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index medicus (289) 289
humans (252) 252
biochemistry & molecular biology (177) 177
acetylation (172) 172
animals (159) 159
proteins (116) 116
cell biology (106) 106
amino acid sequence (85) 85
molecular sequence data (79) 79
n-terminal acetylation (77) 77
yeast (72) 72
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identification (67) 67
article (62) 62
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acetyltransferases - metabolism (59) 59
protein (59) 59
acetyltransferases - genetics (58) 58
gene expression (57) 57
protein processing, post-translational (57) 57
acetyltransferase (55) 55
research (55) 55
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phosphorylation (47) 47
n-terminal acetyltransferase a (46) 46
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genetics & heredity (45) 45
male (45) 45
n-terminal acetyltransferase e - genetics (45) 45
research article (45) 45
multidisciplinary sciences (44) 44
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enzymes (42) 42
n-terminal acetyltransferase (42) 42
n-terminal acetyltransferase a - genetics (42) 42
physiological aspects (40) 40
protein binding (40) 40
biology (38) 38
proteomics (38) 38
cell line, tumor (37) 37
genes (37) 37
genetic aspects (37) 37
n-terminal domain (37) 37
apoptosis (36) 36
signal transduction (36) 36
biophysics (35) 35
medicine (35) 35
cancer (34) 34
n-terminal acetyltransferase e - metabolism (33) 33
n-terminal kinase (33) 33
life sciences (32) 32
alpha-acetyltransferase (31) 31
saccharomyces cerevisiae - genetics (31) 31
base sequence (29) 29
n-terminal acetyltransferase a - metabolism (29) 29
oncology (29) 29
amino acids (28) 28
n-terminal acetyltransferases (28) 28
sequence alignment (28) 28
substrate specificity (28) 28
escherichia-coli (27) 27
expression (27) 27
genetics (27) 27
ard1 (26) 26
protein structure, tertiary (26) 26
science (26) 26
cell cycle (25) 25
gene-expression (25) 25
hela cells (25) 25
microbiology (25) 25
models, molecular (25) 25
biochemical research methods (24) 24
gene expression regulation (24) 24
phenotype (24) 24
review (24) 24
biochemistry (23) 23
cells (23) 23
in-vivo (23) 23
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gene (22) 22
kinases (22) 22
molecular biology (22) 22
cell proliferation (21) 21
crystal-structure (21) 21
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cells, cultured (20) 20
escherichia coli - genetics (20) 20
fungi (20) 20
post-translational modification (20) 20
protein conformation (20) 20
saccharomyces cerevisiae proteins - metabolism (20) 20
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1. Full Text The Role of N-α-acetyltransferase 10 Protein in DNA Methylation and Genomic Imprinting
by Lee, Chen-Cheng and Lee, Chung-Fan and Peng, Shih-Huan and Shen, Li and Du, Ting-Huei and Kang, Ming-Lun and Xu, Guo-Liang and Upadhyay, Anup K and Cheng, Xiaodong and Yan, Yu-Ting and Zhang, Yi and Juan, Li-Jung
Molecular Cell, ISSN 1097-2765, 10/2017, Volume 68, Issue 1, pp. 89 - 103.e7
Genomic imprinting is an allelic gene expression phenomenon primarily controlled by allele-specific DNA methylation at the imprinting control region (ICR), but... 
