Structure of PDB 1bdm Chain A Binding Site BS01
Receptor Information
>1bdm Chain A (length=317) Species:
274
(Thermus thermophilus) [
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MKAPVRVAVTGAAGQIGYSLLFRIAAGEMLGKDQPVILQLLEIPQAMKAL
EGVVMELEDCAFPLLAGLEATDDPDVAFKDADYALLVGAAPLQVNGKIFT
EQGRALAEVAKKDVKVLVVGNPANTNALIAYKNAPGLNPRNFTAMTRLDH
NRAKAQLAKKTGTGVDRIRRMTVWGNHSSIMFPDLFHAEVDGRPALELVD
MEWYEKVFIPTVAQRGAAIIQARGASSAASAANAAIEHIRDWALGTPEGD
WVSMAVPSQGEYGIPEGIVYSFPVTAKDGAYRVVEGLEINEFARKRMEIT
AQELLDEMEQVKALGLI
Ligand information
Ligand ID
NAX
InChI
InChI=1S/C21H31N7O15P2/c22-17-12-19(25-6-24-17)28(7-26-12)21-16(33)14(31)10(42-21)5-40-45(37,38)43-44(35,36)39-4-9-13(30)15(32)20(41-9)27-3-8(18(23)34)1-2-11(27)29/h3,6-7,9-11,13-16,20-21,29-33H,1-2,4-5H2,(H2,23,34)(H,35,36)(H,37,38)(H2,22,24,25)/t9-,10-,11+,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
IDBZKGQRLBFUFQ-VPHRTNKSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)C1=CN([CH](O)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
CACTVS 3.341
NC(=O)C1=CN([C@@H](O)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)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=C(CCC5O)C(=O)N)O)O)O)O)N
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=C(CC[C@@H]5O)C(=O)N)O)O)O)O)N
Formula
C21 H31 N7 O15 P2
Name
BETA-6-HYDROXY-1,4,5,6-TETRHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE
ChEMBL
DrugBank
ZINC
ZINC000008219662
PDB chain
1bdm Chain A Residue 334 [
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Receptor-Ligand Complex Structure
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PDB
1bdm
Determinants of protein thermostability observed in the 1.9-A crystal structure of malate dehydrogenase from the thermophilic bacterium Thermus flavus.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
G10 G13 Q14 I15 E41 I42 V86 V128 G129 N130 M154 H186
Binding residue
(residue number reindexed from 1)
G11 G14 Q15 I16 E42 I43 V87 V119 G120 N121 M145 H177
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
D158 H186
Catalytic site (residue number reindexed from 1)
D149 H177
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:1bdm
,
PDBe:1bdm
,
PDBj:1bdm
PDBsum
1bdm
PubMed
8471603
UniProt
P10584
|MDH_THETH Malate dehydrogenase (Gene Name=mdh)
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