Structure of PDB 1hb2 Chain A Binding Site BS02
Receptor Information
>1hb2 Chain A (length=329) Species:
227321
(Aspergillus nidulans FGSC A4) [
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SVSKANVPKIDVSPLFGDDQAAKMRVAQQIDAASRDTGFFYAVNHGINVQ
RLSQKTKEFHMSITPEEKWDLAIRAYNKEHQDQVRAGYYLSIPGKKAVES
FCYLNPNFTPDHPRIQAKTPTHEVNVWPDETKHPGFQDFAEQYYWDVFGL
SSALLKGYALALGKEENFFARHFKPDDTLASVVLIRYPYLDPYPEAAIKT
AADGTKLSFEWHEDVSLITVLYQSNVQNLQVETAAGYQDIEADDTGYLIN
CGSYMAHLTNNYYKAPIHRVKWVNAERQSLPFFVNLGYDSVIDPFDPREP
NGKSDREPLSYGDYLQNGLVSLINKNGQT
Ligand information
Ligand ID
FE2
InChI
InChI=1S/Fe/q+2
InChIKey
CWYNVVGOOAEACU-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Fe+2]
CACTVS 3.341
[Fe++]
Formula
Fe
Name
FE (II) ION
ChEMBL
DrugBank
DB14510
ZINC
PDB chain
1hb2 Chain A Residue 1334 [
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Receptor-Ligand Complex Structure
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PDB
1hb2
Alternative Oxidation by Isopenicillin N Synthase Observed by X-Ray Diffraction.
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
H214 D216 H270
Binding residue
(residue number reindexed from 1)
H212 D214 H268
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L186 F211 H214 D216 H270
Catalytic site (residue number reindexed from 1)
L184 F209 H212 D214 H268
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:1hb2
,
PDBe:1hb2
,
PDBj:1hb2
PDBsum
1hb2
PubMed
11755401
UniProt
P05326
|IPNA_EMENI Isopenicillin N synthase (Gene Name=ipnA)
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