Solution structure and interface-driven self-assembly of NC2, a new member of the Class II hydrophobin proteins

Proteins: Structure, Function and Bioinformatics

Volumn 82, Issue 6, 2014, Pages 990-1003

  Ren, Qin ^a   Kwan, Ann H ^a   Sunde, Margaret ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

Author keywords

Amphipathic; Hydrophobins; Interface; Monolayer; Self assembly

Indexed keywords

FORMIC ACID; HYDROPHOBIN; NC2 PROTEIN; THIOFLAVINE; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG; FUNGAL PROTEIN; SOLUTION AND SOLUBILITY; SURFACTANT;

AMINO ACID COMPOSITION; AMINO ACID SEQUENCE; ARTICLE; ATOMIC FORCE MICROSCOPY; BIOTECHNOLOGY; CONFORMATIONAL TRANSITION; CONTACT ANGLE; DISULFIDE BOND; GEL PERMEATION CHROMATOGRAPHY; HETERONUCLEAR NUCLEAR MAGNETIC RESONANCE; HYDROGEN BOND; HYPOCREA JECORINA; INFRARED SPECTROSCOPY; LIGHT SCATTERING; NEUROSPORA CRASSA; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; CHEMICAL PHENOMENA; CHEMICAL STRUCTURE; CHEMISTRY; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE; PROTEIN MULTIMERIZATION; PROTEIN QUATERNARY STRUCTURE; SOLUTION AND SOLUBILITY; SURFACE PROPERTY; ULTRASTRUCTURE;

AMINO ACID SEQUENCE; FUNGAL PROTEINS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICROSCOPY, ATOMIC FORCE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NEUROSPORA CRASSA; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; SOLUTIONS; SURFACE PROPERTIES; SURFACE-ACTIVE AGENTS;

EID: 84900562602     PISSN: 08873585     EISSN: 10970134     Source Type: Journal    
DOI: 10.1002/prot.24473     Document Type: Article

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