MAD analysis of FHIT, a putative human tumor suppressor from the HIT protein family.

[1]  L Holm,et al.  Enzyme HIT. , 1997, Trends in biochemical sciences.

[2]  G. Petsko,et al.  Crystal structures of HINT demonstrate that histidine triad proteins are GalT-related nucleotide-binding proteins , 1997, Nature Structural Biology.

[3]  C Sander,et al.  New structure--novel fold? , 1997, Structure.

[4]  C. Croce,et al.  Structure and expression of the human FHIT gene in normal and tumor cells. , 1997, Cancer research.

[5]  R. Gartenhaus.  Allelic loss determination in chronic lymphocytic leukemia by immunomagnetic bead sorting and microsatellite marker analysis , 1997, Oncogene.

[6]  Mary L. Westbrook,et al.  Data acquisition and analysis at the Structural Biology Center , 1996 .

[7]  K. Yanagisawa,et al.  Molecular analysis of the FHIT gene at 3p14.2 in lung cancer cell lines. , 1996, Cancer research.

[8]  R. Lotan,et al.  Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines. , 1996, Cancer research.

[9]  Å. Borg,et al.  The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14. , 1996, Cancer research.

[10]  F. Sarkar,et al.  Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors. , 1996, Cancer research.

[11]  J. Deisenhofer,et al.  The crystal structure of the bifunctional enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase reveals distinct domain homologies. , 1996, Structure.

[12]  P A Frey,et al.  The structure of nucleotidylated histidine-166 of galactose-1-phosphate uridylyltransferase provides insight into phosphoryl group transfer. , 1996, Biochemistry.

[13]  L. D. Barnes,et al.  Fhit, a putative tumor suppressor in humans, is a dinucleoside 5',5"'-P1,P3-triphosphate hydrolase. , 1996, Biochemistry.

[14]  C. Croce,et al.  FHIT gene alterations in head and neck squamous cell carcinomas. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[15]  W. Kuo,et al.  Cloning, mapping, and in vivo localization of a human member of the PKCI-1 protein family (PRKCNH1). , 1996, Genomics.

[16]  C. Croce,et al.  The FHIT gene at 3p14.2 is abnormal in breast carcinomas. , 1996, Cancer research.

[17]  M. Wigler,et al.  Evaluation of the FHIT gene in colorectal cancers. , 1996, Cancer research.

[18]  C. Croce,et al.  Aberrant FHIT transcripts in Merkel cell carcinoma. , 1996, Cancer research.

[19]  C. Lima,et al.  Three-dimensional structure of human protein kinase C interacting protein 1, a member of the HIT family of proteins. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[20]  C. Croce,et al.  The FHIT Gene at 3p14.2 Is Abnormal in Lung Cancer , 1996, Cell.

[21]  C. Croce,et al.  The FHIT Gene, Spanning the Chromosome 3p14.2 Fragile Site and Renal Carcinoma–Associated t(3;8) Breakpoint, Is Abnormal in Digestive Tract Cancers , 1996, Cell.

[22]  L. D. Barnes,et al.  Cloning of the Schizosaccharomyces pombe gene encoding diadenosine 5',5"'-P1,P4-tetraphosphate (Ap4A) asymmetrical hydrolase: sequence similarity with the histidine triad (HIT) protein family. , 1995, The Biochemical journal.

[23]  P. Frey,et al.  Three-dimensional structure of galactose-1-phosphate uridylyltransferase from Escherichia coli at 1.8 A resolution. , 1995, Biochemistry.

[24]  P. Brzoska,et al.  The product of the ataxia-telangiectasia group D complementing gene, ATDC, interacts with a protein kinase C substrate and inhibitor. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[25]  R. Fleischmann,et al.  Whole-genome random sequencing and assembly of Haemophilus influenzae Rd. , 1995, Science.

[26]  S. Howell,et al.  Expression and characterization of maize ZBP14, a member of a new family of zinc-binding proteins. , 1995, Biochemical Journal.