Dnmt1 | development | Ogden syndrome | N-α-acetyltransferase | DNA methylation | developmental delay | genomic imprinting | Naa10p | GENE | REPRESSION | METHYLTRANSFERASES | TERMINAL ACETYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | EMBRYONIC STEM-CELLS | SELF-RENEWAL | MAINTAINS | EXPRESSION | BINDING | DELETION | CELL BIOLOGY | Genomic Imprinting | Developmental Disabilities - metabolism | Embryo, Mammalian | Epigenesis, Genetic | Male | Developmental Disabilities - genetics | Mouse Embryonic Stem Cells - metabolism | DNA (Cytosine-5-)-Methyltransferases - metabolism | Genes, Lethal | DNA Methylation | Developmental Disabilities - pathology | Gene Deletion | Female | Mouse Embryonic Stem Cells - pathology | Disease Models, Animal | Genome-Wide Association Study | N-Terminal Acetyltransferase A - deficiency | DNA (Cytosine-5-)-Methyltransferase 1 | Mice, Inbred C57BL | N-Terminal Acetyltransferase A - genetics | RNA, Long Noncoding - genetics | DNA - metabolism | S Phase - genetics | Mice, Knockout | DNA - genetics | DNA (Cytosine-5-)-Methyltransferases - genetics | Animals | N-Terminal Acetyltransferase E - deficiency | N-Terminal Acetyltransferase E - genetics | Protein Binding | Mice | RNA, Long Noncoding - metabolism
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2. Full Text NAA10 mutation causing a novel intellectual disability syndrome with Long QT due to N-terminal acetyltransferase impairment
by Casey, Jillian P and Støve, Svein I and McGorrian, Catherine and Galvin, Joseph and Blenski, Marina and Dunne, Aimee and Ennis, Sean and Brett, Francesca and King, Mary D and Arnesen, Thomas and Lynch, Sally Ann
Scientific Reports, ISSN 2045-2322, 11/2015, Volume 5, Issue 1, p. 16022
We report two brothers from a non-consanguineous Irish family presenting with a novel syndrome characterised by intellectual disability, facial dysmorphism,... 
GTPASE ARL3P | MEMBRANE-PROTEIN SYS1P | COMPLEX | MENTAL-RETARDATION | ACETYLATION | MULTIDISCIPLINARY SCIENCES | PHENOTYPE | REQUIRES | DEVELOPMENTAL DELAY | SEQUENCING DATA | IDENTIFICATION | Humans | N-Terminal Acetyltransferase A - genetics | Male | Intellectual Disability - genetics | Exome - genetics | Phenotype | N-Terminal Acetyltransferases - genetics | Cell Line, Tumor | Long QT Syndrome - genetics | N-Terminal Acetyltransferase E - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | HeLa Cells | Genotype & phenotype | Enzymes | Scoliosis | Intellectual disabilities | N-terminal acetyltransferase | Acetyltransferase | Heredity | Acetylation | Heart diseases | Microphthalmia
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3. Full Text Chemical inhibition of NAT10 corrects defects of laminopathic cells
by Larrieu, Delphine and Britton, Sébastien and Demir, Mukerrem and Rodriguez, Raphaël and Jackson, Stephen P
Science, ISSN 0036-8075, 2014, Volume 344, Issue 6183, pp. 527 - 532
Down-regulation and mutations of the nuclear-architecture proteins lamin A and C cause misshapen nuclei and altered chromatin organization associated with... 
