Correlation between catalysis and tertiary structure arrangement in an archaeal halophilic subtilase

Biochimie

Volumn 94, Issue 3, 2012, Pages 798-805

  Souza, Tatiana A C B ^a   Okamoto, Débora N ^b   Ruiz, Diego M ^c   Oliveira, Lilian C G ^b   Kondo, Márcia Y ^b   Tersario, Ivarne L S ^d   Juliano, Luiz ^b   De Castro, Rosana E ^c   Gouvea, Iuri E ^b   Murakami, Mário T ^a  

^a BRAZILIAN CENTER FOR RESEARCH IN ENERGY AND MATERIALS CNPEM   (Brazil)

^b FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^c UNIVERSIDAD NACIONAL DE MAR DEL PLATA   (Argentina)

^d UNIVERSIDADE DE MOGI DAS CRUZES   (Brazil)

Author keywords

Extracellular protease; Halophilism; Kinetics; Natrialba magadii; Stability; Structure

Indexed keywords

BACTERIAL ENZYME; EXTRACELLULAR PROTEASE; PROTEINASE; SODIUM CHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; ENZYME ACTIVITY; ENZYME CONFORMATION; ENZYME KINETICS; ENZYME STABILITY; ENZYME STRUCTURE; HALOPHILIC ARCHAEON; HYDRODYNAMICS; HYDROLYSIS; NATRIALBA MAGADII; NONHUMAN; PROTEIN AGGREGATION; PROTEIN FOLDING; SALINITY; TEMPERATURE SENSITIVITY; THERMODYNAMICS; THERMOSTABILITY;

CATALYSIS; ENZYME STABILITY; HALOBACTERIACEAE; HYDROGEN-ION CONCENTRATION; PROTEIN STRUCTURE, TERTIARY; SUBTILISINS; TEMPERATURE;

ARCHAEA; NATRIALBA MAGADII;

EID: 84857050838     PISSN: 03009084     EISSN: 61831638     Source Type: Journal    
DOI: 10.1016/j.biochi.2011.11.011     Document Type: Article

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