Residue-by-residue listing for analyzed_6 Page 1 ---------------------------------------- This listing highlights the residues in the structure which may need investigation. The ideal values and standard deviations against which the structure has been compared are shown in the following table: <------------------------------- I D E A L V A L U E S -------------------------------> Chi-1 dihedral Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality g(-) trans g(+) Chi-2 phi helix psi rt-hand lf-hand bond dihedral en. C-alpha ------------------------------------------------------------------------------------------ Ideal value 64.1 183.6 -66.7 177.4 -65.4 -65.3 -39.4 96.8 -85.8 2.0 180.0 -2.0 33.9 Standard deviation 15.7 16.8 15.0 18.5 11.2 11.9 11.3 14.8 10.7 .1 5.8 .8 3.5 ------------------------------------------------------------------------------------------ In the listing below, properties that deviate from these values are highlighted by asterisks and plus-signs. Each asterisk represents one standard deviation, and each plus-sign represents half a standard deviation. So, a highlight such as +***, indicates that the value of the parameter is between 3.5 and 4.0 standard deviations from the ideal value shown above. Where the deviation is greater than 4.5 standard deviations its numerical value is shown; for example, *5.5*. The final column gives the maximum deviation in each row, while the maximum column deviations are shown at the end of the listing. Also at the end are the keys to the codes used for the secondary structure and Ramachandran plot assignments. Full print-out. ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 1 GLY 1 - - - - - - - - - - - 180.1 - - - 2 HIS 2 ~p - - -113.3 - - - - - - - 180.0 - 34.5 - ** *** *** 3 HIS 3 B - 222.3 - - - - - - - - 180.0 - 34.4 - ** ** 4 HIS 4 B - - -112.8 - - - - - - - 180.0 - 34.4 - *** *** 5 HIS 5 B - - -105.4 - - - - - - - 180.0 -.6 34.4 - +** +* +** 6 HIS 6 b 56.2 - - - - - - - - - 180.0 - 34.4 - 7 HIS 7 B - - -88.4 - - - - - - - 180.0 - 34.4 - * * 8 LEU 8 B - - -72.5 173.4 - - - - - - 179.9 - 34.5 - 9 GLU 9 B - - -117.2 197.3 - - - - - - 180.1 - 34.5 - *** * *** 10 CYS 10 B - 220.0 - - - - - - - - 180.2 - 34.4 - ** ** 11 SER 11 B - - -31.8 - - - - - - - 180.2 - 34.5 - ** ** 12 SER 12 S A - 196.9 - - - - - - - - 179.9 - 34.4 - 13 ASP 13 B - - -95.2 - - - - - - - 180.2 - 34.4 - +* +* 14 SER 14 B - 191.8 - - - - - - - - 179.9 - 34.4 - 15 LEU 15 B - - -105.1 - - - - - - - 180.0 - 34.5 - +** +** 16 GLN 16 B 59.8 - - 129.1 - - - - - - 180.0 - 34.4 - +** +** 17 LEU 17 B - - -60.8 160.6 - - - - - - 179.9 - 34.5 - Residue-by-residue listing for analyzed_6 Page 2 ---------------------------------------- ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 18 HIS 18 E B - - -42.1 - - - - - - - 180.0 -1.8 34.4 - +* +* 19 ASN 19 E B 32.4 - - - - - - - - - 179.9 - 34.5 1 ** * ** 20 VAL 20 E B - 188.2 - - - - - - - - 180.0 -1.3 34.3 - 21 PHE 21 E B - 171.3 - - - - - - - - 179.9 -3.0 34.4 - * * 22 VAL 22 E b - - -55.6 - - - - - - - 180.1 -2.9 34.4 - * * 23 TYR 23 S a 45.4 - - - - - - - - - 180.0 - 34.4 - * * 24 GLY 24 t - - - - - - - - - - - 180.3 - - - 25 SER 25 T A - 190.4 - - - - - - - - 180.1 - 34.4 - 26 PHE 26 T a - - -47.8 - - - - - - - 180.1 - 34.4 - * * 27 GLN 27 t a - 170.4 - 130.5 - - - - - - 179.9 -1.0 34.4 - +** * +** 28 ASP 28 h B - 204.3 - - - - - - - - 180.0 - 34.4 - * * 29 PRO 29 H - - - - - -69.8 -69.8 -22.9 - - - 179.9 - 38.6 - * * * 30 ASP 30 H A - 198.9 - - - -54.7 -48.6 - - - 180.0 - 34.4 - 31 VAL 31 H A 73.5 - - - - -68.5 -28.8 - - - 179.9 - 34.4 - 32 ILE 32 H A - - -71.7 - - -69.7 -40.6 - - - 179.9 -.8 34.3 - +* +* 33 ASN 33 H A - - -102.2 - - -54.0 -42.1 - - - 179.9 -2.5 34.5 - ** ** 34 VAL 34 H A - 182.6 - - - -81.1 -30.4 - - - 180.0 -1.0 34.3 - * * * 35 MET 35 H A - 224.5 - 207.6 - -57.5 -35.4 - - - 180.0 -1.7 34.5 - ** +* ** 36 LEU 36 h a 31.0 - - 135.0 - - - - - - 179.9 -1.8 34.5 1 ** ** * ** 37 ASP 37 t ~a - - -104.0 - - - - - - - 180.1 -.6 34.4 - ** ** +* ** 38 ARG 38 b - - -49.1 231.7 - - - - - - 180.1 - 34.4 - * +** +** 39 THR 39 B - - -51.3 - - - - - - - 179.9 - 34.3 - * * 40 PRO 40 - - - - - -69.8 - - - - - 180.0 - 38.6 - * * 41 GLU 41 e B - 218.7 - 143.1 - - - - - - 180.0 - 34.5 - ** +* ** 42 ILE 42 E B - - -47.8 - - - - - - - 179.9 - 34.3 - * * 43 VAL 43 E B 68.3 - - - - - - - - - 180.1 -3.0 34.3 - * * 44 SER 44 e B - - -65.1 - - - - - - - 179.9 - 34.5 - 45 ALA 45 E B - - - - - - - - - - 180.1 - 34.0 - 46 THR 46 E B - - -60.3 - - - - - - - 180.0 -2.5 34.3 - 47 LEU 47 E b - 167.0 - - - - - - - - 179.8 -3.1 34.5 - * * 48 PRO 48 E - - - - - -69.7 - - - - - 180.0 - 38.6 - * * 49 GLY 49 E - - - - - - - - - - - 180.1 -2.2 - - 50 PHE 50 E B - - -78.6 - - - - - - - 180.1 -.8 34.5 - +* +* Residue-by-residue listing for analyzed_6 Page 3 ---------------------------------------- ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 51 GLN 51 E B - 189.3 - - - - - - - - 180.1 -3.2 34.4 - +* +* 52 ARG 52 E B - 172.3 - 172.4 - - - - - - 180.1 - 34.5 - 53 PHE 53 e B - - -73.7 - - - - - - - 180.1 -1.9 34.4 - 54 ARG 54 B - - -27.9 - - - - - - - 180.0 -.5 34.4 - +** +* +** 55 LEU 55 B 84.4 - - 173.0 - - - - - - 179.9 - 34.5 - * * 56 LYS 56 ~b - 226.2 - 155.9 - - - - - - 179.9 -.5 34.5 - ** +** * ** +** 57 GLY 57 S - - - - - - - - - - - 180.1 - - - 58 ARG 58 S A - 172.1 - - - - - - - - 180.0 -.8 34.5 - +* +* 59 LEU 59 S B - 170.8 - - - - - - - - 180.0 - 34.5 - 60 TYR 60 B - - -37.9 - - - - - - - 179.9 - 34.4 - +* +* 61 PRO 61 - - - - - -69.8 - - - - - 180.0 - 38.6 - * * 62 CYS 62 e b 50.2 - - - - - - - - - 180.1 - 34.5 - 63 ILE 63 E B - - -60.8 - - - - - - - 179.9 - 34.3 - 64 VAL 64 E B - - -62.8 - - - - - - - 179.9 -2.0 34.3 - 65 PRO 65 E - - - - - -69.8 - - - - - 180.2 - 38.6 - * * 66 SER 66 E B - 160.2 - - - - - - - - 180.1 -2.1 34.5 - * * 67 GLU 67 E A - - -104.6 175.5 - - - - - - 180.0 - 34.4 - +** +** 68 LYS 68 E a - - -64.4 198.6 - - - - - - 180.0 - 34.5 - * * 69 GLY 69 E - - - - - - - - - - - 180.2 -.5 - - ** ** 70 GLU 70 E B 60.2 - - - - - - - - - 179.9 - 34.4 - 71 VAL 71 E B - 188.8 - - - - - - - - 180.0 -2.0 34.4 - 72 HIS 72 E B - - -66.5 - - - - - - - 180.1 - 34.4 - 73 GLY 73 e - - - - - - - - - - - 180.1 -1.4 - - 74 LYS 74 E B - - -49.4 - - - - - - - 179.9 -1.3 34.5 - * * 75 VAL 75 E B - 154.1 - - - - - - - - 180.0 -3.2 34.3 - +* +* +* 76 LEU 76 E B - - -40.1 186.1 - - - - - - 179.9 -3.3 34.5 - +* +* +* 77 MET 77 E B - - -88.6 - - - - - - - 180.0 -2.6 34.4 - * * 78 GLY 78 E - - - - - - - - - - - 180.1 - - - 79 VAL 79 E B 84.2 - - - - - - - - - 180.1 -1.5 34.4 - * * 80 THR 80 h B 3.1 - - - - - - - - - 180.1 - 34.3 - +*** +*** 81 SER 81 H A - 188.0 - - - -64.8 -41.9 - - - 179.9 - 34.5 - 82 ASP 82 H A - - -115.2 - - -54.9 -31.4 - - - 180.1 - 34.4 - *** *** 83 GLU 83 H A - - -89.9 - - -76.0 -40.2 - - - 180.0 - 34.4 1 +* * +* 84 LEU 84 H A - 183.3 - - - -52.7 -51.1 - - - 179.9 -1.5 34.5 - * * * 85 GLU 85 H A - - -75.4 155.5 - -68.2 -29.3 - - - 180.0 -1.8 34.5 - * * Residue-by-residue listing for analyzed_6 Page 4 ---------------------------------------- ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 86 ASN 86 H A 118.9 - - - - -73.6 -29.2 - - - 180.0 -.9 34.5 - *** * *** 87 LEU 87 H A - - -72.5 173.7 - -72.2 -51.6 - - - 179.9 -2.3 34.5 - * * 88 ASP 88 H A - 183.4 - - - -56.7 -32.5 - - - 180.0 -1.9 34.4 - 89 ALA 89 H A - - - - - -75.2 -48.0 - - - 180.0 -1.1 34.0 - * * 90 VAL 90 H A - 172.6 - - - -61.4 -48.9 - - - 180.0 -2.2 34.3 - 91 GLU 91 H A - - -103.6 - - -77.6 -22.7 - - - 180.1 -3.2 34.5 1 ** * * * * ** 92 GLY 92 h - - - - - - - - - - - 180.1 -.9 - - +* +* 93 ASN 93 T A - - -88.4 - - - - - - - 180.0 -.8 34.4 - * +* +* 94 GLU 94 T a - - -92.3 200.9 - - - - - - 180.1 -2.5 34.4 - +* * +* 95 TYR 95 t B - - -54.5 - - - - - - - 180.1 -2.7 34.4 - 96 GLU 96 E B - 183.4 - 166.6 - - - - - - 180.1 -.8 34.4 - +* +* 97 ARG 97 E B - 184.5 - 197.1 - - - - - - 180.0 - 34.5 - * * 98 VAL 98 E B - - -74.3 - - - - - - - 180.0 -2.6 34.4 - 99 THR 99 E B - 183.2 - - - - - - - - 179.9 - 34.4 - 100 VAL 100 E B - - -71.6 - - - - - - - 180.0 -1.5 34.3 - 101 GLY 101 E - - - - - - - - - - - 180.0 - - - 102 ILE 102 E B 61.3 - - - - - - - - - 179.9 -2.9 34.3 1 * * * 103 VAL 103 E B - 184.2 - - - - - - - - 180.0 -2.2 34.3 - 104 ARG 104 E B - - -119.3 169.2 - - - - - - 180.0 -1.9 34.5 - +*** +*** 105 GLU 105 e A - - -69.1 184.4 - - - - - - 180.0 -2.8 34.4 - * * 106 ASP 106 T A - 193.0 - - - - - - - - 180.1 -.8 34.4 - +* +* 107 ASN 107 T A 45.5 - - - - - - - - - 180.1 - 34.5 - * * 108 SER 108 T l - 220.3 - - - - - - - - 180.1 -.8 34.4 - ** +* ** 109 GLU 109 E B - - -69.0 - - - - - - - 180.0 -.6 34.4 - +* +* 110 LYS 110 E B 78.7 - - - - - - - - - 179.9 - 34.5 - 111 MET 111 E B - - -107.3 207.3 - - - - - - 179.9 -3.1 34.5 - +** +* * +** 112 ALA 112 E B - - - - - - - - - - 180.0 - 34.0 - 113 VAL 113 E B - - -46.9 - - - - - - - 180.0 -1.4 34.4 - * * 114 LYS 114 E B - - -53.6 - - - - - - - 180.0 -2.1 34.5 - 115 THR 115 E B - 191.4 - - - - - - - - 180.1 -1.8 34.4 - 116 TYR 116 E B - - -36.9 - - - - - - - 179.9 - 34.4 - +* +* 117 MET 117 E B 96.1 - - 192.4 - - - - - - 180.0 -1.1 34.4 - ** * ** 118 TRP 118 B - 206.0 - - - - - - - - 180.0 -2.9 34.4 - * * * 119 ILE 119 S A - - -46.0 - - - - - - - 179.9 - 34.3 - * * Residue-by-residue listing for analyzed_6 Page 5 ---------------------------------------- ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 120 ASN 120 S A - 162.0 - - - - - - - - 179.9 - 34.4 1 * * * 121 LYS 121 l 65.3 - - - - - - - - - 179.9 - 34.5 - 122 ALA 122 a - - - - - - - - - - 179.9 - 34.0 - 123 ASP 123 g b - - -116.2 - - - - - - - 180.0 - 34.4 - *** *** 124 PRO 124 G - - - - - -69.7 - - - - - 180.0 - 38.6 - * * 125 ASP 125 G A - - -103.8 - - - - - - - 180.0 - 34.4 - ** ** 126 MET 126 G A 75.2 - - 215.8 - - - - - - 180.1 -1.6 34.4 - ** ** 127 PHE 127 g B - 190.0 - - - - - - - - 180.0 -1.1 34.4 - * * 128 GLY 128 - - - - - - - - - - - 180.2 -.8 - - +* +* 129 GLU 129 B 56.0 - - 141.6 - - - - - - 180.0 - 34.4 - +* +* 130 TRP 130 h B - - -109.1 - - - - - - - 180.0 - 34.4 - +** +** 131 ASN 131 H A - 228.3 - - - -60.5 -61.4 - - - 180.0 - 34.5 - +** +* +** 132 PHE 132 H A - - -55.7 - - -54.7 -48.5 - - - 180.0 - 34.5 - 133 GLU 133 H A - - -79.4 - - -58.6 -29.2 - - - 180.0 - 34.4 - 134 GLU 134 H A - 197.6 - 190.6 - -59.3 -34.0 - - - 180.1 -1.5 34.4 - 135 TRP 135 H A - 172.7 - - - -69.7 -42.1 - - - 179.9 -1.4 34.4 - 136 LYS 136 H A - 183.0 - - - -53.0 -31.9 - - - 180.0 -1.1 34.5 - * * * 137 ARG 137 H A - 165.1 - 169.2 - -71.0 -51.4 - - - 180.0 -1.1 34.4 - * * * * 138 LEU 138 H A - - -91.5 - - -68.9 -17.9 - - - 179.9 -1.4 34.4 - +* +* +* 139 HIS 139 H A - 179.4 - - - -82.8 -35.2 - - - 180.0 -2.1 34.4 - * * 140 LYS 140 H A - 166.0 - 163.9 - -67.1 -36.7 - - - 179.9 -1.6 34.5 - * * 141 LYS 141 H A - - -117.7 224.0 - -48.4 -31.7 - - - 179.9 -1.4 34.5 - *** +** * *** 142 LYS 142 H A - 201.4 - - - -54.3 -49.2 - - - 180.0 -.8 34.5 - * +* +* 143 PHE 143 H A - - -46.1 - - -76.9 -33.8 - - - 180.0 -1.3 34.5 - * * 144 ILE 144 H A - - -59.2 - - -60.8 -33.2 - - - 179.9 -2.2 34.3 - 145 GLU 145 H A - - -84.1 178.9 - -51.9 -51.7 - - - 180.1 -2.2 34.4 - * * * * 146 THR 146 H A - 181.4 - - - -80.8 -35.7 - - - 180.0 -.6 34.4 - * +* +* 147 PHE 147 H A - - -102.9 - - -61.4 -30.6 - - - 180.0 -2.7 34.5 - ** ** 148 LYS 148 H A - - -106.0 202.8 - -53.6 -36.7 - - - 179.9 -2.7 34.5 - +** * +** 149 LYS 149 H A - - -85.2 203.8 - -73.8 -33.5 - - - 179.9 -1.2 34.5 - * * * * 150 ILE 150 H A - - -58.2 166.1 - -73.8 -40.6 - - - 179.9 -.9 34.3 - * * 151 MET 151 H A 73.7 - - 183.1 - -74.9 -29.1 - - - 180.0 -3.2 34.5 - +* +* Residue-by-residue listing for analyzed_6 Page 6 ---------------------------------------- ................................................................................................................................... Residue Kabsch Region --------- Sander of No. Type Seq sec Ramch. Chi-1 dihedral Chi-2 Proline Phi Helix Chi-3 Chi-3 Disulph Omega H-bond Chirality Bad Max Chain no. struc plot g(-) trans g(+) trans phi helix psi rt-hand lf-hand bond dihedral en. C-alpha contacts dev ----------------------------------------------------------------------------------------------------------------------------------- 152 GLU 152 H A - - -95.8 - - -68.5 -31.5 - - - 180.0 -1.5 34.4 - +* +* 153 CYS 153 H A - 194.3 - - - -66.3 -33.0 - - - 180.0 -1.0 34.4 - * * 154 LYS 154 H A - - -48.5 234.6 - -76.5 -31.3 - - - 179.9 -.7 34.5 - * *** +* *** 155 LYS 155 h b - 200.7 - - - - - - - - 179.9 -1.3 34.5 - * * 156 LYS 156 t b 44.5 - - 146.7 - - - - - - 179.9 -.5 34.5 - * +* ** ** 157 PRO 157 - - - - - -69.7 - - - - - 180.0 - 38.6 - * * 158 GLN 158 b 73.0 - - 203.0 - - - - - - 180.0 -1.1 34.4 - * * * 159 GLY 159 - - - - - - - - - - - 180.1 - - - 160 GLN 160 b - 227.9 - 131.1 - - - - - - 180.0 -.8 34.5 - +** +** +* +** 161 GLY 161 - - - - - - - - - - - 180.1 - - - 162 ASN 162 b - 223.4 - - - - - - - - 179.9 - 34.5 - ** ** 163 ASP 163 B - 236.3 - - - - - - - - 180.0 - 34.4 - *** *** 164 ASP 164 B - - -98.1 - - - - - - - 179.9 - 34.4 - ** ** 165 ILE 165 B - 187.8 - 153.9 - - - - - - 180.1 -.5 34.3 - * +* +* 166 SER 166 B - - -37.8 - - - - - - - 180.0 - 34.5 - +* +* 167 HIS 167 a - - -27.2 - - - - - - - 180.0 - 34.4 1 +** * +** 168 VAL 168 XX - 191.7 - - - - - - - - 180.0 - 34.4 - **** **** 169 LEU 169 B - 179.5 - - - - - - - - 179.9 - 34.5 - 170 ARG 170 b - - -62.7 - - - - - - - 180.1 - 34.5 - 171 GLU 171 B - - -90.5 207.5 - - - - - - 180.0 - 34.5 - +* +* +* 172 ASP 172 b 75.0 - - - - - - - - - 180.1 - 34.4 - 173 GLN 173 - - 216.4 - - - - - - - - - - 34.5 - +* +* ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: **** +*** *** +*** *** * +* ** * * **** ----------------------------------------------------------------------------------------------------------------------------------- Mean values: 63.0 191.5 -75.2 178.9 -69.7 -65.6 -37.3 - - - 180.0 -1.7 34.6 Standard deviations: 23.6 20.2 25.9 27.9 .0 9.5 9.4 - - - .1 .8 .9 Numbers of values: 24 54 72 41 7 42 42 0 0 0 172 89 161 7 Residue-by-residue