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==Overview==
==Overview==
The three-dimensional structure of human carbonic anhydrase II complexed, with azide and with bromide was investigated crystallographically. Both of, these non-protonated inhibitors replace the zinc and the 'deep' water, two, catalytically important water molecules in the active site of the, molecule. Both the azide and the bromide ions bind in a distorted, tetrahedral manner 0.4 and 1.1 A from the zinc water position, respectively, but are in close contact (2.0 and 2.6 A, respectively) with, the zinc ion.
The three-dimensional structure of human carbonic anhydrase II complexed with azide and with bromide was investigated crystallographically. Both of these non-protonated inhibitors replace the zinc and the 'deep' water, two catalytically important water molecules in the active site of the molecule. Both the azide and the bromide ions bind in a distorted tetrahedral manner 0.4 and 1.1 A from the zinc water position, respectively, but are in close contact (2.0 and 2.6 A, respectively) with the zinc ion.


==Disease==
==Disease==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Hakansson, K.]]
[[Category: Hakansson, K.]]
[[Category: Jonsson, B.M.]]
[[Category: Jonsson, B M.]]
[[Category: Liljas, A.]]
[[Category: Liljas, A.]]
[[Category: BR]]
[[Category: BR]]
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[[Category: lyase(oxo-acid)]]
[[Category: lyase(oxo-acid)]]


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