Journal:Acta Cryst F:S2053230X19004618
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As of 2017, tuberculosis has infected 1.7 billion people (23% of the world's population) and has caused 10 million deaths. ''Mycobacterium tuberculosis'' (Mtb) is quickly evolving, and new strains are classified as multi-drug resistant. Thus, the development and discovery of new drugs to combat Mtb is vital to combat the drug-resistant strains. Filamenting temperature-sensitive mutant Z (FtsZ), an important protein involved in cell-division is key for the survival of Mtb. Here, we have solved the crystal structure of MtbFtsZ that exhibit an inter-subunit that plays a biological role in the GTPase activity of MtbFtsZ and have elucidated a novel conformation, involving the T9 loop and the nucleotide binding pocket that breaks up the GTPase active site. This novel conformation can serve as basis for the development of the novel drugs to combat tuberculosis. | As of 2017, tuberculosis has infected 1.7 billion people (23% of the world's population) and has caused 10 million deaths. ''Mycobacterium tuberculosis'' (Mtb) is quickly evolving, and new strains are classified as multi-drug resistant. Thus, the development and discovery of new drugs to combat Mtb is vital to combat the drug-resistant strains. Filamenting temperature-sensitive mutant Z (FtsZ), an important protein involved in cell-division is key for the survival of Mtb. Here, we have solved the crystal structure of MtbFtsZ that exhibit an inter-subunit that plays a biological role in the GTPase activity of MtbFtsZ and have elucidated a novel conformation, involving the T9 loop and the nucleotide binding pocket that breaks up the GTPase active site. This novel conformation can serve as basis for the development of the novel drugs to combat tuberculosis. | ||
| - | <scene name='81/813404/Cv/2'>Asymmetric unit contains 6 protomers that form a dimer of trimers</scene>. Protomers A and C shown in blue, protomer B shown in gray, protomers D and F shown in red, protomer E shown in cyan, GDP are represented by orange spheres, and PO4 by green spheres. | + | <scene name='81/813404/Cv/2'>Asymmetric unit contains 6 protomers that form a dimer of trimers</scene> ([[5v68]]). Protomers A and C shown in blue, protomer B shown in gray, protomers D and F shown in red, protomer E shown in cyan, GDP are represented by orange spheres, and PO4 by green spheres. <scene name='81/813404/Cv/4'>Trimer ABC superimposed onto DEF</scene>. Same color scheme as in previous scene. |
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| + | Comparison of other MtbFtsZ structures with trimer ABC from [[5v68]] reveals that protomers A and B superimposed well but the conformation of protomer C is vastly different. <scene name='81/813404/Cv/23'>Structure 5V68 superimposed onto 4KWE</scene>. Nucleotide for both is GDP. Color scheme is as follows, [[5v68]] blue, [[4kwe]] yellow, nucleotides orange spheres, Glu231 green spheres, phosphate red spheres. <scene name='81/813404/Cv/24'>Click here to see animation of this scene</scene>. <jmol><jmolButton> | ||
| + | <script>if (_animating); anim pause;set echo bottom left; color echo white; font echo 20 sansserif;echo Animation Paused; else; anim resume; set echo off;endif;</script> | ||
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| + | </jmolButton></jmol> The trimer ABC from [[5v68]] is to a curved MtbFtsZ protofilament (PDB [[4kwe]]). Based on an r.m.s.d. of 1.2Å between protomers AB of [[5v68]] and protomers CB of [[4kwe]], protomers A and B from [[5v68]] are similar with protomers C and B of [[4kwe]]. <scene name='81/813404/Cv/25'>Glu231 (shown as green sphere) from protomer C of [[5v68]] and Glu231 from protomer A of [[4kwe]] are far apart</scene>. | ||
