1a8f

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[[Image:1a8f.gif|left|200px]]<br /><applet load="1a8f" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1a8f.gif|left|200px]]
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caption="1a8f, resolution 1.80&Aring;" />
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'''HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE'''<br />
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{{Structure
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|PDB= 1a8f |SIZE=350|CAPTION= <scene name='initialview01'>1a8f</scene>, resolution 1.80&Aring;
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|SITE= <scene name='pdbsite=FE:Ferric+Ion+Binding+Site.+Carbonate+And+ARG+124+Are+Both+...'>FE</scene>
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|LIGAND= <scene name='pdbligand=CO3:CARBONATE+ION'>CO3</scene> and <scene name='pdbligand=FE:FE (III) ION'>FE</scene>
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|ACTIVITY=
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|GENE=
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}}
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'''HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1A8F 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=CO3:'>CO3</scene> and <scene name='pdbligand=FE:'>FE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=FE:Ferric+Ion+Binding+Site.+Carbonate+And+ARG+124+Are+Both+...'>FE</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A8F OCA].
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1A8F is a [[Single protein]] structure of 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=1A8F OCA].
==Reference==
==Reference==
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Two high-resolution crystal structures of the recombinant N-lobe of human transferrin reveal a structural change implicated in iron release., MacGillivray RT, Moore SA, Chen J, Anderson BF, Baker H, Luo Y, Bewley M, Smith CA, Murphy ME, Wang Y, Mason AB, Woodworth RC, Brayer GD, Baker EN, Biochemistry. 1998 Jun 2;37(22):7919-28. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9609685 9609685]
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Two high-resolution crystal structures of the recombinant N-lobe of human transferrin reveal a structural change implicated in iron release., MacGillivray RT, Moore SA, Chen J, Anderson BF, Baker H, Luo Y, Bewley M, Smith CA, Murphy ME, Wang Y, Mason AB, Woodworth RC, Brayer GD, Baker EN, Biochemistry. 1998 Jun 2;37(22):7919-28. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9609685 9609685]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: transferrin]]
[[Category: transferrin]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:42:04 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 09:54:22 2008''

Revision as of 07:54, 20 March 2008


PDB ID 1a8f

Drag the structure with the mouse to rotate
, resolution 1.80Å
Sites:
Ligands: and
Coordinates: save as pdb, mmCIF, xml



HUMAN SERUM TRANSFERRIN, RECOMBINANT N-TERMINAL LOBE


Contents

Overview

The N-lobe of human serum transferrin (hTF/2N) has been expressed in baby hamster kidney cells and crystallized in both orthorhombic (P212121) and tetragonal (P41212) space groups. Both crystal forms diffract to high resolution (1.6 and 1.8 A, respectively) and have been solved by molecular replacement. Subsequent refinement resulted in final models for the structure of hTF/2N that had crystallographic R-factors of 18.1 and 19.7% for the two crystal forms, respectively; these models represent the highest-resolution transferrin structures determined to date. The hTF/2N polypeptide has a folding pattern similar to those of other transferrins, including the presence of a deep cleft that contains the metal-binding site. In contrast to other transferrins, both crystal forms of hTF/2N display disorder at the iron-binding site; model building suggests that this disorder consists of alternative conformations of the synergistically bound carbonate anion, the side chain for Arg-124, and several solvent molecules. Subsequent refinement revealed that conformation A has an occupancy of 0.63-0. 65 and corresponds to the structure of the iron-binding site found in other transferrins. The alternative conformation B has an occupancy of 0.35-0.37; in this structure, the carbonate has rotated 30 degrees relative to the iron and the side chain for Arg-124 has moved to accommodate the new carbonate position. Several water molecules appear to stabilize the carbonate anion in the two conformations. These structures are consistent with the protonation of the carbonate and resulting partial removal of the anion from the metal; these events would occur prior to cleft opening and metal release.

Disease

Known diseases associated with this structure: Atransferrinemia OMIM:[190000], Iron deficiency anemia, susceptibility to OMIM:[190000]

About this Structure

1A8F is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Two high-resolution crystal structures of the recombinant N-lobe of human transferrin reveal a structural change implicated in iron release., MacGillivray RT, Moore SA, Chen J, Anderson BF, Baker H, Luo Y, Bewley M, Smith CA, Murphy ME, Wang Y, Mason AB, Woodworth RC, Brayer GD, Baker EN, Biochemistry. 1998 Jun 2;37(22):7919-28. PMID:9609685

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