Structure of PDB 6zam Chain A Binding Site BS02
Receptor Information
>6zam Chain A (length=328) Species:
227321
(Aspergillus nidulans FGSC A4) [
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VSKANVPKIDVSPLFGDDQAAKMRVAQQIDAASRDTGFFYAVNHGINVQR
LCQKTKEFHMSITPEEKWDLAIRAYNKEHQDQVRAGYYLSIPGKKAVESF
CYLNPNFTPDHPRIQAKTPTHEVNVWPDETKHPGFQDFAEQYYWDVFGLS
SALLKGYALALGKEENFFARHFKPDDTLASVVLIRYPYLDPYPEAAIKTA
ADGTKLSFEWHEDVSLITVLYQSNVQNLQVETAAGYQDIEADDTGYLINC
GSYMAHLTNNYYKAPIHRVKWVNAERQSLPFFVNLGYDSVIDPFDPREPN
GKSDREPLSYGDYLQNGLVSLINKNGQT
Ligand information
Ligand ID
W6X
InChI
InChI=1S/C3H3F3O/c1-2(7)3(4,5)6/h1H3
InChIKey
FHUDAMLDXFJHJE-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
OpenEye OEToolkits 2.0.7
CC(=O)C(F)(F)F
Formula
C3 H3 F3 O
Name
1,1,1-tris(fluoranyl)propan-2-one
ChEMBL
DrugBank
ZINC
ZINC000001693867
PDB chain
6zam Chain A Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
6zam
X-ray free-electron laser studies reveal correlated motion during isopenicillin N synthase catalysis.
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
Q52 C55 Q56
Binding residue
(residue number reindexed from 1)
Q49 C52 Q53
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
F211 H214 D216 H270
Catalytic site (residue number reindexed from 1)
F208 H211 D213 H267
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:6zam
,
PDBe:6zam
,
PDBj:6zam
PDBsum
6zam
PubMed
34417180
UniProt
P05326
|IPNA_EMENI Isopenicillin N synthase (Gene Name=ipnA)
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