listing for analyzed_6 Page 7 ---------------------------------------- KEY TO CODES: ------------ Regions of the Ramachandran plot Secondary structure (extended Kabsch/Sander) -------------------------------- -------------------------------------------- A - Core alpha B - residue in isolated beta-bridge a - Allowed alpha E - extended strand, participates in beta-ladder ~a - Generous alpha ** Generous G - 3-helix (3/10 helix) B - Core beta H - 4-helix (alpha-helix) b - Allowed beta I - 5-helix (pi-helix) ~b - Generous beta ** Generous S - bend L - Core left-handed alpha T - hydrogen-bonded turn l - Allowed left-handed alpha ~l - Generous left-handed alpha ** Generous e - extension of beta-strand p - Allowed epsilon g - extension of 3/10 helix ~p - Generous epsilon ** Generous h - extension of alpha-helix XX - Outside major areas **** Disallowed Residue-by-residue listing for analyzed_6 Page 8 ---------------------------------------- M A I N C H A I N B O N D L E N G T H S A N D B O N D A N G L E S ..................................... Small molecule data ......................................... <---------- Bond lengths ----------> <---------------------- Bond angles ----------------------> C-N C-O CA-C CA-CB N-CA C-N-CA CA-C-N CA-C-O CB-CA-C N-CA-C N-CA-CB O-C-N --------------------------------------------------------------------------------------------------- Any - 1.231 - - - - - - - - - - ( .020) Pro 1.341 - - - 1.466 122.60 116.90 - - 111.80 103.00 122.00 ( .016) ( .015) ( 5.00) ( 1.50) ( 2.50) ( 1.10) ( 1.40) Except Pro 1.329 - - - - - - - - - - 123.00 ( .014) ( 1.60) Gly - - 1.516 - 1.451 120.60 116.40 120.80 - 112.50 - - ( .018) ( .016) ( 1.70) ( 2.10) ( 2.10) ( 2.90) Except Gly - - 1.525 - - - - 120.80 - - - - ( .021) ( 1.70) Ala - - - 1.521 - - - - 110.50 - 110.40 - ( .033) ( 1.50) ( 1.50) Ile,Thr,Val - - - 1.540 - - - - 109.10 - 111.50 - ( .027) ( 2.20) ( 1.70) Except Gly,Pro - - - - 1.458 121.70 116.20 - - 111.20 - - ( .019) ( 1.80) ( 2.00) ( 2.80) The rest - - - 1.530 - - - - 110.10 - 110.50 - ( .020) ( 1.90) ( 1.70) Note. The table above shows the mean values obtained from small molecule data by Engh & Huber (1991). The values shown in brackets are standard deviations ................................................................................................................................... Residue ------------- <---------- Bond lengths ----------> <---------------------- Bond angles ----------------------> No. Type Seq Max Chain no. C-N C-O CA-C CA-CB N-CA C-N-CA CA-C-N CA-C-O CB-CA-C N-CA-C N-CA-CB O-C-N dev ----------------------------------------------------------------------------------------------------------------------------------- 1 GLY 1 - 1.232 1.516 - 1.451 - 116.38 120.64 - 112.46 - 122.98 2 HIS 2 1.329 1.231 1.525 1.530 1.459 121.62 116.22 120.85 109.97 110.87 110.26 122.93 3 HIS 3 1.330 1.231 1.526 1.529 1.458 121.62 116.21 120.81 109.95 110.87 110.34 122.98 4 HIS 4 1.329 1.231 1.526 1.529 1.459 121.59 116.23 120.80 109.94 110.89 110.31 122.97 5 HIS 5 1.329 1.232 1.526 1.529 1.458 121.62 116.20 120.84 109.97 110.88 110.29 122.96 6 HIS 6 1.330 1.232 1.526 1.528 1.458 121.57 116.21 120.82 109.95 110.84 110.36 122.98 7 HIS 7 1.329 1.232 1.526 1.529 1.458 121.59 116.22 120.84 109.92 110.85 110.36 122.94 8 LEU 8 1.328 1.230 1.525 1.530 1.459 121.63 116.25 120.75 109.91 110.95 110.28 123.00 9 GLU 9 1.329 1.232 1.526 1.530 1.458 121.58 116.13 120.84 109.89 110.87 110.35 123.03 10 CYS 10 1.328 1.232 1.526 1.529 1.459 121.60 116.18 120.82 109.94 110.85 110.35 123.00 11 SER 11 1.329 1.231 1.526 1.530 1.458 121.58 116.15 120.86 109.90 110.85 110.29 122.99 12 SER 12 1.329 1.231 1.526 1.530 1.458 121.63 116.13 120.91 109.91 110.87 110.34 122.97 13 ASP 13 1.328 1.230 1.525 1.530 1.458 121.65 116.19 120.83 110.01 110.85 110.34 122.98 14 SER 14 1.329 1.232 1.525 1.529 1.459 121.63 116.14 120.92 109.94 110.88 110.30 122.93 15 LEU 15 1.329 1.231 1.525 1.531 1.458 121.63 116.20 120.75 109.90 110.99 110.25 123.04 16 GLN 16 1.329 1.231 1.526 1.529 1.458 121.58 116.14 120.84 109.98 110.88 110.33 123.02 17 LEU 17 1.329 1.231 1.526 1.530 1.459 121.57 116.21 120.84 109.93 110.92 110.24 122.95 18 HIS 18 1.329 1.231 1.526 1.529 1.458 121.63 116.21 120.78 109.95 110.88 110.33 123.01 19 ASN 19 1.329 1.231 1.525 1.530 1.459 121.61 116.21 120.81 109.91 110.95 110.29 122.98 20 VAL 20 1.329 1.232 1.525 1.540 1.458 121.64 116.17 120.84 109.04 111.15 111.36 122.98 21 PHE 21 1.329 1.231 1.526 1.530 1.458 121.62 116.17 120.90 109.94 110.85 110.33 122.93 22 VAL 22 1.330 1.231 1.525 1.541 1.458 121.61 116.18 120.81 109.00 111.14 111.31 123.01 Residue-by-residue listing for analyzed_6 