| ¿µ¹® | biosynthesis | ÇÑ±Û | »ýÇÕ¼º |
|---|---|---|---|
| ¼³¸í | »ý¹°Ã¼¿¡¼ ¼¼Æ÷ÀÇ ÀÛ¿ëÀ¸·Î À¯±â¹°ÁúÀ» ÇÕ¼ºÇÏ´Â ÀÏ. »ýü ÃßÃ⼺ºÐ¿¡ ÀÇÇÑ »ýü ¿Ü¿¡¼ÀÇ ¹ÝÀÀµµ À̰Ϳ¡ Æ÷ÇÔ½ÃŲ´Ù. È¿¼Ò°¡ ±× ÁÖ¿ªÀ̸ç, »ýü´Â ¿Ü°è¿¡¼ ¼·ÃëÇÑ ¹°ÁúÀ» ¹ÙÅÁÀ¸·Î ¸¹Àº ´Ü°è·Î ÀÌ·ç¾îÁö´Â È¿¼Ò¹ÝÀÀ¿¡ ÀÇÇÏ¿© ¸ñÀû¹°ÁúÀ» Çü¼ºÇÑ´Ù. »ý¸®ÀûÀ¸·Î´Â ºÐÇØ´ë»çÀÇ ¹Ý´ëµÇ´Â ¶æÀ» °¡Áö¸ç, »ýü ±¸¼º¹°Áú°ú ±× ¹ÛÀÇ Çʿ伺ºÐÀÇ ÇÕ¼º-º¸±Þ-ÀúÀå¿¡ °ü¿©ÇÑ´Ù. ÀϹÝÀûÀ¸·Î »ýÇÕ¼º °úÁ¤Àº ¿¡³ÊÁö ¿ä±¸¼ºÀ̸ç, ¹ÝÀÀÀÇ ½ÇÇö¿¡´Â ¿¡³ÊÁö °ø±Þ¹ÝÀÀ°ú ÇÔ²² È£Èí-¹ßÈ¿ µî¿¡ ÀÇÇÏ¿© »ý±â´Â °í¿¡³ÊÁö Àλê°áÇÕ(ATP µî)À» ÇÊ¿ä·Î ÇÏ´Â °æ¿ì°¡ ¸¹´Ù. »ýÇÕ¼ºÀº ÁÖ·Î È¿¼Ò¹ÝÀÀÀ̹ǷΠȿ¼Ò¹ÝÀÀÀÌ °¡Áø ¿©·¯ °¡Áö Ư¼ºÀ» Ÿ³ª³»°í ƯÈ÷ ƯÀ̼ºÀÌ Ç³ºÎÇÏ´Ù. ÀÌ ¼ºÁúÀ» ÀÌ¿ëÇÏ¿© ½ÇÇèÀû ¶Ç´Â °ø¾÷ÀûÀ¸·Îµµ ¿©·¯ °¡Áö ¹°ÁúÀÇ ¼±ÅÃÀû ÇÕ¼ºÀÌ °¡´ÉÇÏ´Ù. |
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| ¿µ¹® | peptide | ÇÑ±Û | ÆéƼµå |
|---|---|---|---|
| ¼³¸í | µÎ °³ÀÌ»óÀÇ ¾Æ¹Ì³ë»ê ºÐÀÚ »çÀÌ¿¡¼, ÇÑÂÊÀÇ ¾Æ¹Ì³ë±â¿Í ´Ù¸¥ ÂÊÀÇ Ä«¸£º¹½Ç±â°¡ ¹° ºÐÀÚ¸¦ ÀÒÀ¸¸é¼ ÃàÇÕÇÏ¿© ÀÌ·ç´Â ¾Æ¹Ìµå °áÇվƹ̳ë»êÀÇ ¼ö°¡ 2, 3, ¡¦ ÀÎ °æ¿ì, °¢°¢ µðÆéƼµå, Æ®¸®ÆéƼµå, ¡¦µîÀ¸·Î ºÎ¸£¸ç, ¿©·¯ °³ÀÇ ¾Æ¹Ì³ë»êÀ¸·Î ±¸¼ºµÇ´Â °ÍÀ» ¿Ã¸®°íÆéƼµå, À̺¸´Ù Å« °ÍÀ» Æú¸®ÆéƼµå¶ó°í ÇÑ´Ù. Á÷¼â»óÀÇ °ÍÀÌ ¸¹Áö¸¸, ȯ»ó ±¸Á¶¸¦ °®´Â ÆéƼµåµµ ÀÖ´Ù. ÀúºÐÀÚÀÇ ÆéƼµå´Â ¹°, »ê, ¾ËÄ®¸® µûÀ§¿¡ Àß ³ì°í ¾ËÄڿÿ¡´Â ³ìÁö ¾ÊÀ¸³ª, °íºÐÀÚÀÇ ÆéƼµå´Â ¹°¿¡ Àß ³ìÁö ¾Ê°í ´Ü¹éÁú°ú ¼ºÁúÀÌ ºñ½ÁÇÏ´Ù. ³úÇϼöüȣ¸£¸ó, ºê¶óµðŰ´Ñ µî°ú °°ÀÌ »ý¸®Àû±â´ÉÀÌ ÇöÀúÇÑ °ÍÀº »ý¸®È°¼ºÆéƼµå(bioactive peptide)¶ó°í ÇÑ´Ù. |
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| ¿µ¹® | nucleic acid | ÇÑ±Û | ÇÙ»ê |
|---|---|---|---|
| ¼³¸í | ¿°±â, ´ç, ÀλêÀ¸·Î ÀÌ·ç¾îÁø ´ºÅ¬·¹¿ÀƼµå°¡ ±ä »ç½½ ¸ð¾çÀ¸·Î ÁßÇÕµÈ °íºÐÀÚ ¹°Áú. À¯ÀüÀ̳ª ´Ü¹éÁú ÇÕ¼ºÀ» Áö¹èÇÏ´Â Áß¿äÇÑ ¹°Áú·Î, »ý¹°ÀÇ Áõ½ÄÀ» ºñ·ÔÇÑ »ý¸í Ȱµ¿ À¯Áö¿¡ Áß¿äÇÑ ÀÛ¿ëÀ» ÇÑ´Ù. ±¸¼º ´çÀÎ ¿Àź´çÀÌ ¸®º¸¿À½ºÀÎ ¸®º¸ÇÙ»ê°ú µð¿Á½Ã¸®º¸¿À½ºÀÎ µð¿Á½Ã¸®º¸ ÇÙ»êÀ¸·Î ³ª´¶´Ù. ÆæÅ佺·Î¼ ¸®º¸½º³ª µ¥¿Á½Ã¸®º¸½º ¾î´À ÇÑÂʸ¸À» Æ÷ÇÔÇϸç ÀüÀÚ¸¦ ¸®º¸ÇÙ»ê(RNA), ÈÄÀÚ¸¦ µ¥¿Á½Ã¸®º¸ÇÙ»ê(deoxyribonucleic acid, DNA)À̶ó ºÎ¸¥´Ù. ¸ðµÎ 4Á¾·ùÀÇ À¯±â¿°±â¿¡ ÀÇÇØ Ư¡Áö¾îÁö¸ç ¾Æµ¥´Ñ, ±¸¾Æ´Ñ ¹× ½ÃÅä½ÅÀº ¾çÀÚ¿¡ °øÅëÀÌ´Ù. Ƽ¹ÎÀº DNA¿¡, ¿ì¶ó½ÇÀº RNA¿¡ Æ÷ÇԵȴÙ. DNA´Â ÁÖ·Î ÇÙ¿¡ Á¸ÀçÇϸç ÇüÁúÀ¯Àü¿¡ ±×¸®°í RNA´Â ¼¼Æ÷Áú¼Ó¿¡¼ ´Ü¹éÁú ÇÕ¼º¿¡ °ü¿©ÇÑ´Ù. ¼·ÃëµÈ ÇÙ»êÀº ¼ÒȰü¿¡¼ ±¸¼ººÐÀڷαîÁö °¡¼öºÐÇØµÇ¾î Èí¼öµÈ´Ù. |
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| NAP | nasion, point A, pogonion [convexity or concavity of the facial profile]; nerve action potential; ne... |
|---|---|
| PBP | penicillin-binding protein; porphyrin biosynthesis pathway; prostate-binding protein; pseudobulbar p... |
| C-Peptide | Connecting Peptide |
| ERP | early receptor potential; effective refractory period; elodoisin-related peptide; endoscopic retrogr... |
| VIP | vasoactive intestinal peptide; vasoinhibitory peptide; venous impedance plethysmography; ventricular... |
