Structure of PDB 1blz Chain A Binding Site BS03
Receptor Information
>1blz Chain A (length=327) Species:
162425
(Aspergillus nidulans) [
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SKANVPKIDVSPLFGDDQAAKMRVAQQIDAASRDTGFFYAVNHGINVQRL
SQKTKEFHMSITPEEKWDLAIRAYNKEHQDQVRAGYYLSIPGKKAVESFC
YLNPNFTPDHPRIQAKTPTHEVNVWPDETKHPGFQDFAEQYYWDVFGLSS
ALLKGYALALGKEENFFARHFKPDDTLASVVLIRYPYLDPYPEAAIKTAA
DGTKLSFEWHEDVSLITVLYQSNVQNLQVETAAGYQDIEADDTGYLINCG
SYMAHLTNNYYKAPIHRVKWVNAERQSLPFFVNLGYDSVIDPFDPREPNG
KSDREPLSYGDYLQNGLVSLINKNGQT
Ligand information
Ligand ID
NO
InChI
InChI=1S/HNO/c1-2/h1H
InChIKey
ODUCDPQEXGNKDN-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
OpenEye OEToolkits 2.0.7
[N]=O
Formula
N O
Name
NITRIC OXIDE;
Nitrogen monoxide
ChEMBL
CHEMBL1234765
DrugBank
ZINC
PDB chain
1blz Chain A Residue 334 [
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Receptor-Ligand Complex Structure
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PDB
1blz
Structure of isopenicillin N synthase complexed with substrate and the mechanism of penicillin formation.
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
H214 H270
Binding residue
(residue number reindexed from 1)
H210 H266
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L186 F211 H214 D216 H270
Catalytic site (residue number reindexed from 1)
L182 F207 H210 D212 H266
Enzyme Commision number
1.21.3.1
: isopenicillin-N synthase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0016216
isopenicillin-N synthase activity
GO:0016491
oxidoreductase activity
GO:0031418
L-ascorbic acid binding
GO:0046872
metal ion binding
Biological Process
GO:0009058
biosynthetic process
GO:0017000
antibiotic biosynthetic process
GO:0042318
penicillin biosynthetic process
GO:0044283
small molecule biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1blz
,
PDBe:1blz
,
PDBj:1blz
PDBsum
1blz
PubMed
9194566
UniProt
P05326
|IPNA_EMENI Isopenicillin N synthase (Gene Name=ipnA)
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