Structure of PDB 5z20 Chain F Binding Site BS01
Receptor Information
>5z20 Chain F (length=336) Species:
287
(Pseudomonas aeruginosa) [
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KVHHHHHMRILFFSSQAYDSESFQASNHRHGFELHFQQAHLQADTAVLAQ
GFEVVCAFVNDDLSRPVLERLAAGGTRLVALRSAGYNHVDLAAAEALGLP
VVHVPAYSPHAVAEHAVGLILTLNRRLHRAYNRTREGDFSLHGLTGFDLH
GKRVGVIGTGQIGETFARIMAGFGCELLAYDPYPNPRIQALGGRYLALDA
LLAESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLINTGRGALVNAAAL
IEALKSGQLGYLGLDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVVVT
AHQAFLTREALAAIADTTLDNIAAWQDGTPRNRVRA
Ligand information
Ligand ID
NAI
InChI
InChI=1S/C21H29N7O14P2/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/h1,3-4,7-8,10-11,13-16,20-21,29-32H,2,5-6H2,(H2,23,33)(H,34,35)(H,36,37)(H2,22,24,25)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BOPGDPNILDQYTO-NNYOXOHSSA-N
SMILES
Software
SMILES
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=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=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
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=CCC(=C5)C(=O)N)O)O)O)O)N
CACTVS 3.341
NC(=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
C21 H29 N7 O14 P2
Name
1,4-DIHYDRONICOTINAMIDE ADENINE DINUCLEOTIDE;
NADH
ChEMBL
CHEMBL1234616
DrugBank
DB00157
ZINC
ZINC000008215403
PDB chain
5z20 Chain F Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5z20
Structural Basis of Sequential Allosteric Transitions in Tetrameric d-Lactate Dehydrogenases from Three Gram-Negative Bacteria.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Y100 G153 Q154 I155 Y173 D174 P175 C205 P206 T211 T232 G233 R234 H295 A297
Binding residue
(residue number reindexed from 1)
Y107 G160 Q161 I162 Y180 D181 P182 C212 P213 T218 T239 G240 R241 H302 A304
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S101 R234 D258 E263 H295
Catalytic site (residue number reindexed from 1)
S108 R241 D265 E270 H302
Enzyme Commision number
1.1.1.28
: D-lactate dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008720
D-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
View graph for
Molecular Function
External links
PDB
RCSB:5z20
,
PDBe:5z20
,
PDBj:5z20
PDBsum
5z20
PubMed
30149697
UniProt
Q9I530
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