|
K +31
|
|
|
7priAAA
|
Carbonic anhydrase from schistosoma mansoni in complex with clorsulon
|
|
K +31
|
|
|
8axzA
|
Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with s-adenosylmethionine, adenosin and diphosphono-aminophosphonic acid.
|
|
K +31
|
|
|
7plfAAA
|
Human carbonic anhydrase i in complex with clorsulon
|
|
K +31
|
|
|
7nh8AAA
|
Crystal structure of human carbonic anhydrase ii with n-((1-(6-((3ar,7r,7as)-7-hydroxy-2,2-dimethyltetrahydro-[1,3]dioxolo[4,5-c]pyridin-5(4h)-yl)hexyl)-1h-1,2,3-triazol-4-yl)methyl)-4-sulfamoylbenzamide
|
|
K +31
|
K 3x +31
|
|
7ng1A
|
Crystal structure of alpha carbonic anhydrase from schistoso ma mansoni bound to 1-(4-iodophenyl)-3-[2-(4-sulfamoylphenyl)ethyl]selenourea
|
|
K +31
|
|
|
7lnhA
|
S-adenosylmethionine synthetase co-crystallized with uppnhp
|
|
K +31
|
|
|
7edcA
|
Crystal structure of mutant trna [gm18] methyltransferase trmh (e107g) in complex with s-adenosyl-l-methionine from escherichia coli
|
|
K +31
|
|
|
7e3tA
|
Crystal structure of trml from mycoplasma capricolum
|
|
K +31
|
|
|
7e3sA
|
Crystal structure of trml from shewanella oneidensis
|
|
K +31
|
|
|
7e3rA
|
Crystal structure of trml from vibrio vulnificus
|
|
K +31
|
|
|
7e3qA
|
Crystal structure of sah bound trml from vibrio vulnificus
|
|
K +31
|
|
|
5nfjA
|
Crystal structure of the methyltransferase subunit of human mitochondrial ribonuclease p (mrpp1) bound to s-adenosyl-methionine (sam)
|
|
K +31
|
|
|
7looA
|
S-adenosyl methionine transferase cocrystallized with atp
|
|
K +31
|
|
|
7d51A
|
Crystal structure of a truly knotted protein: cyclized yibk from haemophilus influenzae
|
|
K +31
|
|
1
|
7cwwA
|
Crystal structure of tsrl
|
|
K +31
|
|
|
7onuF
|
Structure of human mitochondrial rnase p in complex with mitochondrial pre-trna-tyr
|
|
K +31
|
K 3x +31
|
|
7mu3A
|
Human carbonic anhydrase 9 mimic with compound
|
|
K +31
|
|
|
7ockB
|
Mat in complex with samh
|
|
K +31
|
K 4x +31
|
|
6zr9A
|
The crystal structure of the complex of hcavii with 2-(4-benzhydrylpiperazin-1-yl)-n-(4-sulfamoylphenyl)acetamide
|
|
K +31
|
|
|
7mysA
|
Crystal structure of a trna (guanine-n1)-methyltransferase from acinetobacter baumannii ab5075-uw bound to s-adenosyl homocysteine
|
|
K +31
|
|
|
7myqA
|
Crystal structure of a trna (guanine-n1)-methyltransferase from acinetobacter baumannii
|
|
K +31
|
|
|
6jkiA
|
Crystal structure and catalytic mechanism of the essential m1g37 trna methyltransferase trmd from pseudomonas aeruginosa
|
|
K +31
|
|
|
6jofA
|
Crystal structure of trmd from mycobacterium tuberculosis in complex with active-site inhibitor
|
|
K +31
|
|
|
6joeA
|
Crystal structure of trmd from pseudomonas aeruginosa in complex with active-site inhibitor
|
|
K +31
|
|
|
6qowA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with fragment 26 (6-methoxybenzothiazole-2-carboxylic acid)
|
|
K +31
|
|
|
6qrbA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qoeA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with fragment 8 (3-[(2-thienylthio)methyl]benzoic acid)
|
|
K +31
|
|
|
6qqyA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6nw7A
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with s-adenosyl-l-homocysteine
|
|
K +31
|
K 15x +31
|
|
6rrgA
|
Human carbonic anhydrase ii in complex with fluorinated benzenesulfonamide
|
|
K +31
|
|
|
2fg7C
|
N-succinyl-l-ornithine transcarbamylase from b. fragilis complexed with carbamoyl phosphate and n-succinyl-l-norvaline
|
|
K +31
|
|
|
1ipaA
|
Crystal structure of rna 2'-o ribose methyltransferase
|
|
K +31
|
K 3x +31
|
|
6yj3A
|
Metala-carborane di-propyl-sulfonamide
|
|
K +31
|
K 3x +31
|
|
6yokA
|
Para-carborane di-propyl-sulfonamide in complex with ca ix mimic
|
|
K +31
|
K 3x +31
|
|
6y74A
|
X-ray crystal structure of human carbonic anhydrase ix catalytic domain.
