==== Secondary Structure Definition by the program DSSP, updated CMBI version by ElmK / April 1,2000 ==== DATE=4-MAR-2012 . REFERENCE W. KABSCH AND C.SANDER, BIOPOLYMERS 22 (1983) 2577-2637 . HEADER STRUCTURAL GENOMICS, UNKNOWN FUNCTION 29-AUG-11 2LIO . COMPND 2 MOLECULE: UNCHARACTERIZED PROTEIN; . SOURCE 2 ORGANISM_SCIENTIFIC: BACTEROIDES FRAGILIS; . AUTHOR J.L.MILLS,H.LEE,D.LEE,C.CICCOSANTI,H.JANJUA,R.NAIR,B.ROST,T. . 136 1 0 0 0 TOTAL NUMBER OF RESIDUES, NUMBER OF CHAINS, NUMBER OF SS-BRIDGES(TOTAL,INTRACHAIN,INTERCHAIN) . 9670.0 ACCESSIBLE SURFACE OF PROTEIN (ANGSTROM**2) . 94 69.1 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(J) , SAME NUMBER PER 100 RESIDUES . 0 0.0 TOTAL NUMBER OF HYDROGEN BONDS IN PARALLEL BRIDGES, SAME NUMBER PER 100 RESIDUES . 41 30.1 TOTAL NUMBER OF HYDROGEN BONDS IN ANTIPARALLEL BRIDGES, SAME NUMBER PER 100 RESIDUES . 1 0.7 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I-5), SAME NUMBER PER 100 RESIDUES . 2 1.5 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I-4), SAME NUMBER PER 100 RESIDUES . 1 0.7 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I-3), SAME NUMBER PER 100 RESIDUES . 1 0.7 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I-2), SAME NUMBER PER 100 RESIDUES . 0 0.0 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I-1), SAME NUMBER PER 100 RESIDUES . 0 0.0 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+0), SAME NUMBER PER 100 RESIDUES . 0 0.0 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+1), SAME NUMBER PER 100 RESIDUES . 17 12.5 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+2), SAME NUMBER PER 100 RESIDUES . 10 7.4 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+3), SAME NUMBER PER 100 RESIDUES . 24 17.6 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+4), SAME NUMBER PER 100 RESIDUES . 1 0.7 TOTAL NUMBER OF HYDROGEN BONDS OF TYPE O(I)-->H-N(I+5), SAME NUMBER PER 100 RESIDUES . 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 *** HISTOGRAMS OF *** . 0 0 0 2 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 RESIDUES PER ALPHA HELIX . 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 PARALLEL BRIDGES PER LADDER . 0 0 0 1 3 1 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 ANTIPARALLEL BRIDGES PER LADDER . 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 LADDERS PER SHEET . # RESIDUE AA STRUCTURE BP1 BP2 ACC N-H-->O O-->H-N N-H-->O O-->H-N TCO KAPPA ALPHA PHI PSI X-CA Y-CA Z-CA 1 1 A M 0 0 208 0, 0.0 2,-0.4 0, 0.0 103,-0.1 0.000 360.0 360.0 360.0 -54.7 -4.2 24.3 -4.2 2 2 A K - 0 0 167 101,-0.1 103,-0.1 1,-0.0 101,-0.1 -0.960 360.0-104.9-115.7 132.2 -1.2 22.0 -3.3 3 3 A K - 0 0 69 -2,-0.4 2,-0.4 101,-0.1 101,-0.2 -0.128 31.4-132.0 -51.3 144.1 -1.6 18.2 -2.4 4 4 A E