Structure of PDB 4c50 Chain B Binding Site BS01
Receptor Information
>4c50 Chain B (length=716) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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HMKYPVEGGGNQDWWPNRLNLKVLHQNPAVADPMGAAFDYAAEVATIDVD
ALTRDIEEVMTTSQPWWPADYGHYGPLFIRMAWHAAGTYRIHDGRGGAGG
GMQRFAPLNSWPSNASLDKARRLLWPVKKKYGKKLSWADLIVFAGNCALE
SMGFKTFGFGFGRVDQWEPDEVYWGKEATWLGDERYSGKRDLENPLAAVQ
MGLIYVNPEGPNGNPDPMAAAVDIRETFRRMAMNDVETAALIVGGHTFGK
THGAGPADLVGPEPEAAPLEQMGLGWKSSYGTGTGKDAITSGIEVVWTNT
PTKWDNSFLEILYGYEWELTKSPAGAWQYTAKDGAGAGTIPDPFGGPGRS
PTMLATDLSLRVDPIYERITRRWLEHPEELADEFAKAWYKLIHRDMGPVA
RYLGPLVPKQTLLWQDPVPAVSHDLVGEAEIASLKSQIRASGLTVSQLVS
TAWAAASSFRGSDKRGGANGGRIRLQPQVGWEVNDPDGDLRKVIRTLEEI
QESFNSAAPGNIKVSFADLVVLGGCAAIEKAAKAAGHNITVPFTPGRTDA
SQEQTDVESFAVLEPKADGFRNYLGKGNPLPAEYMLLDKANLLTLSAPEM
TVLVGGLRVLGANYKRLPLGVFTEASESLTNDFFVNLLDMGITWEPSPAD
DGTYQGKDGSGKVKWTGSRVDLVFGSNSELRALVEVYGADDAQPKFVQDF
VAAWDKVMNLDRFDVR
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
4c50 Chain B Residue 1741 [
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Receptor-Ligand Complex Structure
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PDB
4c50
Access Channel Residues Ser315 and Asp137 in Mycobacterium Tuberculosis Catalase-Peroxidase (Katg) Control Peroxidatic Activation of the Pro-Drug Isoniazid.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
P100 R104 W107 P232 I266 G269 H270 G273 K274 T275 H276 T314 S315 W321
Binding residue
(residue number reindexed from 1)
P76 R80 W83 P208 I242 G245 H246 G249 K250 T251 H252 T290 S291 W297
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R104 H108 H270 W321 D381
Catalytic site (residue number reindexed from 1)
R80 H84 H246 W297 D357
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
View graph for
Cellular Component
External links
PDB
RCSB:4c50
,
PDBe:4c50
,
PDBj:4c50
PDBsum
4c50
PubMed
24185282
UniProt
P9WIE5
|KATG_MYCTU Catalase-peroxidase (Gene Name=katG)
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