|
|
K +31
|
K 3x +31
|
|
6ymaA
|
Microed structure of acetazolamide-bound human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
6km1A
|
Human carbonic anhydrase ii v143i variant 13 atm co2
|
|
K +31
|
K 3x +31
|
|
6km2A
|
Human carbonic anhydrase ii v143i variant 15 atm co2
|
|
K +31
|
K 3x +31
|
|
6km3A
|
Human carbonic anhydrase ii native 00 atm co2
|
|
K +31
|
K 3x +31
|
|
6km5A
|
Human carbonic anhydrase ii native 13 atm co2
|
|
K +31
|
K 3x +31
|
|
6wq7A
|
Carbonic anhydrase ii complexed with 2-((3-aminopropyl)(phenethyl)amino)-n-(4-fluorobenzyl)-n-(4-sulfamoylphenethyl)acetamide
|
|
K +31
|
K 3x +31
|
|
6otmA
|
Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb10-586b
|
|
K +31
|
K 3x +31
|
|
6otiA
|
Carbonic anhydrase ix mimic complexed with ureic benzene sulfonamide mb9-561b
|
|
K +31
|
K 3x +31
|
|
6oueA
|
Carbonic anhydrase ii complexed with benzene sulfonamide mb11-707a
|
|
K +31
|
K 3x +31
|
|
6rg4A
|
Crystal structure of human carbonic anhydrase ii in complex with (r)-4-(2-benzyl-4-methylpiperazin-1-yl)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6rhjA
|
Crystal structure of human carbonic anhydrase isozyme ii with 4-(4-benzyl-1,4-diazepane-1-carbonyl)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6rofA
|
Human carbonic anhydrase ii mutant t199v bound by 2-(cyclooctylamino)-3,5,6-trifluoro-4-[(2-hydroxyethyl)thio]benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6ux1A
|
Carbonic anhydrase ii complexed with salicylic acid
|
|
K +31
|
K 3x +31
|
|
6r6yA
|
Crystal structure of human carbonic anhydrase isozyme xii with 4-chloro-2-cyclohexylsulfanyl-n-(2-hydroxyethyl)-5-sulfamoyl-benzamide
|
|
K +31
|
K 3x +31
|
|
6vj3A
|
Carbonic anhydrase ii in complex with pyrimidine-based inhibitor
|
|
K +31
|
K 3x +31
|
|
6ugnA
|
Human carbonic anhydrase 2 complexed with sb4-205
|
|
K +31
|
K 3x +31
|
|
6qngA
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6qnlA
|
Three dimensional structure of human carbonic anhydrase xii in complex with benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6qn5A
|
Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6i0jA
|
Crystal structure of human carbonic anhydrase i in complex with the 4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)phenyl sulfamate inhibitor
|
|
K +31
|
K 31x +31
|
|
6i0wA
|
Human carbonic anhydrase ii in complex with 4-methoxybenzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
6qqmA
|
Crystal structure of the alpha carbonic anhydrase from schistosoma mansoni
|
|
K +31
|
K 15x +31
|
|
6hr3A
|
Human carbonic anhydrase ii in complex with 4-propylbenzenesulfonamide
|
|
K +31
|
K 3x +31
|
4
|
6nj4A
|
Thermostable variant of human carbonic anhydrase with disordered tetrazine 2.0 reacted with strained trans-cyclooctene at site 233
|
|
K +31
|
K 3x +31
|
3
|
6nj5A
|
Thermostable variant of human carbonic anhydrase ii with disordered tetrazine 2.0 at site 233
|
|
K +31
|
K 3x +31
|
4
|
6nj2A
|
Thermostable carbonic anhydrase ii variant with tetrazine 2.0 at site 186
|
|
K +31
|
|
|
6uevA
|
Structure of unliganded trna (guanine-n1)-methyltransferase found in anaplasma phagocytophilum
|
|
K +31
|
K 3x +31
|
|
6ql3A
|
Crystal structure of chimeric carbonic anhydrase vi with 3-(cyclooctylamino)-2,5,6-trifluoro-4-[(2-hydroxyethyl)sulfonyl]benzenesulfonamide
|
|
K +31
|
|
|
6qrdA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qrfA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qrcA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqqA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qraA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqrA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qreA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qrgA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qr0A
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qr1A
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqtA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qr3A
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqvA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qr2A
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqwA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
|
|
6qqzA
|
Crystal structure of trmd, a trna-(n1g37) methyltransferase, from mycobacterium abscessus in complex with inhibitor
|
|
K +31
|
K 3x +31
|
|
6hzxA
|
Protein-aromatic foldamer complex crystal structure
|
|
K +31
|
K 3x +31
|
|
6rqnA
|
X-ray crystal structure of protiated (h) small monoclinic unit cell ca ix sv.
