Sandbox2QRU

spinqualitylabelsall models Caption for this structure Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

This is a default text for your page Sandbox2QRU. Click above on edit this page to modify. Be careful with the < and > signs.

You may include any references to papers as in: the use of JSmol in Proteopedia ^[1] or to the article describing Jmol ^[2] to the rescue. The work below details the computational characterization and functional analysis of a protein, 2QRU, with a known crystal structure. Using a variety of computational methods, a variety of key identifiers in the sequences and structure could be isolated to better understand the function of the protein. This is due to the ideology that sequence denotes structure which denotes function.

2QRU is known to be a hydrolase, most active on esterase. The structure is 276 amino acids long, which is approximately 30.14 kDa. Knowing 2QRU is an alpha/beta hydrolase, the literature helped give further information on possible experimental conditions and substrates that can be used to identify activity. However, experimental data has not been obtained yet.

Structure/Sequence Analysis

Sequence Analysis

SPRITE

Chimera

BLAST

Structure Analysis

DALI

DALI analysis showed certain highly conserved sequences among certain related proteins. Among all the highest related proteins, the 2YH2D showed the closest to the 2QRU active site. The 2QRU sequence has some similarity in short bursts, but nothing long-term. Two recurring sequences were HGGG at around 90 and SAGG around 175 that were in coiled regions of the protein.

InterPRO Investigation with InterPro showed the likely family of this enzyme was an alpha/beta hydrolase. Specifically, 2QRU was classified as a GDXG lipolytic enzyme. This family is generally associated with the hydrolysis of short fatty esters up to 8 carbons in length. Enzymes within this family are known to be involved in plant wall degradation and tryptophan synthesis.

SwissDock

SwissDock was used to investigate the active site binding of different substrates. The analysis of 2QRU on this site was performed with orientation parameters of 8x20x10 in a 25x25x25 Å box. The best overall interaction tested was with 4-Methylumbelliferyl 2-acetamido-2-deoxy-beta-D-glucopyranoside that showed an affinity -6.883 kcal/mol. Other significant binding affinities include 4-Nitrophenyl acetate at -5.093 kcal/mol and 4-Nitrophenyl acetate at -5.193 kcal/mol. The greatest binding affinities found were with carbohydrate-based substrates.

Proposed Functionality

Based on the sequence and structural analysis via computational modeling, it is known that the primary function of 2QRU is an alpha/beta hydrolase. Using the Swiss dock, we know the substrates with the highest bonding affinity were sugar-like molecules. This produces bond affinities of -6 or lower. Knowing this, it is hypothesized that 2QRU would be used in biological systems that need to break down sugars for energy, like fermentation or cellular respiration. Where exactly this would occur or on which sugar is unknown at this time, but experimental results may aid in finding what substrate works the best and in what environment.

Relevance