NUCLEOLAR PROTEIN | NUCLEAR MORPHOLOGY | HELA-CELLS | A-TYPE LAMINS | MULTIDISCIPLINARY SCIENCES | FARNESYLATION | HUTCHINSON-GILFORD PROGERIA | MUTATIONS | EXPRESSION | ACETYLTRANSFERASE | FIBROBLASTS | Protein Structure, Tertiary | Chromatin - metabolism | RNA, Small Interfering - genetics | Humans | Progeria - enzymology | Enzyme Inhibitors - pharmacology | Nocodazole - pharmacology | Progeria - genetics | Cell Nucleus - ultrastructure | Hydrazones - chemistry | Hydrazones - pharmacology | N-Terminal Acetyltransferase E - chemistry | Microtubules - metabolism | N-Terminal Acetyltransferase E - antagonists & inhibitors | Cell Nucleus - genetics | Enzyme Inhibitors - chemistry | Lamin Type A - genetics | Cell Line, Tumor | N-Terminal Acetyltransferase E - genetics | Thiazoles - chemistry | Thiazoles - pharmacology | Cell Nucleus - drug effects | Genetic research | Genetic aspects | Research | Gene mutations | Progeria | Proteins | Pathology | Chromatin | Cellular biology | DNA damage | Molecular chemistry | Mutation | Organic chemistry | Chemical Sciences
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4. Full Text Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency
by Saunier, Chloé and Støve, Svein Isungset and Popp, Bernt and Gérard, Bénédicte and Blenski, Marina and Ahmew, Nicholas and de Bie, Charlotte and Goldenberg, Paula and Isidor, Bertrand and Keren, Boris and Leheup, Bruno and Lampert, Laetitia and Mignot, A and Tezcan, Kamer and Mancini, Grazia and Nava, Caroline and Wasserstein, Melissa and Bruel, Ange-Line and Thevenon, Julien and Masurel, Alice and Duffourd, Yannis and Kuentz, Paul and Huet, Frédéric and Riviere, J.-B and Slegtenhorst, Marjon and Faivre, Laurence and Piton, Amélie and Reis, Ané and Arnesen, Thomas and Thauvin-Robinet, Christel and Zweier, Christiane
Human Mutation, ISSN 1059-7794, 01/2016, Volume 37, Issue 8, pp. 755 - 764
textabstractN-terminal acetylation is a common protein modification in eukaryotes associated with numerous cellular processes. Inherited mutations in NAA10,... 
X‐linked | N‐terminal acetylation | NAA10 | intellectual disability | X-linked | Intellectual disability | N-terminal acetylation | GTPASE ARL3P | COMPLEX | FEMALES | IDENTIFICATION | MISSENSE MUTATIONS | MEMBRANE-PROTEIN SYS1P | GENETICS & HEREDITY | REQUIRES | X-CHROMOSOME INACTIVATION | ACETYLTRANSFERASE | Genetic Predisposition to Disease | Genetic Association Studies | N-Terminal Acetyltransferase A - deficiency | Humans | N-Terminal Acetyltransferase A - chemistry | N-Terminal Acetyltransferase A - genetics | Models, Molecular | Male | Mutation, Missense | Intellectual Disability - genetics | N-Terminal Acetyltransferase E - chemistry | Genes, X-Linked | Pedigree | N-Terminal Acetyltransferase E - deficiency | Germ-Line Mutation | N-Terminal Acetyltransferase E - genetics | Female | Mosaicism | Acetylation | Enzymes | Acetates | Genetic aspects | Proteins | Genotype & phenotype | Genetic disorders | Mutation | Life Sciences | Genetics
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5. Full Text De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females
by Popp, Bernt and Støve, Svein I and Endele, Sabine and Myklebust, Line M and Hoyer, Juliane and Sticht, Heinrich and Azzarello-Burri, Silvia and Rauch, Anita and Arnesen, Thomas and Reis, André
European Journal of Human Genetics, ISSN 1018-4813, 05/2015, Volume 23, Issue 5, pp. 602 - 609
Recent studies revealed the power of whole-exome sequencing to identify mutations in sporadic cases with non-syndromic intellectual disability. We now... 
N-TERMINAL ACETYLTRANSFERASE | INTELLECTUAL DISABILITY | ARD1 | COMPLEX | HUMAN GENOME | COFFIN-LOWRY-SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | LENZ MICROPHTHALMIA SYNDROME | ALPHA-ACETYLTRANSFERASE | AUTISM SPECTRUM DISORDERS | SEQUENCING DATA | Phenotypes | Intellectual disabilities | Genes | Licenses | Genomes | Males | Proteins | Genotype & phenotype | Missense mutation | Cell cycle | Genetics | N-terminal acetyltransferase | Acetyltransferase | Mutation | Acetylation
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6. Full Text GSK-3β-regulated N-acetyltransferase 10 is involved in colorectal cancer invasion
by Zhang, Hong and Hou, Wei and Wang, Hua-Li and Liu, Hai-Jing and Jia, Xin-Ying and Zheng, Xing-Zheng and Zou, Yong-Xin and Li, Xin and Hou, Lin and McNutt, Michael A and Zhang, Bo
Clinical cancer research : an official journal of the American Association for Cancer Research, ISSN 1078-0432, 09/2014, Volume 20, Issue 17, pp. 4717 - 4729
Purpose: NAT10 (N-acetyltransferase 10) is a nucleolar protein, but may show subcellular redistribution in colorectal carcinoma. In this study, we evaluated... 
