List of works - Andrew J Sutherland-Smith

An open or closed case for the conformation of calponin homology domains on F-actin?

scientific article

Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.

scientific article published on January 2013

Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes

scientific article published on 13 July 2016

Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.

scientific article published on 13 July 2011

Crystal Structure of the Filamin N-Terminal Region Reveals a Hinge between the Actin Binding and First Repeat Domains ⬇️

scientific article published on October 2, 2012

Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II (α 2 ϵ 2 ) haemoglobin at 2.9 å resolution 1 1Edited by K. Nagai

Cytotoxic aggregation and amyloid formation by the myostatin precursor protein

scientific article

Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions

scientific article published in November 2015

Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.

scientific article published on 18 February 2015

Expression and role in glycolysis of human ADP-dependent glucokinase

scientific article published on 5 January 2012

Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?

scientific article

In Silico Resurrection of the Major Vault Protein Suggests It Is Ancestral in Modern Eukaryotes ⬇️

scientific article published on January 1, 2013

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

scientific article

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

scientific journal article

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

scientific journal article

Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders

scientific article

Structural determination of archaeal UDP-N-acetylglucosamine 4-epimerase from Methanobrevibacter ruminantium M1 in complex with the bacterial cell wall intermediate UDP-N-acetylmuramic acid

scientific article published on 05 October 2018

Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase

scientific article

The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.

scientific article

The Crystal Structures of Dystrophin and Utrophin Spectrin Repeats: Implications for Domain Boundaries ⬇️

scientific article published on July 20, 2012

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

scientific article published in October 2006

The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.

scientific article published on 10 November 2015

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy

scientific article

X-ray crystallographic analyses of the structures of two heme proteins

1998 doctoral thesis by Andrew John Sutherland-Smith at Massey University

List of works by Andrew J Sutherland-Smith

An open or closed case for the conformation of calponin homology domains on F-actin?

Beyond BLASTing: tertiary and quaternary structure analysis helps identify major vault proteins.

Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes

Characterization of a dual-function domain that mediates membrane insertion and excision of Ff filamentous bacteriophage.

Crystal Structure of the Filamin N-Terminal Region Reveals a Hinge between the Actin Binding and First Repeat Domains ⬇️

Crystal structure of a human embryonic haemoglobin: the carbonmonoxy form of gower II (α 2 ϵ 2 ) haemoglobin at 2.9 å resolution 1 1Edited by K. Nagai

Cytotoxic aggregation and amyloid formation by the myostatin precursor protein

Developing a video tracking method to study interactions between close pairs of optically trapped particles in three dimensions

Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA.

Expression and role in glycolysis of human ADP-dependent glucokinase

Filamin structure, function and mechanics: are altered filamin-mediated force responses associated with human disease?

In Silico Resurrection of the Major Vault Protein Suggests It Is Ancestral in Modern Eukaryotes ⬇️

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders

Structural determination of archaeal UDP-N-acetylglucosamine 4-epimerase from Methanobrevibacter ruminantium M1 in complex with the bacterial cell wall intermediate UDP-N-acetylmuramic acid

Structure and Evolution of the Archaeal Lipid Synthesis Enzyme sn-Glycerol-1-phosphate Dehydrogenase

The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability.

The Crystal Structures of Dystrophin and Utrophin Spectrin Repeats: Implications for Domain Boundaries ⬇️

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

The Structural and Functional Characterization of Mammalian ADP-dependent Glucokinase.

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy

X-ray crystallographic analyses of the structures of two heme proteins