[27]  Peter D. Kwong,et al.  Structural basis of cell-cell adhesion by cadherins , 1995, Nature.

[28]  A. Aitken,et al.  Identification of a new protein family which includes bovine protein kinase C inhibitor-1. , 1994, The Biochemical journal.

[29]  J. Navaza,et al.  AMoRe: an automated package for molecular replacement , 1994 .

[30]  C. Orengo,et al.  Alpha plus beta folds revisited: some favoured motifs. , 1993, Structure.

[31]  S V Evans,et al.  SETOR: hardware-lighted three-dimensional solid model representations of macromolecules. , 1993, Journal of molecular graphics.

[32]  J. Correia,et al.  Glu327 is part of a catalytic triad in rat liver fructose-2,6-bisphosphatase. , 1992, The Journal of biological chemistry.

[33]  A. Brunger.  Free R value: a novel statistical quantity for assessing the accuracy of crystal structures. , 1992 .

[34]  M. Walsh,et al.  The major endogenous bovine brain protein kinase C inhibitor is a heat‐labile protein , 1991, FEBS letters.

[35]  K. Sharp,et al.  Protein folding and association: Insights from the interfacial and thermodynamic properties of hydrocarbons , 1991, Proteins.

[36]  W. Hendrickson.  Determination of macromolecular structures from anomalous diffraction of synchrotron radiation. , 1991, Science.

[37]  Sung-Hou Kim,et al.  Sparse matrix sampling: a screening method for crystallization of proteins , 1991 .

[38]  J. Zou,et al.  Improved methods for building protein models in electron density maps and the location of errors in these models. , 1991, Acta crystallographica. Section A, Foundations of crystallography.

[39]  M. Walsh,et al.  Characterization of a novel zinc binding site of protein kinase C inhibitor‐1 , 1991, FEBS letters.

[40]  K. Lin,et al.  Hepatic 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase. Use of site-directed mutagenesis to evaluate the roles of His-258 and His-392 in catalysis. , 1990, The Journal of biological chemistry.

[41]  W A Hendrickson,et al.  Selenomethionyl proteins produced for analysis by multiwavelength anomalous diffraction (MAD): a vehicle for direct determination of three‐dimensional structure. , 1990, The EMBO journal.

[42]  S. Golden,et al.  Different and rapid responses of four cyanobacterial psbA transcripts to changes in light intensity , 1990, Journal of bacteriology.

[43]  R. Heinrikson,et al.  Amino acid sequence and characterization of a protein inhibitor of protein kinase C. , 1990, The Journal of biological chemistry.

[44]  D. Smith,et al.  Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase. , 1988, Gene.

[45]  M. Walsh,et al.  Properties and distribution of the protein inhibitor (Mr 17,000) of protein kinase C. , 1987, The Biochemical journal.

[46]  M. Karplus,et al.  Crystallographic R Factor Refinement by Molecular Dynamics , 1987, Science.

[47]  M. Walsh,et al.  Ca2+-binding proteins from bovine brain including a potent inhibitor of protein kinase C. , 1985, The Biochemical journal.

[48]  A. Beth,et al.  6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase from rat liver. , 1983, The Journal of biological chemistry.

[49]  W. V. D. Van de Ven,et al.  In a Pleomorphic Adenoma of the Parotid Gland Fhit and Hmgic Expression of Reciprocal Hybrid Transcripts of Updated Version Citing Articles E-mail Alerts Expression of Reciprocal Hybrid Transcripts of Hmgic and Fhit in a Pleomorphic Adenoma of the Parotid Gland' , 2013 .

[50]  J. Abrahams,et al.  Methods used in the structure determination of bovine mitochondrial F1 ATPase. , 1996, Acta crystallographica. Section D, Biological crystallography.

[51]  B. Séraphin.  The HIT protein family: a new family of proteins present in prokaryotes, yeast and mammals. , 1992, DNA sequence : the journal of DNA sequencing and mapping.