Wyatt Yue

Principal Investigator / Associate Professor

University of Oxford

Twitter: @Wyatt_Yue

+44 (0)1865 617757

Wyatt Yue is a structural biologist with an MA (Biochemistry) at University of Oxford, and a PhD (Crystallography) at Birkbeck College, University of London. He pursued a postdoc fellowship in Institute of Cancer Research with Prof Laurence Pearl FRS, followed by a stint at the fragment-based drug discovery company Sareum Ltd. In 2008 he joined the Structural Genomics Consortium (SGC), University of Oxford as a Senior Scientist in high throughput protein structure determination. In 2012 he established his own research team ‘Metabolism & Organelle Biogenesis (MOB)’ at the SGC, using structural, biochemical, and chemical biology approaches to study diverse metabolic protein families in the human genome. He specialises in the use of protein structures and biochemistry to understand the molecular basis of human inherited diseases. He collaborates with front line clinicians and industry for the development of small molecule therapy for rare diseases.

Wyatt is featured in:

Research Areas

The Metabolism & Organelle Biogenesis (MOB) group combines structural, biochemical, and chemical biology approaches to study the functions and structure-activity relationships of diverse metabolic protein families in the human genome, with emphasis on understanding the molecular basis of inherited metabolic disorders and potentials of small molecule therapeutics. Research activities in the group include the heterologous expression, chromatography purification, biophysical characterization and crystal structure determination of human metabolic enzymes of medical interest. Current areas of focus include: multiprotein complex machines, glycogen synthesis, vitamin B12 metabolism and Leloir pathway of galactose metabolism.

Our mission statement:
  • We explore how genetic defects lead to disease at the molecular level, by determining the structural and biochemical properties of enzymes and protein complexes linked to genetic errors.
  • We work closely with clinicians, pharmaceutical partners and patient groups to decipher the underlying genetic, biochemical and cellular mechanisms of these diseases.
  • Our long-term goal is to design novel small molecule therapeutic approaches for metabolic diseases with unmet need.

See our structure gallery

Group Members

  • Jolanta Kopec
  • Nicholas Fox
  • Elzbieta Rembeza
  • Hannah Brazier
  • Sabrina MacKinnon
  • Henry Bailey
  • Jack Kelly

Publications

Crystal structure of Porphyromonas gingivalis peptidylarginine deiminase: implications for autoimmunity in rheumatoid arthritis.
Montgomery, AB; Kopec, J; Shrestha, L; Thezenas, ML; Burgess-Brown, NA; Fischer, R; Yue, WW; Venables, PJ;
Annals of the Rheumatic Diseases. 2016 75:1255-1261. doi:
PMID: 26209657

Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design.
Froese, DS; Michaeli, A; McCorvie, TJ; Krojer, T; Sasi, M; Melaev, E; Goldblum, A; Zatsepin, M; Lossos, A; Álvarez, R; Escribá, PV; Minassian, BA; von Delft, F; Kakhlon, O; Yue, WW;
Human Molecular Genetics. 2015 24:5667-5676. doi:
PMID: 26199317

Inter-domain communication of human cystathionine β-synthase: structural basis of S-adenosyl-L-methionine activation.
McCorvie, TJ; Kopec, J; Hyung, SJ; Fitzpatrick, F; Feng, X; Termine, D; Strain-Damerell, C; Vollmar, M; Fleming, J; Janz, JM; Bulawa, C; Yue, WW;
Journal of Biological Chemistry. 2014 289:36018-36030. doi:
PMID: 25336647

Crystal structures of malonyl-coenzyme A decarboxylase provide insights into its catalytic mechanism and disease-causing mutations.
Froese, DS; Forouhar, F; Tran, TH; Vollmar, M; Kim, YS; Lew, S; Neely, H; Seetharaman, J; Shen, Y; Xiao, R; Acton, TB; Everett, JK; Cannone, G; Puranik, S; Savitsky, P; Krojer, T; Pilka, ES; Kiyani, W; Lee, WH; Marsden, BD; von Delft, F; Allerston, CK; Spagnolo, L; Gileadi, O; Montelione, GT; Oppermann, U; Yue, WW; Tong, L;
Structure. 2013 21:1182-1192. doi: 10.1016/j.str.2013.05.001
PMID: 23791943

