Structure of PDB 1oc4 Chain A Binding Site BS01
Receptor Information
>1oc4 Chain A (length=315) Species:
5821
(Plasmodium berghei) [
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APKAKIVLVGSGMIGGVMATLIVQKNLGDVVMFDIVKNMPHGKALDTSHT
NVMAYSNCKVSGSNTYDDLKDADVVIVTAGFTKAPGKSDKEWNRDDLLPL
NNKIMIEIGGHIKNNCPNAFIIVVTNPVDVMVQLLHQHSGVPKNKIVGLG
GVLDTSRLKYYISQKLNVCPRDVNAHIVGAHGNKMVLLKRYITVGGIPLQ
EFINNKKITDQELDAIFDRTINTALEIVNLHASPYVAPAAAIIEMAESYI
RDLRKVLICSTLLEGQYGHKDIFAGTPLVIGGNGVEQVIELQLNADEKKK
FDEAVAETSRMKALI
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
1oc4 Chain A Residue 1330 [
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Receptor-Ligand Complex Structure
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PDB
1oc4
Crystal Structure of Plasmodium Berghei Lactate Dehydrogenase Indicates the Unique Structural Differences of These Enzymes are Shared Across the Plasmodium Genus
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
G27 G29 M30 I31 F52 D53 I54 Y85 T97 A98 G99 F100 T101 V138 N140 L163 L167 H195
Binding residue
(residue number reindexed from 1)
G10 G12 M13 I14 F33 D34 I35 Y66 T78 A79 G80 F81 T82 V124 N126 L149 L153 H181
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
R109 D168 R171 H195
Catalytic site (residue number reindexed from 1)
R94 D154 R157 H181
Enzyme Commision number
1.1.1.27
: L-lactate dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004459
L-lactate dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0051287
NAD binding
Biological Process
GO:0006089
lactate metabolic process
GO:0006090
pyruvate metabolic process
GO:0006096
glycolytic process
GO:0019752
carboxylic acid metabolic process
GO:0042866
pyruvate biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:1oc4
,
PDBe:1oc4
,
PDBj:1oc4
PDBsum
1oc4
PubMed
12967707
UniProt
Q7SI97
|LDH_PLABA L-lactate dehydrogenase (Gene Name=LDH)
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