GLYCOGEN-SYNTHASE KINASE-3-BETA | WNT SIGNALING PATHWAY | TRANSCRIPTIONAL ACTIVATION | PROTEIN | ONCOLOGY | NUCLEOLIN | CELL-SURFACE | RECEPTOR | MECHANISMS | BETA-CATENIN | EXPRESSION | Cell Proliferation - genetics | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Colorectal Neoplasms - genetics | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | N-Terminal Acetyltransferase E - biosynthesis | Glycogen Synthase Kinase 3 beta | Male | Cadherins - biosynthesis | beta Catenin - biosynthesis | Glycogen Synthase Kinase 3 - genetics | Aged, 80 and over | Cell Line, Tumor | N-Terminal Acetyltransferase E - genetics | Adult | Female | Aged | Colorectal Neoplasms - pathology | Neoplasm Invasiveness - genetics
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7. Full Text Phosphoglycerate Kinase 1 Phosphorylates Beclin1 to Induce Autophagy
by Qian, Xu and Li, Xinjian and Cai, Qingsong and Zhang, Chuanbao and Yu, Qiujing and Jiang, Bing-Hua and Jiang, Tao and Jiang, Yuhui and Lee, Jong-Ho and Hawke, David and Wang, Yugang and Xia, Yan and Zheng, Yanhua and Liu, David X and Lu, Zhimin
Molecular Cell, ISSN 1097-2765, 03/2017, Volume 65, Issue 5, pp. 917 - 931.e6
Autophagy is crucial for maintaining cell homeostasis. However, the precise mechanism underlying autophagy initiation remains to be defined. Here, we... 
ARD1 | autophagy | tumor | PGK1 | mTOR | Beclin1 | VPS34 | BREAST-CANCER | NUCLEOTIDE SYNTHESIS | METABOLISM | SIGNALING PATHWAY | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PHOSPHATIDYLINOSITOL 3-KINASE COMPLEXES | GROWTH | TUMOR-CELLS | BETA-CATENIN | TUMORIGENESIS | CELL BIOLOGY | Glioblastoma - enzymology | Glutamine - deficiency | Phosphorylation | Cell Proliferation | TOR Serine-Threonine Kinases - metabolism | Humans | Autophagosomes - enzymology | Brain Neoplasms - pathology | Autophagy | Tumor Hypoxia | TOR Serine-Threonine Kinases - genetics | Transfection | Glioblastoma - genetics | RNA Interference | Time Factors | HEK293 Cells | Female | Acetylation | Phosphoglycerate Kinase - genetics | Brain Neoplasms - enzymology | Signal Transduction | N-Terminal Acetyltransferase A - genetics | Brain Neoplasms - genetics | Class III Phosphatidylinositol 3-Kinases - metabolism | Tumor Burden | Autophagosomes - pathology | Animals | N-Terminal Acetyltransferase A - metabolism | Class III Phosphatidylinositol 3-Kinases - genetics | Mice, Nude | Glioblastoma - pathology | Beclin-1 - genetics | Cell Line, Tumor | N-Terminal Acetyltransferase E - genetics | Protein Binding | Beclin-1 - metabolism | N-Terminal Acetyltransferase E - metabolism | Phosphoglycerate Kinase - metabolism | Enzymes | Medical colleges | Gliomas | Pancreatic cancer | Brain tumors | Physiological aspects | Phospholipids | Protein kinases | Glutamine
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8. Full Text NAA10 controls osteoblast differentiation and bone formation as a feedback regulator of Runx2
by Yoon, Haejin and Kim, Hye-Lim and Chun, Yang-Sook and Shin, Dong Hoon and Lee, Kyoung-Hwa and Shin, Chan Soo and Lee, Dong Yeon and Kim, Hong-Hee and Lee, Zang Hee and Ryoo, Hyun-Mo and Lee, Mi-Ni and Oh, Goo Taeg and Park, Jong-Wan
Nature Communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, p. 5176
Runt-related transcription factor 2 (Runx2) transactivates many genes required for osteoblast differentiation. The role of N-alpha-acetyltransferase 10 (NAA10,... 
