¼±Åà - È»ìǥŰ/¿£ÅÍŰ
´Ý±â - ESC
KMLE °Ë»ö
°Ë»ö ¼³Á¤
¿Â¶óÀÎ ÀÇÇмÀû
ÀÇÇпë¾î »çÀü
ÀÇÇоà¾î
ÀÇÇлçÀü
ÇÑ¿µ/¿µÇÑ»çÀü
¿µ¿µ»çÀü
»çÀÌÆ® ¼Ò°³
Àç°Ë»ö
"biochemical coupling hypothesis"¿¡ ´ëÇÑ ´ëÇÑ»ýÈÇкÐÀÚ»ý¹°ÇÐȸ ÀÇÇпë¾î ¼¼ºÎ °Ë»ö °á°úÀÔ´Ï´Ù
´ëÇÑ»ýÈÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú :
15
ÆäÀÌÁö:
2
¿µ¹®
ÇѱÛ
coupling
¦Áþ±â
coupling constant
¦Áþ±â »ó¼ö(ßÈâ¦)
coupling factor
¦Áþ±â ÀÎÀÚ(ì×í)
coupling inhibition
"¦Áþ±â ÀúÇØ(îÁúª), (ÔÒ) uncompetitive inhibition"
energy coupling
¿¡³ÊÁö ¦Áþ±â
indirect coupling
°£Á¢(ÊàïÈ) ¦Áþ±â
loose coupling
´À½¼ ¦Áþ±â
translational coupling
¹ø¿ª(Ûèæ»)Ä«Çøµ
acetate hypothesis
¾Æ¼¼Æ®»ê(ß«) ¼³(àã)
adapter hypothesis
¾Æ´äÅͼ³(àã)
adenylate charge hypothesis
¾Æµ¥´Ò»ê(ß«)´ëÀü¼³(Óáï³àã)
adenylate control hypothesis
¾Æµ¥´Ò»ê(ß«)Á¶Àý¼³(ðàï½àã)
Akabori hypothesis
¾ÆÄ«º¸¸®¼³(àã)
autocrine hypothesis
ÀÚ°¡ºÐºñ¼³ (í»Ê«ÝÂÝôàã)
Belling's hypothesis
º§¸µ¼³(àã)
ÀÌÀü
´ÙÀ½
ÀÌ ¾Æ·¡ ºÎÅÍ´Â °á°ú°¡ ¾ø½À´Ï´Ù.
´ëÇÑ»ýÈÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö ¸ÂÃã °Ë»ö °á°ú :
0
ÆäÀÌÁö:
2
¿µ¹®
ÇѱÛ
ÀÌÀü
ÅëÇÕ°Ë»ö ¿Ï·á
ÀÌÀü
´ÙÀ½