Structure of PDB 2ij5 Chain A Binding Site BS01
Receptor Information
>2ij5 Chain A (length=392) Species:
1773
(Mycobacterium tuberculosis) [
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VLLEVPFSARGDRIPDAVAELRTREPIRKVRTITGAEAWLVSSYALCTQV
LEDRRFSMKETAAAGAPRLNALTVPPEVVNNMGNIADAGLRKAVMKAITP
KAPGLEQFLRDTANSLLDNLITEGAPADLRNDFADPLATALHCKVLGIPQ
EDGPKLFRSLSIAFMSSADPIPAAKINWDRDIEYMAGILENPNITTGLMG
ELSRLRKDPAYSHVSDELFATIGVTFFGAGVISTGSFLTTALISLIQRPQ
LRNLLHEKPELIPAGVEELLRINLSFADGLPRLATADIQVGDVLVRKGEL
VLVLLEGANFDPEHFPNPGSIELDRPNPTSHLAFGRGQHFCPGSALGRRH
AQIGIEALLKKMPGVDLAVPIDQLVWRTRFQRRIPERLPVLW
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
2ij5 Chain A Residue 462 [
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Receptor-Ligand Complex Structure
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PDB
2ij5
Crystal structure of the Mycobacterium tuberculosis P450 CYP121-fluconazole complex reveals new azole drug-P450 binding mode.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
M62 M86 H146 F230 G234 S237 F241 F280 R286 A337 F338 H343 C345 P346 G347
Binding residue
(residue number reindexed from 1)
M58 M82 H142 F226 G230 S233 F237 F276 R282 A333 F334 H339 C341 P342 G343
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S170 A233 I236 S237 T238 C345 P346 G347 H354 R386
Catalytic site (residue number reindexed from 1)
S166 A229 I232 S233 T234 C341 P342 G343 H350 R382
Enzyme Commision number
1.14.19.70
: mycocyclosin synthase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0008395
steroid hydroxylase activity
GO:0009975
cyclase activity
GO:0016491
oxidoreductase activity
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0016717
oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water
GO:0020037
heme binding
GO:0036199
cholest-4-en-3-one 26-monooxygenase activity
GO:0046872
metal ion binding
GO:0070025
carbon monoxide binding
Biological Process
GO:0006707
cholesterol catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2ij5
,
PDBe:2ij5
,
PDBj:2ij5
PDBsum
2ij5
PubMed
17028183
UniProt
P9WPP7
|CP121_MYCTU Mycocyclosin synthase (Gene Name=cyp121)
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