4Z0L: The murine cyclooxygenase-2

The murine cyclooxygenase-2 complexed with a nido-dicarbaborate-containing indomethacin derivative. Determined by X-ray diffraction at 2.29 Å resolution. Released 10 Jun 2015.

Method
X-ray diffraction
Resolution
2.29 Å
Organism
Mus musculus
Chains
4
Atoms
19,280
Mol. weight
279.78 kDa
Ligands
HEM, NAG, 4LA, N1B
Released
10 Jun 2015

Explore 4Z0L in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4Z0L contains 173 α-helices and 124 β-strands across 4 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: 43 helices, 32 β-strands

ElementResiduesLengthSheet
α-helix451
β-strand46-4941
β-strand55-5841
β-strand64-6522
β-strand71-7222
α-helix74-807
α-helix83-853
α-helix86-938
α-helix97-1037
α-helix106-11914
β-strand13013
β-strand13114
β-strand13414
α-helix139-1435
β-strand14715
β-strand14916
β-strand15013
α-helix153-1564
β-strand16117
β-strand16417
α-helix171-1733
α-helix174-1774
α-helix178-1825
β-strand18318
β-strand18919
β-strand194110
β-strand195111
α-helix196-20611
β-strand212112
β-strand22015
β-strand221112
α-helix231-2344
α-helix238-2447
β-strand245113
α-helix2511
β-strand252113
α-helix2531
β-strand255-257314
β-strand260-262314
β-strand265115
α-helix266-2694
α-helix281-2833
β-strand285115
α-helix296-31924
α-helix325-34319
α-helix344-3485
α-helix349-3535
α-helix363-3664
β-strand37816
α-helix379-3846
α-helix388-3903
β-strand395-397316
β-strand400-402316
α-helix404-4074
α-helix412-4176
α-helix419-42810
β-strand430111
β-strand43219
β-strand44018
α-helix442-4443
α-helix445-45713
α-helix460-4623
α-helix463-4697
α-helix473-4753
α-helix478-4825
α-helix486-49510
α-helix498-5003
α-helix503-5097
α-helix511-5122
α-helix520-53415
α-helix538-5403
α-helix547-5504
α-helix553-5608
α-helix564-5718
β-strand581110
Chain B: 44 helices, 30 β-strands
ElementResiduesLengthSheet
α-helix451
β-strand46-49417
β-strand55-58417
β-strand64-65218
β-strand71-72218
α-helix74-818
α-helix83-853
α-helix86-949
α-helix97-1037
α-helix106-11914
β-strand131119
β-strand134119
α-helix139-1435
β-strand147120
α-helix1481
β-strand149119
α-helix153-1564
β-strand161121
β-strand164121
α-helix171-1733
α-helix174-1774
α-helix178-1825
β-strand183122
β-strand189123
β-strand194124
β-strand195125
α-helix196-20611
β-strand212126
β-strand220120
β-strand221126
α-helix231-2344
α-helix238-2447
β-strand245127
α-helix2511
β-strand252127
α-helix2531
β-strand255-257328
β-strand260-262328
β-strand265129
α-helix266-2694
α-helix281-2833
β-strand285129
α-helix296-31924
α-helix325-34319
α-helix344-3496
α-helix350-3534
α-helix363-3664
β-strand378119
α-helix379-3846
α-helix388-3903
β-strand395-397330
β-strand400-402330
α-helix404-4074
α-helix411-4177
α-helix419-42810
β-strand430125
β-strand432123
β-strand440122
α-helix442-4443
α-helix445-45713
α-helix460-4623
α-helix463-4697
α-helix473-4753
α-helix478-4825
α-helix486-49510
α-helix498-5003
α-helix503-5097
α-helix511-5122
α-helix520-53415
α-helix538-5403
α-helix547-5504
α-helix553-5608
α-helix564-5718
β-strand581124
Chain C: 44 helices, 30 β-strands
ElementResiduesLengthSheet
α-helix451
β-strand46-49431
β-strand55-58431
β-strand64-65232
β-strand71-72232
α-helix74-818
α-helix83-853
α-helix86-938
α-helix97-1048
α-helix106-11914
β-strand130-131233
β-strand134133
α-helix139-1435
β-strand147134
α-helix1481
β-strand149-150233
α-helix153-1564
β-strand161135
β-strand164135
α-helix171-1733
α-helix174-1774
α-helix178-1825
β-strand183136
β-strand189137
β-strand194138
β-strand195139
α-helix196-20611
β-strand212140
β-strand220134
β-strand221140
α-helix231-2344
α-helix238-2447
β-strand245141
α-helix2511
β-strand252141
α-helix2531
β-strand255-257342
β-strand260-262342
β-strand265143
α-helix266-2694
α-helix281-2833
β-strand285143
α-helix292-2943
α-helix296-31924
α-helix325-34319
α-helix344-3496
α-helix350-3534
α-helix363-3664
β-strand378133
α-helix379-3846
α-helix388-3903
β-strand395-397344
β-strand400-402344
α-helix404-4074
α-helix412-42817
β-strand430139
β-strand432137
β-strand440136
α-helix442-4443
α-helix445-45713
α-helix460-4623
α-helix463-4697
α-helix473-4753
α-helix478-4825
α-helix486-49510
α-helix498-5003
α-helix503-5097
α-helix511-5122
α-helix520-53415
α-helix538-5403
α-helix547-5504
α-helix553-5608
α-helix564-5718
β-strand581138
Chain D: 42 helices, 32 β-strands
ElementResiduesLengthSheet
β-strand46-49445
β-strand55-58445
β-strand64-65246
β-strand71-72246
α-helix731
α-helix74-818
α-helix83-853
α-helix86-949
α-helix97-1037
α-helix106-11914
β-strand130-131247
β-strand134147
α-helix139-1435
β-strand147148
β-strand149-150247
α-helix153-1564
β-strand161149
β-strand164149
α-helix171-1733
α-helix174-1774
α-helix178-1825
β-strand183150
β-strand189151
β-strand194152
β-strand195153
α-helix196-20611
β-strand212154
β-strand220148
β-strand221154
α-helix231-2344
α-helix238-2447
β-strand245155
α-helix2511
β-strand252155
α-helix2531
β-strand255-257356
β-strand260-262356
α-helix263-2642
β-strand265157
α-helix266-2694
β-strand285157
α-helix296-31924
α-helix325-34319
α-helix344-3496
α-helix350-3534
α-helix363-3664
β-strand378147
α-helix379-3846
α-helix388-3903
β-strand395-397358
β-strand400-402358
α-helix404-4074
α-helix412-42817
β-strand430153
β-strand432151
β-strand440150
α-helix442-4443
α-helix445-45713
α-helix460-4623
α-helix463-4697
α-helix473-4753
α-helix478-4825
α-helix486-49510
α-helix498-5003
α-helix503-5097
α-helix5111
β-strand512159
β-strand519159
α-helix520-53415
α-helix538-5403
α-helix547-5504
α-helix553-5608
α-helix564-5718
β-strand581152

