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[[Image:4a22.png|left|200px]]


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==Structure of Mycobacterium tuberculosis fructose 1,6-bisphosphate aldolase bound to N-(4-hydroxybutyl)- glycolohydroxamic acid bis- phosphate==
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<StructureSection load='4a22' size='340' side='right'caption='[[4a22]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[4a22]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4A22 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4A22 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=TD4:4-{HYDROXY[(PHOSPHONOOXY)ACETYL]AMINO}BUTYL+DIHYDROGEN+PHOSPHATE'>TD4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
{{STRUCTURE_4a22|  PDB=4a22  |  SCENE=  }}
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4a22 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a22 OCA], [https://pdbe.org/4a22 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4a22 RCSB], [https://www.ebi.ac.uk/pdbsum/4a22 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4a22 ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/ALF_MYCTU ALF_MYCTU] Catalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis (By similarity).
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
The search for anti-TB drugs active against persistent bacilli has led to our interest in metallo-dependent class II fructose-1,6-bisphosphate aldolase (FBA-tb), a key enzyme of gluconeogenesis absent from mammalian cells. Knock-out experiments at the fba-tb locus indicated that this gene is required for the growth of M. tb on gluconeogenetic substrates and in glucose-containing medium. Surface labeling and enzymatic activity measurements revealed that this enzyme is exported to the cell surface of M. tb and is produced under various axenic growth conditions including oxygen depletion, and hence by non-replicating bacilli. Importantly, FBA-tb is also produced in vivo in the lungs of infected guinea pigs and mice. FBA-tb binds human plasmin(ogen) and protects FBA-tb-bound plasmin from regulation by alpha-2-antiplasmin, suggestive of an involvement of this enzyme in host-pathogen interactions. The crystal structures of FBA-tb in the native form and in complex with a hydroxamate substrate analog were determined to 2.35 and 1.9 angstroms resolution, respectively. Whereas inhibitor attachment had no effect on the plasminogen-binding activity of FBA-tb, it competed with the natural substrate of the enzyme, fructose-1,6-bisphosphate, and substantiated a previously unknown reaction mechanism associated with metallo-dependent aldolases involving recruitment of the catalytic zinc ion by the substrate upon active site binding. Altogether, our results highlight the potential of FBA-tb as a novel therapeutic target against both replicating and non-replicating bacilli.


===STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS FRUCTOSE 1,6-BISPHOSPHATE ALDOLASE BOUND TO N-(4-HYDROXYBUTYL)-GLYCOLOHYDROXAMIC ACID BIS-PHOSPHATE===
Glycolytic and non-glycolytic functions of the fructose-1,6-bisphosphate aldolase of Mycobacterium tuberculosis, an essential enzyme produced by replicating and non-replicating bacilli.,Santangelo MD, Gest PM, Guerin ME, Coincon M, Pham H, Ryan G, Puckett SE, Spencer JS, Gonzalez-Juarrero M, Daher R, Lenaerts AJ, Schnappinger D, Therisod M, Ehrt S, Sygusch J, Jackson M J Biol Chem. 2011 Sep 23. PMID:21949126<ref>PMID:21949126</ref>


 
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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{{ABSTRACT_PUBMED_21949126}}
 
==About this Structure==
[[4a22]] is a 4 chain structure of [[Aldolase]] with sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4A22 OCA].


==See Also==
==See Also==
*[[Aldolase]]
*[[Aldolase 3D structures|Aldolase 3D structures]]
 
== References ==
==Reference==
<references/>
<ref group="xtra">PMID:021949126</ref><references group="xtra"/>
__TOC__
[[Category: Fructose-bisphosphate aldolase]]
</StructureSection>
[[Category: Large Structures]]
[[Category: Mycobacterium tuberculosis]]
[[Category: Mycobacterium tuberculosis]]
[[Category: Coincon, M.]]
[[Category: Coincon M]]
[[Category: Daher, R.]]
[[Category: Daher R]]
[[Category: Ehrt, S.]]
[[Category: De la Paz Santangelo M]]
[[Category: Gest, P M.]]
[[Category: Ehrt S]]
[[Category: Gonzalez-Juarrero, M.]]
[[Category: Gest PM]]
[[Category: Guerin, M E.]]
[[Category: Gonzalez-Juarrero M]]
[[Category: Jackson, M.]]
[[Category: Guerin ME]]
[[Category: Lenaerts, A J.]]
[[Category: Jackson M]]
[[Category: Pham, H.]]
[[Category: Lenaerts AJ]]
[[Category: Puckett, S E.]]
[[Category: Pham H]]
[[Category: Ryan, G.]]
[[Category: Puckett SE]]
[[Category: Santangelo, M De La Paz.]]
[[Category: Ryan G]]
[[Category: Schnappinger, D.]]
[[Category: Schnappinger D]]
[[Category: Spencer, J S.]]
[[Category: Spencer JS]]
[[Category: Sygusch, J.]]
[[Category: Sygusch J]]
[[Category: Therisod, M.]]
[[Category: Therisod M]]
[[Category: Lyase]]
[[Category: Lyase-inhibitor complex]]

