Structure of PDB 8sv5 Chain H Binding Site BS01
Receptor Information
>8sv5 Chain H (length=120) Species:
1392
(Bacillus anthracis) [
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MDKIYIHDMEFYGYHGVFPEENKLGQRFKVDLTVELDLKRAGESDDLEHS
VNYGELFELCRKVVEDRTYKLVESIAENIATDILKQYESISRCTIKVIKP
DPPIPGHYRAVAVEITRERP
Ligand information
Ligand ID
PH2
InChI
InChI=1S/C7H9N5O2/c8-7-11-5-4(6(14)12-7)10-3(2-13)1-9-5/h13H,1-2H2,(H4,8,9,11,12,14)
InChIKey
CQQNNQTXUGLUEV-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=NC2=C(N=C(CO)CN2)C(=O)N1
ACDLabs 10.04
O=C1NC(=NC=2NCC(=NC1=2)CO)N
OpenEye OEToolkits 1.5.0
C1C(=NC2=C(N1)N=C(NC2=O)N)CO
Formula
C7 H9 N5 O2
Name
2-AMINO-6-HYDROXYMETHYL-7,8-DIHYDRO-3H-PTERIDIN-4-ONE
ChEMBL
CHEMBL1233322
DrugBank
DB02119
ZINC
PDB chain
8sv5 Chain B Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
8sv5
Crystal structure of Bacillus anthracis dihydroneopterin aldolase in complex with 6-hydroxymethyl-7,8-dihydropterin
Resolution
2.16 Å
Binding residue
(original residue number in PDB)
L47 N52 Y53
Binding residue
(residue number reindexed from 1)
L47 N52 Y53
Annotation score
5
Enzymatic activity
Enzyme Commision number
4.1.2.25
: dihydroneopterin aldolase.
Gene Ontology
Molecular Function
GO:0004150
dihydroneopterin aldolase activity
GO:0016829
lyase activity
Biological Process
GO:0006760
folic acid-containing compound metabolic process
GO:0046654
tetrahydrofolate biosynthetic process
GO:0046656
folic acid biosynthetic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Cellular Component
External links
PDB
RCSB:8sv5
,
PDBe:8sv5
,
PDBj:8sv5
PDBsum
8sv5
PubMed
UniProt
A0A6L7HSV1
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