Structure of PDB 1ege Chain A Binding Site BS02
Receptor Information
>1ege Chain A (length=387) Species:
9606
(Homo sapiens) [
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LGFSFEFTEQQKEFQATARKFAREEIIPVAAEYDKTGEYPVPLIRRAWEL
GLMNTHIPENCGGLGLGTFDACLISEELAYGCTGVQTAIEGNSLGQMPII
IAGNDQQKKKYLGRMTEEPLMCAYCVTEPGAGSDVAGIKTKAEKKGDEYI
INGQKMWITNGGKANWYFLLARSDPDPKAPANKAFTGFIVEADTPGIQIG
RKELNMGQRCSDTRGIVFEDVKVPKENVLIGDGAGFKVAMGAFDKTRPVV
AAGAVGLAQRALDEATKYALERKTFGKLLVEHQAISFMLAEMAMKVELAR
MSYQRAAWEVDSGRRNTYYASIAKAFAGDIANQLATDAVQILGGNGFNTE
YPVEKLMRDAKIYQIYEGTSQIQRLIVAREHIDKYKN
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
1ege Chain B Residue 399 [
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Receptor-Ligand Complex Structure
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PDB
1ege
Crystal structures of the wild type and the Glu376Gly/Thr255Glu mutant of human medium-chain acyl-CoA dehydrogenase: influence of the location of the catalytic base on substrate specificity.
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
T283 F284 L288 H291 Q349 I350 G353
Binding residue
(residue number reindexed from 1)
T274 F275 L279 H282 Q340 I341 G344
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
V135 T136 T255 E376 R388
Catalytic site (residue number reindexed from 1)
V126 T127 T246 E367 R379
Enzyme Commision number
1.3.8.7
: medium-chain acyl-CoA dehydrogenase.
Gene Ontology
Molecular Function
GO:0003995
acyl-CoA dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0042802
identical protein binding
GO:0050660
flavin adenine dinucleotide binding
GO:0070991
medium-chain fatty acyl-CoA dehydrogenase activity
Biological Process
GO:0001889
liver development
GO:0005978
glycogen biosynthetic process
GO:0006082
organic acid metabolic process
GO:0006111
regulation of gluconeogenesis
GO:0006631
fatty acid metabolic process
GO:0006635
fatty acid beta-oxidation
GO:0007507
heart development
GO:0009409
response to cold
GO:0009437
carnitine metabolic process
GO:0009791
post-embryonic development
GO:0019254
carnitine metabolic process, CoA-linked
GO:0033539
fatty acid beta-oxidation using acyl-CoA dehydrogenase
GO:0042594
response to starvation
GO:0045329
carnitine biosynthetic process
GO:0051791
medium-chain fatty acid metabolic process
GO:0051793
medium-chain fatty acid catabolic process
GO:0055007
cardiac muscle cell differentiation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0030424
axon
GO:0031966
mitochondrial membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ege
,
PDBe:1ege
,
PDBj:1ege
PDBsum
1ege
PubMed
8823176
UniProt
P11310
|ACADM_HUMAN Medium-chain specific acyl-CoA dehydrogenase, mitochondrial (Gene Name=ACADM)
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