Insight into S-adenosylmethionine biosynthesis from the crystal structures of the human methionine adenosyltransferase catalytic and regulatory subunits.
Shafqat, N; Muniz, JR; Pilka, ES; Papagrigoriou, E; von Delft, F; Oppermann, U; Yue, WW;
Biochemical Journal. 2013 452:27-36. doi: 10.1042/BJ20121580
PMID: 23425511

Structure of MMACHC reveals an arginine-rich pocket and a domain-swapped dimer for its B12 processing function.
Froese, DS; Krojer, T; Wu, X; Shrestha, R; Kiyani, W; von Delft, F; Gravel, RA; Oppermann, U; Yue, WW;
Biochemistry. 2012 51:5083-5090. doi: 10.1021/bi300150y
PMID: 22642810

Conformational plasticity of glycogenin and its maltosaccharide substrate during glycogen biogenesis.
Chaikuad, A; Froese, DS; Berridge, G; von Delft, F; Oppermann, U; Yue, WW;
Proceedings of the National Academy of Sciences of USA. 2011 108:21028-21033. doi: 10.1073/pnas.1113921108
PMID: 22160680

High-throughput structural biology of metabolic enzymes and its impact on human diseases.
Yue, WW; Oppermann, U;
Journal of Inherited Metabolic Disease. 2011 34:575-581. doi: 10.1007/s10545-011-9296-6
PMID: 21340633

Structural basis of fumarate hydratase deficiency.
Picaud, S; Kavanagh, KL; Yue, WW; Lee, WH; Muller-Knapp, S; Gileadi, O; Sacchettini, J; Oppermann, U;
Journal of Inherited Metabolic Disease. 2011 34:671-676. doi: 10.1007/s10545-011-9294-8
PMID: 21445611

Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.
Froese, DS; Kochan, G; Muniz, JR; Wu, X; Gileadi, C; Ugochukwu, E; Krysztofinska, E; Gravel, RA; Oppermann, U; Yue, WW;
Journal of Biological Chemistry. 2010 285:38204-38213. doi: 10.1074/jbc.M110.177717
PMID: 20876572

Crystal structures of human HMG-CoA synthase isoforms provide insights into inherited ketogenesis disorders and inhibitor design.
Shafqat, N; Turnbull, A; Zschocke, J; Oppermann, U; Yue, WW;
Journal of Molecular Biology. 2010 398:497-506. doi: 10.1016/j.jmb.2010.03.034
PMID: 20346956

2016

Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
Reid, ES; Papandreou, A; Drury, S; Boustred, C; Yue, WW; Wedatilake, Y; Beesley, C; Jacques, TS; Anderson, G; Abulhoul, L; Broomfield, A; Cleary, M; Grunewald, S; Varadkar, SM; Lench, N; Rahman, S; Gissen, P; Clayton, PT; Mills, PB;
Brain: a journal of neurology. 2016 :-. doi:
PMID: 27604308

From structural biology to designing therapy for inborn errors of metabolism.
Y, W; u, W; e, ;
Journal of Inherited Metabolic Disease. 2016 39:489-498. doi:
PMID: 27240455

Structural basis for ligand-dependent dimerization of phenylalanine hydroxylase regulatory domain.
Patel, D; Kopec, J; Fitzpatrick, F; McCorvie, TJ; Yue, WW;
Scientific Reports. 2016 6:23748-. doi:
PMID: 27049649

Molecular basis of classic galactosemia from the structure of human galactose 1-phosphate uridylyltransferase.
McCorvie, TJ; Kopec, J; Pey, AL; Fitzpatrick, F; Patel, D; Chalk, R; Streetha, L; Yue, WW;
Human Molecular Genetics. 2016 :-. doi:
PMID: 27005423

