메뉴 건너뛰기
.. 내서재 .. 알림
소속 기관/학교 인증
인증하면 논문, 학술자료 등을  무료로 열람할 수 있어요.
한국대학교, 누리자동차, 시립도서관 등 나의 기관을 확인해보세요
(국내 대학 90% 이상 구독 중)
로그인 회원가입 고객센터 ENG
주제분류

추천
검색

논문 기본 정보

자료유형
학술저널
저자정보
저널정보
대한생화학·분자생물학회 Experimental and Molecular Medicine Experimental and Molecular Medicine 제35권 제5호
발행연도
2003.1
수록면
421 - 430 (10page)

이용수

표지
📌
연구주제
📖
연구배경
🔬
연구방법
🏆
연구결과
AI에게 요청하기
추천
검색

초록· 키워드

오류제보하기
CDK2 and CDK4 known promoter of cel cycling catalyze phosphorylation of RB protein. Enzyme specificity betwen two CDKs that work at a diferent cel cycle phase is not clearly under-stod. In order to define kinase properties of CDK2 and CDK4 in complex with cycline A or cycline D1 in relation to their respective role in cell cy-ties of both CDK4/cycline D1 and CDK2/cycline A in vitro. Asociation constant, Km for ATP in CDK4/cyclin D1 was found as 418 M, a value un-usualy high whereas CDK2/cyclin A was 23 M, a value close to most of other regulatory protein kinases. Turnover value for both CDK4/cyclin D1 and CDK2/cyclin A were estimated as 3.4 and 3.9 min-1 respectively. Kinetic efficiency estimation in-dicates far over one order magnitude less effici-cycline A (9.3 pM-1 min-1 and 170 pM-1 min-1 respec-tively). In addition, inhibition of celular CDK4 caused increase of cellular levels of ATP, even though inhibition of CDK2 did not change it notice-ably. These data sugest celular CDK4/ cyclin D1 activity is tightly associated with celular ATP concentration. Also, analysis of phosphorylated serine/threonine sites on RB catalyzed by CDK4/ cyclin D1 and CDK2/cyclin A showed significant diferences in their preference of phosphorylation to regulate various celular proteins by binding and this binding is controled by its phosphoryl-ation, these data shown here clearly indicate signi-ficant diference in their biochemical properties betwen CDK4/cyclin D1 and CDK2/cyclin A affec-ting regulation of celular RB function.

목차

등록된 정보가 없습니다.

참고문헌 (0)

참고문헌 신청

함께 읽어보면 좋을 논문

논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!

이 논문의 저자 정보

최근 본 자료

전체보기

댓글(0)

0