Structure of PDB 3ivy Chain A Binding Site BS01
Receptor Information
>3ivy Chain A (length=399) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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PNLPPGFDFTDPAIYAERLPVAEFAELRSAAPIWWNGQDPGKGGGFHDGG
FWAITKLNDVKEISRHSDVFSSYENGVIPRFKNDIAREDIEVQRFVMLNM
DAPHHTRLRKIISRGFTPRAVGRLHDELQERAQKIAAEAAAAGSGDFVEQ
VSCELPLQAIAGLLGVPQEDRGKLFHWSNEMTGNEDPEYAHIDPKASSAE
LIGYAMKMAEEKIVTQLIQADGEKLSDDEFGFFVVMLAVAGNETTRNSIT
QGMMAFAEHPDQWELYKKVRPETAADEIVRWATPVTAFQRTALRDYELSG
VQIKKGQRVVMFYRSANFDEEVFQDPFTFNILRNPNPHVGFGGTGAHYCI
GANLARMTINLIFNAVADHMPDLKPISAPERLRSGWLNGIKHWQVDYTG
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
3ivy Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3ivy
The Structure of Mycobacterium tuberculosis CYP125: molecular basis for cholesterol binding in a P450 needed for host infection.
Resolution
1.352 Å
Binding residue
(original residue number in PDB)
H124 R128 M264 A268 G269 T272 T273 P312 F316 R318 G368 F369 H375 C377 I378 G379 A383
Binding residue
(residue number reindexed from 1)
H105 R109 M236 A240 G241 T244 T245 P284 F288 R290 G340 F341 H347 C349 I350 G351 A355
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G202 A268 E271 T272 T273 C377 I378 G379 T386 L415
Catalytic site (residue number reindexed from 1)
G183 A240 E243 T244 T245 C349 I350 G351 T358 L387
Enzyme Commision number
1.14.15.29
: cholest-4-en-3-one 26-monooxygenase [(25S)-3-oxocholest-4-en-26-oate forming].
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0008395
steroid hydroxylase activity
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037
heme binding
GO:0036199
cholest-4-en-3-one 26-monooxygenase activity
GO:0046872
metal ion binding
Biological Process
GO:0006707
cholesterol catabolic process
GO:0008203
cholesterol metabolic process
GO:0016042
lipid catabolic process
GO:0051701
biological process involved in interaction with host
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3ivy
,
PDBe:3ivy
,
PDBj:3ivy
PDBsum
3ivy
PubMed
19846552
UniProt
P9WPP1
|CP125_MYCTU Steroid C26-monooxygenase (Gene Name=cyp125)
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