|
|
K +31
|
K 3x +31
|
|
6rqqA
|
X-ray crystal structure of protiated (h) large monoclinic unit cell ca ix sv.
|
|
K +31
|
|
1
|
6ac6A
|
Ab initio crystal structure of selenomethionine labelled mycobacterium smegmatis mfd
|
|
K +31
|
|
|
6rxzCN
|
Cryo-em structure of the 90s pre-ribosome (kre33-noc4) from chaetomium thermophilum, state b
|
|
K +31
|
|
|
6rxyCN
|
Cryo-em structure of the 90s pre-ribosome (kre33-noc4) from chaetomium thermophilum, state a
|
|
K +31
|
|
|
6rxxCN
|
Cryo-em structure of the 90s pre-ribosome (kre33-noc4) from chaetomium thermophilum, state c, poly-ala
|
|
K +31
|
|
|
6rxvCN
|
Cryo-em structure of the 90s pre-ribosome (kre33-noc4) from chaetomium thermophilum, state b2
|
|
K +31
|
|
|
6rxtCN
|
Cryo-em structure of the 90s pre-ribosome (kre33-noc4) from chaetomium thermophilum, state a
|
|
K +31
|
|
|
6afkA
|
Crystal structure of trmd from pseudomonas aeruginosa in complex with active-site inhibitor
|
|
K +31
|
K 4x +31
|
|
6h36A
|
The crystal structure of human carbonic anhydrase vii in complex with 4-(4-phenylpiperidine-1-carbonyl)benzenesulfonamide.
|
|
K +31
|
K 3x +31
|
|
6edaA
|
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
|
|
K +31
|
K 3x +31
|
|
6eeaA
|
Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
|
|
K +31
|
K 3x +31
|
|
3iqkA
|
Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
|
|
K +31
|
K 3x +31
|
|
5fl5A
|
Three dimensional structure of human carbonic anhydrase ix in complex with 5-(1-(4-methoxyphenyl)-1h-1,2,3-triazol-4-yl)thiophene-2- sulfonamide
|
|
K +31
|
K 3x +31
|
|
1cakA
|
Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
4mltA
|
Structure of a monodentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii
|
|
K +31
|
K 3x +31
|
|
5eijA
|
Carbonic anhydrase ii in complex with sulfonamide inhibitor
|
|
K +31
|
K 3x +31
|
|
4r59A
|
A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
|
|
K +31
|
K 3x +31
|
|
4mdgA
|
Closo carborane carbonic anhydrase inhibitor
|
|
K +31
|
K 3x +31
|
|
3mnuA
|
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron containing aromatic sulfamide with mammalian isoforms i-xv
|
|
K +31
|
K 3x +31
|
4
|
2nnoA
|
Structure of inhibitor binding to carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
1caoA
|
Crystallographic studies of the binding of protonated and unprotonated inhibitors to carbonic anhydrase using hydrogen sulphide and nitrate anions
|
|
K +31
|
K 3x +31
|
|
3v2jA
|
Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
3konA
|
Crystal structure of cobalt (ii) human carbonic anhydrase ii at ph 11.0
|
|
K +31
|
K 3x +31
|
|
4m2rA
|
Human carbonic anhydrase ii in complex with brinzolamide
|
|
K +31
|
K 3x +31
|
|
2nwoA
|
Structural and kinetic effect of hydrophobic mutations in the active site of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
5msaA
|
Crystal structure of human carbonic anhydrase isozyme xii with 2,3,5,6-tetrafluoro-4-(propylthio)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
5flpA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
|
K +31
|
K 3x +31
|
|
5flrA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
|
K +31
|
K 3x +31
|
|
4xz5A
|
Structure of the thermostable alpha-carbonic anydrase from thiomicrospira crunogena xcl-2 gammaproteobacterium
|
|
K +31
|
K 4x +31
|
|
3ml5A
|
Crystal structure of the c183s/c217s mutant of human ca vii in complex with acetazolamide
|
|
K +31
|
K 3x +31
|
|
4qsbA
|
Crystal structure of human carbonic anhydrase isozyme ii with 3-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
5ty1A
|
Identification of a new zinc binding chemotype by fragment screening
|
|
K +31
|
K 5x +31
|
|
1cnjA
|
X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site
|
|
K +31
|
K 3x +31
|
|
3mhcA
|
Crystal structure of human cabonic anhydrase ii in adduct with an adamantyl analogue of acetazolamide in a novel hydrophobic binding pocket
