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Which part of the ATP molecule breaks free of the rest when an ATP molecule releases energy Part a Part B Part C Part D?

Adenosine triphosphate (ATP) is an important molecule that provides energy for many cellular processes. ATP consists of an adenosine molecule bonded to three phosphate groups (a ribose sugar, adenine base, and three phosphate groups). When ATP is broken down, usually to adenosine diphosphate (ADP) and inorganic phosphate, energy is released which can be used to power biochemical reactions. The specific part of the ATP molecule that breaks free during this process is one of the phosphate groups.

Overview of ATP Structure

The structure of ATP consists of three main components:

  • Adenine – this is one of the nucleobases used in forming nucleotides of nucleic acids.
  • Ribose – the sugar component, a 5-carbon sugar.
  • 3 Phosphate groups – these are bonded together in series, with two phosphoanhydride bonds holding them together. The phosphate groups are labeled alpha, beta, and gamma.

The adenine and ribose combine to form the adenosine nucleoside. The three phosphate groups then bond to the 5′ carbon of the ribose sugar. The bonds between the phosphate groups contain high-energy phosphoanhydride bonds. It is these bonds that are broken when ATP releases energy.

Visual Representation of ATP Structure

Component Structure
3 Phosphates

As seen in the visual representations, ATP contains the purine base adenine bonded to the 5-carbon sugar ribose. Additionally, there are 3 phosphate groups bonded in series through phosphoanhydride bonds. It is this bond between the second and third phosphate groups that is broken when ATP releases energy.

ATP Energy Release

ATP is able to act as an energy currency for cells because the bonds between its phosphate groups contain potential energy. This potential energy can then be converted to kinetic energy to power endergonic reactions when the bonds are broken through hydrolysis.

The bonds between phosphates are known as phosphoanhydride bonds, which are high-energy bonds particularly susceptible to hydrolytic cleavage. Hydrolysis using water can break these anhydride bonds and release energy.

Specifically, it is the bond between the second and third phosphate groups (the beta-gamma phosphoanhydride bond) that is broken when ATP releases energy. This liberates the third phosphate as inorganic phosphate while leaving adenosine diphosphate (ADP) behind.

The reaction can be summarized as:

ATP + H2O → ADP + Pi + Energy (30.5 kJ/mol)

Visualizing ATP Hydrolysis

Molecule Structure
Inorganic Phosphate

As the visuals demonstrate, ATP hydrolysis breaks the bond between the beta and gamma phosphates, releasing a phosphate group and leaving behind ADP. This inorganic phosphate group is what breaks free when ATP releases its energy.

Cellular Usage of ATP

Within cells, ATP is used to provide energy for important processes including:

  • Biosynthesis – ATP is used to power metabolic pathways that build complex molecules like proteins, lipids, and nucleic acids.
  • Motility – Motor proteins use ATP hydrolysis to generate force for muscle contraction and cargo transport.
  • Active transport – ATP powers membrane pumps that establish concentration gradients of ions and molecules.
  • Cell signaling – ATP and its derivatives serve as extracellular signaling molecules.
  • Gene expression – ATP is used by proteins involved in transcription and translation.

By coupling an endergonic reaction with the exergonic reaction of ATP hydrolysis, cells can drive unfavorable reactions forward. Some examples include:

  • Phosphorylation – Adding phosphate groups to proteins often requires ATP.
  • Molecular motors – Myosin uses ATP to walk along actin filaments.
  • Pumps – ATP powers pumps like the sodium-potassium pump to maintain membrane potential.
  • Polymerization – ATP is used to fuel the synthesis of polymers like glycogen and proteins.

In this way, the energy released from ATP hydrolysis allows cells to perform a diverse array of functions.

Factors Affecting ATP Hydrolysis

While ATP readily undergoes hydrolysis to power cellular reactions, there are factors that influence the rate and efficiency of ATP hydrolysis:

Enzyme Catalysis

ATP hydrolysis is dramatically accelerated by enzymes called ATPases. These enzymes catalyze the cleavage of the phosphoanhydride bond. Different classes of ATPases exist for specific functions; for example, the F1F0-ATP synthase generates ATP, while ABC transporters use ATP to transport molecules across membranes.

Mg2+ and Ca2+ Ions

Divalent cations like Mg2+ and Ca2+ stabilize the negative charge on ATP phosphates. This makes the phosphoanhydride bond more susceptible to nucleophilic attack and hydrolysis. Many ATP-dependent enzymes require these ions as enzyme cofactors.

pH Effects

ATP hydrolysis rate is optimal around a neutral pH of 7. Extremely high or low pH can lead to inhibition of ATPases by altering ionization states. ATP itself becomes progressively protonated at lower pH, protecting the phosphates from nucleophilic attack.

Substrate Binding

When an enzyme binds its substrate, it orientates the substrate properly for catalysis. This substrate binding can increase the rate of ATP hydrolysis by optimally positioning water for nucleophilic attack on the phosphoanhydride bond.

Allosteric Regulation

The activity of some ATPases is regulated by allosteric binding of small molecules at sites distal from the active site. This induces conformational changes that alter ATPase activity in response to cellular conditions.

Alternate Forms of Cellular Energy Currency

While ATP is the primary energy currency used by cells, related nucleotide triphosphates also play roles:


Like ATP, guanosine triphosphate (GTP) contains high-energy phosphoanhydride bonds. It is used similarly in processes like protein synthesis and cell signaling. GTP is generated from ATP by nucleoside diphosphate kinase.


Cytidine triphosphate (CTP) provides energy for biosynthesis of phospholipids in cell membranes and aids in lipid metabolism. It transfers high-energy phosphate to form deoxyribonucleotides.


Uridine triphosphate (UTP) is used for glycogen metabolism and glycosylation of proteins. It is also the precursor molecule for RNA synthesis, providing energy for phosphodiester bond formation.

So while ATP is the major energy currency used for biosynthesis, transport, and motility, other NTPs have specialized roles that take advantage of their high-energy phosphates.


In summary, ATP provides usable energy for cells through the hydrolysis of its phosphoanhydride bonds. Specifically, it is the bond between the beta and gamma phosphate groups that is broken when ATP is hydrolyzed to ADP and inorganic phosphate. This liberates the terminal phosphate as energy to drive cellular processes like metabolism, transport, and movement. ATP hydrolysis is accelerated through enzyme catalysis, metal ions, and substrate binding interactions. While ATP is the central energy currency, related NTPs also provide specialized energetic roles.