Structure of PDB 1obn Chain A Binding Site BS01
Receptor Information
>1obn Chain A (length=329) Species:
227321
(Aspergillus nidulans FGSC A4) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SVSKANVPKIDVSPLFGDDQAAKMRVAQQIDAASRDTGFFYAVNHGINVQ
RLSQKTKEFHMSITPEEKWDLAIRAYNKEHQDQVRAGYYLSIPGKKAVES
FCYLNPNFTPDHPRIQAKTPTHEVNVWPDETKHPGFQDFAEQYYWDVFGL
SSALLKGYALALGKEENFFARHFKPDDTLASVVLIRYPYLDPYPEAAIKT
AADGTKLSFEWHEDVSLITVLYQSNVQNLQVETAAGYQDIEADDTGYLIN
CGSYMAHLTNNYYKAPIHRVKWVNAERQSLPFFVNLGYDSVIDPFDPREP
NGKSDREPLSYGDYLQNGLVSLINKNGQT
Ligand information
Ligand ID
ASV
InChI
InChI=1S/C13H21N3O6S/c1-2-8(13(21)22)16-11(18)9(6-23)15-10(17)5-3-4-7(14)12(19)20/h2,7-9,23H,1,3-6,14H2,(H,15,17)(H,16,18)(H,19,20)(H,21,22)/t7-,8+,9-/m0/s1
InChIKey
JJJCGQKXGIRXKN-YIZRAAEISA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(NC(\C=C)C(=O)O)C(NC(=O)CCCC(C(=O)O)N)CS
OpenEye OEToolkits 1.5.0
C=CC(C(=O)O)NC(=O)C(CS)NC(=O)CCCC(C(=O)O)N
OpenEye OEToolkits 1.5.0
C=C[C@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)CCC[C@@H](C(=O)O)N
CACTVS 3.341
N[C@@H](CCCC(=O)N[C@@H](CS)C(=O)N[C@H](C=C)C(O)=O)C(O)=O
CACTVS 3.341
N[CH](CCCC(=O)N[CH](CS)C(=O)N[CH](C=C)C(O)=O)C(O)=O
Formula
C13 H21 N3 O6 S
Name
DELTA-(L-ALPHA-AMINOADIPOYL)-L-CYSTEINYL-D-VINYLGLYCINE
ChEMBL
DrugBank
DB03427
ZINC
ZINC000006363128
PDB chain
1obn Chain A Residue 1332 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1obn
Structural Studies on the Reaction of Isopenicillin N Synthase with the Substrate Analogue Delta-(L-Alpha-Aminoadipoyl)-L-Cysteinyl-D-Alpha-Aminobutyrate.
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
R87 S183 I187 Y189 H214 D216 S281 F285
Binding residue
(residue number reindexed from 1)
R85 S181 I185 Y187 H212 D214 S279 F283
Annotation score
2
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
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1obn
,
PDBe:1obn
,
PDBj:1obn
PDBsum
1obn
PubMed
12622704
UniProt
P05326
|IPNA_EMENI Isopenicillin N synthase (Gene Name=ipnA)
[
Back to BioLiP
]