Skip Nav Destination
Close Modal
Update search
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Article Type
Date
Availability
1-10 of 10
Keywords: binding affinity
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Articles
Putting the pieces into place: Properties of intact zinc metallothionein 1A determined from interaction of its isolated domains with carbonic anhydrase
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2015) 471 (3): 347–356.
Published: 16 October 2015
...-carbonic anhydrase [CA; metal-free CA (apo-CA)] provided the binding affinities for each of the eight sites and showed that CA competed more efficiently for added zinc with the β-domain fragment. The combined effects of the number of sites, chain length and cysteine accessibility modulate the zinc-binding...
Includes: Supplementary data
Articles
Thermodynamics and structural analysis of positive allosteric modulation of the ionotropic glutamate receptor GluA2
Available to PurchaseChristian Krintel, Karla Frydenvang, Lars Olsen, Maria T. Kristensen, Oriol de Barrios, Peter Naur, Pierre Francotte, Bernard Pirotte, Michael Gajhede, Jette S. Kastrup
Journal:
Biochemical Journal
Biochem J (2012) 441 (1): 173–178.
Published: 14 December 2011
... binding affinities and thermodynamic details of binding of modulators of GluA2. A mutant of the LBD of GluA2 (LBD-L483Y-N754S) that forms a stable dimer in solution was used. The potent GluA2 modulator BPAM-97 was used as a reference compound. Evidence that BPAM-97 binds in the same pocket as the well...
Includes: Supplementary data
Articles
Aedes aegypti cadherin serves as a putative receptor of the Cry11Aa toxin from Bacillus thuringiensis subsp. israelensis
Available to PurchaseJianwu Chen, Karlygash G. Aimanova, Luisa E. Fernandez, Alejandra Bravo, Mario Soberon, Sarjeet S. Gill
Journal:
Biochemical Journal
Biochem J (2009) 424 (2): 191–200.
Published: 11 November 2009
... To whom correspondence should be addressed (email [email protected] ). 11 5 2009 18 8 2009 4 9 2009 4 9 2009 © The Authors Journal compilation © 2009 Biochemical Society 2009 Bacillus thuringiensis binding affinity cadherin Cry11Aa toxin midgut receptor...
Includes: Supplementary data
Articles
The chemistry of copper binding to PrP: is there sufficient evidence to elucidate a role for copper in protein function?
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2008) 410 (2): 237–244.
Published: 12 February 2008
... The Authors Journal compilation © 2008 Biochemical Society 2008 binding affinity co-ordination copper octapeptide prion protein (PrP) protein stability PrP (prion protein) is a cell-surface glycoprotein that has been directly implicated in the pathogenesis of a range of neurodegenerative...
Articles
The family 21 carbohydrate-binding module of glucoamylase from Rhizopus oryzae consists of two sites playing distinct roles in ligand binding
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2006) 396 (3): 469–477.
Published: 29 May 2006
... 3 2006 The Biochemical Society, London 2006 binding affinity carbohydrate-binding module (CBM) glucoamylase (GA) homology modelling progressive secondary structure correlation (PSSC) starch-binding domain (SBD) GA (glucoamylase) (1,4-α- D -glucan glucohydrolase, EC 3.2.1.3...
Articles
EGFR kinase possesses a broad specificity for ErbB phosphorylation sites, and ligand increases catalytic-centre activity without affecting substrate binding affinity
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2005) 392 (3): 417–423.
Published: 06 December 2005
...Ying-Xin Fan; Lily Wong; Gibbes R. Johnson We previously found that EGF (epidermal growth factor) increases the EGFR (EGF receptor) kinase-binding affinity towards the major tyrosine phosphorylation sites in downstream adaptor proteins such as Gab1 (Grb2-associated binding protein 1) and Shc [Src...
Articles
Interactions of human replication protein A with single-stranded DNA adducts
Available to PurchaseYiyong LIU, Zhengguan YANG, Christopher D. UTZAT, Yu LIU, Nicholas E. GEACINTOV, Ashis K. BASU, Yue ZOU
Journal:
Biochemical Journal
Biochem J (2005) 385 (2): 519–526.
Published: 07 January 2005
...-aminopyrene-, BPDE (benzo[ a ]pyrene diol epoxide)- and fluorescein that are different in many aspects such as molecular structure and size, DNA disruption mode (e.g. base stacking or non-stacking), as well as chemical properties. Our results showed that RPA has a lower binding affinity for damaged ssDNA than...
Articles
Glucoamylase starch-binding domain of Aspergillus niger B1: molecular cloning and functional characterization
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2003) 372 (3): 905–910.
Published: 15 June 2003
... The Biochemical Society, London ©2003 2003 binding affinity binding reversibility modified starch Abbreviations used: BCA, bicinchoninic acid; CBD, cellulose-binding domain; CBM, carbohydrate-binding module; LB, Luria–Bertani; SBD, starch-binding domain. Biochem. J. (2003) 372, 905 910...
Articles
Tailoring tissue inhibitor of metalloproteinases-3 to overcome the weakening effects of the cysteine-rich domains of tumour necrosis factor-alpha converting enzyme
Available to Purchase
Journal:
Biochemical Journal
Biochem J (2003) 371 (2): 369–376.
Published: 15 April 2003
...-TIMP-3 mutants displayed markedly improved binding affinity with the soluble extracellular domain form of recombinant TACE. With K i (app) values of <0.1nM, these mutants were dramatically better than the wild-type N-TIMP-3 [ K i (app) 1.7nM]. We accounted for this by proposing that Glu 31...
Articles
Engineering N-terminal domain of tissue inhibitor of metalloproteinase (TIMP)-3 to be a better inhibitor against tumour necrosis factor-α-converting enzyme
Available to PurchaseMeng-Huee LEE, Vandana VERMA, Klaus MASKOS, Deepa NATH, Vera KNÄUPER, Philippa DODDS, Augustin AMOUR, Gillian MURPHY
Journal:
Biochemical Journal
Biochem J (2002) 364 (1): 227–234.
Published: 08 May 2002
...Meng-Huee LEE; Vandana VERMA; Klaus MASKOS; Deepa NATH; Vera KNÄUPER; Philippa DODDS; Augustin AMOUR; Gillian MURPHY We previously reported that full-length tissue inhibitor of metalloproteinase-3 (TIMP-3) and its N-terminal domain form (N-TIMP-3) displayed equal binding affinity for tissue...