Sandbox GGC3

Firefly Luciferase

tttaaarrgggetttt to the right plaaccceee and finishh :(

spinqualitylabelsall models Luciferin-4-monooxygenase. The wild-type luciferase in the adenylate-forming conformation with DLSA (PDB 4G36) and the cross-linked luciferase in the second catalytic conformation with DLSA (PDB 4G37) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Firefly luciferase, of the common eastern firefly, is responsible for the ability of the firefly to exhibit bioluminescence. The enzyme luciferin-4-monoxygenase, which catalyzes a multistep oxidative decarboxylation of the luciferyl-AMP intermediate (LH2-AMP) to produce bioluminescence, is a part of the ANL superfamily named so for the acyl-CoA syntheses, the adenylation domains of the modular non-ribosomal peptide synthetases (NRPs), and luciferase. Function The Common Eastern Firefly in a hand emitting a yellow hue, showing bioluminescence. The ANL enzymes catalyze two-step reactions: the first an adenylating step in which an acyl-AMP intermediate is produced; the second step in which the adenylate then serves as a substrate for the multistep oxidative decarboxylation of the luciferyl-AMP (LH2-AMP) intermediate, resulting in bioluminescence. ANL enzymes follow a domain alternation strategy for the first adenylation reaction, in which the reaction is catalyzed by one conformation and following the formation of the adenylate intermediate and release of pyrophosphate (PPi), the C-terminal domain undergoes a rotational transformation that is necessary for the second partial reaction. The active site of ANL enzymes resides between a 400-500 residue N-terminal domain and a smaller C-terminal domain of ~110-130 amino acids. Ten conserved regions of these proteins have been termed the A1-A10 motifs which play critical roles in either or both partial reactions. Two lysine residues are required for each partial reaction suggestive that luciferase similarly adopts a rotational transformation for complete catalysis. A mutation of Lys529, the A10 lysine, impairs only the initial adenylation reaction whereas mutation of Lys443 in the A8 region disrupts the oxidative reaction. Biochemical Mechanism of LH2-AMP Oxidation The generally accepted mechanism of firefly bioluminescence. The first reaction involves the production of an luciferyl-adenylate intermediate (1). The second reaction involves oxidative decarboxylation that emits CO2 and results in bioluminescent properties(2). Nothing but pain. Structural highlights The conserved catalytic lysine for the adenylation reaction, Lys529, interacts with the carbonyl oxygen of the adenylate, the O5 atom that bridges the ribose and sulfamate moiety, and the main chain carbonyl of Gly316. The second conformation observations show that the side chain amine of Lys443 adopts a nearly identical position as Lys529, and Gln448 of the C-terminal domain rotates into the binding pocket where it interacts with a sulfamate oxygen. Altogether (with the inclusion of an ionic interaction between Glu479 and Arg437), these interactions are responsible for the stabilization of the new C-terminal conformation. (going through changes but math is cool :/)The A8 motif harbors the hinge residue at Lys439 and the antiparallel two stranded β-sheet is directed into the active site of the enzyme. The φ/ψ angles of Lys439 change from −73°/−12° in the structure of wild-type luciferase in the adenylate-forming conformation to −69°/158° in the cross- linked structure.this illustrates that a large component of the conformational change occurs with a rotation of the ψ angle of the hinge residue. Additional torsion angle changes are seen in φ angles for Arg437 and Leu441, although the magnitude of the change is not as large as at the hinge residue Lys439. Relevance The Common Eastern Firefly expressing bioluminescence seen giving off a yellow-green hue. Firefly go glow, super duper cool B~) Firefly luciferase has successfully been shown to act as modulatory bioluminescent indicator in the detection and quantification of protein kinase A activation in living cells This is a sample scene created with SAT to color by Group, and another to make a transparent representation of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.