Structure of PDB 2ix5 Chain C Binding Site BS02
Receptor Information
>2ix5 Chain C (length=415) Species:
3702
(Arabidopsis thaliana) [
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KSSYFDLPPMEMSVAFPQATPASTFPPCTSDYYHFNDLLTPEEQAIRKKV
RECMEKEVAPIMTEYWEKAEFPFHITPKLGAMGVAGGSIKGYGCPGLSIT
ANAIATAEIARVDASCSTFILVHSSLGMLTIALCGSEAQKEKYLPSLAQL
NTVACWALTEPDNGSDASGLGTTATKVEGGWKINGQKRWIGNSTFADLLI
IFARNTTTNQINGFIVKKDAPGLKATKIPNKIGLRMVQNGDILLQNVFVP
DEDRLPGVNSFQDTSKVLAVSRVMVAWQPIGISMGIYDMCHRYLKERKQF
GAPLAAFQLNQQKLVQMLGNVQAMFLMGWRLCKLYETGQMTPGQASLGKA
WISSKARETASLGRELLGGNGILADFLVAKAFCDLEPIYTYEGTYDINTL
VTGREVTGIASFKPA
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
2ix5 Chain C Residue 1433 [
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Receptor-Ligand Complex Structure
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PDB
2ix5
Controlling Electron Transfer in Acyl-Coa Oxidases and Dehydrogenases: A Structural View.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
L174 T175 G180 S181 W205 N255 P403 Y407 T410 D412 F428
Binding residue
(residue number reindexed from 1)
L158 T159 G164 S165 W189 N239 P387 Y391 T394 D396 F412
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L174 T175 S287 E408 R420
Catalytic site (residue number reindexed from 1)
L158 T159 S271 E392 R404
Enzyme Commision number
1.3.3.6
: acyl-CoA oxidase.
Gene Ontology
Molecular Function
GO:0003995
acyl-CoA dehydrogenase activity
GO:0003997
acyl-CoA oxidase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0050660
flavin adenine dinucleotide binding
GO:1901149
salicylic acid binding
Biological Process
GO:0006631
fatty acid metabolic process
GO:0006635
fatty acid beta-oxidation
GO:0009793
embryo development ending in seed dormancy
GO:0046459
short-chain fatty acid metabolic process
Cellular Component
GO:0005777
peroxisome
GO:0005829
cytosol
GO:0009514
glyoxysome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ix5
,
PDBe:2ix5
,
PDBj:2ix5
PDBsum
2ix5
PubMed
16887802
UniProt
Q96329
|ACOX4_ARATH Acyl-coenzyme A oxidase 4, peroxisomal (Gene Name=ACX4)
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