Expanding the Genotypic Spectrum of Perrault syndrome.
Demain, LA; Urquhart, JE; O'Sullivan, J; Williams, SG; Bhaskar, SS; Jenkinson, EM; Lourenco, CM; Heiberg, A; Pearce, SH; Shalev, SA; Yue, WW; Mackinnon, S; Munro, KJ; Newbury-Ecob, R; Becker, K; Kim, MJ; O' Keefe, RT; Newman, WG;
Clinical Genetics: an international journal of genetics and molecular medicine. 2016 :-. doi:
PMID: 26970254

Use of Methylmalonyl-CoA Epimerase in Enhancing Crotonase Stereoselectivity.
Hamed, RB; Gomez-Castellanos, JR; Sean Froese, D; Krysztofinska, E; Yue, WW; Schofield, CJ;
ChemBioChem: a European journal of chemical biology. 2016 17:471-473. doi:
PMID: 26716911

Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders.
de Goede, C; Yue, WW; Yan, G; Ariyaratnam, S; Chandler, KE; Downes, L; Khan, N; Mohan, M; Lowe, M; Banka, S;
European Journal of Paediatric Neurology. 2016 20:286-295. doi:
PMID: 26748598

Crystal structure of Porphyromonas gingivalis peptidylarginine deiminase: implications for autoimmunity in rheumatoid arthritis.
Montgomery, AB; Kopec, J; Shrestha, L; Thezenas, ML; Burgess-Brown, NA; Fischer, R; Yue, WW; Venables, PJ;
Annals of the Rheumatic Diseases. 2016 75:1255-1261. doi:
PMID: 26209657

2015

Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation
Riemersma, M; Froese, DS; Van Tol, W; Engelke, UF; Kopec, J; Van Scherpenzeel, M; Ashikov, A; Krojer, T; Von Delft, F; Tessari, M; Buczkowska, A; Swiezewska, E; Jae, LT; Brummelkamp, TR; Manya, H; Endo, T; Van Bokhoven, H; Yue, WW; Lefeber, DJ;
Chemistry and Biology. 2015 22:1643-1652. doi: 10.1016/j.chembiol.2015.10.014
PMID:

Structural Insights into the MMACHC-MMADHC Protein Complex Involved in Vitamin B12 Trafficking.
Froese, DS; Kopec, J; Fitzpatrick, F; Schuller, M; McCorvie, TJ; Chalk, R; Plessl, T; Fettelschoss, V; Fowler, B; Baumgartner, MR; Yue, WW;
Journal of Biological Chemistry. 2015 290:29167-29177. doi:
PMID: 26483544

Proteomic and Biochemical Studies of Lysine Malonylation Suggest Its Malonic Aciduria-associated Regulatory Role in Mitochondrial Function and Fatty Acid Oxidation.
Colak, G; Pougovkina, O; Dai, L; Tan, M; Te Brinke, H; Huang, H; Cheng, Z; Park, J; Wan, X; Liu, X; Yue, WW; Wanders, RJ; Locasale, JW; Lombard, DB; de Boer, VC; Zhao, Y;
Molecular and Cellular Proteomics. 2015 14:3056-3071. doi:
PMID: 26320211

Structural basis of glycogen branching enzyme deficiency and pharmacologic rescue by rational peptide design.
Froese, DS; Michaeli, A; McCorvie, TJ; Krojer, T; Sasi, M; Melaev, E; Goldblum, A; Zatsepin, M; Lossos, A; Álvarez, R; Escribá, PV; Minassian, BA; von Delft, F; Kakhlon, O; Yue, WW;
Human Molecular Genetics. 2015 24:5667-5676. doi:
PMID: 26199317

Mutations in GMPPB cause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies.
Belaya, K; Rodríguez Cruz, PM; Liu, WW; Maxwell, S; McGowan, S; Farrugia, ME; Petty, R; Walls, TJ; Sedghi, M; Basiri, K; Yue, WW; Sarkozy, A; Bertoli, M; Pitt, M; Kennett, R; Schaefer, A; Bushby, K; Parton, M; Lochmüller, H; Palace, J; Muntoni, F; Beeson, D;
Brain: a journal of neurology. 2015 138:2493-2504. doi:
PMID: 26133662

Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation.
Riemersma, M; Froese, DS; van Tol, W; Engelke, UF; Kopec, J; van Scherpenzeel, M; Ashikov, A; Krojer, T; von Delft, F; Tessari, M; Buczkowska, A; Swiezewska, E; Jae, LT; Brummelkamp, TR; Manya, H; Endo, T; van Bokhoven, H; Yue, WW; Lefeber, DJ;
Chemistry and Biology. 2015 22:1643-1652. doi:
PMID: 26687144

Carnosine metabolism in diabetes is altered by reactive metabolites.
Peters, V; Lanthaler, B; Amberger, A; Fleming, T; Forsberg, E; Hecker, M; Wagner, AH; Yue, WW; Hoffmann, GF; Nawroth, P; Zschocke, J; Schmitt, CP;
Amino Acids. 2015 47:2367-2376. doi:
PMID: 26081982

Linking genotypes database with locus-specific database and genotype-phenotype correlation in phenylketonuria.
Wettstein, S; Underhaug, J; Perez, B; Marsden, BD; Yue, WW; Martinez, A; Blau, N;
European Journal of Human Genetics. 2015 23:302-309. doi:
PMID: 24939588

Leri's pleonosteosis, a congenital rheumatic disease, results from microduplication at 8q22.1 encompassing GDF6 and SDC2 and provides insight into systemic sclerosis pathogenesis.
Banka, S; Cain, SA; Carim, S; Daly, SB; Urquhart, JE; Erdem, G; Harris, J; Bottomley, M; Donnai, D; Kerr, B; Kingston, H; Superti-Furga, A; Unger, S; Ennis, H; Worthington, J; Herrick, AL; Merry, CL; Yue, WW; Kielty, CM; Newman, WG;
Annals of the Rheumatic Diseases. 2015 74:1249-1256. doi: 10.1136/annrheumdis-2013-204309
PMID: 24442880

2014

Inter-domain communication of human cystathionine β-synthase: structural basis of S-adenosyl-L-methionine activation.
McCorvie, TJ; Kopec, J; Hyung, SJ; Fitzpatrick, F; Feng, X; Termine, D; Strain-Damerell, C; Vollmar, M; Fleming, J; Janz, JM; Bulawa, C; Yue, WW;
Journal of Biological Chemistry. 2014 289:36018-36030. doi:
PMID: 25336647

Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
Banka, S; de Goede, C; Yue, WW; Morris, AA; von Bremen, B; Chandler, KE; Feichtinger, RG; Hart, C; Khan, N; Lunzer, V; Mataković, L; Marquardt, T; Makowski, C; Prokisch, H; Debus, O; Nosaka, K; Sonwalkar, H; Zimmermann, FA; Sperl, W; Mayr, JA;
Molecular Genetics and Metabolism. 2014 113:301-306. doi:
PMID: 25458521

Enzymatic and structural characterization of rTSγ provides insights into the function of rTSβ.
Wichelecki, DJ; Froese, DS; Kopec, J; Muniz, JR; Yue, WW; Gerlt, JA;
Biochemistry. 2014 53:2732-2738. doi:
PMID: 24697329

Functional characterization and categorization of missense mutations that cause methylmalonyl-CoA mutase (MUT) deficiency.
Forny, P; Froese, DS; Suormala, T; Yue, WW; Baumgartner, MR;
Human Mutation. 2014 35:1449-1458. doi:
PMID: 25125334

Mutation or knock-down of 17β-hydroxysteroid dehydrogenase type 10 cause loss of MRPP1 and impaired processing of mitochondrial heavy strand transcripts.
Deutschmann, AJ; Amberger, A; Zavadil, C; Steinbeisser, H; Mayr, JA; Feichtinger, RG; Oerum, S; Yue, WW; Zschocke, J;
Human Molecular Genetics. 2014 23:3618-3628. doi: 10.1093/hmg/ddu072
PMID: 24549042

The role of protein structural analysis in the next generation sequencing era.
Yue, WW; Froese, DS; Brennan, PE;
Topics in Current Chemistry. 2014 336:67-98. doi: 10.1007/128_2012_326
PMID: 22610134

