Structure of PDB 1mi3 Chain C Binding Site BS01
Receptor Information
>1mi3 Chain C (length=319) [
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SIPDIKLSSGHLMPSIGFGCWKLANATAGEQVYQAIKAGYRLFDGAEDYG
NEKEVGDGVKRAIDEGLVKREEIFLTSKLWNNYHDPKNVETALNKTLADL
KVDYVDLFLIHFPIAFKFVPIEEKYPPGFYCGDGNNFVYEDVPILETWKA
LEKLVAAGKIKSIGVSNFPGALLLDLLRGATIKPAVLQVEHHPYLQQPKL
IEFAQKAGVTITAYSSFGPQSFVEMNQGRALNTPTLFAHDTIKAIAAKYN
KTPAEVLLRWAAQRGIAVIPKSNLPERLVQNRSFNTFDLTKEDFEEIAKL
DIGLRFNDPWDWDNIPIFV
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
1mi3 Chain C Residue 3350 [
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Receptor-Ligand Complex Structure
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PDB
1mi3
Structure of xylose reductase bound to NAD+ and the basis for single and dual co-substrate specificity in family 2 aldo-keto reductases
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
G22 C23 W24 D47 Y52 H114 N170 Q191 Y217 S218 F220 Q223 S224 E227 A257 I272 P273 K274 N276 R280 Q283 N284 N310
Binding residue
(residue number reindexed from 1)
G19 C20 W21 D44 Y49 H111 N167 Q188 Y214 S215 F217 Q220 S221 E224 A254 I269 P270 K271 N273 R277 Q280 N281 N307
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D47 Y52 K81 H114
Catalytic site (residue number reindexed from 1)
D44 Y49 K78 H111
Enzyme Commision number
1.1.1.307
: D-xylose reductase [NAD(P)H].
Gene Ontology
Molecular Function
GO:0004032
aldose reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0032866
D-xylose reductase (NADPH) activity
Biological Process
GO:0042732
D-xylose metabolic process
GO:0042843
D-xylose 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:1mi3
,
PDBe:1mi3
,
PDBj:1mi3
PDBsum
1mi3
PubMed
12733986
UniProt
O74237
|XYL1_CANTE NAD(P)H-dependent D-xylose reductase (Gene Name=XYL1)
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