Structure of PDB 6th2 Chain B Binding Site BS01
Receptor Information
>6th2 Chain B (length=229) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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HHDMAGVKALVTAGGTREPLDPVRFIGNRSSGKQGYAVARVLAQRGADVT
LIAGNTAGLIDPAGVEMVHIGSATQLRDAVSKHAPDANVLVMAAAVADFR
PAHVAAAKIKKGASEPSSIDLVRNDDVLAGAVRARADGQLPNMRAIVGFA
AETGDANGDVLFHARAKLERKGCDLLVVNAVGENRAFEVDHNDGWLLSAD
GTESALEHGSKTLMATRIVDSIAAFLKSQ
Ligand information
Ligand ID
CTP
InChI
InChI=1S/C9H16N3O14P3/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey
PCDQPRRSZKQHHS-XVFCMESISA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]2O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)N=C(N)C=C1)C(O)C2O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]2O
Formula
C9 H16 N3 O14 P3
Name
CYTIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL223533
DrugBank
DB02431
ZINC
ZINC000003861746
PDB chain
6th2 Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6th2
Inhibiting Mycobacterium tuberculosis CoaBC by targeting an allosteric site.
Resolution
1.844 Å
Binding residue
(original residue number in PDB)
K293 K294
Binding residue
(residue number reindexed from 1)
K110 K111
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
N211
Catalytic site (residue number reindexed from 1)
N28
Enzyme Commision number
4.1.1.36
: phosphopantothenoylcysteine decarboxylase.
6.3.2.5
: phosphopantothenate--cysteine ligase (CTP).
External links
PDB
RCSB:6th2
,
PDBe:6th2
,
PDBj:6th2
PDBsum
6th2
PubMed
33420031
UniProt
A0QWT2
|COABC_MYCS2 Coenzyme A biosynthesis bifunctional protein CoaBC (Gene Name=coaBC)
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