Structure of PDB 1mv8 Chain D Binding Site BS02
Receptor Information
>1mv8 Chain D (length=436) Species:
287
(Pseudomonas aeruginosa) [
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MRISIFGLGYVGAVCAGCLSARGHEVIGVDVSSTKIDLINQGKSPIVEPG
LEALLQQGRQTGRLSGTTDFKKAVLDSDVSFICVGTPSKKNGDLDLGYIE
TVCREIGFAIREKSERHTVVVRSTVLPGTVNNVVIPLIEDCSGKKAGVDF
GVGTNPEFLRESTAIKDYDFPPMTVIGELDKQTGDLLEEIYRELDAPIIR
KTVEVAEMIKYTCNVWHAAKVTFANEIGNIAKAVGVDGREVMDVICQDHK
LNLSRYYMRPGFAFGGSCLPKDVRALTYRASQLDVEHPMLGSLMRSNSNQ
VQKAFDLITSHDTRKVGLLGLSFKAGTDDLRESPLVELAEMLIGKGYELR
IFDRNVEYARVHGANKEYIESKIPHVSSLLVSDLDEVVASSDVLVLGNGD
ELFVDLVNKTPSGKKLVDLVGFMPHTTTAQAEGICW
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/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/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[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
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[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
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
1mv8 Chain D Residue 2004 [
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Receptor-Ligand Complex Structure
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PDB
1mv8
The crystal structure of GDP-mannose dehydrogenase: A key enzyme in alginate biosynthesis of P. aeruginosa
Resolution
1.55 Å
Binding residue
(original residue number in PDB)
G7 G9 Y10 V11 D30 V31 K35 V84 T86 Y98 V102 S123 T124
Binding residue
(residue number reindexed from 1)
G7 G9 Y10 V11 D30 V31 K35 V84 T86 Y98 V102 S123 T124
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T124 E161 K210 N214 C268 D272
Catalytic site (residue number reindexed from 1)
T124 E161 K210 N214 C268 D272
Enzyme Commision number
1.1.1.132
: GDP-mannose 6-dehydrogenase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0047919
GDP-mannose 6-dehydrogenase activity
GO:0051287
NAD binding
Biological Process
GO:0006970
response to osmotic stress
GO:0036460
cellular response to cell envelope stress
GO:0042121
alginic acid biosynthetic process
GO:0044010
single-species biofilm formation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1mv8
,
PDBe:1mv8
,
PDBj:1mv8
PDBsum
1mv8
PubMed
12705829
UniProt
P11759
|ALGD_PSEAE GDP-mannose 6-dehydrogenase (Gene Name=algD)
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