Structure of PDB 2nad Chain B Binding Site BS02
Receptor Information
>2nad Chain B (length=383) Species:
33067
(Pseudomonas sp. 101) [
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AKVLCVLYDDPVDGYPKTYARDDLPKIDHYPGGQTLPTPKAIDFTPGQLL
GSVSGELGLRKYLESNGHTLVVTSDKDGPDSVFERELVDADVVISQPFWP
AYLTPERIAKAKNLKLALTAGIGSDHVDLQSAIDRNVTVAEVTYCNSISV
AEHVVMMILSLVRNYLPSHEWARKGGWNIADCVSHAYDLEAMHVGTVAAG
RIGLAVLRRLAPFDVHLHYTDRHRLPESVEKELNLTWHATREDMYPVCDV
VTLNCPLHPETEHMINDETLKLFKRGAYIVNTARGKLCDRDAVARALESG
RLAGYAGDVWFPQPAPKDHPWRTMPYNGMTPHISGTTLTAQARYAAGTRE
ILECFFEGRPIRDEYLIVQGGALAGTGAHSYSK
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
2nad Chain B Residue 394 [
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Receptor-Ligand Complex Structure
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PDB
2nad
High resolution structures of holo and apo formate dehydrogenase.
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
I122 N146 V150 A198 G200 R201 I202 D221 P256 E260 T261 T282 A283 R284 D308 H332 S334 G335 S380
Binding residue
(residue number reindexed from 1)
I122 N146 V150 A198 G200 R201 I202 D221 P256 E260 T261 T282 A283 R284 D308 H332 S334 G335 S380
Annotation score
4
Binding affinity
MOAD
: Ki=0.1uM
Enzymatic activity
Catalytic site (original residue number in PDB)
N146 R284 D308 Q313 H332
Catalytic site (residue number reindexed from 1)
N146 R284 D308 Q313 H332
Enzyme Commision number
1.17.1.9
: formate dehydrogenase.
Gene Ontology
Molecular Function
GO:0008863
formate dehydrogenase (NAD+) 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:0042183
formate catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2nad
,
PDBe:2nad
,
PDBj:2nad
PDBsum
2nad
PubMed
8114093
UniProt
P33160
|FDH_PSESR Formate dehydrogenase
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