PROTEIN SYNTHESIS:During the protein synthesis, the amino acids are connected to form peptides. Later on they disconnect from the mRNA. The polypeptide can either then form into sheets or a helix. Both the sheets and helix shape fold to create proteins .
Thursday, February 2, 2012
BOW 1 (Transcription,Translation and Protein Synthesis)
PROTEIN SYNTHESIS:During the protein synthesis, the amino acids are connected to form peptides. Later on they disconnect from the mRNA. The polypeptide can either then form into sheets or a helix. Both the sheets and helix shape fold to create proteins .
BLAST Gene WS
ELN elastin [ Homo sapiens ](Gene 2)
Gene ID: 2006, updated on 22-Jan-2012Summary
- Official Symbol
- ELNprovided by HGNC
- Official Full Name
- elastinprovided by HGNC
- Primary source
- HGNC:3327
- See related
- Ensembl:ENSG00000049540; HPRD:00556; MIM:130160; Vega:OTTHUMG00000150229
- Gene type
- protein coding
- RefSeq status
- REVIEWED
- Organism
- Homo sapiens
- Lineage
- Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
- Also known as
- WS; WBS; SVAS
- Summary
- This gene encodes a protein that is one of the two components of elastic fibers. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PSEN2 presenilin 2 (Alzheimer disease 4) [ Homo sapiens ](Gene 3)
Gene ID: 5664, updated on 21-Jan-2012Summary
- Official Symbol
- PSEN2provided by HGNC
- Official Full Name
- presenilin 2 (Alzheimer disease 4)provided by HGNC
- Primary source
- HGNC:9509
- See related
- Ensembl:ENSG00000143801; HPRD:02860; MIM:600759; Vega:OTTHUMG00000037563
- Gene type
- protein coding
- RefSeq status
- REVIEWED
- Organism
- Homo sapiens
- Lineage
- Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
- Also known as
- AD4; PS2; AD3L; STM2; CMD1V
- Summary
- Alzheimer's disease (AD) patients with an inherited form of the disease carry mutations in the presenilin proteins (PSEN1 or PSEN2) or the amyloid precursor protein (APP). These disease-linked mutations result in increased production of the longer form of amyloid-beta (main component of amyloid deposits found in AD brains). Presenilins are postulated to regulate APP processing through their effects on gamma-secretase, an enzyme that cleaves APP. Also, it is thought that the presenilins are involved in the cleavage of the Notch receptor such that, they either directly regulate gamma-secretase activity, or themselves act are protease enzymes. Two alternatively spliced transcript variants encoding different isoforms of PSEN2 have been identified. [provided by RefSeq, Jul 2008]
FBN1 fibrillin 1 [ Homo sapiens ](Gene 5)
Gene ID: 2200, updated on 29-Jan-2012Summary
- Official Symbol
- FBN1provided by HGNC
- Official Full Name
- fibrillin 1provided by HGNC
- Primary source
- HGNC:3603
- See related
- Ensembl:ENSG00000166147; HPRD:00618; MIM:134797; Vega:OTTHUMG00000172218
- Gene type
- protein coding
- RefSeq status
- REVIEWED
- Organism
- Homo sapiens
- Lineage
- Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
- Also known as
- FBN; SGS; WMS; MASS; MFS1; OCTD; SSKS; WMS2; ACMICD; GPHYSD2
- Summary
- This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome. [provided by RefSeq, Jul 2008]
RB1 retinoblastoma 1 [ Homo sapiens ](Gene 6)
Gene ID: 5925, updated on 29-Jan-2012Summary
- Official Symbol
- RB1provided by HGNC
- Official Full Name
- retinoblastoma 1provided by HGNC
- Primary source
- HGNC:9884
- Locus tag
- RP11-174I10.1
- See related
- Ensembl:ENSG00000139687; HPRD:01574; MIM:614041; Vega:OTTHUMG00000016900
- Gene type
- protein coding
- RefSeq status
- REVIEWED
- Organism
- Homo sapiens
- Lineage
- Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
- Also known as
- RB; pRb; OSRC; pp110; p105-Rb
- Summary
- The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]
Saturday, January 21, 2012
Osmosis Jones
The three differences that the movie Osmosis Jones is like our system is that when our body is attacked because of germs, our body sends white blood cells to get rid of them. Our body begin with simple symptoms that later on develops into more serious ones. Also, our body tries to prevent bacteria from entering our body. The movie is unlike our immune system because we do not have actual diseases that are left unprotected until it gets very serious. Our body works in different function with the way on how Jones tries to stop the Red Death by actually fighting it in Shane's eye. Also, our body responds immediately and takes full action when a disease occurs
Dominanat/Recessive Genes
A dominant gene is a gene that is more likely to be shown through the offspring. A recessive gene is the gene,that when compared to the dominant, is less like likely to appear in an offspring.
Example: A couple decide to have a child. The father is tall in height (TT) and the mother is not (tt). This means that the domimant trait would be having the height be tall while the recessive would not.
Example: A couple decide to have a child. The father is tall in height (TT) and the mother is not (tt). This means that the domimant trait would be having the height be tall while the recessive would not.
Dangeros Virus
If I were in charge of protecting the Us from a deadly virus, I would try to figure out the main source of the deadly disease and destroy what is causing it. Then, the people tat were infected were to be kept away from the uninfected people until they are treated or a cure was to be discovered. By doing this, it protects the uninfected people from getting the disease and having it spread to healthy people. If killing the main source of the disease, meaning where it started, that it would prevent the disease to continually spread about.
Sunday, January 8, 2012
Benefits of Fungi
Sugar from Chlorophyll
Plants make sugars from chlorophyll. Plants produce sugars in the process of photosynthesis. The chloroplasts capture energy from the sun with the help from the chlorophyll. With this the plant converts the sun"s energy, the water and the carbon dioxide to create glucose (sugars) and oxygen (http://www.sucrose.com/learn.html).
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