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Prostaglandin G/H synthase 2A, B, C, Dprotein587Mus musculusQ05769 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>4Z0L_1 Prostaglandin G/H synthase 2 (chains A, B, C, D)
ANPCCSNPCQNRGECMSTGFDQYKCDCTRTGFYGENCTTPEFLTRIKLLLKPTPNTVHYI
LTHFKGVWNIVNNIPFLRSLIMKYVLTSRSYLIDSPPTYNVHYGYKSWEAFSNLSYYTRA
LPPVADDCPTPMGVKGNKELPDSKEVLEKVLLRREFIPDPQGSNMMFAFFAQHFTHQFFK
TDHKRGPGFTRGLGHGVDLNHIYGETLDRQHKLRLFKDGKLKYQVIGGEVYPPTVKDTQV
EMIYPPHIPENLQFAVGQEVFGLVPGLMMYATIWLREHNRVCDILKQEHPEWGDEQLFQT
SRLILIGETIKIVIEDYVQHLSGYHFKLKFDPELLFNQQFQYQNRIASEFNTLYHWHPLL
PDTFNIEDQEYSFKQFLYNNSILLEHGLTQFVESFTRQIAGRVAGGRNVPIAVQAVAKAS
IDQSREMKYQSLNEYRKRFSLKPYTSFEELTGEKEMAAELKALYSDIDVMELYPALLVEK
PRPDAIFGETMVELGAPFSLKGLMGNPICSPQYWKPSTFGGEVGFKIINTASIQSLICNN
VKGCPFTSFNVQDPQPTKTATINASASHSRLDDINPTVLIKRRSTEL

Ligands and cofactors

IDNameFormulaCopies
HEMProtoporphyrin IX containing FEC34 H32 Fe N4 O44
NAG2-acetamido-2-deoxy-beta-D-glucopyranoseC8 H15 N O68
4LA(R)-7-{[5-methoxy-2-methyl-3-(methoxycarbonylmethyl)-1H-indolyl]carbonyl}-7,8-d…C16 H14 B9 N O44
N1B(S)-7-{[5-methoxy-2-methyl-3-(methoxycarbonylmethyl)-1H-indolyl]carbonyl}-7,8-d…C16 H14 B9 N O44
BOGoctyl beta-D-glucopyranosideC14 H28 O65

Primary citation

nido-Dicarbaborate Induces Potent and Selective Inhibition of Cyclooxygenase-2. Neumann, W., Xu, S., Sarosi, M.B. et al. ChemMedChem (2016) 11:175-178. DOI 10.1002/cmdc.201500199 · PubMed

Other PDB entries of the same protein (UniProt Q05769 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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