Structure of PDB 1egc Chain C Binding Site BS01
Receptor Information
>1egc Chain C (length=387) Species:
9606
(Homo sapiens) [
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LGFSFEFTEQQKEFQATARKFAREEIIPVAAEYDKTGEYPVPLIRRAWEL
GLMNTHIPENCGGLGLGTFDACLISEELAYGCTGVQTAIEGNSLGQMPII
IAGNDQQKKKYLGRMTEEPLMCAYCVTEPGAGSDVAGIKTKAEKKGDEYI
INGQKMWITNGGKANWYFLLARSDPDPKAPANKAFTGFIVEADTPGIQIG
RKELNMGQRCSDTRGIVFEDVKVPKENVLIGDGAGFKVAMGAFDKERPVV
AAGAVGLAQRALDEATKYALERKTFGKLLVEHQAISFMLAEMAMKVELAR
MSYQRAAWEVDSGRRNTYYASIAKAFAGDIANQLATDAVQILGGNGFNTE
YPVEKLMRDAKIYQIYGGTSQIQRLIVAREHIDKYKN
Ligand information
Ligand ID
CO8
InChI
InChI=1S/C29H50N7O17P3S/c1-4-5-6-7-8-9-20(38)57-13-12-31-19(37)10-11-32-27(41)24(40)29(2,3)15-50-56(47,48)53-55(45,46)49-14-18-23(52-54(42,43)44)22(39)28(51-18)36-17-35-21-25(30)33-16-34-26(21)36/h16-18,22-24,28,39-40H,4-15H2,1-3H3,(H,31,37)(H,32,41)(H,45,46)(H,47,48)(H2,30,33,34)(H2,42,43,44)/t18-,22-,23-,24+,28-/m1/s1
InChIKey
KQMZYOXOBSXMII-CECATXLMSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
ACDLabs 10.04
O=C(SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O)CCCCCCC
OpenEye OEToolkits 1.5.0
CCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)CO[P@](=O)(O)O[P@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
CACTVS 3.341
CCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO[P@@](O)(=O)O[P@@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
CACTVS 3.341
CCCCCCCC(=O)SCCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
Formula
C29 H50 N7 O17 P3 S
Name
OCTANOYL-COENZYME A
ChEMBL
DrugBank
DB02910
ZINC
ZINC000096014975
PDB chain
1egc Chain C Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
1egc
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
2.6 Å
Binding residue
(original residue number in PDB)
E99 G100 S142 V144 N191 F245 M249 F252 D253 T326 Y375 G376 R388
Binding residue
(residue number reindexed from 1)
E90 G91 S133 V135 N182 F236 M240 F243 D244 T317 Y366 G367 R379
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
V135 T136 E255 G376 R388
Catalytic site (residue number reindexed from 1)
V126 T127 E246 G367 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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1egc
,
PDBe:1egc
,
PDBj:1egc
PDBsum
1egc
PubMed
8823176
UniProt
P11310
|ACADM_HUMAN Medium-chain specific acyl-CoA dehydrogenase, mitochondrial (Gene Name=ACADM)
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