1uuj

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==Overview==
==Overview==
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Mutations in the Lis1 gene result in lissencephaly (smooth brain), a, debilitating developmental syndrome caused by the impaired ability of, postmitotic neurons to migrate to their correct destination in the, cerebral cortex. Sequence similarities suggest that the LIS1 protein, contains a C-terminal seven-blade beta-propeller domain, while the, structure of the N-terminal fragment includes the LisH (Lis-homology), motif, a pattern found in over 100 eukaryotic proteins with a hitherto, unknown function. We present the 1.75 A resolution crystal structure of, the N-terminal domain of mouse LIS1, and we show that the LisH motif is a, novel, thermodynamically very stable dimerization domain. The structure, explains the molecular basis of a low severity form of lissencephaly.
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Mutations in the Lis1 gene result in lissencephaly (smooth brain), a debilitating developmental syndrome caused by the impaired ability of postmitotic neurons to migrate to their correct destination in the cerebral cortex. Sequence similarities suggest that the LIS1 protein contains a C-terminal seven-blade beta-propeller domain, while the structure of the N-terminal fragment includes the LisH (Lis-homology) motif, a pattern found in over 100 eukaryotic proteins with a hitherto unknown function. We present the 1.75 A resolution crystal structure of the N-terminal domain of mouse LIS1, and we show that the LisH motif is a novel, thermodynamically very stable dimerization domain. The structure explains the molecular basis of a low severity form of lissencephaly.
==About this Structure==
==About this Structure==
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[[Category: Mus musculus]]
[[Category: Mus musculus]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Cooper, D.R.]]
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[[Category: Cooper, D R.]]
[[Category: Derewenda, U.]]
[[Category: Derewenda, U.]]
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[[Category: Derewenda, Z.S.]]
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[[Category: Derewenda, Z S.]]
[[Category: Devedjiev, Y.]]
[[Category: Devedjiev, Y.]]
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[[Category: Kim, M.H.]]
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[[Category: Kim, M H.]]
[[Category: ACT]]
[[Category: ACT]]
[[Category: BEZ]]
[[Category: BEZ]]
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[[Category: platelet-activating factor acetylhydrolase]]
[[Category: platelet-activating factor acetylhydrolase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:08:09 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:28:28 2008''

Revision as of 13:28, 21 February 2008


1uuj, resolution 1.75Å

Drag the structure with the mouse to rotate

N-TERMINAL DOMAIN OF LISSENCEPHALY-1 PROTEIN (LIS-1)

Overview

Mutations in the Lis1 gene result in lissencephaly (smooth brain), a debilitating developmental syndrome caused by the impaired ability of postmitotic neurons to migrate to their correct destination in the cerebral cortex. Sequence similarities suggest that the LIS1 protein contains a C-terminal seven-blade beta-propeller domain, while the structure of the N-terminal fragment includes the LisH (Lis-homology) motif, a pattern found in over 100 eukaryotic proteins with a hitherto unknown function. We present the 1.75 A resolution crystal structure of the N-terminal domain of mouse LIS1, and we show that the LisH motif is a novel, thermodynamically very stable dimerization domain. The structure explains the molecular basis of a low severity form of lissencephaly.

About this Structure

1UUJ is a Single protein structure of sequence from Mus musculus with , and as ligands. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

The structure of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications., Kim MH, Cooper DR, Oleksy A, Devedjiev Y, Derewenda U, Reiner O, Otlewski J, Derewenda ZS, Structure. 2004 Jun;12(6):987-98. PMID:15274919

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