Structure of PDB 2ivi Chain B Binding Site BS01
Receptor Information
>2ivi Chain B (length=329) Species:
227321
(Aspergillus nidulans FGSC A4) [
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SVSKANVPKIDVSPLFGDDQAAKMRVAQQIDAASRDTGFFYAVNHGINVQ
RLSQKTKEFHMSITPEEKWDLAIRAYNKEHQDQVRAGYYLSIPGKKAVES
FCYLNPNFTPDHPRIQAKTPTHEVNVWPDETKHPGFQDFAEQYYWDVFGL
SSALLKGYALALGKEENFFARHFKPDDTLASVVLIRYPYLDPYPEAAIKT
AADGTKLSFEWHEDVSLITVLYQSNVQNLQVETAAGYQDIEADDTGYLIN
CGSYMAHLTNNYYKAPIHRVKWVNAERQSLPFFVNLGYDSVIDPFDPREP
NGKSDREPLSYGDYLQNGLVSLINKNGQT
Ligand information
Ligand ID
ACW
InChI
InChI=1S/C15H25N3O6S/c1-15(5-6-15)11(14(23)24)18-12(20)9(7-25)17-10(19)4-2-3-8(16)13(21)22/h8-9,11,25H,2-7,16H2,1H3,(H,17,19)(H,18,20)(H,21,22)(H,23,24)/t8-,9-,11-/m0/s1
InChIKey
RSWNRYJZSUJOPA-QXEWZRGKSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC1(CC1)[C@H](C(=O)O)NC(=O)[C@H](CS)NC(=O)CCC[C@@H](C(=O)O)N
OpenEye OEToolkits 1.5.0
CC1(CC1)C(C(=O)O)NC(=O)C(CS)NC(=O)CCCC(C(=O)O)N
CACTVS 3.341
CC1(CC1)[C@@H](NC(=O)[C@H](CS)NC(=O)CCC[C@H](N)C(O)=O)C(O)=O
ACDLabs 10.04
O=C(NC(C(=O)O)C1(C)CC1)C(NC(=O)CCCC(C(=O)O)N)CS
CACTVS 3.341
CC1(CC1)[CH](NC(=O)[CH](CS)NC(=O)CCC[CH](N)C(O)=O)C(O)=O
Formula
C15 H25 N3 O6 S
Name
D-(L-A-AMINOADIPOYL)-L-CYSTEINYL-B-METHYL-D-CYCLOPROPYLGLYCINE
ChEMBL
DrugBank
ZINC
ZINC000016052188
PDB chain
2ivi Chain B Residue 1332 [
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Receptor-Ligand Complex Structure
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PDB
2ivi
Interactions of Isopenicillin N Synthase with Cyclopropyl-Containing Substrate Analogues Reveal New Mechanistic Insight.
Resolution
1.3 Å
Binding residue
(original residue number in PDB)
R87 S183 I187 Y189 H214 D216 L223 V272 S281 F285 L324
Binding residue
(residue number reindexed from 1)
R85 S181 I185 Y187 H212 D214 L221 V270 S279 F283 L322
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
F211 H214 D216 H270
Catalytic site (residue number reindexed from 1)
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
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ivi
,
PDBe:2ivi
,
PDBj:2ivi
PDBsum
2ivi
PubMed
17397141
UniProt
P05326
|IPNA_EMENI Isopenicillin N synthase (Gene Name=ipnA)
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