Structure of PDB 1bmd Chain A Binding Site BS01
Receptor Information
>1bmd Chain A (length=327) Species:
274
(Thermus thermophilus) [
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MKAPVRVAVTGAAGQIGYSLLFRIAAGEMLGKDQPVILQLLEIPQAMKAL
EGVVMELEDCAFPLLAGLEATDDPDVAFKDADYALLVGAAPRKAGMERRD
LLQVNGKIFTEQGRALAEVAKKDVKVLVVGNPANTNALIAYKNAPGLNPR
NFTAMTRLDHNRAKAQLAKKTGTGVDRIRRMTVWGNHSSTMFPDLFHAEV
DGRPALELVDMEWYEKVFIPTVAQRGAAIIQARGASSAASAANAAIEHIR
DWALGTPEGDWVSMAVPSQGEYGIPEGIVYSFPVTAKDGAYRVVEGLEIN
EFARKRMEITAQELLDEMEQVKALGLI
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
1bmd Chain A Residue 334 [
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Receptor-Ligand Complex Structure
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PDB
1bmd
Determinants of protein thermostability observed in the 1.9-A crystal structure of malate dehydrogenase from the thermophilic bacterium Thermus flavus.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G10 G13 Q14 I15 E41 I42 V86 G87 V128 G129 N130 M154 H186
Binding residue
(residue number reindexed from 1)
G11 G14 Q15 I16 E42 I43 V87 G88 V129 G130 N131 M155 H187
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D158 N185 H186
Catalytic site (residue number reindexed from 1)
D159 N186 H187
Enzyme Commision number
1.1.1.37
: malate dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0016491
oxidoreductase activity
GO:0016615
malate dehydrogenase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0030060
L-malate dehydrogenase (NAD+) activity
Biological Process
GO:0006099
tricarboxylic acid cycle
GO:0006107
oxaloacetate metabolic process
GO:0006108
malate metabolic process
GO:0006734
NADH metabolic process
GO:0019752
carboxylic acid metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1bmd
,
PDBe:1bmd
,
PDBj:1bmd
PDBsum
1bmd
PubMed
8471603
UniProt
P10584
|MDH_THETH Malate dehydrogenase (Gene Name=mdh)
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