2c91

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 4: Line 4:
|PDB= 2c91 |SIZE=350|CAPTION= <scene name='initialview01'>2c91</scene>, resolution 2.30&Aring;
|PDB= 2c91 |SIZE=350|CAPTION= <scene name='initialview01'>2c91</scene>, resolution 2.30&Aring;
|SITE= <scene name='pdbsite=AC1:Mes+Binding+Site+For+Chain+J'>AC1</scene>
|SITE= <scene name='pdbsite=AC1:Mes+Binding+Site+For+Chain+J'>AC1</scene>
-
|LIGAND= <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene>, <scene name='pdbligand=TLA:L(+)-TARTARIC+ACID'>TLA</scene>, <scene name='pdbligand=MES:2-(N-MORPHOLINO)-ETHANESULFONIC+ACID'>MES</scene> and <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>
+
|LIGAND= <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MES:2-(N-MORPHOLINO)-ETHANESULFONIC+ACID'>MES</scene>, <scene name='pdbligand=NAP:NADP+NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NAP</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=TLA:L(+)-TARTARIC+ACID'>TLA</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
 +
|DOMAIN=
 +
|RELATEDENTRY=
 +
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2c91 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2c91 OCA], [http://www.ebi.ac.uk/pdbsum/2c91 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2c91 RCSB]</span>
}}
}}
Line 25: Line 28:
[[Category: Lapthorn, A J.]]
[[Category: Lapthorn, A J.]]
[[Category: Zhu, X.]]
[[Category: Zhu, X.]]
-
[[Category: GOL]]
 
-
[[Category: MES]]
 
-
[[Category: NAP]]
 
-
[[Category: PO4]]
 
-
[[Category: TLA]]
 
[[Category: akr]]
[[Category: akr]]
[[Category: aldo/keto reductase]]
[[Category: aldo/keto reductase]]
Line 39: Line 37:
[[Category: tartrate]]
[[Category: tartrate]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 16:12:26 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:18:07 2008''

Revision as of 23:18, 30 March 2008


PDB ID 2c91

Drag the structure with the mouse to rotate
, resolution 2.30Å
Sites:
Ligands: , , , ,
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



MOUSE SUCCINIC SEMIALDEHYDE REDUCTASE, AKR7A5


Overview

The aldo-keto reductases make up a superfamily of enzymes which can reduce a variety of aldehydes and ketones to their corresponding alcohols. Within each family are distinct preferences for certain substrates, presumably reflecting their role within the cell. The original member of the AKR7A subfamily was purified from liver as an aflatoxin dialdehyde reductase AKR7A1. However, recent additions to the family have revealed that even closely related enzymes have clear substrate preferences with AKR7A2, AKR7A4, and AKR7A5 showing much higher affinities for succinic semialdehyde (SSA) than does AKR7A1. To investigate the structural basis of this specificity, the crystal structure of mouse AKR7A5 has been determined to better than 2.5 A resolution. The structure is of the ternary complex of the enzyme with NADP+ and tartrate as an inhibitor. This structure has the same overall fold as the previously determined structure of AKR7A1; however, there are a number of differences in loops around the active site that contribute to observed differences in the substrate specificity between the AKR7A enzymes. Several differences are the result of bulky hydrophobic residues found in AKR7A5, namely, Met44, Trp77, and Trp224, which significantly restrict the size and modify the architecture of the substrate-binding pocket, producing a tighter or less flexible binding site for SSA than in AKR7A1. Site-directed mutagenesis was used to introduce Met44, Trp77, and Trp224 individually into AKR7A1, to test if they improved the affinity of the enzyme for SSA. Each mutation showed improved affinity for SSA, with Trp77Met having the largest effect. This confirms the role of these amino acids as substrate determinants for SSA.

About this Structure

2C91 is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

Reference

Crystal structure of mouse succinic semialdehyde reductase AKR7A5: structural basis for substrate specificity., Zhu X, Lapthorn AJ, Ellis EM, Biochemistry. 2006 Feb 14;45(6):1562-70. PMID:16460003

Page seeded by OCA on Mon Mar 31 02:18:07 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools