4irp: Difference between revisions
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{{STRUCTURE_4irp| PDB=4irp | SCENE= }} | |||
===Crystal structure of catalytic domain of human beta1,4-galactosyltransferase-7 in open conformation with manganses and UDP=== | |||
The entry | ==Disease== | ||
[[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. | |||
==Function== | |||
[[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. | |||
==About this Structure== | |||
[[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]. | |||
[[Category: Homo sapiens]] | |||
[[Category: Qasba, P K.]] | |||
[[Category: Ramakrishnan, B.]] | |||
[[Category: Tsutsui, Y.]] | |||
[[Category: Glycosyltransferase]] | |||
[[Category: Golgi]] | |||
[[Category: Gt-a fold]] | |||
[[Category: Manganese and udp complex]] | |||
[[Category: Open conformation]] | |||
[[Category: Transferase]] | |||
Revision as of 08:18, 29 September 2013
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.
