Structure of PDB 1kij Chain B Binding Site BS01
Receptor Information
>1kij Chain B (length=384) Species:
274
(Thermus thermophilus) [
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AIRVLKGLEGVRHRPAMYIGGTGVEGYHHLFKEILDNAVDEALAGYATEI
LVRLNEDGSLTVEDNGRGIPVDLMPEEGKPAVEVIYNTLHSGGKFEQGAY
KVSGGLHGVGASVVNALSEWTVVEVFREGKHHRIAFSRGEVTEPLRVVGE
APRGKTGTRVTFKPDPEIFGNLRFDPSKIRARLREVAYLVAGLKLVFQDR
QHGKEEVFLDKGGVASFAKALAEGEDLLYEKPFLIRGTHGEVEVEVGFLH
TQGYNAEILTYANMIPTRDGGTHLTAFKSAYSRALNQYAKKAGLNKEKGP
QPTGDDLLEGLYAVVSVKLPNPQFEGQTKGKLLNPEAGTAVGQVVYERLL
EILEENPRIAKAVYEKALRAAQAREAARKARELV
Ligand information
Ligand ID
NOV
InChI
InChI=1S/C31H36N2O11/c1-14(2)7-8-16-13-17(9-11-19(16)34)27(37)33-21-22(35)18-10-12-20(15(3)24(18)42-28(21)38)41-29-23(36)25(43-30(32)39)26(40-6)31(4,5)44-29/h7,9-13,23,25-26,29,34-36H,8H2,1-6H3,(H2,32,39)(H,33,37)/t23-,25+,26-,29-/m1/s1
InChIKey
YJQPYGGHQPGBLI-KGSXXDOSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
Cc1c(ccc2c1OC(=O)C(=C2O)NC(=O)c3ccc(c(c3)CC=C(C)C)O)O[C@H]4[C@@H]([C@@H]([C@H](C(O4)(C)C)OC)OC(=O)N)O
CACTVS 3.370
CO[CH]1[CH](OC(N)=O)[CH](O)[CH](Oc2ccc3C(=C(NC(=O)c4ccc(O)c(CC=C(C)C)c4)C(=O)Oc3c2C)O)OC1(C)C
ACDLabs 12.01
O=C(c1ccc(O)c(c1)C\C=C(/C)C)NC3=C(O)c4ccc(OC2OC(C(OC)C(OC(=O)N)C2O)(C)C)c(c4OC3=O)C
CACTVS 3.370
CO[C@@H]1[C@@H](OC(N)=O)[C@@H](O)[C@H](Oc2ccc3C(=C(NC(=O)c4ccc(O)c(CC=C(C)C)c4)C(=O)Oc3c2C)O)OC1(C)C
OpenEye OEToolkits 1.7.0
Cc1c(ccc2c1OC(=O)C(=C2O)NC(=O)c3ccc(c(c3)CC=C(C)C)O)OC4C(C(C(C(O4)(C)C)OC)OC(=O)N)O
Formula
C31 H36 N2 O11
Name
NOVOBIOCIN;
4-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)benzamido]-8-methylcoumarin-7-yl 3-O-carbamoyl-5,5-di-C-methyl-alpha-l-lyxofuranoside
ChEMBL
CHEMBL36506
DrugBank
DB01051
ZINC
ZINC000014879999
PDB chain
1kij Chain B Residue 444 [
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Receptor-Ligand Complex Structure
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PDB
1kij
An open conformation of the Thermus thermophilus gyrase B ATP-binding domain.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
N45 E49 D72 R75 P78 D80 R135
Binding residue
(residue number reindexed from 1)
N37 E41 D64 R67 P70 D72 R127
Annotation score
1
Enzymatic activity
Enzyme Commision number
5.6.2.2
: DNA topoisomerase (ATP-hydrolyzing).
Gene Ontology
Molecular Function
GO:0003677
DNA binding
GO:0003918
DNA topoisomerase type II (double strand cut, ATP-hydrolyzing) activity
GO:0005524
ATP binding
Biological Process
GO:0006265
DNA topological change
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1kij
,
PDBe:1kij
,
PDBj:1kij
PDBsum
1kij
PubMed
11850422
UniProt
Q5SHZ4
|GYRB_THET8 DNA gyrase subunit B (Gene Name=gyrB)
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