全文获取类型
收费全文 | 306篇 |
免费 | 28篇 |
出版年
2022年 | 3篇 |
2021年 | 7篇 |
2019年 | 2篇 |
2018年 | 10篇 |
2017年 | 3篇 |
2016年 | 8篇 |
2015年 | 7篇 |
2014年 | 12篇 |
2013年 | 13篇 |
2012年 | 26篇 |
2011年 | 28篇 |
2010年 | 15篇 |
2009年 | 8篇 |
2008年 | 17篇 |
2007年 | 23篇 |
2006年 | 17篇 |
2005年 | 19篇 |
2004年 | 23篇 |
2003年 | 29篇 |
2002年 | 24篇 |
2001年 | 6篇 |
2000年 | 4篇 |
1999年 | 3篇 |
1998年 | 3篇 |
1997年 | 3篇 |
1996年 | 4篇 |
1995年 | 1篇 |
1994年 | 2篇 |
1993年 | 2篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1987年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1976年 | 1篇 |
排序方式: 共有334条查询结果,搜索用时 203 毫秒
1.
2.
Ivano Bertini Bertini Luchinat Mario Piccioli Margarita Vicens Oliver Maria Silvia Viezzoli 《European biophysics journal : EBJ》1991,20(5):269-279
Human copper-cobalt superoxide dismutase in the reduced form has been investigated through 1H NMR techniques. The aim is to monitor the structural properties of this derivative and to compare them with those of reduced and oxidized native superoxide dismutases. The observed signals of the cobalt ligands have been assigned as well as the signals of the histidines bound to copper(I). The latter signals experience little pseudocontact shifts which allow a rough orientation of the magnetic susceptibility tensor in the molecular frame. The connectivities indicate that, although the histidine bridge is broken in the reduced form, the interproton distances between ligands of both ions are essentially the same.Abbreviations WEFT
water eliminated Fourier transform
- NOE
nuclear Overhauser effect
- NOESY
NOE spectroscopy
- COSY
correlation spectroscopy
- TOCSY
total correlation spectroscopy
- SOD
superoxide dismutase
- E2Co(II)SOD
SOD with empty copper site (E=empty) and with cobalt(II) in the Zinc(II) site
Offprint requests to: I. Bertini 相似文献
3.
4.
5.
The effect of omeprazole on the mitochondrial carnitine/acylcarnitine transporter has been studied in proteoliposomes. Externally added omeprazole inhibited the carnitine/carnitine antiport catalysed by the transporter. The inhibition was partially reversed by DTE indicating that it was caused by the covalent reaction of omeprazole with Cys residue(s). Inhibition of the C-less mutant transporter indicated also the occurrence of an alternative non-covalent mechanism. The IC50 of the inhibition of the WT and the C-less CACT by omeprazole were 5.4 µM and 29 µM, respectively. Inhibition kinetics showed non competitive inhibition of the WT and competitive inhibition of the C-less. The presence of carnitine or acylcarnitines during the incubation of the proteoliposomes with omeprazole increased the inhibition. Using site-directed Cys mutants it was demonstrated that C283 and C136 were essential for covalent inhibition. Molecular docking of omeprazole with CACT indicated the formation of both covalent interactions with C136 and C283 and non-covalent interactions in agreement with the experimental data. 相似文献
6.
7.
Interspecific reproductive barriers between sympatric populations of wild tomato species (Solanum section Lycopersicon)
下载免费PDF全文
![点击此处可从《American journal of botany》网站下载免费的PDF全文](/ch/ext_images/free.gif)
8.
9.
Arendt Y Banci L Bertini I Cantini F Cozzi R Del Conte R Gonnelli L 《FEBS letters》2007,581(24):4723-4726
The solution structure of the catalytic domain of MMP-20, a member of the matrix metalloproteinases family not yet structurally characterized, complexed with N-Isobutyl-N-(4-methoxyphenylsulfonyl)glycyl hydroxamic acid (NNGH), is here reported and compared with other MMPs-NNGH adducts. The backbone dynamic has been characterized as well. We have found that, despite the same fold and very high overall similarity, the present structure experiences specific structural and dynamical similarities with some MMPs and differences with others, around the catalytic cavity. The present solution structure, not only contributes to fill the gap of structural knowledge on human MMPs, but also provides further information to design more selective and efficient inhibitors for a specific member of this class of proteins. 相似文献
10.
Banci L Bertini I Cantini F Della-Malva N Migliardi M Rosato A 《The Journal of biological chemistry》2007,282(32):23140-23146
ATP7A is a P-type ATPase involved in copper(I) homeostasis in humans. It possesses a long N-terminal cytosolic tail containing six domains that are individually folded and capable of binding one copper(I) ion each. We investigated the entire N-terminal tail (MNK1-6) in solution by NMR spectroscopy and addressed its interaction with copper(I) and with copper(I)-HAH1, the physiological partner of ATP7A. At copper(I)-HAH1:MNK1-6 ratios of up to 3:1, thus encompassing the range of protein ratios in vivo, both the first and fourth domain of the tail formed a metal-mediated adduct with HAH1 whereas the sixth domain was simultaneously able to partly remove copper(I) from HAH1. These processes are not dependent on one another. In particular, formation of the adducts is not necessary for copper(I) transfer from HAH1 to the sixth domain. The present data, together with available in vivo studies, suggest that the localization of ATP7A between the trans-Golgi network and the plasma membrane may be regulated by the accumulation of the adducts with HAH1, whereas the main role of domains 5 and 6 is to assist copper(I) translocation. 相似文献