Default: Biochemistry

ISSN: 0006-2960

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Biochemistry Q1 Unclaimed

American Chemical Society United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Biochemistry is a journal indexed in SJR in Biochemistry with an H index of 274. It has a price of 3678 €. It has an SJR impact factor of 1,042 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,042.

Biochemistry focuses its scope in these topics and keywords: protein, human, structure, peptide, escherichia, acid, formation, binding, activity, receptor, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Scopus WOS
Categories: Biochemistry (Q1)
Price

3678 €

Inmediate OA

1839 €

Embargoed OA

0 €

Non OA

Metrics

Biochemistry

1,042

SJR Impact factor

274

H Index

350

Total Docs (Last Year)

1116

Total Docs (3 years)

18613

Total Refs

2914

Total Cites (3 years)

1076

Citable Docs (3 years)

2.69

Cites/Doc (2 years)

53.18

Ref/Doc

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Aims and Scope


protein, human, structure, peptide, escherichia, acid, formation, binding, activity, receptor, coli, synthesis, rna, active, dna, characterization, proteins, cell, functional, mechanism, interactions, surface,



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Abscisic Acid Analogues That Act as Universal or Selective Antagonists of Phytohormone Receptors

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Inhibition of the Class C beta-Lactamase fromAcinetobacterspp.: Insights into Effective Inhibitor Design

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A Streptavidin Binding Site Mutation Yields an Unexpected Result: An Ionized Asp128 Residue Is Not Essential for Strong Biotin Binding

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Modulation of Conformational Equilibria in the S-Adenosylmethionine (SAM) II Riboswitch by SAM, Mg2+, and Trimethylamine N-Oxide

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Following the Reactions of Mechanism-Based Inhibitors with beta-Lactamase by Raman Crystallography†

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Mechanism and Kinetics of d-Lysin Interaction with Phospholipid Vesicles†

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Overcoming Resistance to beta-Lactamase Inhibitors: Comparing Sulbactam to Novel Inhibitors against Clavulanate Resistant SHV Enzymes with Substitutions at Ambler Position 244†

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Platelet-Activating Factor Acetylhydrolases: Broad Substrate Specificity and Lipoprotein Binding Does Not Modulate the Catalytic Properties of the Plasma Enzyme

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Modulator-Induced Interference in Functional Cross Talk between the Substrate and the ATP Sites of Human P-glycoprotein†

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Domain Motions of the Mip Protein fromLegionella pneumophila†,‚Ä°

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Carbapenems and SHV-1 beta-Lactamase Form Different Acyl-Enzyme Populations in Crystals and Solution†

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