Page 9 ---------------------------------------- ................................................................................................................................... Residue ------------- <---------- Bond lengths ----------> <---------------------- Bond angles ----------------------> No. Type Seq Max Chain no. C-N C-O CA-C CA-CB N-CA C-N-CA CA-C-N CA-C-O CB-CA-C N-CA-C N-CA-CB O-C-N dev ----------------------------------------------------------------------------------------------------------------------------------- 23 TYR 23 1.327 1.230 1.525 1.530 1.459 121.62 116.11 120.94 109.94 110.93 110.30 122.95 24 GLY 24 1.329 1.230 1.516 - 1.452 120.73 116.35 120.68 - 112.48 - 122.97 25 SER 25 1.330 1.230 1.526 1.530 1.459 121.62 116.11 120.91 109.96 110.87 110.33 122.98 26 PHE 26 1.330 1.230 1.526 1.530 1.458 121.63 116.13 120.78 109.92 110.89 110.34 123.09 27 GLN 27 1.329 1.232 1.525 1.529 1.458 121.56 116.20 120.81 109.94 110.92 110.34 122.99 28 ASP 28 1.328 1.231 1.526 1.529 1.459 121.61 116.18 121.65 109.96 110.87 110.34 122.17 29 PRO 29 1.342 1.231 1.524 1.531 1.466 122.67 116.25 120.82 110.46 112.36 103.35 122.93 30 ASP 30 1.329 1.232 1.526 1.530 1.458 121.65 116.21 120.85 109.98 110.86 110.34 122.94 31 VAL 31 1.329 1.232 1.525 1.540 1.459 121.64 116.19 120.78 109.01 111.09 111.36 123.03 32 ILE 32 1.329 1.230 1.525 1.540 1.458 121.56 116.20 120.82 109.03 111.14 111.42 122.98 33 ASN 33 1.328 1.232 1.525 1.530 1.459 121.62 116.23 120.88 109.91 110.87 110.29 122.89 34 VAL 34 1.329 1.230 1.525 1.540 1.458 121.69 116.17 120.81 109.05 111.11 111.40 123.02 35 MET 35 1.329 1.233 1.525 1.530 1.458 121.57 116.28 120.80 109.92 110.85 110.32 122.92 36 LEU 36 1.328 1.231 1.525 1.530 1.459 121.68 116.23 120.79 109.90 110.95 110.22 122.98 37 ASP 37 1.329 1.231 1.525 1.529 1.458 121.62 116.16 120.84 109.99 110.86 110.35 123.00 38 ARG 38 1.329 1.231 1.526 1.530 1.459 121.59 116.20 120.87 109.93 110.89 110.31 122.93 39 THR 39 1.329 1.231 1.524 1.540 1.457 121.68 116.25 121.54 109.03 111.16 111.42 122.21 40 PRO 40 1.341 1.230 1.525 1.531 1.466 122.70 116.16 120.78 110.46 112.31 103.38 123.06 41 GLU 41 1.330 1.231 1.527 1.530 1.459 121.54 116.14 120.79 109.88 110.86 110.36 123.06 42 ILE 42 1.329 1.231 1.525 1.540 1.458 121.55 116.16 120.88 109.04 111.10 111.46 122.96 43 VAL 43 1.329 1.230 1.525 1.541 1.458 121.60 116.16 120.85 109.04 111.10 111.40 123.00 44 SER 44 1.329 1.230 1.526 1.530 1.458 121.62 116.13 120.90 109.94 110.82 110.30 122.97 45 ALA 45 1.329 1.232 1.525 1.522 1.457 121.61 116.27 120.83 110.34 111.12 110.32 122.90 46 THR 46 1.329 1.232 1.525 1.540 1.457 121.67 116.23 120.77 109.03 111.17 111.40 122.99 47 LEU 47 1.328 1.232 1.525 1.530 1.459 121.63 116.21 121.63 109.95 110.86 110.26 122.16 48 PRO 48 1.341 1.230 1.524 1.531 1.465 122.71 116.25 120.82 110.47 112.40 103.43 122.93 49 GLY 49 1.330 1.231 1.516 - 1.451 120.78 116.34 120.69 - 112.53 - 122.97 50 PHE 50 1.329 1.231 1.526 1.531 1.458 121.60 116.14 120.82 109.92 110.88 110.31 123.04 51 GLN 51 1.330 1.231 1.526 1.529 1.458 121.54 116.20 120.81 109.93 110.87 110.33 123.00 52 ARG 52 1.329 1.231 1.526 1.531 1.458 121.59 116.17 120.84 109.88 110.84 110.31 122.99 53 PHE 53 1.329 1.231 1.526 1.530 1.458 121.63 116.15 120.88 109.92 110.89 110.33 122.97 54 ARG 54 1.329 1.231 1.526 1.529 1.458 121.62 116.17 120.84 109.91 110.89 110.33 122.99 55 LEU 55 1.328 1.231 1.526 1.530 1.459 121.61 116.19 120.84 109.92 110.92 110.27 122.97 56 LYS 56 1.328 1.230 1.526 1.530 1.458 121.68 116.19 120.79 109.87 110.92 110.30 123.02 57 GLY 57 1.329 1.230 1.515 - 1.452 120.75 116.34 120.68 - 112.49 - 122.99 58 ARG 58 1.329 1.232 1.525 1.530 1.458 121.61 116.21 120.87 109.93 110.89 110.29 122.92 59 LEU 59 1.329 1.231 1.526 1.530 1.459 121.67 116.17 120.78 109.92 110.94 110.28 123.05 60 TYR 60 1.328 1.231 1.526 1.530 1.458 121.60 116.14 121.66 109.94 110.91 110.34 122.20 61 PRO 61 1.341 1.232 1.525 1.531 1.466 122.71 116.23 120.75 110.43 112.33 103.42 123.02 62 CYS 62 1.328 1.232 1.526 1.529 1.458 121.60 116.19 120.77 109.91 110.86 110.32 123.04 63 ILE 63 1.329 1.231 1.525 1.540 1.458 121.54 116.14 120.87 109.02 111.11 111.42 122.99 64 VAL 64 1.329 1.231 1.525 1.540 1.458 121.58 116.16 121.64 109.08 111.09 111.37 122.20 65 PRO 65 1.342 1.232 1.525 1.531 1.466 122.68 116.25 120.78 110.42 112.35 103.43 122.96 66 SER 66 1.329 1.231 1.526 1.530 1.459 121.62 116.11 120.83 109.93 110.82 110.32 123.05 67 GLU 67 1.329 1.231 1.526 1.530 1.458 121.55 116.11 120.93 109.90 110.89 110.38 122.96 68 LYS 68 1.329 1.230 1.525 1.531 1.458 121.67 116.22 120.82 109.90 110.93 110.30 122.96 69 GLY 69 1.329 1.230 1.516 - 1.452 120.73 116.34 120.63 - 112.48 - 123.03 