are given Roman numerals. For example the two enzymes isolated from the R strain of E. Coli are designated Eco RI and Eco RII.
(10 Mar 1998)
restriction enzyme cutting site <molecular biology> A specific nucleotide sequence of DNA at which a particular restriction enzyme cuts the DNA.
Some sites occur frequently in DNA (for example, every several hundred basepairs), others much less frequently (rare-cutter, for example, every 10,000 base pairs).
(10 Mar 1998)
restriction enzyme, endonuclease A protein that recognises specific, short nucleotide sequences and cuts DNA at those sites. Bacteria contain over 400 such enzymes that recognise and cut over 100 different DNA sequences. See restriction enzyme cutting site.
(05 Mar 2000)
P enzyme <enzyme> Enzyme that catalyses the sequential removal of glycosyl residues from glycogen to yield one glucose-1-phosphate per reaction. Its activity is controlled by phosphorylation (by phosphorylase kinase).
(21 Jun 2000)
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    ÇѱÛ
  • public key
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  • related key
    (ÁÖÀ½ µî°ú °¡±î¿î °ü°è°¡ ÀÖ´Â)±ÙÄ£(°ü°è)Á¶
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    °èÀü Ű
  • skeleton key
    (¿©·¯ ÀÚ¹°¼è¿¡ ¸Â´Â) °ç¼è
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