Kenji Mizuguchi

Prof. Kenji Mizuguchi

National Institutes of Biomedical Innovation, Health and Nutrition
orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 August 2022 in Nature Communications
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KHKoji Hosomi
Koji Hosomi
MSMayu Saito
Mayu Saito
JPJonguk Park
Jonguk Park
HMHaruka Murakami
Haruka Murakami
NSNaoko Shibata
Naoko Shibata
JKJun Kunisawa
Jun Kunisawa
The gut microbiome is an important determinant in various diseases. Here we perform a cross-sectional study of Japanese adults and identify the Blautia genus, especially B. wexlerae, as a commensal bacterium that is inversely correlated with obesity and type 2 diabetes mellitus. Oral administration of B. wexlerae to mice induce metabolic changes and anti-inflammatory effects that decrease both high-fat diet–induced obesity and diabetes. The beneficial effects of B. wexlerae are correlated with unique amino-acid metabolism to produce S-adenosylmethionine, acetylcholine, and l-ornithine and carbohydrate metabolism resulting in the accumulation of amylopectin and production of succinate, lactate, and acetate, with simultaneous modification of the gut bacterial composition. These findings reveal unique regulatory pathways of host and microbial metabolism that may provide novel strategies in preventive and therapeutic approaches for metabolic disorders.

1 November 1998 in Protein Science
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Journal Article
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KMKenji Mizuguchi
Kenji Mizuguchi
CDCharlotte M. Deane
Charlotte M. Deane
TBTom L. Blundell
Tom L. Blundell
JOJohn Overington
John Overington
We describe a database of protein structure alignments for homologous families. The database HOMSTRAD presently contains 130 protein families and 590 aligned structures, which have been selected on the basis of quality of the X‐ray analysis and accuracy of the structure. For each family, the database provides a structure‐based alignment derived using COMPARER and annotated with JOY in a special format that represents the local structural environment of each amino acid residue. HOMSTRAD also provides a set of superposed atomic coordinates obtained using MNYFIT, which can be viewed with a graphical user interface or used for comparative modeling studies. The database is freely available on the World Wide Web at: http://www‐cryst. bioc. cam. ac. uk/homstrad/, with search facilities and links to other databases.

17 October 2006 in Molecular Psychiatry
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LCL M Camargo
L M Camargo
VCV Collura
V Collura
JRJ-C Rain
J-C Rain
KMKenji Mizuguchi
Kenji Mizuguchi
HHHenning Hermjakob
Henning Hermjakob
NBN J Brandon
N J Brandon
Disrupted in Schizophrenia 1 (DISC1) is a schizophrenia risk gene associated with cognitive deficits in both schizophrenics and the normal ageing population. In this study, we have generated a network of protein–protein interactions (PPIs) around DISC1. This has been achieved by utilising iterative yeast-two hybrid (Y2H) screens, combined with detailed pathway and functional analysis. This so-called ‘DISC1 interactome’ contains many novel PPIs and provides a molecular framework to explore the function of DISC1. The network implicates DISC1 in processes of cytoskeletal stability and organisation, intracellular transport and cell-cycle/division. In particular, DISC1 looks to have a PPI profile consistent with that of an essential synaptic protein, which fits well with the underlying molecular pathology observed at the synaptic level and the cognitive deficits seen behaviourally in schizophrenics. Utilising a similar approach with dysbindin (DTNBP1), a second schizophrenia risk gene, we show that dysbindin and DISC1 share common PPIs suggesting they may affect common biological processes and that the function of schizophrenia risk genes may converge.

1 January 1998 in Bioinformatics
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KMKenji Mizuguchi
Kenji Mizuguchi
CDC M Deane
C M Deane
TBT L Blundell
T L Blundell
MJM S Johnson
M S Johnson
JOJohn Overington
John Overington
MOTIVATION: JOY is a program to annotate protein sequence alignments with three-dimensional (3D) structural features. It was developed to display 3D structural information in a sequence alignment and to help understand the conservation of amino acids in their specific local environments. RESULTS:: The JOY representation now constitutes an essential part of the two databases of protein structure alignments: HOMSTRAD (http://www-cryst.bioc.cam.ac.uk/homstrad ) and CAMPASS (http://www-cryst.bioc.cam.ac. uk/campass). It has also been successfully used for identifying distant evolutionary relationships. AVAILABILITY: The program can be obtained via anonymous ftp from torsa.bioc.cam.ac.uk from the directory /pub/joy/. The address for the JOY server is http://www-cryst.bioc.cam.ac.uk/cgi-bin/joy.cgi. CONTACT: kenji@cryst.bioc.cam.ac.uk

5 July 2007 in Genome Biology
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RLRachel Lyne
Rachel Lyne
RSRichard Smith
Richard Smith
KRKim Rutherford
Kim Rutherford
MWMatthew Wakeling
Matthew Wakeling
AVAndrew Varley
Andrew Varley
GMGos Micklem
Gos Micklem
FlyMine is a data warehouse that addresses one of the important challenges of modern biology: how to integrate and make use of the diversity and volume of current biological data. Its main focus is genomic and proteomics data for Drosophila and other insects. It provides web access to integrated data at a number of different levels, from simple browsing to construction of complex queries, which can be executed on either single items or lists.