This is the same Lowe-Thorneley kinetic scheme as the 3D docking simulator, but drawn the way biochemists actually diagram it: as a circular reaction-coordinate wheel, not a protein dock/undock animation. Each catalytic site is a dot that orbits the wheel through eight electron-accumulation stations E0 → E7, closing the loop through a resolving arc at E8:
N2 + 8 H+ + 8 e- + 16 MgATP + 16 H2O
-> 2 NH3 + H2 + 16 MgADP + 16 Pi
fluxTerm = flux / (flux + K), K = 0.6
P(N2 fixed | E8 reached) = fluxTerm × [N2 atm]
- Reaction wheel (left) — every dot's angular position is its live progress through the 8-electron cycle; dwell time per station is cycleTime/8 with cycleTime = 1.2/flux, identical to the population field in the 3D version. Color still ramps blue (E0) → gold (E7); gray dots have been permanently knocked out by O₂.
- E-state histogram (top right) — a live bar count of how many sites currently sit in each of the 8 states, the same distribution the wheel encodes spatially, read as a quantitative population snapshot.
- Production-rate strip chart (bottom right) — a scrolling trace of NH₃ and H₂ output rate (molecules/s across the population), sampled every 0.25s from the same discrete turnover events driving the wheel — a real derivative of the cumulative totals, not a decorative animation.
- Electron flux / N₂ pressure sliders and O₂ exposure — identical meaning and identical formulas to the 3D model: higher flux both speeds the cycle and biases the E8 branch toward productive N₂ reduction; low N₂ or low flux defaults sites to unproductive H₂ evolution (4 H₂ per turnover instead of 1 NH₂+1 H₂); O₂ exposure inactivates active sites at random with the same 6%·dt per-frame hazard, irreversibly.
Real-world relevance: nitrogenase is the only enzyme family that breaks the N≡N triple bond at ambient temperature and pressure, and its obligate 1 H₂-per-N₂ waste and extreme O₂ sensitivity are exactly the two properties this reaction wheel is built to make legible at a glance.