Saturday, May 14, 2022

How To Draw A Dna Strand

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A Little More About Dna

How to draw a DNA Strand in 3 Easy Steps | #shorts

Heres a model of DNA:

This model is made from data giving the position of the atoms in a crystal of DNA using X-ray crystallography one way to take a picture of molecule. Its the real deal, in detail we can see where every atom is.

There are several forms of DNA. The best-known are A, B and Z.

The classical form, the one that most of DNA our genes are made of is in, is B-form DNA like that in the animated model above and the illustration to the left.

You can see that DNA is made of two helical chains with the DNA bases in the middle.

B-form DNA has two grooves of different sizes: the major and minor grooves, as marked in the illustration to the left.

Reminds you of keys in music, right?

The major groove is the wider valley between the phosphate backbones.

The minor groove is the narrow one.

Next Draw The Inner Structure Of The Dna

For this second part of your DNA drawing, we will be drawing the inner ladder of the drawing. These straight structures are what actually contains the information of the DNA strand.

Using a ruler, you can draw the first two of these rungs in the upper-most part of the molecule. With the way the backbone is curled in this section, we wont see the very ends of these rungs.

It will be a different story for the next section, as seeing as we will see the inner section of the backbone, we will actually see the ends of these strands.

Then you can draw the next section of rungs as they appear, and then we can move on to step 3!

Learn To Draw Dna For Science Class

See our collection of How-To-Draw tutorial instructions for young kids! Check out our collection of free coloring pages for kids while youre here too. Were a group of independent illustrators that create coloring pages, how to draw tutorials, craft printables, and educational worksheets for kids. We update our resource library regularly so feel free to check back as we add more and more content. Were currently at over 1000+ coloring pages and 500+ how-to-draw stuff guides for kids!

  • Draw a diagonal wave with two troughs and one crest. The wave must be made with two curved lines closely parallel to each other, enclosed with curves on each opposite end.
  • Repeat step one, but this time draw it behind the first wave without overlapping and in the opposite direction. The waves look like they are crossing each other, forming the backbone of the human DNA.
  • In between the backbone, draw pairs of horizontal baselines closely parallel to each other two at the bottom and four on the spaces at the middle and on top. These baselines will have different sizes because of the irregularities the backbones have. You can also make some base pairs a little slanted to add more art.
  • Our DNA has a color combination, so lets add some colors to it! Color the bases from bottom to top with this color sequence green, yellow, green, yellow, red, green, yellow, red, green, yellow. Then, color the DNAs backbone with red and light blue.
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    Making A Model Using Styrofoam Balls

  • 1Gather your supplies. For this version of the project, you will need small styrofoam balls, a needle and thread, paint, and toothpicks.XResearch source
  • 2Paint your styrofoam balls. Choose 6 different colors to represent the sugar and phosphate groups, and the 4 nitrogenous bases. They can be any 6 colors of your choice.
  • You will need to paint 16 sugar balls, 14 phosphate balls, and 4 different colors for each of the nitrogenous bases .
  • You could choose to have one of the colors be white, so that you don’t have to paint some of the styrofoam. This might be easiest for the sugar balls, as it will greatly reduce your total amount of work.
  • 3Pair off the nitrogenous bases. Once the paint has dried, designate 1 color for each of the nitrogenous bases, and then pair them with their matching base. Cytosine always goes with guanine, and thymine always goes with adenine.
  • The order of the colors does not matter, as long as they are in the correct pairs.
  • Stick a toothpick between each of the pairs, leaving a little extra space at the sharp ends of the toothpicks.
  • 4Make the double helix. Using the needle and string, cut a piece that is long enough to go the length of 15 styrofoam balls. Tie a knot at one end of the string, and thread the needle on the other.
  • Line up the styrofoam sugar and phosphate balls, so that they alternate in sets of 15. There should be more sugar balls than phosphate balls.
  • Draw A Complementary Right Side Of The Molecule 6

    How to draw a DNA molecule
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      Specific Sequences Of Nitrogenous Bases That Code For Particular Proteins Or Regulatory Rna Molecules Are Called Genes

      Each strand of DNA is like a recipe book for synthesizing proteins. Certain sequences of nitrogenous bases along the strand encode particular RNA molecules. These sequences are called genes. mRNA molecules transcribed from genes are translated into proteins later.

      Chromosomes can vary widely in their number of base pairs and genes. The longest chromosome in human cells, Chromosome 1, is around 249 million base pairs long and has between 2000 and 2100 distinct genes. Chromosome 21, the shortest human chromosome, consists of 48 million base pairs and contains between 200 and 300 genes. Overall, prokaryotic cells have shorter chromosomes with fewer genes. For example, the bacterium Carsonella rudii has only 159,662 base pairs and 182 genes in its entire genome.

