H R Faber
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Explore the profile of H R Faber including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
242
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Recent Articles
1.
Feese M, Faber H, Bystrom C, Pettigrew D, Remington S
Structure
. 1998 Nov;
6(11):1407-18.
PMID: 9817843
Background: Glycerol kinase (GK) from Escherichia coli is a velocity-modulated (V system) enzyme that has three allosteric effectors with independent mechanisms: fructose-1,6-bisphosphate (FBP); the phosphocarrier protein IIAGlc; and adenosine nucleotides....
2.
Faber H, Baker C, Day C, Tweedie J, Baker E
Biochemistry
. 1996 Nov;
35(46):14473-9.
PMID: 8931543
A conserved arginine residue helps to form the synergistic anion binding site in transferrins. To probe the importance of this residue for anion binding and iron binding, Arg 121 has...
3.
Dobbs A, Anderson B, Faber H, Baker E
Acta Crystallogr D Biol Crystallogr
. 1996 Mar;
52(Pt 2):356-68.
PMID: 15299707
The three-dimensional structures of two cytochromes c' have been determined in order to analyse the common features of proteins of this family and their relationship with other four-helix bundle structures....
4.
Faber H, Bland T, Day C, Norris G, Tweedie J, Baker E
J Mol Biol
. 1996 Feb;
256(2):352-63.
PMID: 8594202
The crystal structure of a site-specific mutant of the N-terminal half-molecule of human lactoferrin, Lf(N), in which the iron ligand Asp60 has been mutated to Ser, has been determined at...
5.
McLenachan P, Lockhart P, Faber H, Mansfield B
J Mol Evol
. 1996 Feb;
42(2):273-80.
PMID: 8919879
The pregnancy-specific beta 1-glycoproteins (PSG) form a large family of closely related proteins. Using newly developed methods of sequence analysis, in combination with protein modeling, we provide a framework for...
6.
Faber H, Groom C, BAKER H, Morgan W, Smith A, Baker E
Structure
. 1995 Jun;
3(6):551-9.
PMID: 8590016
Background: Haemopexin is a serum glycoprotein that binds haem reversibly and delivers it to the liver where it is taken up by receptor-mediated endocytosis. Haemopexin has two homologous domains, each...
7.
Hurley J, Faber H, Worthylake D, Meadow N, Roseman S, Pettigrew D, et al.
Science
. 1993 Jan;
259(5095):673-7.
PMID: 8430315
The phosphocarrier protein IIIGlc is an integral component of the bacterial phosphotransferase (PTS) system. Unphosphorylated IIIGlc inhibits non-PTS carbohydrate transport systems by binding to diverse target proteins. The crystal structure...
8.
Jacobson R, Matsumura M, Faber H, Matthews B
Protein Sci
. 1992 Jan;
1(1):46-57.
PMID: 1304882
The engineered disulfide bridge between residues 21 and 142 of phage T4 lysozyme spans the active-site cleft and can be used as a switch to control the activity of the...
9.
Bell J, Wilson K, Zhang X, Faber H, Nicholson H, Matthews B
Proteins
. 1991 Jan;
10(1):10-21.
PMID: 2062826
Crystals of bacteriophage T4 lysozyme used for structural studies are routinely grown from concentrated phosphate solutions. It has been found that crystals in the same space group can also be...
10.
Faber H, Matthews B
Nature
. 1990 Nov;
348(6298):263-6.
PMID: 2234094
Phage T4 lysozyme consists of two domains between which is formed the active-site cleft of the enzyme. The crystallographically determined thermal displacement parameters for the protein suggested that the amino...