E -A 103 0A 108 99,-1.8 99,-2.1 2,-0.0 2,-0.4 -0.887 13.0-126.5-103.7 132.3 -1.3 17.2 1.3 5 5 A K E +A 102 0A 130 -2,-0.4 2,-0.4 97,-0.2 97,-0.2 -0.677 34.1 179.4 -76.6 125.9 0.9 14.2 2.4 6 6 A I E -A 101 0A 16 95,-2.6 95,-2.5 -2,-0.4 2,-0.6 -0.996 21.8-152.3-135.0 123.5 -1.2 11.8 4.6 7 7 A H E -A 100 0A 96 -2,-0.4 2,-0.6 93,-0.2 93,-0.2 -0.899 17.6-151.5 -95.7 115.8 -0.1 8.5 6.3 8 8 A L E -A 99 0A 2 91,-2.6 91,-2.0 -2,-0.6 2,-0.5 -0.804 6.8-152.7 -96.5 115.8 -3.1 6.2 6.7 9 9 A E E -A 98 0A 93 -2,-0.6 2,-0.4 89,-0.2 89,-0.2 -0.770 12.3-175.4 -92.3 125.2 -2.8 3.7 9.6 10 10 A Y E -A 97 0A 18 87,-2.1 87,-1.9 -2,-0.5 2,-0.8 -0.986 23.0-133.5-118.3 129.3 -4.7 0.4 9.5 11 11 A L E -A 96 0A 70 -2,-0.4 2,-0.4 85,-0.2 116,-0.2 -0.740 25.0-168.5 -85.9 106.4 -4.7 -2.1 12.5 12 12 A L E -A 95 0A 13 83,-2.2 83,-2.1 -2,-0.8 116,-0.1 -0.844 23.9-112.0 -96.4 135.9 -3.9 -5.6 11.1 13 13 A N > - 0 0 42 -2,-0.4 3,-1.5 114,-0.3 82,-0.1 -0.196 23.2-110.8 -67.6 155.4 -4.4 -8.6 13.5 14 14 A A T 3 S+ 0 0 55 1,-0.3 -1,-0.1 80,-0.1 -2,-0.0 0.647 115.9 69.1 -60.2 -19.7 -1.5 -10.8 14.9 15 15 A T T 3 S+ 0 0 114 2,-0.1 2,-0.3 0, 0.0 -1,-0.3 0.869 90.6 72.5 -61.4 -40.6 -2.9 -13.7 12.7 16 16 A S S < S- 0 0 19 -3,-1.5 79,-0.1 1,-0.1 -4,-0.1 -0.658 72.8-159.3 -84.7 131.2 -1.7 -11.7 9.6 17 17 A K > - 0 0 126 -2,-0.3 3,-0.7 77,-0.0 -1,-0.1 -0.101 38.6 -86.5 -93.9-168.8 2.1 -11.4 8.9 18 18 A N T >> S+ 0 0 41 1,-0.2 4,-1.8 2,-0.1 3,-0.8 0.745 110.1 85.5 -70.0 -26.7 4.2 -9.0 6.8 19 19 A I H 3> S+ 0 0 110 1,-0.2 4,-1.5 2,-0.2 -1,-0.2 0.718 70.3 81.7 -53.1 -24.4 3.6 -11.0 3.6 20 20 A L H <4 S+ 0 0 61 -3,-0.7 -1,-0.2 1,-0.2 -2,-0.1 0.919 115.8 7.6 -44.0 -65.6 0.3 -9.0 3.0 21 21 A W H X4 S+ 0 0 75 -3,-0.8 3,-0.7 1,-0.2 -1,-0.2 0.518 120.2 73.1 -99.8 -13.6 1.9 -5.9 1.4 22 22 A S H >< S+ 0 0 31 -4,-1.8 3,-0.9 1,-0.2 4,-0.2 0.709 87.0 70.8 -68.2 -19.0 5.5 -7.5 1.2 23 23 A A G >< S+ 0 0 14 -4,-1.5 3,-1.6 -5,-0.2 7,-0.6 0.771 80.8 71.1 -63.3 -30.4 3.8 -9.5 -1.7 24 24 A I G < S+ 0 0 8 -3,-0.7 -1,-0.2 1,-0.3 -2,-0.1 0.698 87.2 65.1 -66.9 -19.5 3.6 -6.4 -4.0 25 25 A S G < S+ 0 0 48 -3,-0.9 -1,-0.3 -4,-0.2 -2,-0.2 0.644 101.7 57.5 -74.2 -20.3 7.5 -6.5 -4.5 26 26 A T S <> S- 0 0 67 -3,-1.6 4,-2.2 -4,-0.2 5,-0.2 -0.856 81.7-128.6-113.5 150.7 7.2 -9.9 -6.3 27 27 A P H > S+ 0 0 43 0, 0.0 4,-2.5 0, 0.0 5,-0.3 0.988 109.9 41.6 -56.4 -64.7 5.2 -10.9 -9.5 28 28 A T H 4 S+ 0 0 104 1,-0.2 4,-0.3 2,-0.2 -4,-0.1 0.707 116.8 51.7 -60.3 -25.4 3.3 -14.0 -8.1 29 29 A G H 4 S+ 0 0 14 -6,-0.3 -1,-0.2 2,-0.1 -5,-0.2 0.905 115.2 39.7 -73.4 -45.9 2.7 -12.1 -4.8 30 30 A L H >X S+ 0 0 11 -4,-2.2 3,-2.1 -7,-0.6 4,-1.1 0.968 113.2 50.7 -69.7 -56.2 1.2 -9.0 -6.5 31 31 A E T 3< S+ 0 0 46 -4,-2.5 -1,-0.2 1,-0.3 -3,-0.1 0.596 94.2 77.2 -63.3 -13.0 -1.0 -10.7 -9.3 32 32 A D T 34 