2013

5-Carboxy-8-hydroxyquinoline is a broad spectrum 2-oxoglutarate oxygenase inhibitor which causes iron translocation
Hopkinson, RJ; Tumber, A; Yapp, C; Chowdhury, R; Aik, W; Che, KH; Li, XS; Kristensen, JBL; King, ONF; Chan, MC; Yeoh, KK; Choi, H; Walport, LJ; Thinnes, CC; Bush, JT; Lejeune, C; Rydzik, AM; Rose, NR; Bagg, EA; McDonough, MA; Krojer, TJ; Yue, WW; Ng, SS; Olsen, L; Brennan, PE; Oppermann, U; Müller, S; Klose, RJ; Ratcliffe, PJ; Schofield, CJ; Kawamura, A;
Chemical Science. 2013 4:3110-3117. doi: 10.1039/c3sc51122g
PMID: 26682036

Crystal structures of malonyl-coenzyme A decarboxylase provide insights into its catalytic mechanism and disease-causing mutations.
Froese, DS; Forouhar, F; Tran, TH; Vollmar, M; Kim, YS; Lew, S; Neely, H; Seetharaman, J; Shen, Y; Xiao, R; Acton, TB; Everett, JK; Cannone, G; Puranik, S; Savitsky, P; Krojer, T; Pilka, ES; Kiyani, W; Lee, WH; Marsden, BD; von Delft, F; Allerston, CK; Spagnolo, L; Gileadi, O; Montelione, GT; Oppermann, U; Yue, WW; Tong, L;
Structure. 2013 21:1182-1192. doi: 10.1016/j.str.2013.05.001
PMID: 23791943

Insight into S-adenosylmethionine biosynthesis from the crystal structures of the human methionine adenosyltransferase catalytic and regulatory subunits.
Shafqat, N; Muniz, JR; Pilka, ES; Papagrigoriou, E; von Delft, F; Oppermann, U; Yue, WW;
Biochemical Journal. 2013 452:27-36. doi: 10.1042/BJ20121580
PMID: 23425511

A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency.
Shafqat, N; Kavanagh, KL; Sass, JO; Christensen, E; Fukao, T; Lee, WH; Oppermann, U; Yue, WW;
Journal of Inherited Metabolic Disease. 2013 36:983-987. doi: 10.1007/s10545-013-9589-z
PMID: 23420214

LRIG2 mutations cause urofacial syndrome.
Stuart, HM; Roberts, NA; Burgu, B; Daly, SB; Urquhart, JE; Bhaskar, S; Dickerson, JE; Mermerkaya, M; Silay, MS; Lewis, MA; Olondriz, MB; Gener, B; Beetz, C; Varga, RE; Gülpınar, O; Süer, E; Soygür, T; Ozçakar, ZB; Yalçınkaya, F; Kavaz, A; Bulum, B; Gücük, A; Yue, WW; Erdogan, F; Berry, A; Hanley, NA; McKenzie, EA; Hilton, EN; Woolf, AS; Newman, WG;
American Journal of Human Genetics. 2013 92:259-264. doi: 10.1016/j.ajhg.2012.12.002
PMID: 23313374

2012

ENZYMATIC CHARACTERIZATION AND THERMAL STABILITY ASSAYS ESTABLISH METHYLMALONYL-COA MUTASE MUTATIONS AS A TARGET FOR PHARMACOLOGICAL CHAPERONE SCREENING
Forny, P; Froese, DS; Suormala, T; Yue, WW; Baumgartner, MR;
Journal of Inherited Metabolic Disease. 2012 35:S9-S9. doi:
PMID:

Structure of human aspartyl aminopeptidase complexed with substrate analogue: insight into catalytic mechanism, substrate specificity and M18 peptidase family.
Chaikuad, A; Pilka, ES; De Riso, A; von Delft, F; Kavanagh, KL; Vénien-Bryan, C; Oppermann, U; Yue, WW;
BMC Structural Biology. 2012 12:14-. doi: 10.1186/1472-6807-12-14
PMID: 22720794

