Evidence map›Paper›PMID 23988152›Full record

ArticleBiochemistry2013

Structure and dynamics of the N-terminal domain of the Cu(I) binding protein CusB.

Melek N Ucisik, Dhruva K Chakravorty, Kenneth M Merz

Open access · greenAbstract read
In one paragraph

Article in Biochemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Melek N UcisikDepartment of Chemistry and Quantum Theory Project, University of Florida , 2328 New Physics Building, P.O. Box 118435, Gainesville, Florida 32611-8435, United States.
Dhruva K Chakravorty
Kenneth M Merz
University of Florida · US

Funding

Mettalloenzyme Structure/FunctionR01GM044974 · NIGMS · UNIVERSITY OF FLORIDA · PI MERZ, KENNETH M. · 1997 to 2010
$2.0M
The Bioinorganic Chemistry of Nickel: The UreasesR01GM066859 · NIGMS · UNIVERSITY OF FLORIDA · PI DEUMENS, ERIK · 2003 to 2011
$1.9M
THEORETICAL STUDY--METALLOENZYME STRUCTURE AND FUNCTIONR29GM044974 · NIGMS · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI MERZ, KENNETH M · 1991 to 1995
–
NIGMS NIH HHS GM044974NIGMS NIH HHS GM066859NIGMS NIH HHS R01 GM044974NIGMS NIH HHS R01 GM066859
6 · The paper itself

Abstract

CusCFBA is one of the metal efflux systems in Escherichia coli that is highly specific for its substrates, Cu(I) and Ag(I). It serves to protect the bacteria in environments that have lethal concentrations of these metals. The membrane fusion protein CusB is the periplasmic piece of CusCFBA, which has not been fully characterized by crystallography because of its extremely disordered N-terminal region. This region has both structural and functional importance because it has been experimentally proven to transfer the metal by itself from the metallochaperone CusF and to induce a structural change in the rest of CusB to increase Cu(I)/Ag(I) resistance. Understanding metal uptake from the periplasm is critical to gain insight into the mechanism of the whole CusCFBA pump, which makes resolving a structure for the N-terminal region necessary because it contains the metal binding site. We ran extensive molecular dynamics simulations to reveal the structural and dynamic properties of both the apo and Cu(I)-bound versions of the CusB N-terminal region. In contrast to its functional companion CusF, Cu(I) binding to the N-terminus of CusB causes only a slight, local stabilization around the metal site. The trajectories were analyzed in detail, revealing extensive structural disorder in both the apo and holo forms of the protein. CusB was further analyzed by breaking the protein up into three subdomains according to the extent of the observed disorder: the N- and C-terminal tails, the central beta strand motif, and the M21-M36 loop connecting the two metal-coordinating methionine residues. Most of the observed disorder was traced back to the tail regions, leading us to hypothesize that the latter two subdomains (residues 13-45) may form a functionally competent metal-binding domain because the tail regions appear to play no role in metal binding.

Indexed as

Molecular Dynamics SimulationEscherichia coli ProteinsMembrane Transport ProteinsModels, MolecularProtein ConformationCusB protein, E coliEscherichia coli ProteinsMembrane Transport Proteins

Identifiers

PMID23988152
PMCPMC3817623
OpenAlexW2018292030

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.