Found 40 chains in Knotted chains table. Displaying 1 - 40. Applied filters: Probabilistic
Search results query: topological notation: S +31 11x +31
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#pdbid|chain|deposition date|is S/K-not|(slip)knot types;
2gd8|A|2018-10-20|S|+3.1;
1ydd|A|2018-10-20|S|+3.1;
1fql|A|2018-10-20|S|+3.1;
1hea|A|2018-10-20|S|+3.1;
1bn4|A|2018-10-20|S|+3.1;
1bn3|A|2018-10-20|S|+3.1;
3nj9|A|2018-10-20|S|+3.1;
4yxi|A|2018-10-20|S|+3.1;
1bn1|A|2018-10-20|S|+3.1;
4jss|A|2018-10-19|S|+3.1;
1okn|A|2018-10-19|S|+3.1;
4yx4|A|2018-10-19|S|+3.1;
2q1b|A|2018-10-19|S|+3.1;
1okm|A|2018-10-19|S|+3.1;
4qy3|A|2018-10-19|S|+3.1;
2hnc|A|2018-10-19|S|+3.1;
4yxu|A|2018-10-19|S|+3.1;
1bnw|A|2018-10-19|S|+3.1;
4fvn|A|2018-10-19|S|+3.1;
1mua|A|2018-10-19|S|+3.1;
1a42|A|2018-10-18|S|+3.1;
1cny|A|2018-10-18|S|+3.1;
2hkk|A|2018-10-18|S|+3.1;
1cnw|A|2018-10-18|S|+3.1;
2hl4|A|2018-10-18|S|+3.1;
1bnm|A|2018-10-17|S|+3.1;
2h15|A|2018-10-17|S|+3.1;
4yxo|A|2018-10-17|S|+3.1;
4yyt|A|2018-10-17|S|+3.1;
8ca2|A|2018-10-17|S|+3.1;
2fmg|A|2018-10-03|S|+3.1;
1if8|A|2018-10-03|S|+3.1;
1heb|A|2018-10-03|S|+3.1;
1i8z|A|2018-10-03|S|+3.1;
4fvo|A|2018-10-03|S|+3.1;
1avn|A|2018-10-03|S|+3.1;
2q1q|A|2018-10-01|S|+3.1;
1ugf|A|2018-09-29|S|+3.1;
1bic|A|2018-09-29|S|+3.1;
2abe|A|2018-09-26|S|+3.1;
Knot types |
Knot loop types |
| pdb | Title |
S +31
|
S 11x +31
|
|
2gd8A
|
Crystal structure analysis of the human carbonic anhydrase ii in complex with a 2-substituted estradiol bis-sulfamate
|
S +31
|
S 11x +31
|
|
1yddA
|
Structural basis of inhibitor affinity to variants of human carbonic anhydrase ii
|
S +31
|
S 11x +31
|
|
1fqlA
|
X-ray crystal structure of zinc-bound f95m/w97v carbonic anhydrase (caii) variant
|
S +31
|
S 11x +31
|
|
1heaA
|
Carbonic anhydrase ii (carbonate dehydratase) (hca ii) (e.c.4.2.1.1) mutant with leu 198 replaced by arg (l198r)
|
S +31
|
S 11x +31
|
|
1bn4A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 11x +31
|
|
1bn3A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 11x +31
|
|
3nj9A
|
Crystal structure of carbonic anhydrase ii in complex with a nir inhibitor
|
S +31
|
S 11x +31
|
|
4yxiA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (2).
|
S +31
|
S 11x +31
|
|
1bn1A
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 11x +31
|
|
4jssA
|
Human carbonic anhydrase ii h94d bound to a bidentate inhibitor
|
S +31
|
S 11x +31
|
|
1oknA
|
Carbonic anhydrase ii complex with the 1okn inhibitor 4-sulfonamide-[1-(4-n-(5-fluorescein thiourea)butane)]
|
S +31
|
S 11x +31
|
|
4yx4A
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (1).
|
S +31
|
S 11x +31
|
|
2q1bA
|
Carbonic anhydrase ii in complex with saccharin
|
S +31
|
S 11x +31
|
|
1okmA
|
Carbonic anhydrase ii complex with the 1okm inhibitor 4-sulfonamide-[1-(4-aminobutane)]benzamide
|
S +31
|
S 11x +31
|
|
4qy3A
|
The crystal structure of the complex of hcaii with an ortho-substituted benzoic acid
|
S +31
|
S 11x +31
|
|
2hncA
|
Crystal structure of the human carbonic anhydrase ii in complex with the 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.
