Structure of PDB 3rnm Chain D Binding Site BS01
Receptor Information
>3rnm Chain D (length=468) Species:
9606
(Homo sapiens) [
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PIDADVTVIGSGPGGYVAAIKAAQLGFKTVCIEKNETLGGTCLNVGCIPS
KALLNNSHYYHMAHGKDFASRGIEMSEVRLNLDKMMEQKSTAVKALTGGI
AHLFKQNKVVHVNGYGKITGKNQVTATKADGGTQVIDTKNILIATGSEVT
PFPGITIDEDTIVSSTGALSLKKVPEKMVVIGAGVIGVELGSVWQRLGAD
VTAVEFLGHVGGVGIDMEISKNFQRILQKQGFKFKLNTKVTGATKKSDGK
IDVSIEAGKAEVITCDVLLVCIGRRPFTKNLGLEELGIELDPRGRIPVNT
RFQTKIPNIYAIGDVVAGPMLAHKAEDEGIICVEGMAGGAVHIDYNCVPS
VIYTHPEVAWVGKSEEQLKEEGIEYKVGKFPFAANSRAKTNADTDGMVKI
LGQKSTDRVLGAHILGPGAGEMVNEAALALEYGASCEDIARVCHAHPTLS
EAFREANLAASFGKSINF
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
3rnm Chain D Residue 480 [
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Receptor-Ligand Complex Structure
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PDB
3rnm
Structural and Thermodynamic Basis for Weak Interactions between Dihydrolipoamide Dehydrogenase and Subunit-binding Domain of the Branched-chain {alpha}-Ketoacid Dehydrogenase Complex.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
I12 G15 P16 G17 E36 K37 N38 G43 T44 C45 G49 C50 K54 Y118 G119 T148 G149 S168 I189 R280 F283 G319 D320 M326 L327 A328 H329
Binding residue
(residue number reindexed from 1)
I9 G12 P13 G14 E33 K34 N35 G40 T41 C42 G46 C47 K51 Y115 G116 T145 G146 S165 I186 R274 F277 G313 D314 M320 L321 A322 H323
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
L41 C45 C50 S53 V188 E192 H450 H452 E457
Catalytic site (residue number reindexed from 1)
L38 C42 C47 S50 V185 E189 H444 H446 E451
Enzyme Commision number
1.8.1.4
: dihydrolipoyl dehydrogenase.
Gene Ontology
Molecular Function
GO:0004148
dihydrolipoyl dehydrogenase activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016668
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0034604
pyruvate dehydrogenase (NAD+) activity
GO:0047101
branched-chain alpha-keto acid dehydrogenase activity
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0006086
acetyl-CoA biosynthetic process from pyruvate
GO:0006120
mitochondrial electron transport, NADH to ubiquinone
GO:0006508
proteolysis
GO:0007369
gastrulation
GO:0009083
branched-chain amino acid catabolic process
GO:0042391
regulation of membrane potential
GO:0048240
sperm capacitation
Cellular Component
GO:0001669
acrosomal vesicle
GO:0005634
nucleus
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0005929
cilium
GO:0031410
cytoplasmic vesicle
GO:0031514
motile cilium
GO:0043159
acrosomal matrix
GO:0045252
oxoglutarate dehydrogenase complex
GO:0045254
pyruvate dehydrogenase complex
GO:0160157
branched-chain alpha-ketoacid dehydrogenase complex
GO:0160167
oxoadipate dehydrogenase complex
GO:1902493
acetyltransferase complex
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Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3rnm
,
PDBe:3rnm
,
PDBj:3rnm
PDBsum
3rnm
PubMed
21543315
UniProt
P09622
|DLDH_HUMAN Dihydrolipoyl dehydrogenase, mitochondrial (Gene Name=DLD)
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