Structure of PDB 6u01 Chain B Binding Site BS01
Receptor Information
>6u01 Chain B (length=296) Species:
197
(Campylobacter jejuni) [
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KNIIIGAMTALITPFKNGKVDEQSYARLIKRQIENGIDAVVPVGTTGESA
TLTHEEHRTCIEIAVETCKGTKVKVLAGAGSDATHEAVGLAKFAKEHGAD
GILSVAPYYNKPTQQGLYEHYKAIAQSVDIPVLLYNVPGRTGCEISTDTI
IKLFRDCENIYGVKEASGNIDKCVDLLAHEPRMMLISGEDAINYPILSNG
GKGVISVTSNLLPDMISALTHFALDENYKEAKKINDELYNINKILFCESN
PIPIKTAMYLAGLIESLEFRLPLCSPSKENFAKIEEVMKKYKIKGF
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
6u01 Chain B Residue 303 [
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Receptor-Ligand Complex Structure
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PDB
6u01
Asparagine-84, a regulatory allosteric site residue, helps maintain the quaternary structure of Campylobacter jejuni dihydrodipicolinate synthase.
Resolution
1.87 Å
Binding residue
(original residue number in PDB)
S189 E191 D192 N195 I207
Binding residue
(residue number reindexed from 1)
S187 E189 D190 N193 I205
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T47 Y111 Y137 R142 K166 I207
Catalytic site (residue number reindexed from 1)
T45 Y109 Y135 R140 K164 I205
Enzyme Commision number
4.3.3.7
: 4-hydroxy-tetrahydrodipicolinate synthase.
Gene Ontology
Molecular Function
GO:0008840
4-hydroxy-tetrahydrodipicolinate synthase activity
GO:0016829
lyase activity
Biological Process
GO:0009085
lysine biosynthetic process
GO:0009089
lysine biosynthetic process via diaminopimelate
GO:0019877
diaminopimelate biosynthetic process
GO:0044281
small molecule metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6u01
,
PDBe:6u01
,
PDBj:6u01
PDBsum
6u01
PubMed
31678256
UniProt
Q9PPB4
|DAPA_CAMJE 4-hydroxy-tetrahydrodipicolinate synthase (Gene Name=dapA)
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