Structure of PDB 2ayl Chain B Binding Site BS03
Receptor Information
>2ayl Chain B (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
MNH
InChI
InChI=1S/C34H34N4O4.Mn/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;+6/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
UIBYYPDLEONCGQ-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.2
Cc1c2cc3[n+]4c(cc5c(c(c6n5[Mn@+2]47n2c(c1CCC(=O)O)cc8[n+]7c(c6)C(=C8CCC(=O)O)C)C=C)C)C(=C3C)C=C
CACTVS 3.370
CC1=C(CCC(O)=O)C2=CC3=[N@+]4C(=Cc5n6c(C=C7C(=C(C)C8=[N@+]7[Mn@@++]46[N@]2C1=C8)C=C)c(C)c5C=C)C(=C3CCC(O)=O)C
ACDLabs 12.01
O=C(O)CCC=1c4[n+]3C(C=1C)=Cc8c(c(c7cc2C(=C(C6=[n+]2[Mn+2]3(n5c(c4)C(=C(C5=C6)C)CCC(=O)O)n78)C)/C=C)C)/C=C
CACTVS 3.370
CC1=C(CCC(O)=O)C2=CC3=[N+]4C(=Cc5n6c(C=C7C(=C(C)C8=[N+]7[Mn++]46[N]2C1=C8)C=C)c(C)c5C=C)C(=C3CCC(O)=O)C
OpenEye OEToolkits 1.7.2
Cc1c2cc3[n+]4c(cc5c(c(c6n5[Mn+2]47n2c(c1CCC(=O)O)cc8[n+]7c(c6)C(=C8CCC(=O)O)C)C=C)C)C(=C3C)C=C
Formula
C34 H32 Mn N4 O4
Name
MANGANESE PROTOPORPHYRIN IX
ChEMBL
DrugBank
ZINC
PDB chain
2ayl Chain B Residue 1601 [
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Receptor-Ligand Complex Structure
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PDB
2ayl
2.0 angstroms structure of prostaglandin H2 synthase-1 reconstituted with a manganese porphyrin cofactor.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
A1202 Q1203 H1207 K1211 T1212 L1295 H1386 H1388 M1391 I1444 V1447 D1450
Binding residue
(residue number reindexed from 1)
A171 Q172 H176 K180 T181 L264 H355 H357 M360 I413 V416 D419
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q1203 H1207 L1384 Y1385 H1388 G1526 S1530
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:2ayl
,
PDBe:2ayl
,
PDBj:2ayl
PDBsum
2ayl
PubMed
16421446
UniProt
P05979
|PGH1_SHEEP Prostaglandin G/H synthase 1 (Gene Name=PTGS1)
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