| PNA | Peptide Nucleic Acid |
|---|---|
| PBAN | Pheromone Biosynthesis Activating Neuropeptide |
| NASBA | Nucleic Acid Sequence Based Amplification |
| NA | Nucleic acid |
| NAT | Nucleic acid testing |
corticotropin-releasing factor (ºÎ½Å ÇÇÁú È£¸£¸ó À¯¸® ¿ä¼Ò, ºÎ½Å ÇÇÁú È£¸£¸ó À¯¸® ÀÎÀÚ
| biosynthesis | <biochemistry> The building up of a chemical compound in the physiologic processes of a living organism. (18 Nov 1997) |
|---|---|
| regulatory sequences, nucleic acid | DNA sequences involved in regulating the expression of other genes. (12 Dec 1998) |
| repetitive sequences, nucleic acid | Nucleotide sequences present in multiple copies in the genome. They include direct, inverted, tandem, and terminal repeat sequences and the alu family repeat (named for the restriction endonuclease cleavage enzyme alu I). (12 Dec 1998) |
| minus-strand nucleic acid | <molecular biology> An RNA or DNA strand which has the opposite sense of (would be complementary to) the mRNA of a virus. (12 Jan 1998) |
| sequence homology, nucleic acid | The sequential correspondence of nucleotide triplets in a nucleic acid molecule which permits nucleic acid hybridization. Sequence homology is important in the study of mechanisms of oncogenesis and also as an indication of the evolutionary relatedness of different organisms. The concept includes viral homology. (12 Dec 1998) |
| nucleic acid | <biochemistry, molecular biology> Linear polymers of nucleotides, linked by 3', 5' phosphodiester linkages. In DNA, deoxyribonucleic acid, the sugar group is deoxyribose and the bases of the nucleotides adenine, guanine, thymine and cytosine. RNA, ribonucleic acid, has ribose as the sugar and uracil replaces thymine. DNA functions as a stable repository of genetic information in the form of base sequence. RNA has a similar function in some viruses but more usually serves as an informational intermediate (mRNA), a transporter of amino acids (tRNA), in a structural capacity or, in some newly discovered instances, as an enzyme. The spontaneous loss of the amino groups of cytosine (yielding uracil), methyl cytosine (yielding thymine) or of adenine (yielding hypoxanthine). It can be argued that the presence of thymine in DNA in place of the uracil of RNA stabilises genetic information against this lesion, since repair enzymes would restore the GU base pair to GC. (18 Nov 1997) |
| nucleic acid base | A purine or pyrimidine; found in naturally occurring nucleic acids such as DNA. (05 Mar 2000) |
| nucleic acid conformation | The characteristic 3-dimensional shape of a nucleic acid or polynucleotide. Its secondary structure is due to the formation of hydrogen bonds between nucleotides, resulting in base pairing and areas with alpha helix structure. (12 Dec 1998) |
