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. Author manuscript; available in PMC: 2010 Dec 6.
Published in final edited form as: Cell Mol Bioeng. 2008 Mar 1;1(1):84–92. doi: 10.1007/s12195-008-0008-8

Table 1.

Bacterial chemotaxis reactions

Reaction Rate (forward) Rate (reverse) Description
A2 <-> A2* Immediate equilibration (13.2% active) CheA activation
A2p <-> A2*p Immediate equilibration (13.2% active) CheAp activation
A2* -> A2*p 34 s−1 - CheA autophosphorylation7,21
Y + A2p -> Yp + A2 1 × 108 M−1s−1 - Phosphotransfer24
Y + A2*p -> Yp + A2* 1 × 108 M−1s−1 - Phosphotransfer24
Yp + Z2 <=> Z2Yp 2 × 107 M−1s−1 0.5 s−1 Complex formation
Yp + Z2Yp <=> Z2Yp2 1 × 107 M−1s−1 0.5 s−1 Complex formation
Z2Yp -> Y + Z2 5 s−1 - CheYp hydrolysis
Z2Yp2 -> Y + Z2Yp 5 s−1 - CheYp hydrolysis

Reactions labeled with `immediate equilibration' are the system's input: Every 10 ms throughout the simulation, the ratio of the two indicated molecular species was adjusted stochastically. The following abbreviations are used: Y, CheY; Yp, CheYp, phosphorylated CheY; A2, CheA dimer, inactive; A2*, CheA dimer, active; A2p, phospho-CheA dimer, inactive; A2*p, phospho-CheA dimer, active; Z2 CheZ dimer; Z2Yp, complex of CheZ and CheYp; Z2Yp2, complex of CheZ and two CheYp.