Structure of PDB 7aau Chain D Binding Site BS03
Receptor Information
>7aau Chain D (length=378) Species:
3055
(Chlamydomonas reinhardtii) [
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MSETAGKPIECKAAIAWEAKKPLEVRTVTVAPPGPGEVRVQIKATALCQT
DAYTLGGLDPEGRFPCILGHEAAGVVESVGEGVTSVKPGDHVIPCYQAYC
GECKFCKHPESNLCVSVRAFTGKGVMKSDGKPRFTVDGKPIYHFMGTSTF
SEYTVVHEQSVAKIDVNAPLDKVCLLGCGVSTGWGAVFNTAKVTAGSTVA
VFGLGAVGLAVIEAAKRAGASRIIAVDIDPTKFPTAKEFGATDCINPKDH
EKPIQQVIVEMTEWGCDYTFECIGNTAVMRAALECAHRGWGTSVIVGVAA
AGQEISTRPFQLVTGRRWMGTAFGGYKSRVQVPDLVTDYMSGATLLDKYI
THNMKFDQINEAFELLHAGECLRCVLTF
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
7aau Chain D Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
7aau
Structural and functional insights into nitrosoglutathione reductase from Chlamydomonas reinhardtii.
Resolution
2.301 Å
Binding residue
(original residue number in PDB)
T182 G205 V207 D227 I228 K232 C272 I273 V296 G297 V298 A322 F323 R373
Binding residue
(residue number reindexed from 1)
T182 G205 V207 D227 I228 K232 C272 I273 V296 G297 V298 A322 F323 R373
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C48 T50 Y53 H70 C178
Catalytic site (residue number reindexed from 1)
C48 T50 Y53 H70 C178
Enzyme Commision number
1.1.1.284
: S-(hydroxymethyl)glutathione dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004022
alcohol dehydrogenase (NAD+) activity
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0051903
S-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
GO:0106321
S-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity
GO:0106322
S-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity
Biological Process
GO:0044281
small molecule metabolic process
GO:0046294
formaldehyde catabolic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7aau
,
PDBe:7aau
,
PDBj:7aau
PDBsum
7aau
PubMed
33316743
UniProt
A0A2K3D6R4
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