Structure of PDB 2a94 Chain A Binding Site BS01
Receptor Information
>2a94 Chain A (length=315) Species:
5833
(Plasmodium falciparum) [
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APKAKIVLVGSGMIGGVMATLIVQKNLGDVVLFDIVKNMPHGKALDTSHT
NVMAYSNCKVSGSNTYDDLAGADVVIVTAGFTKAPGKSDKEWNRDDLLPL
NNKIMIEIGGHIKKNCPNAFIIVVTNPVDVMVQLLHQHSGVPKNKIIGLG
GVLDTSRLKYYISQKLNVCPRDVNAHIVGAHGNKMVLLKRYITVGGIPLQ
EFINNKLISDAELEAIFDRTVNTALEIVNLHASPYVAPAAAIIEMAESYL
KDLKKVLICSTLLEGQYGHSDIFGGTPVVLGANGVEQVIELQLNSEEKAK
FDEAIAETKRMKALA
Ligand information
Ligand ID
AP0
InChI
InChI=1S/C22H30N6O14P2/c1-10(29)11-3-2-4-27(5-11)21-17(32)15(30)12(40-21)6-38-43(34,35)42-44(36,37)39-7-13-16(31)18(33)22(41-13)28-9-26-14-19(23)24-8-25-20(14)28/h2,4-5,8-9,12-13,15-18,21-22,30-33H,3,6-7H2,1H3,(H,34,35)(H,36,37)(H2,23,24,25)/t12-,13-,15-,16-,17-,18-,21-,22-/m1/s1
InChIKey
CIWXCGUGRDQCHH-RBEMOOQDSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(=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
ACDLabs 12.01
Nc1ncnc2c1ncn2C1OC(COP(=O)(O)OP(=O)(O)OCC2OC(N3C=C(CC=C3)C(C)=O)C(O)C2O)C(O)C1O
OpenEye OEToolkits 2.0.7
CC(=O)C1=CN(C=CC1)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O
OpenEye OEToolkits 2.0.7
CC(=O)C1=CN(C=CC1)[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
CACTVS 3.385
CC(=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
C22 H30 N6 O14 P2
Name
ACETYL PYRIDINE ADENINE DINUCLEOTIDE, REDUCED
ChEMBL
DrugBank
ZINC
ZINC000150348266
PDB chain
2a94 Chain A Residue 336 [
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Receptor-Ligand Complex Structure
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PDB
2a94
Structure of Lactate Dehydrogenase from Plasmodium vivax: Complexes with NADH and APADH.
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
G29 M30 I31 F52 D53 I54 Y85 T97 A98 G99 F100 V138 N140 V142 L163 H195
Binding residue
(residue number reindexed from 1)
G12 M13 I14 F33 D34 I35 Y66 T78 A79 G80 F81 V124 N126 V128 L149 H181
Annotation score
3
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
Biological Process
GO:0006089
lactate metabolic process
GO:0006090
pyruvate metabolic process
GO:0019752
carboxylic acid metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2a94
,
PDBe:2a94
,
PDBj:2a94
PDBsum
2a94
PubMed
16331982
UniProt
Q27743
|LDH_PLAFD L-lactate dehydrogenase
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