Structure of MMACHC reveals an arginine-rich pocket and a domain-swapped dimer for its B12 processing function.
Froese, DS; Krojer, T; Wu, X; Shrestha, R; Kiyani, W; von Delft, F; Gravel, RA; Oppermann, U; Yue, WW;
Biochemistry. 2012 51:5083-5090. doi: 10.1021/bi300150y
PMID: 22642810

3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals.
Grünert, SC; Stucki, M; Morscher, RJ; Suormala, T; Bürer, C; Burda, P; Christensen, E; Ficicioglu, C; Herwig, J; Kölker, S; Möslinger, D; Pasquini, E; Santer, R; Schwab, KO; Wilcken, B; Fowler, B; Yue, WW; Baumgartner, MR;
Orphanet Journal of Rare Diseases. 2012 7:31-. doi: 10.1186/1750-1172-7-31
PMID: 22642865

Crystal structure of the secretory isozyme of mammalian carbonic anhydrases CA VI: implications for biological assembly and inhibitor development.
Pilka, ES; Kochan, G; Oppermann, U; Yue, WW;
Biochemical and Biophysical Research Communications. 2012 419:485-489. doi: 10.1016/j.bbrc.2012.02.038
PMID: 22366092

2011

Conformational plasticity of glycogenin and its maltosaccharide substrate during glycogen biogenesis.
Chaikuad, A; Froese, DS; Berridge, G; von Delft, F; Oppermann, U; Yue, WW;
Proceedings of the National Academy of Sciences of USA. 2011 108:21028-21033. doi: 10.1073/pnas.1113921108
PMID: 22160680

Structural and evolutionary basis for the dual substrate selectivity of human KDM4 histone demethylase family.
Hillringhaus, L; Yue, WW; Rose, NR; Ng, SS; Gileadi, C; Loenarz, C; Bello, SH; Bray, JE; Schofield, CJ; Oppermann, U;
Journal of Biological Chemistry. 2011 286:41616-41625. doi: 10.1074/jbc.M111.283689
PMID: 21914792

Interactive JIMD articles using the iSee concept: turning a new page on structural biology data
Lee, WH; Yue, WW; Raush, E; Totrov, M; Abagyan, R; Oppermann, U; Marsden, BD;
Journal of Inherited Metabolic Disease. 2011 :1-3. doi: 10.1007/s10545-011-9334-4
PMID: 21509537

Structural basis of fumarate hydratase deficiency.
Picaud, S; Kavanagh, KL; Yue, WW; Lee, WH; Muller-Knapp, S; Gileadi, O; Sacchettini, J; Oppermann, U;
Journal of Inherited Metabolic Disease. 2011 34:671-676. doi: 10.1007/s10545-011-9294-8
PMID: 21445611

Structure and kinetic characterization of human sperm-specific glyceraldehyde-3-phosphate dehydrogenase, GAPDS.
Chaikuad, A; Shafqat, N; Al-Mokhtar, R; Cameron, G; Clarke, AR; Brady, RL; Oppermann, U; Frayne, J; Yue, WW;
Biochemical Journal. 2011 435:401-409. doi: 10.1042/BJ20101442
PMID: 21269272

DELINEATING THE MITOCHONDRIAL VITAMIN B12 PATHWAY THROUGH STRUCTURAL AND INTERACTION STUDIES
Froese, DS; Kochan, G; Muniz, JRC; Chaikuad, A; Wu, X; Gileadi, C; Ugochukwu, E; Krysztofinska, E; Gravel, RA; Oppermann, U; Yue, WW;
Journal of Inherited Metabolic Disease. 2011 34:S119-S119. doi:
PMID:

INTERACTIVE 3D VISUALISATIONS OF PROTEIN STRUCTURES TO AID THE STUDY OF INBORN ERRORS OF METABOLISM
Lee, WH; Raush, E; Totrov, M; Abagyan, R; Marsden, BD; Oppermann, U; Yue, WW;
Journal of Inherited Metabolic Disease. 2011 34:S240-S240. doi:
PMID:

