Structure of PDB 3zwa Chain A Binding Site BS01
Receptor Information
>3zwa Chain A (length=727) Species:
10116
(Rattus norvegicus) [
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VPRGSHMAEYLRLPHSLAMIRLCNPPVNAVSPTVIREVRNGLQKAGSDHT
VKAIVICGANGNFCAGADIHGFSAFTPGLALGSLVDEIQRYQKPVLAAIQ
GVALGGGLELALGCHYRIANAKARVGLPEVTLGILPGARGTQLLPRVVGV
PVALDLITSGKYLSADEALRLGILDAVVKSDPVEEAIKFAQKIIDKPIEP
RRIFNKPVPSLPNMDSVFAEAIAKVRKQYPGVLAPETCVRSIQASVKHPY
EVGIKEEEKLFMYLRASGQAKALQYAFFAEKSANKWSTPSGASWKTASAQ
PVSSVGVLGLGTMGRGIAISFARVGISVVAVESDPKQLDAAKKIITFTLE
KEASRAHQNGQASAKPKLRFSSSTKELSTVDLVVEAVFEDMNLKKKVFAE
LSALCKPGAFLCTNTSALNVDDIASSTDRPQLVIGTHFFSPAHVMRLLEV
IPSRYSSPTTIATVMSLSKKIGKIGVVVGNCYGFVGNRMLAPYYNQGFFL
LEEGSKPEDVDGVLEEFGFKMGPFRVSDLAGLDVGWKIRKGQGLTGPSLP
PGTPVRKRGNSRYSPLGDMLCEAGRFGQKTGKGWYQYDKPLGRIHKPDPW
LSTFLSQYREVHHIEQRTISKEEILERCLYSLINEAFRILEEGMAARPEH
IDVIYLHGYGWPRHKGGPMFYAASVGLPTVLEKLQKYYRQNPDIPQLEPS
DYLRRLVAQGSPPLKEWQSLAGPHGSK
Ligand information
Ligand ID
3H9
InChI
InChI=1S/C27H46N7O18P3S/c1-4-5-15(35)10-18(37)56-9-8-29-17(36)6-7-30-25(40)22(39)27(2,3)12-49-55(46,47)52-54(44,45)48-11-16-21(51-53(41,42)43)20(38)26(50-16)34-14-33-19-23(28)31-13-32-24(19)34/h13-16,20-22,26,35,38-39H,4-12H2,1-3H3,(H,29,36)(H,30,40)(H,44,45)(H,46,47)(H2,28,31,32)(H2,41,42,43)/p-4/t15-,16+,20+,21+,22-,26+/m0/s1
InChIKey
VAAHKRMGOFIORX-IKTBLOROSA-J
SMILES
Software
SMILES
CACTVS 3.370
CCC[CH](O)CC(=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
CACTVS 3.370
CCC[C@H](O)CC(=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
OpenEye OEToolkits 1.7.2
CCC[C@@H](CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([O-])OP(=O)([O-])OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)([O-])[O-])O)O
OpenEye OEToolkits 1.7.2
CCCC(CC(=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)O
Formula
C27 H42 N7 O18 P3 S
Name
(S)-3-Hydroxyhexanoyl-CoA
ChEMBL
DrugBank
ZINC
PDB chain
3zwa Chain A Residue 1725 [
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Receptor-Ligand Complex Structure
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PDB
3zwa
The Isomerase and Hydratase Reaction Mechanism of the Crotonase Active Site of the Multifunctional Enzyme (Type-1), as Deduced from Structures of Complexes with 3S-Hydroxy- Acyl-Coa.
Resolution
2.47 Å
Binding residue
(original residue number in PDB)
V21 A59 G60 A61 D62 I63 L98 E103 R118 E123 L126 G131 Y156
Binding residue
(residue number reindexed from 1)
V27 A65 G66 A67 D68 I69 L104 E109 R124 E129 L132 G137 Y162
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
A61 F66 G76 G100 E103 P122 E123 P130 G131 K249 S410 H431 E443 N481
Catalytic site (residue number reindexed from 1)
A67 F72 G82 G106 E109 P128 E129 P136 G137 K255 S416 H437 E449 N487
Enzyme Commision number
1.1.1.35
: 3-hydroxyacyl-CoA dehydrogenase.
4.2.1.17
: enoyl-CoA hydratase.
5.3.3.8
: Delta(3)-Delta(2)-enoyl-CoA isomerase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003857
3-hydroxyacyl-CoA dehydrogenase activity
GO:0004165
delta(3)-delta(2)-enoyl-CoA isomerase activity
GO:0004300
enoyl-CoA hydratase activity
GO:0016491
oxidoreductase activity
GO:0016509
long-chain-3-hydroxyacyl-CoA dehydrogenase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0016829
lyase activity
GO:0016853
isomerase activity
GO:0016863
intramolecular oxidoreductase activity, transposing C=C bonds
GO:0019899
enzyme binding
GO:0070403
NAD+ binding
Biological Process
GO:0006631
fatty acid metabolic process
GO:0006635
fatty acid beta-oxidation
Cellular Component
GO:0005777
peroxisome
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3zwa
,
PDBe:3zwa
,
PDBj:3zwa
PDBsum
3zwa
PubMed
23351063
UniProt
P07896
|ECHP_RAT Peroxisomal bifunctional enzyme (Gene Name=Ehhadh)
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