      Although genes get most of the credit for what DNA does, they make up only about 1% of DNA . Genes are separated from one another by sequences of nitrogenous bases that dont provide instructions for RNA synthesis. These are called intergenic regions. Even within genes, there are regions of noncoding DNA called introns.

      Noncoding regions of DNA are important because they provide binding sites for proteins that help activate or deactivate the process of transcription. They can also provide protection for the coding regions. For instance, telomeres consist of repetitive sequences that protect the genetic information on each DNA molecule from being damaged during cell division.

      Only Dna Replication In The 5

      The need for accuracy probably explains why replication occurs only in the 5-to-3 direction. If there were a that added deoxyribonucleoside triphosphates in the 3-to-5 direction, the growing 5-chain end, rather than the incoming mononucleotide, would carry the activating triphosphate. In this case, the mistakes in polymerization could not be simply hydrolyzed away, because the bare 5-chain end thus created would immediately terminate DNA synthesis . It is therefore much easier to correct a mismatched that has just been added to the 3 end than one that has just been added to the 5 end of a DNA chain. Although the mechanism for DNA replication seems at first sight much more than the incorrect mechanism depicted earlier in , it is much more accurate because all DNA synthesis occurs in the 5-to-3 direction.

      An explanation for the 5-to-3 direction of DNA chain growth. Growth in the 5-to-3 direction, shown on the right, allows the chain to continue to be elongated when a mistake in polymerization has been removed by exonucleolytic

      Despite these safeguards against replication errors, DNA polymerases occasionally make mistakes. However, as we shall see later, cells have yet another chance to correct these errors by a process called . Before discussing this mechanism, however, we describe the other types of proteins that function at the .

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      The Sequences Of Nitrogenous Bases On The Two Strands Of A Dna Molecule Are Complementary

      The sequence of nitrogenous bases on one strand of a DNA molecules double helix matches up in a particular way with the sequence on the other strand. Adenine pairs with thymine and cytosine pairs with guanine.

      Why do the nitrogenous bases pair in this specific way? The bases on each strand are joined to the bases on the other strand with hydrogen bonds, but different bases have different chemical structures. Cytosine and thymine are pyrimidines, containing one ring. Adenine and guanine are purines, containing two rings. The pyrimidines pair with the purines: cytosine and guanine form three hydrogen bonds, and adenine and thymine form two.

      By Step Instructions For Drawing Dna

      How to make a DNA strand in After Effects tutorial

      1. Begin by drawing a pair of straight lines, placed diagonally and parallel to one another. These guide lines will help you to draw the DNA.

      2. Draw pairs of parallel, curved lines between the two straight lines. These lines should be placed diagonally in relation to the straight lines.

      3. Begin drawing additional pairs of parallel, curved lines on the opposite diagonal from the first. These lines should appear to form an “X” shape with the first lines.

      4. Continue drawing pairs of parallel, curved lines until you reach the bottom of the figure. There, draw an additional set of lines that look as if they will cross each other if they were to continue. Enclose the end of each set with a short line.

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      Finish Off Your Dna Drawing

      Now its time to finish off the structure of the molecule in this step of our guide on how to drawDNA! First, you can draw two more rungs of the DNA ladder, as shown in our reference image.

      Then we will draw some more of the backbone for this final section around the ends of them. This strand of the backbone will flow logically from where it would join to the previous section.

      Finally, you can add the last rung of the ladder and draw the ends of the backbone. Then you have finished the drawing!

      There are also a few ways in which you could take this drawing even further, though.

      One idea would be to look up a labeled diagram of DNA and label your own drawing. You could also draw some additional detailing or even add some more strands in the background!

      These are just a few ideas that you could go for, but what else can you think of to finish it off?

      So What Does It Mean To Be A Complementary Strand

      Suppose we have a DNA strand 5 GGTACTTGCCAT 3 for this strand of DNA the complementary strand is 3 CCATGAACGGTA 5. This is because we all know that there are 4 base pairs in DNA: Adenine , Guanine , Cytosine , and Thymine , these base pairs bonds together these bonds follow the lock and key principle.in DNA A=T and GC

      In the process of DNA Replication, both of the strands are unzipped by an enzyme named helicase and both of them serve as a template strand for new DNA .

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      How Dna Is Arranged In The Cell

      DNA is a working molecule it must be replicated when a cell is ready to divide, and it must be read to produce the molecules, such as proteins, to carry out the functions of the cell. For this reason, the DNA is protected and packaged in very specific ways. In addition, DNA molecules can be very long. Stretched end-to-end, the DNA molecules in a single human cell would come to a length of about 2 meters. Thus, the DNA for a cell must be packaged in a very ordered way to fit and function within a structure that is not visible to the naked eye. The chromosomes of prokaryotes are much simpler than those of eukaryotes in many of their features . Most prokaryotes contain a single, circular chromosome that is found in an area in the cytoplasm called the nucleoid.

