Structure of PDB 2ccd Chain B Binding Site BS01
Receptor Information
>2ccd Chain B (length=715) Species:
1773
(Mycobacterium tuberculosis) [
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MKYPVEGGGNQDWWPNRLNLKVLHQNPAVADPMGAAFDYAAEVATIDVDA
LTRDIEEVMTTSQPWWPADYGHYGPLFIRMAWHAAGTYRIHDGRGGAGGG
MQRFAPLNSWPDNASLDKARRLLWPVKKKYGKKLSWADLIVFAGNCALES
MGFKTFGFGFGRVDQWEPDEVYWGKEATWLGDERYSGKRDLENPLAAVQM
GLIYVNPEGPNGNPDPMAAAVDIRETFRRMAMNDVETAALIVGGHTFGKT
HGAGPADLVGPEPEAAPLEQMGLGWKSSYGTGTGKDAITTGIEVVWTNTP
TKWDNSFLEILYGYEWELTKSPAGAWQYTAKDGAGAGTIPDPFGGPGRSP
TMLATDLSLRVDPIYERITRRWLEHPEELADEFAKAWYKLIHRDMGPVAR
YLGPLVPKQTLLWQDPVPAVSHDLVGEAEIASLKSQIRASGLTVSQLVST
AWAAASSFRGSDKRGGANGGRIRLQPQVGWEVNDPDGDLRKVIRTLEEIQ
ESFNSAAPGNIKVSFADLVVLGGCAAIEKAAKAAGHNITVPFTPGRTDAS
QEQTDVESFAVLEPKADGFRNYLGKGNPLPAEYMLLDKANLLTLSAPEMT
VLVGGLRVLGANYKRLPLGVFTEASESLTNDFFVNLLDMGITWEPSPADD
GTYQGKDGSGKVKWTGSRVDLVFGSNSELRALVEVYGADDAQPKFVQDFV
AAWDKVMNLDRFDVR
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
2ccd Chain B Residue 1741 [
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Receptor-Ligand Complex Structure
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PDB
2ccd
Hydrogen Peroxide-Mediated Isoniazid Activation Catalyzed by Mycobacterium Tuberculosis Catalase- Peroxidase (Katg) and its S315T Mutant.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
P100 I103 R104 W107 V230 P232 F252 L265 G269 H270 K274 T275 H276 T314 T315 W321 F408 W412
Binding residue
(residue number reindexed from 1)
P75 I78 R79 W82 V205 P207 F227 L240 G244 H245 K249 T250 H251 T289 T290 W296 F383 W387
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R104 H108 H270 W321 D381
Catalytic site (residue number reindexed from 1)
R79 H83 H245 W296 D356
Enzyme Commision number
1.11.1.21
: catalase peroxidase.
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0005515
protein binding
GO:0016677
oxidoreductase activity, acting on a heme group of donors, nitrogenous group as acceptor
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0070402
NADPH binding
GO:0070404
NADH binding
Biological Process
GO:0006979
response to oxidative stress
GO:0042744
hydrogen peroxide catabolic process
GO:0045739
positive regulation of DNA repair
GO:0046677
response to antibiotic
GO:0070301
cellular response to hydrogen peroxide
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005576
extracellular region
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0009274
peptidoglycan-based cell wall
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ccd
,
PDBe:2ccd
,
PDBj:2ccd
PDBsum
2ccd
PubMed
16566587
UniProt
P9WIE5
|KATG_MYCTU Catalase-peroxidase (Gene Name=katG)
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