|
|
K +31
|
K 3x +31
|
|
5flsA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
|
K +31
|
K 3x +31
|
|
5umcA
|
Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
|
|
K +31
|
K 3x +31
|
4
|
5tt3A
|
Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with ethoxzolamide
|
|
K +31
|
K 3x +31
|
|
5g01A
|
An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
|
|
K +31
|
K 3x +31
|
|
4ywpA
|
Sucrose binding site in genetically engineered carbonic anhydrase ix
|
|
K +31
|
K 11x +31
|
|
4mdlA
|
Meta carborane carbonic anhydrase inhibitor
|
|
K +31
|
K 11x +31
|
|
4fptA
|
Carbonic anhydrase ii in complex with ethyl (2z,4r)-2-(sulfamoylimino)-1,3-thiazolidine-4-carboxylate
|
|
K +31
|
K 3x +31
|
4
|
3s72B
|
The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
|
|
K +31
|
K 3x +31
|
|
3dazA
|
Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
|
|
K +31
|
K 3x +31
|
|
2vvbX
|
Human carbonic anhydrase ii in complex with bicarbonate
|
|
K +31
|
K 3x +31
|
|
4z1eA
|
Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
|
|
K +31
|
K 3x +31
|
|
3kkxA
|
Neutron structure of human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
4kp5A
|
Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
4l5vA
|
The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
|
|
K +31
|
K 3x +31
|
|
3u3aX
|
Structure of human carbonic anhydrase ii v143i
|
|
K +31
|
K 3x +31
|
|
3hknA
|
Human carbonic anhydrase ii in complex with (2,3,4,6-tetra-o-acetyl-beta-d-galactopyranosyl) -(1-4)-1,2,3,6-tetra-o-acetyl-1-thio-beta-d-glucopyranosylsulfonamide
|
|
K +31
|
K 3x +31
|
|
5tfxA
|
New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase
|
|
K +31
|
K 3x +31
|
|
2fnnA
|
Activation of human carbonic anhydrase ii by exogenous proton donors
|
|
K +31
|
K 29x +31
|
30
|
5jdfA
|
Structural mechanisms of extracellular ion exchange and induced binding-site occlusion in the sodium-calcium exchanger ncx_mj soaked with 2.5 mm na+ and 1mm ca2+
|
|
K +31
|
K 3x +31
|
|
1ugdA
|
Human carbonic anhydrase ii[hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by ser (a65s)
|
|
K +31
|
K 3x +31
|
|
3p3jA
|
Human carbonic anhydrase ii in complex with p-(5-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
5jesB
|
Human carbonic anhydrase ii (v121t) complexed with benzo[d]thiazole-2-sulfonamide
|
|
K +31
|
K 3x +31
|
|
3gz0A
|
Apo-human carbonic anhydrase ii revisited: implications of the loss of a metal in protein structure, stability and solvent network
|
|
K +31
|
K 3x +31
|
|
4qk1A
|
Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - k170p
|
|
K +31
|
K 3x +31
|
|
5floA
|
Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
|
|
K +31
|
K 3x +31
|
|
5th4A
|
Crystal structure of 1-hydroxypyridine-2(1h)-thione bound to human carbonic anhydrase 2 l198g
|
|
K +31
|
K 3x +31
|
|
5cjfA
|
The crystal structure of the human carbonic anhydrase xiv in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor.
|
|
K +31
|
K 3x +31
|
|
1z97A
|
Human carbonic anhydrase iii: structural and kinetic study of catalysis and proton transfer.
|
|
K +31
|
K 3x +31
|
|
5sz5A
|
Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide
|
|
K +31
|
K 3x +31
|
|
1fsqA
|
X-ray crystal structure of cobalt-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
|
|
K +31
|
K 3x +31
|
|
3ryjB
|
Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
|
|
K +31
|
K 7x +31
|
|
1ze8A
|
Carbonic anhydrase ii in complex with a membrane-impermeant sulfonamide inhibitor
|
|
K +31
|
K 3x +31
|
|
4ygnA
|
Nai--interactions between hofmeister anions and the binding pocket of a protein
|
|
K +31
|
K 3x +31
|
|
5lmdA
|
The crystal structure of hca ii in complex with a benzoxaborole inhibitor
|
|
K +31
|
K 3x +31
|
4
|
5jgsB
|
Human carbonic anhydrase ii (f131y/l198a) complexed with benzo[d]thiazole-2-sulfonamide
|
