Structure of PDB 3ijp Chain B Binding Site BS01
Receptor Information
>3ijp Chain B (length=267) Species:
38323
(Bartonella henselae) [
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SMRLTVVGANGRMGRELITAIQRRKDVELCAVLVRKGSSFVDKDASILIG
SDFLGVRITDDPESAFSNTEGILDFSQPQASVLYANYAAQKSLIHIIGTT
GFSKTEEAQIADFAKYTTIVKSGNMSLGVNLLANLVKRAAKALDDDFDIE
IYEMHHANKVDSPSGTALLLGQAAAEGRNIMLKNVSVNGRSGHTGKREKG
TIGFACSRGGTVIGDHSITFAGENERIVLSHIAQERSIFANGALKAALWA
KNHENGLYSMLDVLGLN
Ligand information
Ligand ID
NA
InChI
InChI=1S/Na/q+1
InChIKey
FKNQFGJONOIPTF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Na+]
Formula
Na
Name
SODIUM ION
ChEMBL
DrugBank
DB14516
ZINC
PDB chain
3ijp Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
3ijp
The crystal structure of dihydrodipicolinate reductase from the human-pathogenic bacterium Bartonella henselae strain Houston-1 at 2.3 angstrom resolution.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
I20 Q21 R23 V26 E27
Binding residue
(residue number reindexed from 1)
I21 Q22 R24 V27 E28
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H154 K158
Catalytic site (residue number reindexed from 1)
H155 K159
Enzyme Commision number
1.17.1.8
: 4-hydroxy-tetrahydrodipicolinate reductase.
Gene Ontology
Molecular Function
GO:0008839
4-hydroxy-tetrahydrodipicolinate reductase
GO:0016491
oxidoreductase activity
GO:0016726
oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor
GO:0050661
NADP binding
GO:0051287
NAD binding
Biological Process
GO:0009085
lysine biosynthetic process
GO:0009089
lysine biosynthetic process via diaminopimelate
GO:0019877
diaminopimelate biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3ijp
,
PDBe:3ijp
,
PDBj:3ijp
PDBsum
3ijp
PubMed
27917836
UniProt
Q6G2G3
|DAPB_BARHE 4-hydroxy-tetrahydrodipicolinate reductase (Gene Name=dapB)
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