1cyc

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(New page: 200px<br /><applet load="1cyc" size="450" color="white" frame="true" align="right" spinBox="true" caption="1cyc, resolution 2.3&Aring;" /> '''THE CRYSTAL STRUCTURE...)
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[[Image:1cyc.gif|left|200px]]<br /><applet load="1cyc" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1cyc, resolution 2.3&Aring;" />
caption="1cyc, resolution 2.3&Aring;" />
'''THE CRYSTAL STRUCTURE OF BONITO (KATSUO) FERROCYTOCHROME C AT 2.3 ANGSTROMS RESOLUTION. II. STRUCTURE AND FUNCTION'''<br />
'''THE CRYSTAL STRUCTURE OF BONITO (KATSUO) FERROCYTOCHROME C AT 2.3 ANGSTROMS RESOLUTION. II. STRUCTURE AND FUNCTION'''<br />
==Overview==
==Overview==
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The structure analysis of bonito heart ferrocytochrome c was carried out, at 2.3 A resolution by X-ray diffraction, and a Kendrew-type skeletal, model was built up. This molecule has an overall egg shape, 35 A in, height, 30 A in width and 23 A in thickness; the 5th ligand of the heme, iron atom is the N-epsilon atom of the His-18 imidazole ring and the 6th, is the Met-80 sulfur atom. Distinct alpha-helix regions are found between, the N-terminus and reside 11, between 60 and 69, and between 90 and the, C-terminus. The most distinct difference between the conformation of the, present molecule and that of the horse oxidized molecule is the location, of the Phe-82 phenyl ring. In the present reduced molecule, the phyenyl, ring is in closer contact with the iron atom and gives influences on the, character of the iron atom. Inside the molecule, at the lower part of the, heme pocket, there is an extended hydrogen bond network including the, propionic acid residues of the heme group. Both Phe-82 and the hydrogen, bond network may play a key role in the function of this molecule.
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The structure analysis of bonito heart ferrocytochrome c was carried out at 2.3 A resolution by X-ray diffraction, and a Kendrew-type skeletal model was built up. This molecule has an overall egg shape, 35 A in height, 30 A in width and 23 A in thickness; the 5th ligand of the heme iron atom is the N-epsilon atom of the His-18 imidazole ring and the 6th is the Met-80 sulfur atom. Distinct alpha-helix regions are found between the N-terminus and reside 11, between 60 and 69, and between 90 and the C-terminus. The most distinct difference between the conformation of the present molecule and that of the horse oxidized molecule is the location of the Phe-82 phenyl ring. In the present reduced molecule, the phyenyl ring is in closer contact with the iron atom and gives influences on the character of the iron atom. Inside the molecule, at the lower part of the heme pocket, there is an extended hydrogen bond network including the propionic acid residues of the heme group. Both Phe-82 and the hydrogen bond network may play a key role in the function of this molecule.
==About this Structure==
==About this Structure==
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1CYC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Katsuwonus_pelamis Katsuwonus pelamis] with HEM as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1CYC OCA].
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1CYC is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Katsuwonus_pelamis Katsuwonus pelamis] with <scene name='pdbligand=HEM:'>HEM</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1CYC OCA].
==Reference==
==Reference==
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The crystal structure of bonito (katsuo) ferrocytochrome c at 2.3 A resolution. II. Structure and function., Tanaka N, Yamane T, Tsukihara T, Ashida T, Kakudo M, J Biochem (Tokyo). 1975 Jan 1;77(1?):147-62. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=166072 166072]
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The crystal structure of bonito (katsuo) ferrocytochrome c at 2.3 A resolution. II. Structure and function., Tanaka N, Yamane T, Tsukihara T, Ashida T, Kakudo M, J Biochem. 1975 Jan 1;77(1?):147-62. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=166072 166072]
[[Category: Katsuwonus pelamis]]
[[Category: Katsuwonus pelamis]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: electron transport]]
[[Category: electron transport]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Nov 20 12:50:52 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:10:57 2008''

Revision as of 10:10, 21 February 2008


1cyc, resolution 2.3Å

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THE CRYSTAL STRUCTURE OF BONITO (KATSUO) FERROCYTOCHROME C AT 2.3 ANGSTROMS RESOLUTION. II. STRUCTURE AND FUNCTION

Overview

The structure analysis of bonito heart ferrocytochrome c was carried out at 2.3 A resolution by X-ray diffraction, and a Kendrew-type skeletal model was built up. This molecule has an overall egg shape, 35 A in height, 30 A in width and 23 A in thickness; the 5th ligand of the heme iron atom is the N-epsilon atom of the His-18 imidazole ring and the 6th is the Met-80 sulfur atom. Distinct alpha-helix regions are found between the N-terminus and reside 11, between 60 and 69, and between 90 and the C-terminus. The most distinct difference between the conformation of the present molecule and that of the horse oxidized molecule is the location of the Phe-82 phenyl ring. In the present reduced molecule, the phyenyl ring is in closer contact with the iron atom and gives influences on the character of the iron atom. Inside the molecule, at the lower part of the heme pocket, there is an extended hydrogen bond network including the propionic acid residues of the heme group. Both Phe-82 and the hydrogen bond network may play a key role in the function of this molecule.

About this Structure

1CYC is a Single protein structure of sequence from Katsuwonus pelamis with as ligand. Full crystallographic information is available from OCA.

Reference

The crystal structure of bonito (katsuo) ferrocytochrome c at 2.3 A resolution. II. Structure and function., Tanaka N, Yamane T, Tsukihara T, Ashida T, Kakudo M, J Biochem. 1975 Jan 1;77(1?):147-62. PMID:166072

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