This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.

Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


4irq

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
'''Unreleased structure'''
+
{{STRUCTURE_4irq| PDB=4irq | SCENE= }}
 +
===Crystal structure of catalytic domain of human beta1,4galactosyltransferase 7 in closed conformation in complex with manganese and UDP===
-
The entry 4irq is ON HOLD until Paper Publication
+
==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.
-
Authors: Tsutsui, Y., Ramakrishnan, B., Qasba, P.K.
+
==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.
-
Description: Crystal structure of catalytic domain of human beta1,4galactosyltransferase 7 in closed conformation in complex with manganese and UDP
+
==About this Structure==
 +
[[4irq]] is a 4 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=4IRQ OCA].
 +
[[Category: Homo sapiens]]
 +
[[Category: Qasba, P K.]]
 +
[[Category: Ramakrishnan, B.]]
 +
[[Category: Tsutsui, Y.]]
 +
[[Category: Closed conformation]]
 +
[[Category: Glycosyltransferase]]
 +
[[Category: Golgi]]
 +
[[Category: Gt-a fold]]
 +
[[Category: Manganese and udp complex]]
 +
[[Category: Transferase]]

Revision as of 08:18, 29 September 2013

Template:STRUCTURE 4irq

Contents

Crystal structure of catalytic domain of human beta1,4galactosyltransferase 7 in closed conformation in complex with manganese 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

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

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/4irq"
Personal tools