70 GLU 70 1.329 1.230 1.526 1.530 1.459 121.56 116.11 120.90 109.93 110.86 110.37 122.99 71 VAL 71 1.330 1.232 1.524 1.541 1.459 121.57 116.21 120.82 109.03 111.15 111.33 122.96 72 HIS 72 1.329 1.230 1.526 1.530 1.458 121.64 116.18 120.82 109.92 110.87 110.35 122.99 73 GLY 73 1.329 1.231 1.516 - 1.452 120.71 116.35 120.72 - 112.47 - 122.93 74 LYS 74 1.328 1.231 1.526 1.531 1.459 121.65 116.19 120.80 109.86 110.88 110.28 123.01 75 VAL 75 1.329 1.232 1.525 1.540 1.458 121.61 116.18 120.87 109.06 111.12 111.35 122.95 76 LEU 76 1.328 1.231 1.525 1.529 1.459 121.68 116.24 120.83 109.95 110.89 110.27 122.93 77 MET 77 1.329 1.230 1.526 1.530 1.458 121.64 116.21 120.83 109.96 110.83 110.33 122.97 Residue-by-residue listing for analyzed_6 Page 10 ---------------------------------------- ................................................................................................................................... Residue ------------- <---------- Bond lengths ----------> <---------------------- Bond angles ----------------------> No. Type Seq Max Chain no. C-N C-O CA-C CA-CB N-CA C-N-CA CA-C-N CA-C-O CB-CA-C N-CA-C N-CA-CB O-C-N dev ----------------------------------------------------------------------------------------------------------------------------------- 78 GLY 78 1.330 1.231 1.516 - 1.451 120.74 116.33 120.69 - 112.53 - 122.97 79 VAL 79 1.329 1.231 1.525 1.540 1.458 121.61 116.15 120.89 108.99 111.12 111.39 122.96 80 THR 80 1.329 1.231 1.525 1.540 1.458 121.64 116.22 120.78 109.03 111.11 111.41 123.00 81 SER 81 1.329 1.231 1.526 1.530 1.458 121.62 116.13 120.85 109.91 110.87 110.33 123.01 82 ASP 82 1.328 1.230 1.526 1.530 1.458 121.63 116.18 120.77 109.99 110.88 110.34 123.05 83 GLU 83 1.329 1.232 1.526 1.531 1.458 121.58 116.15 120.86 109.94 110.90 110.37 122.99 84 LEU 84 1.328 1.231 1.525 1.530 1.458 121.63 116.22 120.80 109.91 110.94 110.28 122.98 85 GLU 85 1.329 1.230 1.526 1.531 1.458 121.59 116.17 120.85 109.87 110.91 110.36 122.98 86 ASN 86 1.329 1.233 1.526 1.530 1.458 121.61 116.21 120.84 109.89 110.87 110.31 122.95 87 LEU 87 1.328 1.231 1.525 1.530 1.459 121.64 116.17 120.81 109.91 110.92 110.22 123.01 88 ASP 88 1.329 1.231 1.526 1.529 1.458 121.60 116.20 120.79 109.97 110.82 110.32 123.00 89 ALA 89 1.329 1.231 1.525 1.521 1.457 121.59 116.23 120.80 110.36 111.11 110.29 122.97 90 VAL 90 1.329 1.230 1.524 1.540 1.458 121.64 116.14 120.85 109.06 111.13 111.40 123.00 91 GLU 91 1.330 1.230 1.526 1.531 1.459 121.54 116.17 120.91 109.91 110.89 110.31 122.91 92 GLY 92 1.330 1.230 1.516 - 1.451 120.77 116.37 120.66 - 112.46 - 122.97 93 ASN 93 1.329 1.230 1.526 1.529 1.459 121.63 116.20 120.82 109.93 110.88 110.32 122.99 94 GLU 94 1.330 1.232 1.526 1.530 1.458 121.58 116.16 120.90 109.87 110.89 110.38 122.95 95 TYR 95 1.329 1.230 1.526 1.530 1.458 121.65 116.13 120.84 109.95 110.94 110.29 123.02 96 GLU 96 1.329 1.231 1.526 1.530 1.458 121.56 116.13 120.89 109.88 110.83 110.41 122.98 97 ARG 97 1.329 1.231 1.526 1.530 1.459 121.59 116.17 120.85 109.90 110.86 110.32 122.98 98 VAL 98 1.329 1.232 1.525 1.540 1.458 121.60 116.19 120.92 109.02 111.09 111.39 122.89 99 THR 99 1.329 1.230 1.525 1.540 1.457 121.66 116.16 120.85 108.99 111.12 111.39 122.99 100 VAL 100 1.330 1.230 1.525 1.539 1.458 121.59 116.18 120.86 109.03 111.10 111.39 122.96 101 GLY 101 1.330 1.231 1.516 - 1.451 120.73 116.33 120.59 - 112.44 - 123.08 102 ILE 102 1.329 1.230 1.525 1.540 1.457 121.55 116.15 120.87 109.00 111.13 111.43 122.98 103 VAL 103 1.329 1.231 1.524 1.540 1.459 121.63 116.18 120.81 109.09 111.10 111.41 123.01 104 ARG 104 1.329 1.230 1.526 1.529 1.458 121.63 116.22 120.79 109.88 110.88 110.36 122.99 105 GLU 105 1.330 1.231 1.526 1.530 1.459 121.58 116.12 120.84 109.89 110.93 110.35 123.04 106 ASP 106 1.329 1.230 1.526 1.529 1.459 121.58 116.16 120.78 109.98 110.85 110.29 123.06 107 ASN 107 1.329 1.231 1.526 1.530 1.459 121.56 116.15 120.81 109.92 110.88 110.29 123.03 108 SER 108 1.329 1.230 1.526 1.529 1.459 121.57 116.13 120.82 109.92 110.84 110.34 123.05 109 GLU 109 1.330 1.231 1.526 1.530 1.458 121.57 116.20 120.92 109.90 110.90 110.39 122.88 110 LYS 110 1.329 1.230 1.525 1.530 1.458 121.68 116.21 120.85 109.86 110.87 110.26 122.94 111 MET 111 1.330 1.230 1.526 1.531 1.457 121.59 116.20 120.79 109.91 110.86 110.35 123.01 112 ALA 112 1.330 1.231 1.526 1.521 1.457 121.57 116.19 120.80 110.36 111.10 110.29 123.01 113 VAL 113 1.329 1.231 1.525 1.540 1.458 121.57 116.13 120.89 109.02 111.11 111.36 122.98 114 LYS 114 1.329 1.231 1.526 1.531 1.458 121.63 116.18 120.91 109.90 110.85 110.28 122.91 115 THR 115 1.330 1.231 1.525 1.540 1.458 121.60 116.16 120.81 109.02 111.11 111.36 123.02 116 TYR 116 