2G24: Renin

Ketopiperazine-Based Renin Inhibitors: Optimization of the "C" Ring. Determined by X-ray diffraction at 1.9 Å resolution. Released 13 Jun 2006.

Method
X-ray diffraction
Resolution
1.9 Å
Organism
Homo sapiens
Chains
2
Atoms
5,214
Mol. weight
73.49 kDa
Ligands
7IG
Released
13 Jun 2006

Explore 2G24 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2G24 contains 29 α-helices and 63 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: 15 helices, 32 β-strands

ElementResiduesLengthSheet
β-strand4-741
β-strand8-1032
β-strand14-1632
β-strand17-2153
β-strand26-3383
β-strand39-4243
β-strand4314
α-helix51-544
β-strand5914
α-helix61-633
β-strand68-78113
β-strand81-94143
β-strand97-108123
α-helix111-1144
β-strand121-12443
α-helix128-1303
α-helix132-1343
α-helix135-1373
α-helix138-1436
β-strand152-15761
α-helix158-1603
β-strand167-17151
α-helix176-1783
β-strand179-18791
β-strand18815
β-strand195-19845
β-strand200-20346
β-strand20916
β-strand214-21855
β-strand225-22735
α-helix229-23911
β-strand242-24327
β-strand248-25147
α-helix252-2576
α-helix258-2603
β-strand261-26556
β-strand268-27256
α-helix274-2774
β-strand27818
β-strand288-29037
β-strand29118
β-strand293-29535
α-helix298-2992
β-strand306-30835
α-helix310-3134
β-strand316-32161
β-strand326-33271
Chain B: 14 helices, 31 β-strands
ElementResiduesLengthSheet
β-strand4-749
β-strand8-10310
β-strand14-16310
β-strand17-21511
β-strand26-33811
β-strand39-42411
β-strand43112
α-helix52-554
β-strand59112
α-helix61-633
β-strand68111
β-strand73-77511
β-strand82-941311
β-strand97-1081211
α-helix111-1144
β-strand121-124411
α-helix128-1303
α-helix132-1343
α-helix138-1447
β-strand152-15769
α-helix158-1603
β-strand167-17159
α-helix176-1783
β-strand179-18799
β-strand188113
β-strand195-203913
β-strand206-209413
β-strand214-218513
β-strand225-227313
α-helix229-23911
β-strand242-243214
β-strand248-251414
α-helix252-2576
α-helix259-2602
β-strand261-265513
β-strand269-272413
α-helix274-2774
β-strand278-279214
β-strand288-291414
β-strand293-295313
α-helix298-2992
β-strand306-308313
α-helix310-3156
β-strand316-32169
β-strand326-33279

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
ReninA, Bprotein333Homo sapiensP00797 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>2G24_1 Renin (chains A, B)
SSVILTNYMDTQYYGEIGIGTPPQTFKVVFDTGSSNVWVPSSKCSRLYTACVYHKLFDAS
DSSSYKHNGTELTLRYSTGTVSGFLSQDIITVGGITVTQMFGEVTEMPALPFMLAEFDGV
VGMGFIEQAIGRVTPIFDNIISQGVLKEDVFSFYYNRDSENSQSLGGQIVLGGSDPQHYE
GNFHYINLIKTGVWQIQMKGVSVGSSTLLCEDGCLALVDTGASYISGSTSSIEKLMEALG
AKKRLFDYVVKCNEGPTLPDISFHLGGKEYTLTSADYVFQESYSSKKLCTLAIHAMDIPP
PTGPTWALGATFIRKFYTEFDRRNNRIGFALAR

Ligands and cofactors

IDNameFormulaCopies
7IG5-{4-[(3,5-difluorobenzyl)amino]phenyl}-6-ethylpyrimidine-2,4-diamineC19 H19 F2 N51

Primary citation

Ketopiperazine-Based Renin Inhibitors: Optimization of the C Ring. Holsworth, D.D., Cai, C., Cheng, X.M. et al. Bioorg Med Chem Lett (2006) 16:2500-2504. DOI 10.1016/j.bmcl.2006.01.084 · PubMed

Other PDB entries of the same protein (UniProt P00797 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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