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| + | <scene name='81/813404/Cv/26'>5V68 with bound GDP superimposed onto 2Q1Y with bound GTP</scene>. Color scheme is as follows, [[5v68]] blue, [[2q1y]] green, nucleotides orange spheres, Glu231 green spheres, phosphate red spheres. <scene name='81/813404/Cv/27'>Click here to see animation of this scene</scene>. <jmol><jmolButton> | ||
| + | <script>if (_animating); anim pause;set echo bottom left; color echo white; font echo 20 sansserif;echo Animation Paused; else; anim resume; set echo off;endif;</script> | ||
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| + | </jmolButton></jmol> To generate this trimer ([[2q1y]]), A1 A2 A3, the crystal symmetry molecules neighboring chain A2 that exhibit the inter-subunit interface were used. Only chains A1 and A2 were used for the superimposition. Again, protomers A and B from present study are similar with the top two protomers A1 and A2 from [[2q1y]] with an r.m.s.d of 2.1Å. <scene name='81/813404/Cv/29'>The distance of their respective Glu231</scene> is approximately 63Å. | ||
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| + | <scene name='81/813404/Cv/21'>4KWE with bound GDP superimposed onto 2Q1Y with bound GTP</scene>. Color scheme is as follows, [[4kwe]] yellow, [[2q1y]] green, nucleotides orange spheres, Glu231 green spheres. <scene name='81/813404/Cv/22'>Click here to see animation of this scene</scene>. <jmol><jmolButton> | ||
| + | <script>if (_animating); anim pause;set echo bottom left; color echo white; font echo 20 sansserif;echo Animation Paused; else; anim resume; set echo off;endif;</script> | ||
| + | <text>Toggle Animation</text> | ||
| + | </jmolButton></jmol> Superimposition of [[4kwe]] and [[2q1y]] reveals an r.m.s.d. of 2.8Å between the trimers and a 12.5Å <scene name='81/813404/Cv/30'>distance between their respective Glu231’s of A and A3</scene>, showing that these structures are relatively similar. The distances between Glu231 of [[5v68]] from protomer C is far greater than 12.5Å and the interaction with the middle protomers of [[4kwe]] and [[2q1y]] with protomer C of [[5v68]] involve the T9 loop residue Glu231, which is not the case in the other structures. | ||
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| + | <scene name='81/813404/Cv1/3'>Crystal structure of protomers A and B of 5V68</scene> (gray). <scene name='81/813404/Cv1/6'>A zoom-in of the inter-subunit interface with bound GDP</scene> (orange). Helix H11 is shown in green. Helices η1, H7, and loop T6 are shown in blue. Switch I (T3 loop) is disordered surrounded by a cloud. Switch II (sH2) is shown in magenta. The top two protomers of all three structures (AB for [[5v68]], A1 A2 for [[2q1y]], and CB for [[4kwe]]) all exhibit a similar inter-subunit interface. This interaction between protomers A and B of 5V68 involve the T6 and T7 loops, helices: H11, η1, and H7. Protomer A of our structure “sits” on the helices η1, H7 and loop T6 (all shown in blue) from protomer B. This brings the T7 loop’s (shown in red) residues <scene name='81/813404/Cv1/9'>Asn205, Asp207 and Asp210</scene> of protomer A of [[5v68]] within 16Å of GDP from protomer B, forming the GTPase active site. The T3 loop is disordered or in its OFF position (surrounded by magenta cloud). Helix sH2 is also OFF because there is no hydrogen network (shown in magenta). | ||
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| + | <scene name='81/813404/Cv1/11'>Crystal structure of protomer B and C of 5V68</scene>. Protomer B is shown in gray, the T9 loop in brown, T11 in cyan; and the N-terminal of protomer C is shown in green, C-terminal blue, helix H8 yellow, the T7 loop red, and the switches in magenta. <scene name='81/813404/Cv1/12'>PO4 binding site</scene>. Glu231 from protomer B is shown in brown, while Glu274 from protomer is in gray. The residues in green are from protomer C. | ||
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| + | '''PDB reference:''' FtsZ from ''Mycobacterium tuberculosis'', [[5v68]] | ||
<b>References</b><br> | <b>References</b><br> | ||
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