Pages that link to "Q44112912"

The following pages link to Effect of N-terminal truncation and solution conditions on chemokine dimer stability: nuclear magnetic resonance structural analysis of macrophage inflammatory protein 1 beta mutants (Q44112912):

Displaying 23 items.

• Structural rearrangement of human lymphotactin, a C chemokine, under physiological solution conditions (Q24292437) (← links)
• Identification of amino acid residues critical for aggregation of human CC chemokines macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, and RANTES. Characterization of active disaggregated chemokine variants (Q27618367) (← links)
• The solution structure of the anti-HIV chemokine vMIP-II (Q27620649) (← links)
• NMR structure of the pseudo-receiver domain of CikA (Q27643902) (← links)
• Structural and functional studies of the potent anti-HIV chemokine variant P2-RANTES (Q27657257) (← links)
• Total chemical synthesis and high-resolution crystal structure of the potent anti-HIV protein AOP-RANTES (Q27766504) (← links)
• Natural truncation of the chemokine MIP-1 beta /CCL4 affects receptor specificity but not anti-HIV-1 activity (Q28205217) (← links)
• Identification of human macrophage inflammatory proteins 1alpha and 1beta as a native secreted heterodimer (Q28207703) (← links)
• Human nucleotide excision repair protein XPA: NMR spectroscopic studies of an XPA fragment containing the ERCC1-binding region and the minimal DNA-binding domain (M59-F219). (Q30699239) (← links)
• Biochemical characterization and N-terminomics analysis of leukolysin, the membrane-type 6 matrix metalloprotease (MMP25): chemokine and vimentin cleavages enhance cell migration and macrophage phagocytic activities (Q34172720) (← links)
• Effects of temperature and salt concentration on the structural stability of human lymphotactin: insights from molecular simulations (Q37011062) (← links)
• The binding surface and affinity of monomeric and dimeric chemokine macrophage inflammatory protein 1 beta for various glycosaminoglycan disaccharides (Q38361416) (← links)
• Biochemical analysis of matrix metalloproteinase activation of chemokines CCL15 and CCL23 and increased glycosaminoglycan binding of CCL16. (Q39432022) (← links)
• The Effect of N-Terminal Cyclization on the Function of the HIV Entry Inhibitor 5P12-RANTES. (Q40115327) (← links)
• Multi-step purification strategy for RANTES wild-type and mutated analogues expressed in a baculovirus system. (Q40899741) (← links)
• Backbone dynamics of the human CC chemokine eotaxin: fast motions, slow motions, and implications for receptor binding (Q41776124) (← links)
• Recognition of a CXCR4 sulfotyrosine by the chemokine stromal cell-derived factor-1alpha (SDF-1alpha/CXCL12) (Q41907503) (← links)
• The monomer-dimer equilibrium of stromal cell-derived factor-1 (CXCL 12) is altered by pH, phosphate, sulfate, and heparin (Q43058079) (← links)
• CC and CX3C chemokines differentially interact with the N terminus of the human cytomegalovirus-encoded US28 receptor (Q45152598) (← links)
• Recombinant guinea pig CCL5 (RANTES) differentially modulates cytokine production in alveolar and peritoneal macrophages (Q46513429) (← links)
• The human CC chemokine MIP-1beta dimer is not competent to bind to the CCR5 receptor (Q51795920) (← links)
• Elucidating the structural mechanisms for biological activity of the chemokine family (Q52066466) (← links)
• Structure-function guided modeling of chemokine-GPCR specificity for the chemokine XCL1 and its receptor XCR1 (Q93085849) (← links)