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1lxt

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==Overview==
==Overview==
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Data between 6.0 and 2.4 A resolution, collected at 253 K, wer used to, refine a revised atomic model of muscle phosphoglucomutase: final, crystallographic R factor = 16.3% (Rfree = 19.1%); final r.m.s. deviations, from ideal bond lengths and angles = 0.018 A and 3.2 degrees, respectively. Features of the protein that were recognized only in the, revised model include: the disposition of water molecules within, domain-domain interfaces; two ion pairs buried in domain-domain, interfaces, one of which is a structural arginine around which the, active-site phosphoserine loop is wound; the basic architecture of the, active-site 'crevice', which is a groove in a 1(1/3)-turn helix, open at, both ends, that is produced by the interfacing of the four domains; the, distorted hexacoordinate ligand sphere of the active-site Mg2+, where the, enzymic phosphate group acts as a bidentate ligand; a pair of arginine, residues in domain IV that form part of the enzymic phosphate-binding site, (distal subsite) whose disposition in the two monomers of the asymmetric, unit is affected unequally by distant crystallographic contacts;, structural differences throughout domain IV, produced by these differing, contacts, that may mimic solution differences induced by substrate, binding; large differences in individually refined Debye-Waller thermal, factors for corresponding main-chain atoms in monomers (1) and (2), suggesting a dynamic disorder within the crystal that may involve, domain-size groups of residues; and a 'nucleophilic elbow' in the active, site that resides in a topological environment differing from previous, descriptions of this type of structure in other proteins.
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Data between 6.0 and 2.4 A resolution, collected at 253 K, wer used to refine a revised atomic model of muscle phosphoglucomutase: final crystallographic R factor = 16.3% (Rfree = 19.1%); final r.m.s. deviations from ideal bond lengths and angles = 0.018 A and 3.2 degrees, respectively. Features of the protein that were recognized only in the revised model include: the disposition of water molecules within domain-domain interfaces; two ion pairs buried in domain-domain interfaces, one of which is a structural arginine around which the active-site phosphoserine loop is wound; the basic architecture of the active-site 'crevice', which is a groove in a 1(1/3)-turn helix, open at both ends, that is produced by the interfacing of the four domains; the distorted hexacoordinate ligand sphere of the active-site Mg2+, where the enzymic phosphate group acts as a bidentate ligand; a pair of arginine residues in domain IV that form part of the enzymic phosphate-binding site (distal subsite) whose disposition in the two monomers of the asymmetric unit is affected unequally by distant crystallographic contacts; structural differences throughout domain IV, produced by these differing contacts, that may mimic solution differences induced by substrate binding; large differences in individually refined Debye-Waller thermal factors for corresponding main-chain atoms in monomers (1) and (2), suggesting a dynamic disorder within the crystal that may involve domain-size groups of residues; and a 'nucleophilic elbow' in the active site that resides in a topological environment differing from previous descriptions of this type of structure in other proteins.
==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Baranidharan, S.]]
[[Category: Baranidharan, S.]]
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[[Category: Junior, W.J.Ray.]]
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[[Category: Junior, W J.Ray.]]
[[Category: Liu, Y.]]
[[Category: Liu, Y.]]
[[Category: CD]]
[[Category: CD]]
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[[Category: phosphotransferase]]
[[Category: phosphotransferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 09:53:26 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:49:27 2008''

Revision as of 11:49, 21 February 2008


1lxt, resolution 2.7Å

Drag the structure with the mouse to rotate

STRUCTURE OF PHOSPHOTRANSFERASE PHOSPHOGLUCOMUTASE FROM RABBIT

Overview

Data between 6.0 and 2.4 A resolution, collected at 253 K, wer used to refine a revised atomic model of muscle phosphoglucomutase: final crystallographic R factor = 16.3% (Rfree = 19.1%); final r.m.s. deviations from ideal bond lengths and angles = 0.018 A and 3.2 degrees, respectively. Features of the protein that were recognized only in the revised model include: the disposition of water molecules within domain-domain interfaces; two ion pairs buried in domain-domain interfaces, one of which is a structural arginine around which the active-site phosphoserine loop is wound; the basic architecture of the active-site 'crevice', which is a groove in a 1(1/3)-turn helix, open at both ends, that is produced by the interfacing of the four domains; the distorted hexacoordinate ligand sphere of the active-site Mg2+, where the enzymic phosphate group acts as a bidentate ligand; a pair of arginine residues in domain IV that form part of the enzymic phosphate-binding site (distal subsite) whose disposition in the two monomers of the asymmetric unit is affected unequally by distant crystallographic contacts; structural differences throughout domain IV, produced by these differing contacts, that may mimic solution differences induced by substrate binding; large differences in individually refined Debye-Waller thermal factors for corresponding main-chain atoms in monomers (1) and (2), suggesting a dynamic disorder within the crystal that may involve domain-size groups of residues; and a 'nucleophilic elbow' in the active site that resides in a topological environment differing from previous descriptions of this type of structure in other proteins.

About this Structure

1LXT is a Single protein structure of sequence from Oryctolagus cuniculus with and as ligands. Active as Phosphoglucomutase, with EC number 5.4.2.2 Known structural/functional Sites: and . Full crystallographic information is available from OCA.

Reference

Structure of rabbit muscle phosphoglucomutase refined at 2.4 A resolution., Liu Y, Ray WJ Jr, Baranidharan S, Acta Crystallogr D Biol Crystallogr. 1997 Jul 1;53(Pt 4):392-405. PMID:15299905

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