Wada H, Yeh E T, Kamitani T
Department of Internal Medicine, Institute of Molecular Medicine for the Prevention of Human Diseases, Houston, Texas 77030, USA.
Biochem Biophys Res Commun. 1999 Apr 2;257(1):100-5. doi: 10.1006/bbrc.1999.0339.
NEDD8 is a novel ubiquitin-like protein that has been shown to conjugate to nuclear proteins in a manner analogous to ubiquitination and sentrinization. Recently, human cullin-4A was reported to be conjugated by a single molecule of NEDD8. Here, we show that human cullin-2 is also conjugated by a single molecule of the NEDD8. The C-terminal 171-amino-acid residues in human cullin-2 are sufficient for NEDD8-conjugation. In addition, the equivalent C-terminal fragments of other cullins have been shown to be conjugated by NEDD8. Mapping of the NEDD8-conjugation site revealed that Lys-689 in human cullin-2 is conjugated by NEDD8. Interestingly, the Lys residue at position 689 in cullin-2 is conserved in all cullin family members, including human cullin-1, -2, -3, -4A, -4B, and -5 and yeast cullin (Cdc53), suggesting the possibility that other cullin family members are conjugated by NEDD8/Rub1 at a Lys residue of equivalent position.
NEDD8是一种新型的类泛素蛋白,已被证明能以类似于泛素化和类泛素化的方式与核蛋白结合。最近,据报道人类cullin-4A能被单个NEDD8分子结合。在此,我们表明人类cullin-2也能被单个NEDD8分子结合。人类cullin-2中C末端的171个氨基酸残基足以进行NEDD8结合。此外,其他cullin的等效C末端片段已被证明能被NEDD8结合。NEDD8结合位点的定位显示,人类cullin-2中的赖氨酸-689能被NEDD8结合。有趣的是,cullin-2中第689位的赖氨酸残基在所有cullin家族成员中都是保守的,包括人类cullin-1、-2、-3、-4A、-4B和-5以及酵母cullin(Cdc53),这表明其他cullin家族成员有可能在等效位置的赖氨酸残基处被NEDD8/Rub1结合。