Structure of PDB 6ynz Chain e Binding Site BS01
Receptor Information
>6ynz Chain e (length=417) Species:
5911
(Tetrahymena thermophila) [
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KRKKTSGDLDNYDVLFVGANLGGICSNHFDKDTHGKYKCFVSFDQPINQI
YSVRIPYEQQRVRKSEYIHFSKKSINQFTPSEMLAVKEILPEQNAVVLSS
GRRIGYNQLVLATGLKHDFSQIKGFYEALEHPEHPVYANRDPETWRSAQH
KYSKYISNFKSGDGYFCIPEYPYAGEVECFNFFVSDEVWKWAQHHGALSP
KHTFTIVNANEKFVHYCDSADAFIKERLEKRGIRVEYNTKLLEVHQDGQK
ATFINTKTGEKSVRDYNNLYSIVPSKRQEFLDKAGLTNGNGLLNVDHQTL
QHKKYKNIFGLGDAADLPTTKTFWAGWYQIAVVRNNVKRNLQGQTLNAHY
DGFSKVPLFTGHQTLTYVAHSYGGVGNWQHLKHNNGGILAWMRYRSWAKG
MAKKFQDFYNGARLGPP
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
6ynz Chain e Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
6ynz
Type III ATP synthase is a symmetry-deviated dimer that induces membrane curvature through tetramerization.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
G44 N46 L47 S68 F69 D70 Q71 Y77 A111 V112 A138 T139 G140 H143 N165 A200 G201 E204 Q304 F306 G338 D339 T348
Binding residue
(residue number reindexed from 1)
G18 N20 L21 S42 F43 D44 Q45 Y51 A85 V86 A112 T113 G114 H117 N139 A174 G175 E178 Q278 F280 G312 D313 T322
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
GO:0070224
sulfide:quinone oxidoreductase activity
GO:0071949
FAD binding
Biological Process
GO:0070221
sulfide oxidation, using sulfide:quinone oxidoreductase
Cellular Component
GO:0005739
mitochondrion
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6ynz
,
PDBe:6ynz
,
PDBj:6ynz
PDBsum
6ynz
PubMed
33093501
UniProt
I7LVQ8
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