4ob9

<StructureSection load='4ob9' size='340' side='right'caption='[[4ob9]], [[Resolution|resolution]] 2.50&Aring;' scene=''>

<table><tr><td colspan='2'>[[4ob9]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Acinetobacter_baumannii_ATCC_19606_=_CIP_70.34_=_JCM_6841 Acinetobacter baumannii ATCC 19606 = CIP 70.34 = JCM 6841]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4OB9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4OB9 FirstGlance]. <br>

</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4ob9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4ob9 OCA], [https://pdbe.org/4ob9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4ob9 RCSB], [https://www.ebi.ac.uk/pdbsum/4ob9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4ob9 ProSAT]</span></td></tr>

== Function ==

[https://www.uniprot.org/uniprot/D0C7F3_ACIB2 D0C7F3_ACIB2] Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system.[HAMAP-Rule:MF_00300]

==See Also==

*[[Chorismate synthase|Chorismate synthase]]

[[Category: Acinetobacter baumannii ATCC 19606 = CIP 70 34 = JCM 6841]]

[[Category: Large Structures]]

[[Category: Bhushan A]]

[[Category: Chaudhary A]]

[[Category: Kaur P]]

[[Category: Sharma S]]

[[Category: Shukla PK]]

[[Category: Singh N]]

[[Category: Singh TP]]

[[Category: Sinha M]]