Faster access than browser!
37 relations: ACTC1, Alanine, Alpha helix, Amino acid, Arthrogryposis, ATPase, C-terminus, Calcium, Cardiac muscle, Coiled coil, Contractility, Diastole, Gene, Heart failure, Muscle contraction, MYH7, Myosin, Nemaline myopathy, PDLIM7, Phosphorylation, Protein, Protein isoform, Protein–protein interaction, RRAD, Sarcoplasmic reticulum, Serine, Skeletal muscle, Striated muscle tissue, Systole, TNNI3, TNNT2, TNNT3, TPM1, Troponin, Troponin C type 1, Ventricle (heart), Ventricular hypertrophy.
ACTC1
ACTC1 encodes cardiac muscle alpha actin.
New!!: TPM2 and ACTC1 · See more »
Alanine
Alanine (symbol Ala or A) is an α-amino acid that is used in the biosynthesis of proteins.
New!!: TPM2 and Alanine · See more »
Alpha helix
The alpha helix (α-helix) is a common motif in the secondary structure of proteins and is a righthand-spiral conformation (i.e. helix) in which every backbone N−H group donates a hydrogen bond to the backbone C.
New!!: TPM2 and Alpha helix · See more »
Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
New!!: TPM2 and Amino acid · See more »
Arthrogryposis
Arthrogryposis multiplex congenital (AMC), or simply arthrogryposis, describes congenital joint contracture in two or more areas of the body.
New!!: TPM2 and Arthrogryposis · See more »
ATPase
ATPases (adenylpyrophosphatase, ATP monophosphatase, triphosphatase, SV40 T-antigen, adenosine 5'-triphosphatase, ATP hydrolase, complex V (mitochondrial electron transport), (Ca2+ + Mg2+)-ATPase, HCO3−-ATPase, adenosine triphosphatase) are a class of enzymes that catalyze the decomposition of ATP into ADP and a free phosphate ion.
New!!: TPM2 and ATPase · See more »
C-terminus
The C-terminus (also known as the carboxyl-terminus, carboxy-terminus, C-terminal tail, C-terminal end, or COOH-terminus) is the end of an amino acid chain (protein or polypeptide), terminated by a free carboxyl group (-COOH).
New!!: TPM2 and C-terminus · See more »
Calcium
Calcium is a chemical element with symbol Ca and atomic number 20.
New!!: TPM2 and Calcium · See more »
Cardiac muscle
Cardiac muscle (heart muscle) is one of the three major types of muscle, the others being skeletal and smooth muscle.
New!!: TPM2 and Cardiac muscle · See more »
Coiled coil
A coiled coil is a structural motif in proteins in which 2–7 alpha-helices are coiled together like the strands of a rope (dimers and trimers are the most common types).
New!!: TPM2 and Coiled coil · See more »
Contractility
Contractility refers to the ability for self-contraction, especially of the muscles, or similar active biological tissue.
New!!: TPM2 and Contractility · See more »
Diastole
Diastole is the part of the cardiac cycle during which the heart refills with blood after the emptying done during systole (contraction).
New!!: TPM2 and Diastole · See more »
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
New!!: TPM2 and Gene · See more »
Heart failure
Heart failure (HF), often referred to as congestive heart failure (CHF), is when the heart is unable to pump sufficiently to maintain blood flow to meet the body's needs.
New!!: TPM2 and Heart failure · See more »
Muscle contraction
Muscle contraction is the activation of tension-generating sites within muscle fibers.
New!!: TPM2 and Muscle contraction · See more »
MYH7
MYH7 is a gene encoding a myosin heavy chain beta (MHC-β) isoform (slow twitch) expressed primarily in the heart, but also in skeletal muscles (type I fibers).
New!!: TPM2 and MYH7 · See more »
Myosin
Myosins are a superfamily of motor proteins best known for their roles in muscle contraction and in a wide range of other motility processes in eukaryotes.