N-TERMINAL ACETYLTRANSFERASE | ARD1 | OSTEOCALCIN GENE | ACETYLATION | PHOSPHORYLATION | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | GROWTH | RECEPTOR | MOLECULAR-BASIS | MORPHOGENETIC PROTEIN-2 | N-Terminal Acetyltransferase A - physiology | Bone Regeneration - physiology | Osteogenesis - physiology | N-Terminal Acetyltransferase E - physiology | N-Terminal Acetyltransferases - deficiency | Molecular Sequence Data | Male | Skull - physiology | N-Terminal Acetyltransferases - genetics | Skull - injuries | Female | Osteoblasts - cytology | Cell Differentiation - physiology | Amino Acid Sequence | N-Terminal Acetyltransferase A - deficiency | Osteoblasts - physiology | Cells, Cultured | Core Binding Factor Alpha 1 Subunit - physiology | N-Terminal Acetyltransferase A - genetics | Rats | Mice, Transgenic | Rats, Sprague-Dawley | Mice, Knockout | Animals | N-Terminal Acetyltransferase E - deficiency | N-Terminal Acetyltransferase E - genetics | Signal Transduction - physiology | Mice | Wound Healing - physiology | Feedback, Physiological - physiology | N-Terminal Acetyltransferases - physiology
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9. Full Text Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies
by Cheng, Hanyin and Dharmadhikari, Avinash V and Varland, Sylvia and Ma, Ning and Domingo, Deepti and Kleyner, Robert and Rope, Alan F and Yoon, Margaret and Stray-Pedersen, Asbjørg and Posey, Jennifer E and Crews, Sarah R and Eldomery, Mohammad K and Akdemir, Zeynep Coban and Lewis, Andrea M and Sutton, Vernon R and Rosenfeld, Jill A and Conboy, Erin and Agre, Katherine and Xia, Fan and Walkiewicz, Magdalena and Longoni, Mauro and High, Frances A and van Slegtenhorst, Marjon A and Mancini, Grazia M.S and Finnila, Candice R and van Haeringen, Arie and den Hollander, Nicolette and Ruivenkamp, Claudia and Naidu, Sakkubai and Mahida, Sonal and Palmer, Elizabeth E and Murray, Lucinda and Lim, Derek and Jayakar, Parul and Parker, Michael J and Giusto, Stefania and Stracuzzi, Emanuela and Romano, Corrado and Beighley, Jennifer S and Bernier, Raphael A and Küry, Sébastien and Nizon, Mathilde and Corbett, Mark A and Shaw, Marie and Gardner, Alison and Barnett, Christopher and Armstrong, Ruth and Kassahn, Karin S and Van Dijck, Anke and Vandeweyer, Geert and Kleefstra, Tjitske and Schieving, Jolanda and Jongmans, Marjolijn J and de Vries, Bert B.A and Pfundt, Rolph and Kerr, Bronwyn and Rojas, Samantha K and Boycott, Kym M and Person, Richard and Willaert, Rebecca and Eichler, Evan E and Kooy, R. Frank and Yang, Yaping and Wu, Joseph C and Lupski, James R and Arnesen, Thomas and Cooper, Gregory M and Chung, Wendy K and Gecz, Jozef and Stessman, Holly A.F and Meng, Linyan and Lyon, Gholson J
The American Journal of Human Genetics, ISSN 0002-9297, 05/2018, Volume 102, Issue 5, pp. 985 - 994
N-alpha-acetylation is a common co-translational protein modification that is essential for normal cell function in humans. We previously identified the... 
