Structure of PDB 3ej6 Chain D Binding Site BS01
Receptor Information
>3ej6 Chain D (length=681) Species:
5141
(Neurospora crassa) [
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EVDARQRLKEVEVDDNGQFMTTDFGGNIEEQFSLKAGGRGSTLLEDFIFR
QKLQHFDHERIPERVVHARGAGAHGIFTSYGDWSNITAASFLGAKDKQTP
VFVRFSTVAGSRGSADTARDVHGFATRFYTDEGNFDIVGNNIPVFFIQDA
IRFPDLIHSVKPSPDNEVPQAATAHDSAWDFFSSQPSALHTLFWAMSGNG
IPRSYRHMDGFGIHTFRLVTEDGKSKLVKWHWKTKQGKAALVWEEAQVLA
GKNADFHRQDLWDAIESGNAPSWELAVQLIDEDKAQAYGFDLLDPTKFLP
EEFAPLQVLGEMTLNRNPMNYFAETEQISFQPGHIVRGVDFTEDPLLQGR
LYSYLDTQLNRHRGPNFEQLPINRPVSGVHNNHRDGQGQAWIHKNIHHYS
PSYLNKGYPAQANQTVGRGFFTTPGRTASGVLNRELSATFDDHYTQPRLF
FNSLTPVEQQFVINAIRFEASHVTNEQVKKNVLEQLNKISNDVAKRVAVA
LGLEAPQPDPTYYHNNVTRGVSIFNESLPTIATLRVGVLSTTKGGSLDKA
KALKEQLEKDGLKVTVIAEYLASGVDQTYSAADATAFDAVVVAEGAERVF
SGKGAMSPLFPAGRPSQILTDGYRWGKPVAAVGSAKKALQSIGVEEKEAG
VYAGAQDEVIKGVEEGLKVFKFLERFAVDGD
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
3ej6 Chain D Residue 4003 [
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Receptor-Ligand Complex Structure
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PDB
3ej6
Structure-Function Relationships in Fungal Large-Subunit Catalases
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
R99 V101 H102 R139 V173 G174 N175 F180 F188 I248 H249 F365 L381 G384 R385 S388 Y389 T392 Q393 R396
Binding residue
(residue number reindexed from 1)
R64 V66 H67 R104 V138 G139 N140 F145 F153 I213 H214 F330 L346 G349 R350 S353 Y354 T357 Q358 R361
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H102 N175 Q366
Catalytic site (residue number reindexed from 1)
H67 N140 Q331
Enzyme Commision number
1.11.1.6
: catalase.
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006979
response to oxidative stress
GO:0042744
hydrogen peroxide catabolic process
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3ej6
,
PDBe:3ej6
,
PDBj:3ej6
PDBsum
3ej6
PubMed
19109972
UniProt
Q9C169
|CAT3_NEUCR Catalase-3 (Gene Name=cat-3)
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