New!!: TPM2 and Myosin · See more »
Nemaline myopathy
Nemaline myopathy (also called rod myopathy or nemaline rod myopathy) is a congenital, hereditary neuromuscular disorder with many symptoms that can occur such as muscle weakness, hypoventilation, swallowing dysfunction, and impaired speech ability.
New!!: TPM2 and Nemaline myopathy · See more »
PDLIM7
PDZ and LIM domain protein 7 is a protein that in humans is encoded by the PDLIM7 gene.
New!!: TPM2 and PDLIM7 · See more »
Phosphorylation
In chemistry, phosphorylation of a molecule is the attachment of a phosphoryl group.
New!!: TPM2 and Phosphorylation · See more »
Protein
Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.
New!!: TPM2 and Protein · See more »
Protein isoform
A protein isoform, or "protein variant" is a member of a set of highly similar proteins that originate from a single gene or gene family and are the result of genetic differences.
New!!: TPM2 and Protein isoform · See more »
Protein–protein interaction
Protein–protein interactions (PPIs) are the physical contacts of high specificity established between two or more protein molecules as a result of biochemical events steered by electrostatic forces including the hydrophobic effect.
New!!: TPM2 and Protein–protein interaction · See more »
RRAD
GTP-binding protein RAD is a protein that in humans is encoded by the RRAD gene.
New!!: TPM2 and RRAD · See more »
Sarcoplasmic reticulum
The sarcoplasmic reticulum (SR) is a membrane-bound structure found within muscle cells that is similar to the endoplasmic reticulum in other cells.
New!!: TPM2 and Sarcoplasmic reticulum · See more »
Serine
Serine (symbol Ser or S) is an ɑ-amino acid that is used in the biosynthesis of proteins.
New!!: TPM2 and Serine · See more »
Skeletal muscle
Skeletal muscle is one of three major muscle types, the others being cardiac muscle and smooth muscle.
New!!: TPM2 and Skeletal muscle · See more »
Striated muscle tissue
Striated muscle tissue is a muscle tissue that features repeating functional units called sarcomeres, in contrast with smooth muscle tissue which does not.
New!!: TPM2 and Striated muscle tissue · See more »
Systole
The systole is that part of the cardiac cycle during which some chambers of the heart muscle contract after refilling with blood.
New!!: TPM2 and Systole · See more »
TNNI3
Troponin I, cardiac muscle is a protein that in humans is encoded by the TNNI3 gene.
New!!: TPM2 and TNNI3 · See more »
TNNT2
Cardiac muscle troponin T (cTnT), is a protein which in humans is encoded by the TNNT2 gene.
New!!: TPM2 and TNNT2 · See more »
TNNT3
Fast skeletal muscle troponin T (fTnT) is a protein that in humans is encoded by the TNNT3 gene.
New!!: TPM2 and TNNT3 · See more »
TPM1
Tropomyosin alpha-1 chain is a protein that in humans is encoded by the TPM1 gene.
New!!: TPM2 and TPM1 · See more »
Troponin
bibcode.
New!!: TPM2 and Troponin · See more »
Troponin C type 1
Troponin C, also known as TN-C or TnC, is a protein that resides in the troponin complex on actin thin filaments of striated muscle (cardiac, fast-twitch skeletal, or slow-twitch skeletal) and is responsible for binding calcium to activate muscle contraction.
New!!: TPM2 and Troponin C type 1 · See more »
Ventricle (heart)
A ventricle is one of two large chambers in the heart that collect and expel blood received from an atrium towards the peripheral beds within the body and lungs.
New!!: TPM2 and Ventricle (heart) · See more »
Ventricular hypertrophy
Ventricular hypertrophy (VH) is thickening of the walls of a ventricle (lower chamber) of the heart.
New!!: TPM2 and Ventricular hypertrophy · See more »
Redirects here:
References
[1] https://en.wikipedia.org/wiki/TPM2