|
S +31
|
S 11x +31
|
|
4yxuA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (4).
|
S +31
|
S 11x +31
|
|
1bnwA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 11x +31
|
|
4fvnA
|
Carbonic anhydrase ii in complex with n-(tetrahydropyrimidin-2(1h)-ylidene)sulfuric diamide
|
S +31
|
S 11x +31
|
|
1muaA
|
Structure and energetics of a non-proline cis-peptidyl linkage in an engineered protein
|
S +31
|
S 11x +31
|
|
1a42A
|
Human carbonic anhydrase ii complexed with brinzolamide
|
S +31
|
S 11x +31
|
|
1cnyA
|
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants
|
S +31
|
S 11x +31
|
|
2hkkA
|
Carbonic anhydrase activators: solution and x-ray crystallography for the interaction of andrenaline with various carbonic anhydrase isoforms
|
S +31
|
S 11x +31
|
|
1cnwA
|
Secondary interactions significantly removed from the sulfonamide binding pocket of carbonic anhydrase ii influence binding constants
|
S +31
|
S 11x +31
|
|
2hl4A
|
Crystal structure analysis of human carbonic anhydrase ii in complex with a benzenesulfonamide derivative
|
S +31
|
S 11x +31
|
|
1bnmA
|
Carbonic anhydrase ii inhibitor
|
S +31
|
S 11x +31
|
|
2h15A
|
Carbonic anhydrase inhibitors: clashing with ala65 as a means of designing isozyme-selective inhibitors that show low affinity for the ubiquitous isozyme ii
|
S +31
|
S 11x +31
|
|
4yxoA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (3).
|
S +31
|
S 11x +31
|
|
4yytA
|
Human carbonic anhydrase ii complexed with an inhibitor with a benzenesulfonamide group (5).
|
S +31
|
S 11x +31
|
|
8ca2A
|
Engineering the hydrophobic pocket of carbonic anhydrase ii
|
S +31
|
S 11x +31
|
|
2fmgA
|
Carbonic anhydrase activators. activation of isoforms i, ii, iv, va, vii and xiv with l- and d- phenylalanine and crystallographic analysis of their adducts with isozyme ii: sterospecific recognition within the active site of an enzyme and its consequences for the drug design, structure with l-phenylalanine
|
S +31
|
S 11x +31
|
|
1if8A
|
Carbonic anhydrase ii complexed with (s)-n-(3-indol-1-yl-2-methyl-propyl)-4-sulfamoyl-benzamide
|
S +31
|
S 11x +31
|
|
1hebA
|
Structural consequences of hydrophilic amino-acid substitutions in the hydrophobic pocket of human carbonic anhydrase ii
|
S +31
|
S 11x +31
|
|
1i8zA
|
Carbonic anhydrase ii complexed with al-6629 2h-thieno[3,2-e]-1,2-thiazine-6-sulfonamide, 2-(3-methoxyphenyl)-3-(4-morpholinyl)-, 1,1-dioxide
|
S +31
|
S 11x +31
|
|
4fvoA
|
Carbonic anhydrase ii in complex with n-[(2e)-3,4-dihydroquinazolin-2(1h)-ylidene]sulfuric diamide
|
S +31
|
S 11x +31
|
|
1avnA
|
Human carbonic anhydrase ii complexed with the histamine activator
|
S +31
|
S 11x +31
|
|
2q1qA
|
Carbonic anhydrase inhibitors. interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: kinetic and x-ray crystallographic studies
|
S +31
|
S 11x +31
|
|
1ugfA
|
Human carbonic anhydrase ii [hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by thr (a65t)
|
S +31
|
S 11x +31
|
|
1bicA
|
Crystallographic analysis of thr-200-> his human carbonic anhydrase ii and its complex with the substrate, hco3-
|
S +31
|
S 11x +31
|
|
2abeA
|
Carbonic anhydrase activators: x-ray crystal structure of the adduct of human isozyme ii with l-histidine as a platform for the design of stronger activators
|