Formate Dehydrogenase: The Role of the AMP Cofactor Fragment in Stabilization of the Transition State for Enzyme-Catalyzed Hydride Transfer

We report experiments that probe the role of the NAD+-driven protein conformational change in the formate dehydrogenase (FDH)-catalyzed hydride transfer. The binding interactions between FDH and the ADP fragment of NAD+ provide an 11.9 kcal/mol stabilization of the transition state for FDH-catalyzed hydride transfer from formate to NAD+ and a 7.9 kcal/mol stabilization of the complex between FDH and the putative transition state analogue azide anion. The binding interactions between FDH and the AMP cofactor piece likewise provide a 5.6 kcal/mol stabilization of the transition state for FDH-catalyzed hydride transfer from formate to nicotinamide riboside (NR) and a 1.4 kcal/mol stabilization of the complex between FDH and the azide anion. The results provide support for the conclusion that binding of NAD+ or the AMP cofactor fragment to FDH drives a change in protein conformation from a flexible open conformation to the tight closed conformation that locks the active site side chains into positions that provide optimal stabilization of both the hydride transfer transition state and the azide anion mimic for this transition state.

Authors

Institutions

Publication Details

Journal
ACS Omega
Published
2026-04-26
DOI
https://doi.org/10.1021/acsomega.6c02728
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Formate Dehydrogenase: The Role of the AMP Cofactor Fragment in Stabilization of the Transition State for Enzyme-Catalyzed Hydride Transfer

Astrid P. Koudelka, John P. Richard, Rania Hegazy
ACS Omega
Enzyme Catalysis and Immobilization
article

Formate Dehydrogenase: The Role of the AMP Cofactor Fragment in Stabilization of the Transition State for Enzyme-Catalyzed Hydride Transfer

Astrid P. Koudelka, John P. Richard, Rania Hegazy
article en

Abstract

We report experiments that probe the role of the NAD+-driven protein conformational change in the formate dehydrogenase (FDH)-catalyzed hydride transfer. The binding interactions between FDH and the ADP fragment of NAD+ provide an 11.9 kcal/mol stabilization of the transition state for FDH-catalyzed hydride transfer from formate to NAD+ and a 7.9 kcal/mol stabilization of the complex between FDH and the putative transition state analogue azide anion. The binding interactions between FDH and the AMP cofactor piece likewise provide a 5.6 kcal/mol stabilization of the transition state for FDH-catalyzed hydride transfer from formate to nicotinamide riboside (NR) and a 1.4 kcal/mol stabilization of the complex between FDH and the azide anion. The results provide support for the conclusion that binding of NAD+ or the AMP cofactor fragment to FDH drives a change in protein conformation from a flexible open conformation to the tight closed conformation that locks the active site side chains into positions that provide optimal stabilization of both the hydride transfer transition state and the azide anion mimic for this transition state.

ACS Omega
University at Buffalo, State University of New York (US)
Clean water and sanitation
Openalex Percentile: Top 7%
Enzyme Catalysis and Immobilization
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.