NAA10 | neurodevelopmental disorder | Ogden syndrome | N-terminal acetylation (NTA) | NAA15 | NatA complex | N-terminal acetyltransferases (NATs) | intellectual disability | autism | congenital heart defects | N-TERMINAL ACETYLATION | HEART-DISEASE | DE-NOVO MUTATIONS | ARF-LIKE GTPASE | GENES | GENETICS & HEREDITY | CELLULAR-PROTEINS | MODEL | IDENTIFICATION | SACCHAROMYCES-CEREVISIAE | ACETYLTRANSFERASE 10 PROTEIN | Humans | Middle Aged | Male | RNA, Messenger - metabolism | Intellectual Disability - genetics | Genetic Variation | Saccharomyces cerevisiae - metabolism | Adult | Female | Child | Abnormalities, Multiple - genetics | Autism Spectrum Disorder - genetics | Cell Line | Genetic Predisposition to Disease | RNA, Messenger - genetics | Gene Expression Regulation | N-Terminal Acetyltransferase A - genetics | Exons - genetics | Mutation - genetics | Phenotype | N-Terminal Acetyltransferase A - metabolism | Pedigree | Adolescent | N-Terminal Acetyltransferase E - genetics | N-Terminal Acetyltransferase E - metabolism | Genetic variation | Physiological aspects | Genetic aspects | Acetylation | Research | Mental retardation | Risk factors | Report
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10. Full Text N‐terminal acetylome analysis reveals the specificity of Naa50 (Nat5) and suggests a kinetic competition between N‐terminal acetyltransferases and methionine aminopeptidases
by Damme, Petra and Hole, Kristine and Gevaert, Kris and Arnesen, Thomas
PROTEOMICS, ISSN 1615-9853, 07/2015, Volume 15, Issue 14, pp. 2436 - 2446
Cotranslational N‐terminal (Nt‐) acetylation of nascent polypeptides is mediated by N‐terminal acetyltransferases (NATs). The very N‐terminal amino acid... 
NAT | Naa50 | N‐terminomics | Methionine aminopeptidase | Acetylation | Nt‐acetylome | N‐terminal acetyltransferase | N-terminomics | N-terminal acetyltransferase | Nt-acetylome | COMPLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | ALPHA-ACETYLTRANSFERASE | IDENTIFICATION | NASCENT POLYPEPTIDE-CHAINS | YEAST | PEPTIDES | IN-VIVO | PROTEINS | PROTEOMICS | Saccharomyces cerevisiae - genetics | Humans | Glycoproteins - metabolism | Molecular Sequence Data | Substrate Specificity | Saccharomyces cerevisiae - metabolism | N-Terminal Acetyltransferase D - genetics | Gene Deletion | Aminopeptidases - chemistry | Glycoproteins - chemistry | Aminopeptidases - metabolism | Recombinant Proteins - metabolism | Amino Acid Sequence | Gene Expression | Methionine - metabolism | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Saccharomyces cerevisiae Proteins - genetics | Saccharomyces cerevisiae - chemistry | N-Terminal Acetyltransferase D - metabolism | N-Terminal Acetyltransferase E - chemistry | N-Terminal Acetyltransferase D - chemistry | Saccharomyces cerevisiae Proteins - metabolism | N-Terminal Acetyltransferase E - genetics | Kinetics | N-Terminal Acetyltransferase E - metabolism | Saccharomyces cerevisiae Proteins - chemistry | Proteins | Amino acids | Aminopeptidases | Analysis | Competition | Yeast | Polypeptides | Substrate specificity | Deduction | Methionine | Amino acid sequence | Catalysis | Substrates
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11. Full Text A Saccharomyces cerevisiae model reveals in vivo functional impairment of the Ogden syndrome N-terminal acetyltransferase NAA10 Ser37Pro mutant
by Van Damme, Petra and Støve, Svein I and Glomnes, Nina and Gevaert, Kris and Arnesen, Thomas
Molecular and Cellular Proteomics, ISSN 1535-9476, 2014, Volume 13, Issue 8, pp. 2031 - 2041
N-terminal acetylation (Nt-acetylation) occurs on the majority of eukaryotic proteins and is catalyzed by N-terminal acetyltransferases (NATs). Nt-acetylation... 
