3E7M: Nitric oxide synthase, inducible

Structure of murine iNOS oxygenase domain with inhibitor AR-C95791. Determined by X-ray diffraction at 2.0 Å resolution. Released 7 Oct 2008.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Mus musculus
Chains
2
Atoms
7,484
Mol. weight
102.74 kDa
Ligands
AT2, H4B, HEM, ZN
Released
7 Oct 2008

Explore 3E7M in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3E7M contains 59 α-helices and 50 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 30 helices, 25 β-strands

ElementResiduesLengthSheet
β-strand79-8241
β-strand8312
β-strand89-9241
α-helix94-974
α-helix117-1193
β-strand12013
α-helix127-1293
α-helix130-14516
α-helix153-17018
α-helix177-18913
α-helix197-1993
β-strand204-20744
α-helix214-22916
α-helix230-2323
β-strand237-24044
α-helix242-2443
β-strand252-25325
β-strand25714
β-strand26116
β-strand263-26537
β-strand271-27337
α-helix275-2773
α-helix278-2869
α-helix289-2913
α-helix2971
β-strand29816
α-helix299-3002
β-strand301-30445
α-helix308-3103
β-strand311-31335
α-helix314-3163
α-helix317-3193
β-strand322-32438
α-helix331-3366
β-strand339-34138
β-strand345-34624
β-strand350-35349
β-strand356-35839
β-strand363-36424
β-strand367-368210
α-helix369-3702
α-helix371-3766
α-helix377-3782
α-helix386-3927
α-helix400-4023
α-helix404-42219
β-strand427-428210
α-helix430-44819
α-helix455-4584
α-helix464-4663
α-helix468-4714
β-strand47212
β-strand482-48439
β-strand48513
α-helix489-4924
Chain B: 29 helices, 25 β-strands
ElementResiduesLengthSheet
β-strand79-82411
β-strand83112
β-strand89-92411
α-helix94-974
α-helix117-1193
β-strand120113
α-helix127-1293
α-helix130-14617
α-helix153-17018
α-helix177-18913
α-helix197-1993
β-strand204-207414
α-helix214-22916
α-helix230-2323
β-strand237-240414
α-helix241-2444
β-strand252-253215
β-strand257114
β-strand261116
β-strand263-265317
β-strand271-273317
α-helix275-2773
α-helix278-2869
α-helix2971
β-strand298116
α-helix299-3002
β-strand301-304415
α-helix308-3103
β-strand311-313315
α-helix314-3163
α-helix317-3193
β-strand322-324318
α-helix331-3366
β-strand339-341318
β-strand345-346214
β-strand350-353419
β-strand356-358319
β-strand363-364214
β-strand367-368220
α-helix369-3702
α-helix371-3766
α-helix377-3782
α-helix386-3927
α-helix400-4023
α-helix404-42219
β-strand427-428220
α-helix430-44819
α-helix455-4584
α-helix464-4663
α-helix468-4714
β-strand472112
β-strand482-484319
β-strand485113
α-helix489-4913

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Nitric oxide synthase, inducibleA, Bprotein433Mus musculusP29477 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>3E7M_1 Nitric oxide synthase, inducible (chains A, B)
LDKLHVTSTRPQYVRIKNWGSGEILHDTLHHKATSDFTCKSKSCLGSIMNPKSLTRGPRD
KPTPLEELLPHAIEFINQYYGSFKEAKIEEHLARLEAVTKEIETTGTYQLTLDELIFATK
MAWRNAPRCIGRIQWSNLQVFDARNCSTAQEMFQHICRHILYATNNGNIRSAITVFPQRS
DGKHDFRLWNSQLIRYAGYQMPDGTIRGDAATLEFTQLCIDLGWKPRYGRFDVLPLVLQA
DGQDPEVFEIPPDLVLEVTMEHPKYEWFQELGLKWYALPAVANMLLEVGGLEFPACPFNG
WYMGTEIGVRDFCDTQRYNILEEVGRRMGLETHTLASLWKDRAVTEINVAVLHSFQKQNV
TIMDHHTASESFMKHMQNEYRARGGCPADWIWLVPPVSGSITPVFHQEMLNYVLSPFYYY
QIEPWKTHIWQNE

Ligands and cofactors

IDNameFormulaCopies
AT2Ethyl 4-[(4-methylpyridin-2-yl)amino]piperidine-1-carboxylateC14 H21 N3 O22
H4B5,6,7,8-tetrahydrobiopterinC9 H15 N5 O32
HEMProtoporphyrin IX containing FEC34 H32 Fe N4 O42
ZNZinc ionZn2

Water and common crystallization additives (EDO) are not listed.

Primary citation

Anchored plasticity opens doors for selective inhibitor design in nitric oxide synthase. Garcin, E.D., Arvai, A.S., Rosenfeld, R.J. et al. Nat Chem Biol (2008) 4:700-707. DOI 10.1038/nchembio.115 · PubMed

Other PDB entries of the same protein (UniProt P29477 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

About this viewer

MolViewer shows 3E7M directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.