Structure of PDB 7r5t Chain BBB Binding Site BS01
Receptor Information
>7r5t Chain BBB (length=383) Species:
511145
(Escherichia coli str. K-12 substr. MG1655) [
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ANRMILNETAWFGRGAVGALTDEVKRRGYQKALIVTDKTLVQCGVVAKVT
DKMDAAGLAWAIYDGVVPNPTITVVKEGLGVFQNSGADYLIAIGGGSPQD
TCKAIGIISNNPEFADVRSLEGLSPTNKPSVPILAIPTTAGTAAEVTINY
VITDEEKRRKFVCVDPHDIPQVAFIDADMMDGMPPALKAATGVDALTHAI
EGYITRGAWALTDALHIKAIEIIAGALRGSVAGDKDAGEEMALGQYVAGM
GISNVGLGLVHGMAHPLGAFYNTPHGVANAILLPHVMRYNADFTGEKYRD
IARVMGVKVEGMSLEEARNAAVEAVFALNRDVGIPPHLRDVGVRKEDIPA
LAQAALDDVCTGGNPREATLEDIVELYHTAWTS
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
7r5t Chain BBB Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
7r5t
Structures of lactaldehyde reductase, FucO, link enzyme activity to hydrogen bond networks and conformational dynamics.
Resolution
1.85 Å
Binding residue
(original residue number in PDB)
D39 L42 G97 G98 S99 D102 T140 T141 T144 A146 N151 Y152 K162 G184 M185 L189 H277
Binding residue
(residue number reindexed from 1)
D37 L40 G95 G96 S97 D100 T138 T139 T142 A144 N149 Y150 K160 G182 M183 L187 H275
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.1.1.77
: lactaldehyde reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004022
alcohol dehydrogenase (NAD+) activity
GO:0008198
ferrous iron binding
GO:0008912
lactaldehyde reductase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0052660
R-lactaldehyde reductase activity
GO:0052661
S-lactaldehyde reductase activity
Biological Process
GO:0006004
fucose metabolic process
GO:0019301
rhamnose catabolic process
GO:0019317
fucose catabolic process
GO:0042355
L-fucose catabolic process
GO:0042846
glycol catabolic process
GO:0051143
propanediol metabolic 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:7r5t
,
PDBe:7r5t
,
PDBj:7r5t
PDBsum
7r5t
PubMed
36002154
UniProt
P0A9S1
|FUCO_ECOLI Lactaldehyde reductase (Gene Name=fucO)
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