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
"sequence hypothesis"¿¡ ´ëÇÑ ´ëÇÑ»ýÈÇкÐÀÚ»ý¹°ÇÐȸ ÀÇÇпë¾î ¼¼ºÎ °Ë»ö °á°úÀÔ´Ï´Ù
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
swquence hypothesis
´ëÇÑ»ýÈÇкÐÀÚ»ý¹°ÇÐȸ ¿ë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú :
15
ÆäÀÌÁö:
3
¿µ¹®
ÇѱÛ
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)
biochemical coupling hypothesis
»ýÈÇÐÀû(ßæûùùÊîÜ) ¦ÁöÀ½¼³(àã)
biochemical deletion hypothesis
»ýÈÇÐÀû(ßæûùùÊîÜ)°á½Ç¼³(ÌÀã÷àã)
biogenic amine hypothesis
»ýü(ßæô÷)¾Æ¹Î¼³(àã)
bookmark hypothesis
¼Ç¥¼³(ßöøöàã)
catabolic deletion hypothesis
ÀÌÈ´ë»çÀû °á¼Õ¼³(ì¶ûùÓÛÞóîÜ ÌÀáßàâ)
chemical coupling hypothesis
ÈÇÐ(ûùùÊ) Ä«Çøµ¼³(àã)
chemiosmotic coupling hypothesis
ÈÇлïÅõ(ûùùÊß¶÷â) ¦ÁöÀ½¼³(àã)
conformational coupling hypothesis
ÀÔüÇüÅÂ(Ø¡ô÷û¡÷¾) Ä«Çøµ¼³(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:
3
¿µ¹®
ÇѱÛ
ÀÌÀü
ÅëÇÕ°Ë»ö ¿Ï·á
ÀÌÀü
´ÙÀ½