| nucleic acid denaturation | Disorganization of secondary structures of nucleic acids through cleavage of hydrogen bonds and hydrophobic linkages. Denatured DNA appears to be a single-stranded flexible structure. The effects of denaturation on RNA are similar though less pronounced and largely reversible. (12 Dec 1998) |
| nucleic acid heteroduplexes | Double-stranded nucleic acid molecules (DNA-DNA or DNA-RNA) which contain regions of nucleotide mismatches (non-complementary). In vivo, these heteroduplexes can result from mutation or genetic recombination; in vitro, they are formed by nucleic acid hybridization. Electron microscopic analysis of the resulting heteroduplexes facilitates the mapping of regions of base sequence homology of nucleic acids. (12 Dec 1998) |
| nucleic acid hybridization | Widely used technique which exploits the ability of complementary sequences in single-stranded dnas or rnas to pair with each other to form a double helix. Hybridization can take place between two complimentary DNA sequences, between a single-stranded DNA and a complementary RNA, or between two RNA sequences. The technique is used to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. (kendrew, encyclopedia of molecular biology, 1994, p503; dorlands, 28th ed, p781) (12 Dec 1998) |
| nucleic acid precursors | Use for nucleic acid precursors in general or for which there is no specific heading. (12 Dec 1998) |
| nucleic acid probe | A nucleic acid fragment, labelled by a radioisotope, biotin, etc., that is complementary to a sequence in another nucleic acid (fragment) and that will, by hydrogen binding to the latter, locate or identify it and be detected; a diagnostic technique based on the fact that every species of microbe possesses some unique nucleic acid sequences which differentiate it from all others, and thus can be used as identifying markers or "fingerprints." (05 Mar 2000) |
| nucleic acid probes | Nucleic acid which complements a specific mRNA or DNA molecule, or fragment thereof; used for hybridization studies in order to identify microorganisms and for genetic studies. (12 Dec 1998) |
| nucleic acid renaturation | The reformation of all, or part of, the native conformation of a nucleic acid molecule after the molecule has undergone denaturation. (12 Dec 1998) |
Synonyms : Extraribosomal Peptide Biosynthesis, Nonribosomal Peptide Biosynthesis, Nucleic Acid-Independent Peptide Biosynthesis, Biosynthesis, Extra-Ribosomal Peptide, Extra-Ribosomal Peptide Biosynthesis, Non-Ribosomal Peptide Biosynthesis
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