The solution NMR structure of a blue-green algae hepatotoxin, microcystin-RR - A comparison with the structure of microcystin-LR
被引:14
作者:
Trogen, GB
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机构:Umea Univ, Dept Organ Chem, S-90187 Umea, Sweden
Trogen, GB
Edlund, U
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机构:Umea Univ, Dept Organ Chem, S-90187 Umea, Sweden
Edlund, U
Larsson, G
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机构:Umea Univ, Dept Organ Chem, S-90187 Umea, Sweden
Larsson, G
Sethson, I
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机构:
Umea Univ, Dept Organ Chem, S-90187 Umea, SwedenUmea Univ, Dept Organ Chem, S-90187 Umea, Sweden
Sethson, I
[1
]
机构:
[1] Umea Univ, Dept Organ Chem, S-90187 Umea, Sweden
[2] Umea Univ, Dept Med Biochem & Biophys, S-90187 Umea, Sweden
来源:
EUROPEAN JOURNAL OF BIOCHEMISTRY
|
1998年
/
258卷
/
02期
关键词:
microcystins;
cyanobacteria;
protein phosphatase;
three-dimensional structure;
simulated annealing;
D O I:
10.1046/j.1432-1327.1998.2580301.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The microcystin-RR structures are compared with the structures of microcystin-LR in solution as well as in the crystal structure of the complex with protein phosphatase. The gross structures of the two peptides are similar, but with a more accentuated and compact saddle structure for microcystin-RR. The structural differences affect the hydrogen-bond pattern in the peptides and the location of the side chain of N-methyldehydroalanine, both of which are important for the ability of the peptide to form a tight complex with protein phosphatase. These structural differences may contribute to the observed differences in toxicity of microcystin-RR and microcystin-LR.