Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 46 min ago
Peer-reviewedCC BYComptes rendus. Chimie (Print)

Structural factors governing alkane substrate specificity in the alkane monooxygenase (AlkB) family

  1. 1Department of Chemistry, University of Vermont, Burlington, VT, 05405, USA
  2. 2Department of Chemistry, Barnard College, New York, NY 10027 USA

Abstract

Alkane monooxygenases (AlkB) are a family of integral membrane non-heme diiron enzymes that catalyze the initial step in the oxidation of alkanes by numerous microorganisms. They play a key role in the global carbon cycle, but the scope of this role is unknown. The AlkB family is thought to catalyze the oxidation of alkanes from pentane to C 44 H 90 ; implicit in this assertion is the idea that an individual AlkB only catalyzes the oxidization of a relatively narrow range of substrates. The structural basis of this discrimination is unclear. In this paper, eight AlkBs for which we possess reliable biochemical information about their substrate ranges were selected and AlphaFold3 was used to predict their three-dimensional structure. Several different cavity-determining programs were used to identify and measure the substrate channel in these predicted structures. Correlations between substrate selectivity and structure have been made. Combining information available from different sources enables new hypotheses about the factors that control substrate selectivity in this important family of metalloenzymes to be made.

Related

  1. S-glycosyltransferase UGT74B1 can glycosylate both S- and O-acceptors: mechanistic insights through substrate specificity
    P. Lafite, S. Marroun, G. Coadou +7
    Molecular CatalysisPeer-reviewedLicence not statedFull text18 citedOrganic chemistryHAL
  2. Exploring the substrate specificity and catalytic mechanism in a PAPS independent ASST from Salmonella typhimurium
    N. M. Nimbona, H. Obeid, D. Balci +7
    bioRxivPreprintCC BY-NC-NDFull textMaterials & polymersbioRxiv
  3. Structural mechanism defining product specificity in glycoside hydrolase family 66 cycloisomaltotetraose glucanotransferase
    R. Yasukochi, T. Kashima, T. Mori +4
    bioRxivPreprintAll rights reservedFull textOrganic chemistrybioRxiv
  4. Redox Properties of the Copper Centers in Particulate Methane Monooxygenase
    Divyansh Prakash, Joseph D. Groom, Frank J. Tucci +3
    Journal of the American Chemical SocietyPeer-reviewedLicence not statedFull textInorganic & organometallic chemistryPMC
  5. Reactive molecular dynamics simulations of atenolol first steps degradation by 9CL6 ammonia monooxygenase
    Pascal Brault, Matthieu Wolf, Yana Gouzi +2
    HALPreprintCC BY 4.0Full textBioinformatics & computational biologyPhysical chemistryHALarXiv
BibTeX
@article{stanczak2026structural,
  title = {{Structural factors governing alkane substrate specificity in the alkane monooxygenase (AlkB) family}},
  author = {Agnieszka Stańczak and Stella Bailey and Cameron Heanue and Noga Rafalin and Eliana Weinsaft and Clorice Reinhardt and Rachel Narehood Austin},
  journal = {Comptes rendus. Chimie (Print)},
  year = {2026},
  month = nov,
  doi = {10.5802/crchim.455},
  url = {https://doi.org/10.5802/crchim.455},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Structural factors governing alkane substrate specificity in the alkane monooxygenase (AlkB) family
AU  - Agnieszka Stańczak
AU  - Stella Bailey
AU  - Cameron Heanue
AU  - Noga Rafalin
AU  - Eliana Weinsaft
AU  - Clorice Reinhardt
AU  - Rachel Narehood Austin
PY  - 2026
DA  - 2026/11/02
JO  - Comptes rendus. Chimie (Print)
DO  - 10.5802/crchim.455
UR  - https://doi.org/10.5802/crchim.455
AB  - Alkane monooxygenases (AlkB) are a family of integral membrane non-heme diiron enzymes that catalyze the initial step in the oxidation of alkanes by numerous microorganisms. They play a key role in the global carbon cycle, but the scope of this role is unknown. The AlkB family is thought to catalyze the oxidation of alkanes from pentane to C 44 H 90 ; implicit in this assertion is the idea that an individual AlkB only catalyzes the oxidization of a relatively narrow range of substrates. The structural basis of this discrimination is unclear. In this paper, eight AlkBs for which we possess reliable biochemical information about their substrate ranges were selected and AlphaFold3 was used to predict their three-dimensional structure. Several different cavity-determining programs were used to identify and measure the substrate channel in these predicted structures. Correlations between substrate selectivity and structure have been made. Combining information available from different sources enables new hypotheses about the factors that control substrate selectivity in this important family of metalloenzymes to be made.
SN  - 1631-0748
SN  - 1878-1543
ER  -