High-throughput structural biology of metabolic enzymes and its impact on human diseases.
Yue, WW; Oppermann, U;
Journal of Inherited Metabolic Disease. 2011 34:575-581. doi: 10.1007/s10545-011-9296-6
PMID: 21340633

2010

Structures of the human GTPase MMAA and vitamin B12-dependent methylmalonyl-CoA mutase and insight into their complex formation.
Froese, DS; Kochan, G; Muniz, JR; Wu, X; Gileadi, C; Ugochukwu, E; Krysztofinska, E; Gravel, RA; Oppermann, U; Yue, WW;
Journal of Biological Chemistry. 2010 285:38204-38213. doi: 10.1074/jbc.M110.177717
PMID: 20876572

Structural impact of human and Escherichia coli biotin carboxyl carrier proteins on biotin attachment.
Healy, S; McDonald, MK; Wu, X; Yue, WW; Kochan, G; Oppermann, U; Gravel, RA;
Biochemistry. 2010 49:4687-4694. doi: 10.1021/bi901612y
PMID: 20443544

Crystal structures of human HMG-CoA synthase isoforms provide insights into inherited ketogenesis disorders and inhibitor design.
Shafqat, N; Turnbull, A; Zschocke, J; Oppermann, U; Yue, WW;
Journal of Molecular Biology. 2010 398:497-506. doi: 10.1016/j.jmb.2010.03.034
PMID: 20346956

Crystal structure of the PHF8 Jumonji domain, an Nepsilon-methyl lysine demethylase.
Yue, WW; Hozjan, V; Ge, W; Loenarz, C; Cooper, CD; Schofield, CJ; Kavanagh, KL; Oppermann, U; McDonough, MA;
FEBS Letters. 2010 584:825-830. doi: 10.1016/j.febslet.2009.12.055
PMID: 20067792

2009

Crystal structure of human carbonic anhydrase-related protein VIII reveals the basis for catalytic silencing.
Picaud, SS; Muniz, JR; Kramm, A; Pilka, ES; Kochan, G; Oppermann, U; Yue, WW;
Proteins: Structure, Function, and Bioinformatics. 2009 76:507-511. doi: 10.1002/prot.22411
PMID: 19360879

Structural snapshots for the conformation-dependent catalysis by human medium-chain acyl-coenzyme A synthetase ACSM2A.
Kochan, G; Pilka, ES; von Delft, F; Oppermann, U; Yue, WW;
Journal of Molecular Biology. 2009 388:997-1008. doi: 10.1016/j.jmb.2009.03.064
PMID: 19345228

Dynamic protein methylation in chromatin biology.
Ng, SS; Yue, WW; Oppermann, U; Klose, RJ;
Cellular and Molecular Life Sciences. 2009 66:407-422. doi: 10.1007/s00018-008-8303-z
PMID: 18923809

2007

Crystal structure of the retinoblastoma protein N domain provides insight into tumor suppression, ligand interaction, and holoprotein architecture.
Hassler, M; Singh, S; Yue, WW; Luczynski, M; Lakbir, R; Sanchez-Sanchez, F; Bader, T; Pearl, LH; Mittnacht, S;
Molecular Cell. 2007 28:371-385. doi: 10.1016/j.molcel.2007.08.023
PMID: 17996702

Insights into histone code syntax from structural and biochemical studies of CARM1 methyltransferase.
Yue, WW; Hassler, M; Roe, SM; Thompson-Vale, V; Pearl, LH;
The EMBO Journal. 2007 26:4402-4412. doi: 10.1038/sj.emboj.7601856
PMID: 17882261

2004

Recognition of iron-free siderophores by TonB-dependent iron transporters.
Schalk, IJ; Yue, WW; Buchanan, SK;
Molecular Microbiology. 2004 54:14-22. doi: 10.1111/j.1365-2958.2004.04241.x
PMID: 15458401

2003

Structural evidence for iron-free citrate and ferric citrate binding to the TonB-dependent outer membrane transporter FecA.
Yue, WW; Grizot, S; Buchanan, SK;
Journal of Molecular Biology. 2003 332:353-368. doi:
PMID: 12948487

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