4irp

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'''Unreleased structure'''
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{{STRUCTURE_4irp| PDB=4irp | SCENE= }}
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===Crystal structure of catalytic domain of human beta1,4-galactosyltransferase-7 in open conformation with manganses and UDP===
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The entry 4irp is ON HOLD until Paper Publication
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==Disease==
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[[http://www.uniprot.org/uniprot/B4GT7_HUMAN B4GT7_HUMAN]] Ehlers-Danlos syndrome, progeroid type. The disease is caused by mutations affecting the gene represented in this entry.
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Authors: Tsutsui, Y., Ramakrishnan, B., Qasba, P.K.
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==Function==
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[[http://www.uniprot.org/uniprot/B4GT7_HUMAN B4GT7_HUMAN]] Required for the biosynthesis of the tetrasaccharide linkage region of proteoglycans, especially for small proteoglycans in skin fibroblasts.
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Description: Crystal structure of catalytic domain of human beta1,4-galactosyltransferase-7 in open conformation with manganses and UDP
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==About this Structure==
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[[4irp]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IRP OCA].
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[[Category: Homo sapiens]]
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[[Category: Qasba, P K.]]
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[[Category: Ramakrishnan, B.]]
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[[Category: Tsutsui, Y.]]
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[[Category: Glycosyltransferase]]
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[[Category: Golgi]]
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[[Category: Gt-a fold]]
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[[Category: Manganese and udp complex]]
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[[Category: Open conformation]]
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[[Category: Transferase]]

Revision as of 08:18, 29 September 2013

Template:STRUCTURE 4irp

Contents

Crystal structure of catalytic domain of human beta1,4-galactosyltransferase-7 in open conformation with manganses and UDP

Disease

[B4GT7_HUMAN] Ehlers-Danlos syndrome, progeroid type. The disease is caused by mutations affecting the gene represented in this entry.

Function

[B4GT7_HUMAN] Required for the biosynthesis of the tetrasaccharide linkage region of proteoglycans, especially for small proteoglycans in skin fibroblasts.

About this Structure

4irp is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

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