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The histone H3-H4 tetramer is a copper reductase enzyme
期刊论文
, 2020, 卷号: 369, 期号: 6499
作者:
Attar N.
;
Campos O.A.
;
Vogelauer M.
;
Cheng C.
;
Xue Y.
;
Schmollinger S.
;
Salwinski L.
;
Mallipeddi N.V.
;
Boone B.A.
;
Yen L.
;
Yang S.
;
Zikovich S.
;
Dardine J.
;
Carey M.F.
;
Merchant S.S.
;
Kurdistani S.K.
收藏
  |  
浏览/下载:28/0
  |  
提交时间:2020/07/28
copper
copper oxidase
copper zinc superoxide dismutase
histone
MAC1 protein, S cerevisiae
nuclear protein
oxidoreductase
recombinant protein
Saccharomyces cerevisiae protein
transcription factor
animal
biocatalysis
chemistry
enzyme active site
enzymology
gain of function mutation
genetics
metabolism
mitochondrion
protein multimerization
Saccharomyces cerevisiae
Xenopus laevis
Animals
Biocatalysis
Catalytic Domain
Copper
Gain of Function Mutation
Histones
Mitochondria
Nuclear Proteins
Oxidoreductases
Protein Multimerization
Recombinant Proteins
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Superoxide Dismutase-1
Transcription Factors
Xenopus laevis
Structural evidence for a dynamic metallocofactor during N2 reduction by Mo-nitrogenase
期刊论文
, 2020, 卷号: 368, 期号: 6497
作者:
Kang W.
;
Lee C.C.
;
Jasniewski A.J.
;
Ribbe M.W.
;
Hu Y.
收藏
  |  
浏览/下载:48/0
  |  
提交时间:2020/07/28
ammonia
catalysis
crystal structure
enzyme activity
ligand
physiological response
sulfur
ligand
molybdenum iron protein
nitrogen
sulfur
Azotobacter vinelandii
biocatalysis
chemistry
enzymology
oxidation reduction reaction
protein multimerization
X ray crystallography
Azotobacter vinelandii
Biocatalysis
Crystallography, X-Ray
Ligands
Molybdoferredoxin
Nitrogen
Oxidation-Reduction
Protein Multimerization
Sulfur
Determination of the melanocortin-4 receptor structure identifies Ca2+ as a cofactor for ligand binding
期刊论文
, 2020, 卷号: 368, 期号: 6489
作者:
Yu J.
;
Gimenez L.E.
;
Hernandez C.C.
;
Wu Y.
;
Wein A.H.
;
Han G.W.
;
McClary K.
;
Mittal S.R.
;
Burdsall K.
;
Stauch B.
;
Wu L.
;
Stevens S.N.
;
Peisley A.
;
Williams S.Y.
;
Chen V.
;
Millhauser G.L.
;
Zhao S.
;
Cone R.D.
;
Stevens R.C.
收藏
  |  
浏览/下载:38/0
  |  
提交时间:2020/07/28
alpha intermedin
calcium ion
cyclic AMP
G protein coupled receptor
heterotrimeric guanine nucleotide binding protein
inwardly rectifying potassium channel
inwardly rectifying potassium channel subunit Kir7.1
melanocortin 4 receptor
n acetyl alpha intermedin[4-10]cyclo[4 norleucine 5 aspartic acid 7 [3 (2 naphthyl)alanine] 10 lysinamide]
unclassified drug
calcium
G protein coupled receptor
intermedin
inwardly rectifying potassium channel
Kir7.1 channel
ligand
melanocortin 4 receptor
n acetyl alpha intermedin[4-10]cyclo[4 norleucine 5 aspartic acid 7 [3 (2 naphthyl)alanine] 10 lysinamide]
protein binding
calcium
chemical binding
homeostasis
hormone
ligand
obesity
peptide
protein
Article
binding affinity
complex formation
crystallization
drug structure
extracellular calcium
human
ligand binding
priority journal
protein structure
receptor blocking
signal transduction
chemistry
genetics
mutation
protein multimerization
protein secondary structure
X ray crystallography
Calcium
Crystallography, X-Ray
Cyclic AMP
Humans
Ligands
Melanocyte-Stimulating Hormones
Mutation
Potassium Channels, Inwardly Rectifying
Protein Binding
Protein Multimerization
Protein Structure, Secondary
Receptor, Melanocortin, Type 4
Receptors, G-Protein-Coupled
Signal Transduction
Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2
期刊论文
, 2020, 卷号: 367, 期号: 6485
作者:
Yan R.
;
Zhang Y.
;
Li Y.
;
Xia L.
;
Guo Y.
;
Zhou Q.
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2020/07/28
angiotensin converting enzyme 2
coronavirus spike glycoprotein
heterodimer
homodimer
amino acid transporter
angiotensin converting enzyme 2
dipeptidyl carboxypeptidase
protein binding
SLC6A19 protein, human
spike protein, SARS-CoV-2
virus receptor
enzyme
gene
gene expression
protein
ultrastructure
virus
Article
binding site
complex formation
controlled study
coronavirus disease 2019
cryoelectron microscopy
dimerization
embryo
enzyme structure
human
human cell
nonhuman
priority journal
protein domain
SARS-related coronavirus
Severe acute respiratory syndrome coronavirus 2
amino acid sequence
Betacoronavirus
Coronavirus infection
molecular model
pandemic
protein multimerization
SARS coronavirus
sequence alignment
ultrastructure
virus pneumonia
Coronavirus
SARS coronavirus
Amino Acid Sequence
Amino Acid Transport Systems, Neutral
Betacoronavirus
Coronavirus Infections
Cryoelectron Microscopy
Humans
Models, Molecular
Pandemics
Peptidyl-Dipeptidase A
Pneumonia, Viral
Protein Binding
Protein Domains
Protein Multimerization
Receptors, Virus
SARS Virus
Sequence Alignment
Spike Glycoprotein, Coronavirus
Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation
期刊论文
, 2020, 卷号: 367, 期号: 6483
作者:
Wrapp D.
;
Wang N.
;
Corbett K.S.
;
Goldsmith J.A.
;
Hsieh C.-L.
;
Abiona O.
;
Graham B.S.
;
McLellan J.S.
收藏
  |  
浏览/下载:36/0
  |  
提交时间:2020/07/28
2019 nCoV S protein
angiotensin converting enzyme 2
unclassified drug
viral protein
angiotensin converting enzyme 2
coronavirus spike glycoprotein
dipeptidyl carboxypeptidase
monoclonal antibody
protein binding
severe acute respiratory syndrome coronavirus 2
virus antibody
virus receptor
antibody
detection method
electron microscopy
protein
public health
severe acute respiratory syndrome
virus
Article
binding affinity
biophysics
corona virus disease 2019
coronavirus disease 2019
Coronavirus infection
cross reaction
cryoelectron microscopy
molecular dynamics
nonhuman
priority journal
protein binding
protein structure
SARS coronavirus
Severe acute respiratory syndrome coronavirus 2
virus transmission
virus virulence
Betacoronavirus
chemistry
cryoelectron microscopy
image processing
immunology
metabolism
molecular model
protein conformation
protein domain
protein multimerization
ultrastructure
Coronavirus
SARS coronavirus
Antibodies, Monoclonal
Antibodies, Viral
Betacoronavirus
Cross Reactions
Cryoelectron Microscopy
Image Processing, Computer-Assisted
Models, Molecular
Peptidyl-Dipeptidase A
Protein Binding
Protein Conformation
Protein Domains
Protein Multimerization
Receptors, Virus
SARS Virus
Spike Glycoprotein, Coronavirus