S+ 0 0 132 -5,-0.3 -1,-0.3 -4,-0.3 -2,-0.2 0.741 123.3 2.5 -64.3 -25.9 -2.5 -12.9 -6.5 33 33 A W T <4 S+ 0 0 122 -3,-2.1 2,-0.4 -4,-0.2 -2,-0.2 0.212 124.6 73.0-148.0 12.5 -4.7 -9.9 -5.5 34 34 A F S < S- 0 0 75 -4,-1.1 -1,-0.2 1,-0.1 0, 0.0 -0.980 97.7 -35.1-138.7 123.5 -3.8 -7.1 -8.1 35 35 A A S S- 0 0 41 -2,-0.4 -1,-0.1 1,-0.1 3,-0.1 0.053 81.1 -73.6 62.6-175.3 -4.8 -7.0 -11.9 36 36 A D S S- 0 0 112 1,-0.3 2,-0.3 12,-0.1 13,-0.2 0.920 111.0 -0.4 -75.5 -52.5 -5.2 -10.1 -14.2 37 37 A K E -B 48 0A 95 11,-1.4 11,-2.5 2,-0.0 2,-0.4 -0.987 55.0-159.5-142.1 144.8 -1.4 -10.8 -14.6 38 38 A V E -B 47 0A 5 -2,-0.3 2,-0.6 9,-0.2 9,-0.2 -0.949 9.5-172.0-127.1 109.7 1.9 -9.2 -13.4 39 39 A V E -B 46 0A 79 7,-2.5 7,-1.8 -2,-0.4 2,-0.1 -0.913 18.4-154.2 -99.3 117.6 5.1 -10.1 -15.4 40 40 A S E +B 45 0A 57 -2,-0.6 2,-0.3 5,-0.2 5,-0.2 -0.485 18.2 179.9 -95.1 161.1 8.2 -8.8 -13.6 41 41 A D E > -B 44 0A 116 3,-2.2 3,-1.3 -2,-0.1 2,-0.1 -0.880 52.4 -59.7-141.0 171.6 11.7 -7.7 -14.8 42 42 A D T 3 S- 0 0 114 -2,-0.3 3,-0.0 1,-0.2 0, 0.0 -0.398 119.5 -15.5 -57.7 126.5 14.8 -6.4 -12.8 43 43 A K T 3 S+ 0 0 153 -2,-0.1 16,-1.0 15,-0.1 2,-0.3 0.524 126.8 85.9 51.7 15.9 13.8 -3.1 -10.9 44 44 A T E < -BC 41 58A 25 -3,-1.3 -3,-2.2 14,-0.2 2,-0.5 -0.984 62.7-154.1-146.2 128.8 10.7 -2.8 -13.1 45 45 A V E -BC 40 57A 10 12,-2.3 12,-1.7 -2,-0.3 2,-0.6 -0.911 10.2-159.2-105.3 119.8 7.1 -4.3 -12.7 46 46 A T E -BC 39 56A 26 -7,-1.8 -7,-2.5 -2,-0.5 2,-0.4 -0.878 6.4-154.2-106.0 111.3 5.1 -4.9 -16.0 47 47 A F E -BC 38 55A 10 8,-2.0 8,-1.5 -2,-0.6 2,-0.4 -0.698 9.9-169.9 -85.6 131.4 1.3 -5.2 -15.4 48 48 A C E +BC 37 54A 20 -11,-2.5 -11,-1.4 -2,-0.4 6,-0.2 -0.974 13.4 167.8-128.7 114.4 -0.7 -7.2 -18.1 49 49 A W S S- 0 0 102 4,-0.7 -1,-0.1 -2,-0.4 4,-0.1 0.898 78.6 -18.6 -88.0 -83.6 -4.5 -7.2 -18.2 50 50 A G S S- 0 0 55 2,-0.7 2,-0.2 3,-0.3 3,-0.1 -0.148 95.8 -92.8-122.2 37.1 -6.0 -8.7 -21.5 51 51 A K S S+ 0 0 189 2,-0.1 2,-0.5 1,-0.1 3,-0.1 0.083 108.1 96.5 70.2 -23.3 -2.8 -8.4 -23.8 52 52 A T S S+ 0 0 115 1,-0.2 -2,-0.7 -2,-0.2 -3,-0.2 -0.883 91.0 6.1 -90.5 125.4 -4.2 -4.9 -24.9 53 53 A E S S- 0 0 126 -2,-0.5 -4,-0.7 1,-0.1 2,-0.4 0.933 71.7-173.3 66.3 100.5 -2.6 -2.0 -22.9 54 54 A Q E -C 48 0A 105 -6,-0.2 2,-0.2 -3,-0.1 -6,-0.2 -0.985 7.4-153.9-124.5 137.7 0.3 -3.1 -20.5 55 55 A R E -C 47 0A 90 -8,-1.5 -8,-2.0 -2,-0.4 2,-0.3 -0.662 3.4-150.7-113.6 160.1 1.9 -0.7 -18.0 56 56 A Q E -C 46 0A 88 -10,-0.2 17,-1.7 -2,-0.2 18,-0.5 -0.993 9.4-176.1-132.7 143.6 5.4 -0.5 -16.2 57 57 A A E -CD 45 72A 2 -12,-1.7 -12,-2.3 -2,-0.3 15,-0.3 -0.982 15.3-143.8-141.6 124.0 6.4 1.0 -12.8 58 58 A G E -CD 44 71A 12 13,-1.5 13,-1.8 -2,-0.4 2,-0.4 -0.585 21.3-117.8 -85.2 148.5 9.9 1.2 -11.4 59 59 A I E - 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