1bke

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|PDB= 1bke |SIZE=350|CAPTION= <scene name='initialview01'>1bke</scene>, resolution 3.15&Aring;
|PDB= 1bke |SIZE=350|CAPTION= <scene name='initialview01'>1bke</scene>, resolution 3.15&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=MYR:MYRISTIC+ACID'>MYR</scene> and <scene name='pdbligand=B3I:2,3,5-TRIIODOBENZOIC ACID'>B3I</scene>
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|LIGAND= <scene name='pdbligand=B3I:2,3,5-TRIIODOBENZOIC+ACID'>B3I</scene>, <scene name='pdbligand=MYR:MYRISTIC+ACID'>MYR</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
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|DOMAIN=
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1bke FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1bke OCA], [http://www.ebi.ac.uk/pdbsum/1bke PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1bke RCSB]</span>
}}
}}
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==Overview==
==Overview==
Human serum albumin (HSA) is the most abundant protein in the circulatory system. Its principal function is to transport fatty acids, but it is also capable of binding a great variety of metabolites and drugs. Despite intensive efforts, the detailed structural basis of fatty acid binding to HSA has remained elusive. We have now determined the crystal structure of HSA complexed with five molecules of myristate at 2.5 A resolution. The fatty acid molecules bind in long, hydrophobic pockets capped by polar side chains, many of which are basic. These pockets are distributed asymmetrically throughout the HSA molecule, despite its symmetrical repeating domain structure.
Human serum albumin (HSA) is the most abundant protein in the circulatory system. Its principal function is to transport fatty acids, but it is also capable of binding a great variety of metabolites and drugs. Despite intensive efforts, the detailed structural basis of fatty acid binding to HSA has remained elusive. We have now determined the crystal structure of HSA complexed with five molecules of myristate at 2.5 A resolution. The fatty acid molecules bind in long, hydrophobic pockets capped by polar side chains, many of which are basic. These pockets are distributed asymmetrically throughout the HSA molecule, despite its symmetrical repeating domain structure.
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==Disease==
 
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Known diseases associated with this structure: Analbuminemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103600 103600]], Dysalbuminemic hyperthyroxinemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103600 103600]], Dysalbuminemic hyperzincemia OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103600 103600]]
 
==About this Structure==
==About this Structure==
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[[Category: Franks, N.]]
[[Category: Franks, N.]]
[[Category: Mandelkow, H.]]
[[Category: Mandelkow, H.]]
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[[Category: B3I]]
 
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[[Category: MYR]]
 
[[Category: lipid-binding]]
[[Category: lipid-binding]]
[[Category: metal-binding]]
[[Category: metal-binding]]
[[Category: plasma protein]]
[[Category: plasma protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:12:17 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:02:50 2008''

Revision as of 16:02, 30 March 2008


PDB ID 1bke

Drag the structure with the mouse to rotate
, resolution 3.15Å
Ligands: ,
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



HUMAN SERUM ALBUMIN IN A COMPLEX WITH MYRISTIC ACID AND TRI-IODOBENZOIC ACID


Overview

Human serum albumin (HSA) is the most abundant protein in the circulatory system. Its principal function is to transport fatty acids, but it is also capable of binding a great variety of metabolites and drugs. Despite intensive efforts, the detailed structural basis of fatty acid binding to HSA has remained elusive. We have now determined the crystal structure of HSA complexed with five molecules of myristate at 2.5 A resolution. The fatty acid molecules bind in long, hydrophobic pockets capped by polar side chains, many of which are basic. These pockets are distributed asymmetrically throughout the HSA molecule, despite its symmetrical repeating domain structure.

About this Structure

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

Reference

Crystal structure of human serum albumin complexed with fatty acid reveals an asymmetric distribution of binding sites., Curry S, Mandelkow H, Brick P, Franks N, Nat Struct Biol. 1998 Sep;5(9):827-35. PMID:9731778

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