Structure of PDB 4fw8 Chain A Binding Site BS01
Receptor Information
>4fw8 Chain A (length=427) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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SFLARQLGVPQPETLRRYRAGEPPLTGSLLIGGAGRVVEPLRAALEKDYD
LVGDSFGGLVFDATGITEPAGLKGLHEFFTPVLRNLGRCGRVVVVGGTPE
AAASTNERIAQRALEGFTRSLGKELRRGATTALVYLSPDAKPAATGLEST
MRFLLSAKSAYVDGQVFSVGADDSTPPADWEKPLDGKVAIVTGAARGIGA
TIAEVFARDGAHVVAIDVESAAENLAETASKVGGTALWLDVTADDAVDKI
SEHLRDHHGGKADILVNNAGITRDKLLANMDDARWDAVLAVNLLAPLRLT
EGLVGNGSIGEGGRVIGLSSIAGIAGNRGQTNYATTKAGMIGITQALAPG
LAAKGITINAVAPGFIETQMTAAIPLATREVGRRLNSLLQGGQPVDVAEA
IAYFASPASNAVTGNVIRVCGQAMIGA
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
Formula
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
4fw8 Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
4fw8
Crystal structure of hexanoyl-CoA bound to beta-ketoacyl reductase FabG4 of Mycobacterium tuberculosis
Resolution
2.79 Å
Binding residue
(original residue number in PDB)
G220 R223 I225 D244 L266 V268 N295 A296 G297 L345 Y360 K364 P390
Binding residue
(residue number reindexed from 1)
G193 R196 I198 D217 L239 V241 N268 A269 G270 L318 Y333 K337 P363
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S347 Y360 K364
Catalytic site (residue number reindexed from 1)
S320 Y333 K337
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004316
3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
Biological Process
GO:0030497
fatty acid elongation
GO:0035336
long-chain fatty-acyl-CoA metabolic process
GO:0046459
short-chain fatty acid metabolic process
GO:0046677
response to antibiotic
Cellular Component
GO:0005576
extracellular region
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0009274
peptidoglycan-based cell wall
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4fw8
,
PDBe:4fw8
,
PDBj:4fw8
PDBsum
4fw8
PubMed
23163771
UniProt
O53665
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