Structure of PDB 4cuk Chain A Binding Site BS01
Receptor Information
>4cuk Chain A (length=330) Species:
90370
(Salmonella enterica subsp. enterica serovar Typhi) [
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MKLAVYSTKQYDKKYLQQVNEAFGFELEFFDFLLTEKTAKTANGCEAVCI
FVNDDGSRPVLEELKKHGVKYIALRCAGFNNVDLDAAKELGLQVVRVPAY
SPEAVAEHAIGMMMTLNRRIHRAYQRTRDANFSLEGLTGFTMHGKTAGVI
GTGKIGVAALRILKGFGMRLLAFDPYPSTAALDLGVEYVDLQTLFAESDV
ISLHCPLTPENYHLLNHAAFDQMKNGVMIINTSRGALIDSQAAIEALKNQ
KIGSLGMDVYENERDLFFEDKSVDVIQDDVFRRLSACHNVLFTGHQAFLT
AEALISISETTLQNLSQLEKGEACPNALFK
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
4cuk Chain A Residue 1331 [
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Receptor-Ligand Complex Structure
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PDB
4cuk
The Structure of Salmonella D-Lactate Dehydrogenase
Resolution
2.18 Å
Binding residue
(original residue number in PDB)
Y100 G153 K154 I155 F173 D174 P175 H204 C205 P206 N211 T232 Y260 H295 A297
Binding residue
(residue number reindexed from 1)
Y100 G153 K154 I155 F173 D174 P175 H204 C205 P206 N211 T232 Y260 H295 A297
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
S101 R234 D258 E263 H295
Catalytic site (residue number reindexed from 1)
S101 R234 D258 E263 H295
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
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:4cuk
,
PDBe:4cuk
,
PDBj:4cuk
PDBsum
4cuk
PubMed
UniProt
Q8Z780
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