2i17

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(New page: 200px<br /> <applet load="2i17" size="450" color="white" frame="true" align="right" spinBox="true" caption="2i17, resolution 0.81&Aring;" /> '''Human aldose reduct...)
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caption="2i17, resolution 0.81&Aring;" />
caption="2i17, resolution 0.81&Aring;" />
'''Human aldose reductase in complex with NADP+ and the inhibitor IDD594 at temperature of 60K'''<br />
'''Human aldose reductase in complex with NADP+ and the inhibitor IDD594 at temperature of 60K'''<br />
==Overview==
==Overview==
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Two X-ray data sets for a complex of human aldose reductase (h-AR) with, the inhibitor IDD 594 and the cofactor NADP(+) were collected from two, different parts of the same crystal to a resolution of 0.81 A at 15 and 60, K using cold helium gas as cryogen. The contribution of temperature to the, atomic B values was estimated by comparison of the independently refined, models. It was found that although being slightly different for different, kinds of atoms, the differences (deltaB) in the isotropic equivalents B of, atomic displacement parameters (ADPs) were approximately constant (about, 1.7 A(2)) for well ordered atoms as the temperature was increased from 15, to 60 K. The mean value of this difference varied according to the number, of non-H atoms covalently bound to the parent atom. Atoms having a B value, of higher than 8 A(2) at 15 K showed much larger deviations of deltaB from, the average value, which might reflect partial occupancy of atomic sites., An analysis of the anisotropy of ADPs for individual atoms revealed an, increase in the isotropy of ADPs with the increase of the temperature from, 15 to 60 K. In a separate experiment, a 0.93 A resolution data set was, collected from a different crystal of the same complex at 100 K using cold, nitrogen as a cryogen. The effects of various errors on the atomic B, values were estimated by comparison of the refined models and the, temperature-dependent component was inferred. It was found that both, decreasing the data redundancy and increasing the resolution cutoff led to, an approximately constant increase in atomic B values for well ordered, atoms.
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Two X-ray data sets for a complex of human aldose reductase (h-AR) with the inhibitor IDD 594 and the cofactor NADP(+) were collected from two different parts of the same crystal to a resolution of 0.81 A at 15 and 60 K using cold helium gas as cryogen. The contribution of temperature to the atomic B values was estimated by comparison of the independently refined models. It was found that although being slightly different for different kinds of atoms, the differences (deltaB) in the isotropic equivalents B of atomic displacement parameters (ADPs) were approximately constant (about 1.7 A(2)) for well ordered atoms as the temperature was increased from 15 to 60 K. The mean value of this difference varied according to the number of non-H atoms covalently bound to the parent atom. Atoms having a B value of higher than 8 A(2) at 15 K showed much larger deviations of deltaB from the average value, which might reflect partial occupancy of atomic sites. An analysis of the anisotropy of ADPs for individual atoms revealed an increase in the isotropy of ADPs with the increase of the temperature from 15 to 60 K. In a separate experiment, a 0.93 A resolution data set was collected from a different crystal of the same complex at 100 K using cold nitrogen as a cryogen. The effects of various errors on the atomic B values were estimated by comparison of the refined models and the temperature-dependent component was inferred. It was found that both decreasing the data redundancy and increasing the resolution cutoff led to an approximately constant increase in atomic B values for well ordered atoms.
==About this Structure==
==About this Structure==
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2I17 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with NDP, LDT and CIT as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Aldehyde_reductase Aldehyde reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.21 1.1.1.21] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2I17 OCA].
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2I17 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=NDP:'>NDP</scene>, <scene name='pdbligand=LDT:'>LDT</scene> and <scene name='pdbligand=CIT:'>CIT</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Aldehyde_reductase Aldehyde reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.21 1.1.1.21] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2I17 OCA].
==Reference==
==Reference==
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[[Category: Hasemann, I.]]
[[Category: Hasemann, I.]]
[[Category: Joachimiak, A.]]
[[Category: Joachimiak, A.]]
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[[Category: Lunin, V.Y.]]
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[[Category: Lunin, V Y.]]
[[Category: Mitshler, A.]]
[[Category: Mitshler, A.]]
[[Category: Petrova, T.]]
[[Category: Petrova, T.]]
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 22:39:37 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:48:03 2008''

Revision as of 15:48, 21 February 2008


2i17, resolution 0.81Å

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Human aldose reductase in complex with NADP+ and the inhibitor IDD594 at temperature of 60K

Overview

Two X-ray data sets for a complex of human aldose reductase (h-AR) with the inhibitor IDD 594 and the cofactor NADP(+) were collected from two different parts of the same crystal to a resolution of 0.81 A at 15 and 60 K using cold helium gas as cryogen. The contribution of temperature to the atomic B values was estimated by comparison of the independently refined models. It was found that although being slightly different for different kinds of atoms, the differences (deltaB) in the isotropic equivalents B of atomic displacement parameters (ADPs) were approximately constant (about 1.7 A(2)) for well ordered atoms as the temperature was increased from 15 to 60 K. The mean value of this difference varied according to the number of non-H atoms covalently bound to the parent atom. Atoms having a B value of higher than 8 A(2) at 15 K showed much larger deviations of deltaB from the average value, which might reflect partial occupancy of atomic sites. An analysis of the anisotropy of ADPs for individual atoms revealed an increase in the isotropy of ADPs with the increase of the temperature from 15 to 60 K. In a separate experiment, a 0.93 A resolution data set was collected from a different crystal of the same complex at 100 K using cold nitrogen as a cryogen. The effects of various errors on the atomic B values were estimated by comparison of the refined models and the temperature-dependent component was inferred. It was found that both decreasing the data redundancy and increasing the resolution cutoff led to an approximately constant increase in atomic B values for well ordered atoms.

About this Structure

2I17 is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as Aldehyde reductase, with EC number 1.1.1.21 Full crystallographic information is available from OCA.

Reference

Ultrahigh-resolution study of protein atomic displacement parameters at cryotemperatures obtained with a helium cryostat., Petrova T, Ginell S, Mitschler A, Hazemann I, Schneider T, Cousido A, Lunin VY, Joachimiak A, Podjarny A, Acta Crystallogr D Biol Crystallogr. 2006 Dec;62(Pt 12):1535-44. Epub 2006, Nov 23. PMID:17139089

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