Structure of PDB 3n8x Chain A Binding Site BS01
Receptor Information
>3n8x Chain A (length=553) Species:
9940
(Ovis aries) [
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PVNPCCYYPCQHQGICVRFGLDRYQCDCTRTGYSGPNCTIPEIWTWLRTT
LRPSPSFIHFLLTHGRWLWDFVNATFIRDTLMRLVLTVRSNLIPSPPTYN
IAHDYISWESFSNVSYYTRILPSVPRDCPTPMGTKGKKQLPDAEFLSRRF
LLRRKFIPDPQGTNLMFAFFAQHFTHQFFKTSGKMGPGFTKALGHGVDLG
HIYGDNLERQYQLRLFKDGKLKYQMLNGEVYPPSVEEAPVLMHYPRGIPP
QSQMAVGQEVFGLLPGLMLYATIWLREHNRVCDLLKAEHPTWGDEQLFQT
ARLILIGETIKIVIEEYVQQLSGYFLQLKFDPELLFGAQFQYRNRIAMEF
NQLYHWHPLMPDSFRVGPQDYSYEQFLFNTSMLVDYGVEALVDAFSRQPA
GRIGGGRNIDHHILHVAVDVIKESRVLRLQPFNEYRKRFGMKPYTSFQEL
TGEKEMAAELEELYGDIDALEFYPGLLLEKCHPNSIFGESMIEMGAPFSL
KGLLGNPICSPEYWKASTFGGEVGFNLVKTATLKKLVCLNTKTCPYVSFH
VPD
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
3n8x Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
3n8x
Comparison of Cyclooxygenase-1 Crystal Structures: Cross-Talk between Monomers Comprising Cyclooxygenase-1 Homodimers
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
A202 Q203 H207 F210 K211 T212 L295 N382 Y385 H386 H388 M391 I444 V447
Binding residue
(residue number reindexed from 1)
A171 Q172 H176 F179 K180 T181 L264 N351 Y354 H355 H357 M360 I413 V416
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q203 H207 L384 Y385 H388 G526 S530
Catalytic site (residue number reindexed from 1)
Q172 H176 L353 Y354 H357 G495 S499
Enzyme Commision number
1.14.99.1
: prostaglandin-endoperoxide synthase.
Gene Ontology
Molecular Function
GO:0004601
peroxidase activity
GO:0004666
prostaglandin-endoperoxide synthase activity
GO:0016702
oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
GO:0020037
heme binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0001516
prostaglandin biosynthetic process
GO:0006979
response to oxidative stress
GO:0008217
regulation of blood pressure
GO:0019371
cyclooxygenase pathway
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0016020
membrane
GO:0043005
neuron projection
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3n8x
,
PDBe:3n8x
,
PDBj:3n8x
PDBsum
3n8x
PubMed
20669977
UniProt
P05979
|PGH1_SHEEP Prostaglandin G/H synthase 1 (Gene Name=PTGS1)
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