YEAST | ARD1 | COMPLEX | SPECIFICITIES | ACETYLATION | BIOCHEMICAL RESEARCH METHODS | CELL-CYCLE | ALPHA-ACETYLTRANSFERASE | IDENTIFICATION | MOLECULAR-BASIS | METHIONINE AMINOPEPTIDASE | Species Specificity | Proline - metabolism | Saccharomyces cerevisiae - genetics | Humans | N-Terminal Acetyltransferase A - genetics | Saccharomyces cerevisiae Proteins - genetics | N-Terminal Acetyltransferases - metabolism | Serine - metabolism | Phenotype | N-Terminal Acetyltransferase A - metabolism | N-Terminal Acetyltransferases - genetics | Saccharomyces cerevisiae Proteins - metabolism | N-Terminal Acetyltransferase E - genetics | Acetylation | N-Terminal Acetyltransferase E - metabolism | Saccharomyces cerevisiae - growth & development | Amino Acid Substitution
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12. Full Text Implications for the evolution of eukaryotic amino-terminal acetyltransferase (NAT) enzymes from the structure of an archaeal ortholog
by Glen Liszczak and Ronen Marmorstein
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2013, Volume 110, Issue 36, pp. 14652 - 14657
Amino-terminal acetylation is a ubiquitous modification in eukaryotes that is involved in a growing number of biological processes.There are six known... 
Proteins | Enzymes | Active sites | Substrate specificity | Archaea | Evolution | Acetylation | Catalysis | Enzyme substrates | Cartoons | X-ray crystallography | Evolutionary biology | Enzymology | Structural biology | YEAST | COMPLEX | evolutionary biology | ACETYLATION | MULTIDISCIPLINARY SCIENCES | structural biology | N-ACETYLTRANSFERASE | enzymology | PROTEOMICS | N-Terminal Acetyltransferase A - chemistry | Protein Multimerization | Archaeal Proteins - chemistry | Molecular Sequence Data | Crystallography, X-Ray | N-Terminal Acetyltransferases - chemistry | N-Terminal Acetyltransferases - metabolism | N-Terminal Acetyltransferases - genetics | Archaeal Proteins - genetics | Acetyl Coenzyme A - chemistry | Archaeal Proteins - metabolism | Eukaryotic Cells - enzymology | Protein Structure, Tertiary | Amino Acid Sequence | Catalytic Domain - genetics | N-Terminal Acetyltransferase A - genetics | Models, Molecular | Sulfolobus solfataricus - enzymology | Acetyl Coenzyme A - metabolism | Sequence Homology, Amino Acid | N-Terminal Acetyltransferase E - chemistry | N-Terminal Acetyltransferase A - metabolism | N-Terminal Acetyltransferase E - genetics | Protein Binding | Kinetics | Mutation | N-Terminal Acetyltransferase E - metabolism | Evolution, Molecular | Microbial genetics | Transferases | Bacteria, Thermophilic | Crystals | Physiological aspects | Evolutionary genetics | Genetic aspects | Research | Structure | Index Medicus | Biological Sciences
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