Crystal structure of p-hydroxybenzoate hydroxylase

RK Wierenga, RJ De Jong, KH Kalk, WGJ Hol… - Journal of molecular …, 1979 - Elsevier
The structure of the enzyme p-hydroxybenzoate hydroxylase (EC 1.14.13.2) in a complex with
its substrate has been determined at a resolution of 2.5 Å. The molecular weight is 43,000 …

Mutation update on ACAT1 variants associated with mitochondrial acetoacetyl‐CoA thiolase (T2) deficiency

…, RK Harijan, S Yamaguchi, RK Wierenga… - Human …, 2019 - Wiley Online Library
Mitochondrial acetoacetyl‐CoA thiolase (T2, encoded by the ACAT1 gene) deficiency is an
inherited disorder of ketone body and isoleucine metabolism. It typically manifests with …

[HTML][HTML] A community proposal to integrate structural bioinformatics activities in ELIXIR (3D-Bioinfo Community)

…, JM Thornton, P Tuffery, G Tusnady, R Wierenga… - …, 2020 - ncbi.nlm.nih.gov
Structural bioinformatics provides the scientific methods and tools to analyse, archive,
validate, and present the biomolecular structure data generated by the structural biology …

[HTML][HTML] Neutron structures of Leishmania mexicana triosephosphate isomerase in complex with reaction-intermediate mimics shed light on the proton-shuttling steps

…, O Caldararu, MP Blakeley, N Coquelle, RK Wierenga… - IUCrJ, 2021 - scripts.iucr.org
Triosephosphate isomerase (TIM) is a key enzyme in glycolysis that catalyses the
interconversion of glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. This simple …

Structures of lactaldehyde reductase, FucO, link enzyme activity to hydrogen bond networks and conformational dynamics

…, S Sridhar, TR Kiema, RK Wierenga… - The FEBS …, 2023 - Wiley Online Library
A group‐III iron containing 1,2‐propanediol oxidoreductase, FucO, (also known as
lactaldehyde reductase) from Escherichia coli was examined regarding its structure–dynamics–…

Development of MLPA for human ACAT1 gene and identification of a heterozygous Alu-mediated deletion of exons 3 and 4 in a patient with mitochondrial acetoacetyl …

…, K Murase, T Hori, RK Harijan, RK Wierenga… - Molecular genetics and …, 2013 - Elsevier
Mitochondrial acetoacetyl-CoA thiolase deficiency is an autosomal recessive disorder,
characterized by intermittent ketoacidosis. We developed a multiplex ligation-dependent probe …

Crystallographic binding studies of rat peroxisomal multifunctional enzyme type 1 with 3-ketodecanoyl-CoA: capturing active and inactive states of its hydratase and …

…, U Bergmann, TR Kiema, RK Wierenga - … Section D: Structural …, 2020 - scripts.iucr.org
The peroxisomal multifunctional enzyme type 1 (MFE1) catalyzes two successive reactions
in the β-oxidation cycle: the 2E-enoyl-CoA hydratase (ECH) and NAD+-dependent 3S-…

[HTML][HTML] Crystal Structure of a Monomeric Thiolase-Like Protein Type 1 (TLP1) from Mycobacterium smegmatis

N Janardan, RK Harijan, RK Wierenga, MRN Murthy - 2012 - journals.plos.org
An analysis of the Mycobacterium smegmatis genome suggests that it codes for several
thiolases and thiolase-like proteins. Thiolases are an important family of enzymes that are …

Structural characterization of a mitochondrial 3-ketoacyl-CoA (T1)-like thiolase from Mycobacterium smegmatis

…, RK Harijan, TR Kiema, RK Wierenga… - … Section D: Biological …, 2015 - scripts.iucr.org
Thiolases catalyze the degradation and synthesis of 3-ketoacyl-CoA molecules. Here, the
crystal structures of a T1-like thiolase (MSM-13 thiolase) from Mycobacterium smegmatis in …

A Master of Science course on macromolecular X-ray crystallography resembling a realistic research project

…, E Daniel, E Obaji, R Venkatesan, RK Wierenga… - 2023 - osf.io
Macromolecular X-ray crystallography is a robust method to understand protein functions at
the molecular level, deciphering their various roles in biochemical processes. This makes …