Latest revision as of 13:45, 9 May 2024

Structure of Mycobacterium tuberculosis fructose 1,6-bisphosphate aldolase bound to N-(4-hydroxybutyl)- glycolohydroxamic acid bis- phosphateStructure of Mycobacterium tuberculosis fructose 1,6-bisphosphate aldolase bound to N-(4-hydroxybutyl)- glycolohydroxamic acid bis- phosphate

Structural highlights

4a22 is a 4 chain structure with sequence from Mycobacterium tuberculosis. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 1.9Å
Ligands:, , ,
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

ALF_MYCTU Catalyzes the aldol condensation of dihydroxyacetone phosphate (DHAP or glycerone-phosphate) with glyceraldehyde 3-phosphate (G3P) to form fructose 1,6-bisphosphate (FBP) in gluconeogenesis and the reverse reaction in glycolysis (By similarity).

Publication Abstract from PubMed

The search for anti-TB drugs active against persistent bacilli has led to our interest in metallo-dependent class II fructose-1,6-bisphosphate aldolase (FBA-tb), a key enzyme of gluconeogenesis absent from mammalian cells. Knock-out experiments at the fba-tb locus indicated that this gene is required for the growth of M. tb on gluconeogenetic substrates and in glucose-containing medium. Surface labeling and enzymatic activity measurements revealed that this enzyme is exported to the cell surface of M. tb and is produced under various axenic growth conditions including oxygen depletion, and hence by non-replicating bacilli. Importantly, FBA-tb is also produced in vivo in the lungs of infected guinea pigs and mice. FBA-tb binds human plasmin(ogen) and protects FBA-tb-bound plasmin from regulation by alpha-2-antiplasmin, suggestive of an involvement of this enzyme in host-pathogen interactions. The crystal structures of FBA-tb in the native form and in complex with a hydroxamate substrate analog were determined to 2.35 and 1.9 angstroms resolution, respectively. Whereas inhibitor attachment had no effect on the plasminogen-binding activity of FBA-tb, it competed with the natural substrate of the enzyme, fructose-1,6-bisphosphate, and substantiated a previously unknown reaction mechanism associated with metallo-dependent aldolases involving recruitment of the catalytic zinc ion by the substrate upon active site binding. Altogether, our results highlight the potential of FBA-tb as a novel therapeutic target against both replicating and non-replicating bacilli.

Glycolytic and non-glycolytic functions of the fructose-1,6-bisphosphate aldolase of Mycobacterium tuberculosis, an essential enzyme produced by replicating and non-replicating bacilli.,Santangelo MD, Gest PM, Guerin ME, Coincon M, Pham H, Ryan G, Puckett SE, Spencer JS, Gonzalez-Juarrero M, Daher R, Lenaerts AJ, Schnappinger D, Therisod M, Ehrt S, Sygusch J, Jackson M J Biol Chem. 2011 Sep 23. PMID:21949126[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Santangelo MD, Gest PM, Guerin ME, Coincon M, Pham H, Ryan G, Puckett SE, Spencer JS, Gonzalez-Juarrero M, Daher R, Lenaerts AJ, Schnappinger D, Therisod M, Ehrt S, Sygusch J, Jackson M. Glycolytic and non-glycolytic functions of the fructose-1,6-bisphosphate aldolase of Mycobacterium tuberculosis, an essential enzyme produced by replicating and non-replicating bacilli. J Biol Chem. 2011 Sep 23. PMID:21949126 doi:10.1074/jbc.M111.259440

4a22, resolution 1.90Å

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