Structure of PDB 1vs1 Chain D Binding Site BS01
Receptor Information
>1vs1 Chain D (length=271) Species:
56636
(Aeropyrum pernix) [
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PVAGFKGVKLALKSEERRETVVEVEGVRIGGGSKAVIAGPCSVESWEQVR
EAALAVKEAGAHMLRGGAFKPRTSPYSFQGLGLEGLKLLRRAGDEAGLPV
VTEVLDPRHVETVSRYADMLQIGARNMQNFPLLREVGRSGKPVLLKRGFG
NTVEELLAAAEYILLEGNWQVVLVERGIRTFEPSTRFTLDVAAVAVLKEA
THLPVIVDPSHPAGRRSLVPALAKAGLAAGADGLIVEVHPNPEEALSDAK
QQLTPGEFARLMGELRWHRLL
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
1vs1 Chain D Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1vs1
Crystal structure of 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase (DAHP synthase) from Aeropyrum pernix in complex with Mn2+ and PEP
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
C46 H216 E242 D253
Binding residue
(residue number reindexed from 1)
C41 H211 E237 D248
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.5.1.54
: 3-deoxy-7-phosphoheptulonate synthase.
Gene Ontology
Molecular Function
GO:0003849
3-deoxy-7-phosphoheptulonate synthase activity
GO:0016740
transferase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0009058
biosynthetic process
GO:0009073
aromatic amino acid family biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:1vs1
,
PDBe:1vs1
,
PDBj:1vs1
PDBsum
1vs1
PubMed
UniProt
Q9YEJ7
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