      The size of the genome in one of the most well-studied prokaryotes, Escherichia coli, is 4.6 million base pairs, which would extend a distance of about 1.6 mm if stretched out. So how does this fit inside a small bacterial cell? The DNA is twisted beyond the double helix in what is known as supercoiling. Some proteins are known to be involved in the supercoiling other proteins and enzymes help in maintaining the supercoiled structure.

      The High Fidelity Of Dna Replication Requires Several Proofreading Mechanisms

      How to Draw DNA – Very Easy For kids

      As discussed at the beginning of this chapter, the fidelity of copying during replication is such that only about 1 mistake is made for every 109 nucleotides copied. This fidelity is much higher than one would expect, on the basis of the accuracy of -pairing. The standard complementary base pairs are not the only ones possible. For example, with small changes in helix geometry, two hydrogen bonds can form between and T in DNA. In addition, rare tautomeric forms of the four DNA bases occur transiently in ratios of 1 part to 104 or 105. These forms mispair without a change in helix geometry: the rare tautomeric form of C pairs with A instead of G, for example.

      If the did nothing special when a mispairing occurred between an incoming deoxyribonucleoside triphosphate and the DNA , the wrong would often be incorporated into the new DNA chain, producing frequent mutations. The high fidelity of DNA replication, however, depends not only on -pairing but also on several proofreading mechanisms that act sequentially to correct any initial mispairing that might have occurred.

      Editing by DNA polymerase. Outline of the structures of DNA polymerase complexed with the DNA template in the polymerizing mode and the editing mode . The catalytic site for the exonucleolytic and the polymerization reactions are

      The Three Steps That Give Rise to High-Fidelity DNA Synthesis.

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      A Moving Dna Polymerase Molecule Stays Connected To The Dna By A Sliding Ring

      On their own, most molecules will synthesize only a short string of nucleotides before falling off the DNA . The tendency to dissociate quickly from a DNA allows a DNA polymerase molecule that has just finished synthesizing one Okazaki fragment on the to be recycled quickly, so as to begin the synthesis of the next Okazaki fragment on the same strand. This rapid dissociation, however, would make it difficult for the polymerase to synthesize the long DNA strands produced at a were it not for an accessory that functions as a regulated clamp. This clamp keeps the polymerase firmly on the DNA when it is moving, but releases it as soon as the polymerase runs into a double-stranded region of DNA ahead.

      How can a clamp prevent the polymerase from dissociating without at the same time impeding the polymerase’s rapid movement along the ? The three-dimensional structure of the clamp , by x-ray diffraction, reveals that it forms a large ring around the DNA helix. One side of the ring binds to the back of the , and the whole ring slides freely along the DNA as the polymerase moves. The assembly of the clamp around DNA requires ATP hydrolysis by a special protein , the clamp loader, which hydrolyzes ATP as it loads the clamp on to a primer- junction .

      Different Types Of Dna In Different Organisms:

      Studies on DNA of viruses, bacteria and eukaryotes have given rise to a number of surprising findings. One is that viral and bacterial DNAs are very simple. Molecular weight is very low and approximate number of gene is relatively few. DNA is not associated with any proteins, i.e., a naked DNA thread. It is sometimes called genophore.

      Second is that eukaryotic DNA is very complex. Molecular weight is comparatively high and the DNA contains several genes. It always makes a complex with basic histone protein.

      Besides this, a number of variations still exist with respect to the structure of DNA that serves as genome material in viruses, bacteria and eukaryotic organisms.

      Viral DNA:

      Viruses contain either DNA or genetic RNA, never both. Some of the viral DNA are double- stranded as in prokaryotic and eukaryotic cells and others are single-stranded . Among them some are linear and others circular . Hence a number of possibilities exist with respect to structure of DNA. Some of the more common viral DNA with brief description are listed in Table 10.3.

      The DNAs of lamda bacteriophages and x 174 have received much attention. The former is a linear duplex DNA with molecular weight of 32 million. The DNA of x 174 viruswhich is one of the smallest DNA viruses known is circular and single-stranded with molecular weight of 1.7 million.

      Bacterial DNA:

      The clustering of genes in this ordered manner, therefore, requires only a single regulatory switch for coordinate expression.

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      How To Spot A Badly

      By Grant Jacobs 22/07/2013

      The DNA double helix is one of the icons of our time. Youd wish people would draw it right.

      Youd think getting it wrong would make the artist feel like a complete mug, as if theyd drawn the Statue of Liberty holding up a lump of coal instead of a flaming torch.

      But the DNA helix in all sorts of places is simply wrong.

      You dont need to be a TV drama-smart science geek to know which artists have screwed up.

      Let me show you an easy way.

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