Structure of PDB 2qd2 Chain A Binding Site BS03
Receptor Information
>2qd2 Chain A (length=359) Species:
9606
(Homo sapiens) [
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RKPKTGILMLNMGGPETLGDVHDFLLRLFLDRDLMTLPIQNKLAPAIAKR
RTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDELSPNTAPHKYYIGFR
YVHPLTEEAIEEMERDGLERAIAFTQYPQYSCSTTGSSLNAIYRYYNQVG
RKPTMKWSTIDRWPTHHLLIQCFADHILKELDHFPLEKRSEVVILFSAHS
LPMSVVNRGDPYPQEVSATVQKVMERLEYCNPYRLVWQSKVGPMPWLGPQ
TDESIKGLCERGRKNILLVPIAFTSDHIETLYELDIEYSQVLAKECGVEN
IRRAESLNGNPLFSKALADLVHSHIQSNELCSKQLTLSCPLCVNPVCRET
KSFFTSQQL
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
2qd2 Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
2qd2
A pi-Helix Switch Selective for Porphyrin Deprotonation and Product Release in Human Ferrochelatase.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
M76 L92 L98 R115 I119 Y191 S197 T198 H263 L265 P266 Y276 F337 H341 I342
Binding residue
(residue number reindexed from 1)
M12 L28 L34 R51 I55 Y127 S133 T134 H199 L201 P202 Y212 F273 H277 I278
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
M76 L92 L98 R164 Y165 H263 D340 E343 E347
Catalytic site (residue number reindexed from 1)
M12 L28 L34 R100 Y101 H199 D276 E279 E283
Enzyme Commision number
4.98.1.1
: protoporphyrin ferrochelatase.
Gene Ontology
Molecular Function
GO:0004325
ferrochelatase activity
Biological Process
GO:0006783
heme biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2qd2
,
PDBe:2qd2
,
PDBj:2qd2
PDBsum
2qd2
PubMed
17884090
UniProt
P22830
|HEMH_HUMAN Ferrochelatase, mitochondrial (Gene Name=FECH)
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