Structure of PDB 4gl4 Chain B Binding Site BS03
Receptor Information
>4gl4 Chain B (length=378) Species:
3702
(Arabidopsis thaliana) [
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ATQGQVITCKAAVAYEPNKPLVIEDVQVAPPQAGEVRIKILYTALCHTDA
YTWSGKDPEGLFPCILGHEAAGIVESVGEGVTEVQAGDHVIPCYQAECRE
CKFCKSGKTNLCGKVRSATGVGIMMNDRKSRFSVNGKPIYHFMGTSTFSQ
YTVVHDVSVAKIDPTAPLDKVCLLGCGVPTGLGAVWNTAKVEPGSNVAIF
GLGTVGLAVAEGAKTAGASRIIGIDIDSKKYETAKKFGVNEFVNPKDHDK
PIQEVIVDLTDGGVDYSFECIGNVSVMRAALECCHKGWGTSVIVGVAASG
QEISTRPFQLVTGRVWKGTAFGGFKSRTQVPWLVEKYMNKEIKVDEYITH
NLTLGEINKAFDLLHEGTCLRCVLDTSK
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
4gl4 Chain B Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
4gl4
Crystal structure and kinetic behavior of alcohol dehydrogenase III/S-nitrosoglutathione reductase from arabidopsis thalina
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H48 Y95 C177 T181 G204 V206 D226 I227 C271 I272 G296 V297 A321
Binding residue
(residue number reindexed from 1)
H47 Y94 C176 T180 G203 V205 D225 I226 C270 I271 G295 V296 A320
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C47 H48 T49 Y52 H69 E70 C99 C102 C105 C113 R117 C177 T181 R372
Catalytic site (residue number reindexed from 1)
C46 H47 T48 Y51 H68 E69 C98 C101 C104 C112 R116 C176 T180 R371
Enzyme Commision number
1.1.1.-
1.1.1.1
: alcohol dehydrogenase.
1.1.1.284
: S-(hydroxymethyl)glutathione dehydrogenase.
Gene Ontology
Molecular Function
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:0080007
S-nitrosoglutathione reductase (NADH) 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:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:4gl4
,
PDBe:4gl4
,
PDBj:4gl4
PDBsum
4gl4
PubMed
UniProt
Q96533
|ADHX_ARATH Alcohol dehydrogenase class-3 (Gene Name=ADH2)
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