1.328 1.230 1.526 1.528 1.459 121.61 116.11 120.89 109.95 110.90 110.32 122.99 117 MET 117 1.329 1.232 1.526 1.530 1.458 121.59 116.24 120.72 109.91 110.93 110.32 123.04 118 TRP 118 1.327 1.231 1.524 1.530 1.458 121.57 116.21 120.77 109.93 110.93 110.31 123.01 119 ILE 119 1.329 1.230 1.526 1.540 1.458 121.56 116.17 120.84 109.02 111.13 111.46 122.98 120 ASN 120 1.329 1.232 1.526 1.529 1.459 121.65 116.18 120.86 109.95 110.86 110.32 122.97 121 LYS 121 1.328 1.230 1.526 1.530 1.458 121.65 116.20 120.79 109.88 110.91 110.30 123.01 122 ALA 122 1.329 1.231 1.525 1.521 1.458 121.60 116.26 120.79 110.39 111.07 110.31 122.95 123 ASP 123 1.329 1.231 1.526 1.530 1.458 121.63 116.21 121.58 109.95 110.87 110.33 122.22 124 PRO 124 1.341 1.231 1.525 1.530 1.466 122.70 116.22 120.80 110.49 112.37 103.40 122.98 125 ASP 125 1.329 1.231 1.526 1.530 1.458 121.62 116.20 120.76 109.93 110.83 110.34 123.04 126 MET 126 1.328 1.232 1.525 1.530 1.458 121.61 116.23 120.83 109.94 110.89 110.34 122.93 127 PHE 127 1.329 1.231 1.526 1.530 1.459 121.65 116.16 120.88 109.93 110.87 110.31 122.95 128 GLY 128 1.330 1.231 1.516 - 1.452 120.70 116.37 120.60 - 112.45 - 123.03 129 GLU 129 1.330 1.231 1.526 1.529 1.458 121.55 116.15 120.83 109.90 110.85 110.36 123.02 130 TRP 130 1.328 1.231 1.524 1.529 1.459 121.59 116.28 120.75 110.02 110.92 110.29 122.97 131 ASN 131 1.329 1.231 1.526 1.530 1.458 121.64 116.15 120.85 109.90 110.90 110.30 122.99 132 PHE 132 1.329 1.230 1.526 1.530 1.458 121.61 116.15 120.82 109.88 110.89 110.33 123.03 Residue-by-residue listing for analyzed_6 Page 11 ---------------------------------------- ................................................................................................................................... Residue ------------- <---------- Bond lengths ----------> <---------------------- Bond angles ----------------------> No. Type Seq Max Chain no. C-N C-O CA-C CA-CB N-CA C-N-CA CA-C-N CA-C-O CB-CA-C N-CA-C N-CA-CB O-C-N dev ----------------------------------------------------------------------------------------------------------------------------------- 133 GLU 133 1.329 1.231 1.526 1.530 1.458 121.58 116.15 120.82 109.90 110.91 110.40 123.03 134 GLU 134 1.330 1.230 1.526 1.530 1.458 121.56 116.12 120.86 109.94 110.90 110.34 123.02 135 TRP 135 1.328 1.232 1.525 1.529 1.459 121.59 116.28 120.81 109.94 110.90 110.33 122.91 136 LYS 136 1.329 1.231 1.526 1.530 1.458 121.72 116.21 120.78 109.84 110.87 110.30 123.01 137 ARG 137 1.329 1.232 1.526 1.529 1.458 121.61 116.18 120.86 109.90 110.85 110.36 122.96 138 LEU 138 1.328 1.232 1.525 1.529 1.459 121.66 116.22 120.82 109.96 110.89 110.27 122.96 139 HIS 139 1.329 1.230 1.526 1.529 1.458 121.62 116.15 120.86 109.94 110.91 110.32 122.99 140 LYS 140 1.329 1.231 1.526 1.530 1.459 121.62 116.21 120.86 109.89 110.88 110.25 122.93 141 LYS 141 1.329 1.230 1.525 1.531 1.458 121.64 116.21 120.84 109.89 110.91 110.25 122.96 142 LYS 142 1.328 1.231 1.526 1.530 1.458 121.71 116.19 120.81 109.90 110.88 110.33 123.00 143 PHE 143 1.329 1.231 1.526 1.531 1.458 121.57 116.14 120.82 109.91 110.87 110.29 123.03 144 ILE 144 1.329 1.230 1.525 1.541 1.457 121.57 116.17 120.75 109.02 111.12 111.42 123.08 145 GLU 145 1.329 1.231 1.526 1.530 1.458 121.57 116.12 120.95 109.91 110.89 110.38 122.93 146 THR 146 1.330 1.231 1.525 1.541 1.456 121.61 116.21 120.81 109.01 111.16 111.38 122.98 147 PHE 147 1.328 1.231 1.526 1.530 1.459 121.64 116.18 120.87 109.93 110.83 110.31 122.95 148 LYS 148 1.328 1.231 1.525 1.531 1.458 121.69 116.23 120.85 109.90 110.87 110.29 122.92 149 LYS 149 1.329 1.232 1.525 1.530 1.458 121.71 116.22 120.79 109.93 110.90 110.30 122.99 150 ILE 150 1.328 1.230 1.526 1.540 1.459 121.59 116.16 120.77 109.02 111.11 111.43 123.06 151 MET 151 1.329 1.230 1.525 1.530 1.458 121.54 116.23 120.81 109.89 110.90 110.33 122.97 152 GLU 152 1.330 1.232 1.526 1.531 1.457 121.60 116.19 120.81 109.89 110.88 110.38 123.00 153 CYS 153 1.328 1.231 1.525 1.529 1.458 121.64 116.16 120.90 109.97 110.92 110.32 122.93 154 LYS 154 1.329 1.231 1.525 1.530 1.458 121.64 116.25 120.83 109.88 110.89 110.24 122.92 155 LYS 155 1.329 1.231 1.525 1.530 1.458 121.73 116.23 120.81 109.90 110.90 110.31 122.96 156 LYS 156 1.328 1.231 1.526 1.530 1.458 121.69 116.24 121.53 109.88 110.91 110.34 122.23 157 PRO 157 1.340 1.230 1.525 1.530 1.466 122.69 116.21 120.74 110.47 112.34 103.41 123.06 158 GLN 158 1.329 1.230 1.525 1.529 1.459 121.56 116.18 120.85 109.98 110.90 110.29 122.98 159 GLY 159 1.329 1.231 1.516 - 1.452 120.75 116.37 120.60 - 112.48 - 123.04 160 GLN 160 1.329 1.230 1.524 1.530 1.457 121.58 116.24 120.81 109.92 110.96 110.31 122.96 161 GLY 161 1.329 1.230 1.516 - 1.451 120.74 116.34 120.64 - 112.48 - 123.02 162 ASN 162 1.329 1.231 1.526 1.530 1.458 121.59 116.19 120.86 109.92 110.89 110.29 122.95 163 ASP 163 1.329 1.231 1.525 1.530 1.458 121.63 116.19 120.86 109.97 110.85 110.31 122.95 164 ASP 164 1.329 1.232 1.525 1.529 1.459 121.66 116.22 120.78 109.99 110.83 110.32 123.00 165 ILE 165 1.329 1.231 1.525 1.541 1.457 121.60 116.17 120.87 109.04 111.14 111.42 122.95 166 SER 166 1.329 1.231 1.526 1.530 1.458 121.64 116.10 120.93 109.95 110.88 110.29 122.97 167 HIS 167 1.329 1.231 1.526 1.529 1.459 121.59 116.20 120.85 109.96 110.82 110.35 122.95 168 VAL 168 1.330 1.231 1.525 1.541 1.458 121.61 116.14 120.84 109.06 111.15 111.35 123.02 169 LEU 169 1.328 1.230 1.526 1.530 1.459 121.60 116.20 120.81 109.95 110.90 110.27 122.99 170 ARG 170 1.329 1.230 1.526 1.530 1.457 121.62 116.18 120.76 109.89 110.90 110.33 123.06 171 GLU 171 1.329 1.231 1.526 1.530 1.459 121.52 116.14 120.87 109.90 110.87 110.34 122.99 172 ASP 172 1.328 1.231 1.526 1.530 1.458 121.60 116.21 120.76 109.92 110.86 110.35 123.04 173 GLN 173 1.329 - 1.525 1.530 1.458 121.58 - - 109.93 110.93 110.28 - ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: ----------------------------------------------------------------------------------------------------------------------------------- Residue-by-residue listing for analyzed_6 Page 12 ---------------------------------------- A N A L Y S I S O F M A I N C H A I N B O N D L E N G T H S A N D B O N D A N G L E S +------------------+ | BOND LENGTHS | +------------------+ ------------------------------------------------------------------------------------------------------------- (Small molecule data) Number of Min Max Mean Standard Bond X-PLOR labelling Mean St. dev values value value value deviation ------------------------------------------------------------------------------------------------------------- C-N C-NH1 (except Pro) 1.329 .014 165 1.327 1.330 1.329 .001 C-N (Pro) 1.341 .016 7 1.340 1.342 1.341 .000 C-O C-O 1.231 .020 172 1.230 1.233 1.231 .001 CA-C CH1E-C (except Gly) 1.525 .021 161 1.524 1.527 1.525 .001 CH2G*-C (Gly) 1.516 .018 12 1.515 1.516 1.516 .000 CA-CB CH1E-CH3E (Ala) 1.521 .033 4 1.521 1.522 1.521 .000 CH1E-CH1E (Ile,Thr,Val) 1.540 .027 29 1.539 1.541 1.540 .000 CH1E-CH2E (the rest) 1.530 .020 128 1.528 1.531 1.530 .001 N-CA NH1-CH1E (except Gly,Pro)1.458 .019 154 1.456 1.459 1.458 .001 NH1-CH2G* (Gly) 1.451 .016 12 1.451 1.452 1.451 .000 N-CH1E (Pro) 1.466 .015 7 1.465 1.466 1.466 .000 ------------------------------------------------------------------------------------------------------------- +-----------------+ | BOND ANGLES | +-----------------+ ------------------------------------------------------------------------------------------------------------- (Small molecule data) Number of Min Max Mean Standard Angle X-PLOR labelling Mean St. dev values value value value deviation ------------------------------------------------------------------------------------------------------------- CA-C-N CH1E-C-NH1 (except Gly,Pro)116.2 2.0 153 116.10 116.28 116.18 .04 CH2G*-C-NH1 (Gly) 116.4 2.1 12 116.33 116.38 116.35 .02 CH1E-C-N (Pro) 116.9 1.5 7 116.16 116.25 116.22 .03 O-C-N O-C-NH1 (except Pro) 123.0 1.6 165 122.16 123.09 122.95 .16 O-C-N (Pro) 122.0 1.4 7 122.93 123.06 122.99 .05 C-N-CA C-NH1-CH1E (except Gly,Pro)121.7 1.8 154 121.52 121.73 121.61 .04 C-NH1-CH2G* (Gly) 120.6 1.7 11 120.70 120.78 120.74 .02 C-N-CH1E (Pro) 122.6 5.0 7 122.67 122.71 122.70 .02 CA-C-O CH1E-C-O (except Gly) 120.8 1.7 160 120.72 121.66 120.87 .16 CH2G*-C-O (Gly) 120.8 2.1 12 120.59 120.72 120.65 .04 CB-CA-C CH3E-CH1E-C (Ala) 110.5 1.5 4 110.34 110.39 110.36 .02 CH1E-CH1E-C (Ile,Thr,Val) 109.1 2.2 29 108.99 109.09 109.03 .02 CH2E-CH1E-C (the rest) 110.1 1.9 128 109.84 110.49 109.95 .13 N-CA-C NH1-CH1E-C (except Gly,Pro)111.2 2.8 154 110.82 111.17 110.93 .10 NH1-CH2G*-C (Gly) 112.5 2.9 12 112.44 112.53 112.48 .03 N-CH1E-C (Pro) 111.8 2.5 7 112.31 112.40 112.35 .03 N-CA-CB NH1-CH1E-CH3E (Ala) 110.4 1.5 4 110.29 110.32 110.30 .01 NH1-CH1E-CH1E (Ile,Thr,Val) 111.5 1.7 29 111.31 111.46 111.39 .04 N-CH1E-CH2E (Pro) 103.0 1.1 7 103.35 103.43 103.40 .03 NH1-CH1E-CH2E (the rest) 110.5 1.7 121 110.22 110.41 110.32 .04 ------------------------------------------------------------------------------------------------------------- The small molecule data used in the above analysis is from Engh & Huber (1991). The atom labelling follows that used in the X-PLOR dictionary, with some additional atoms (marked with an asterisk) as defined by Engh & Huber. Residue-by-residue listing for analyzed_6 Page 13 ---------------------------------------- B A D C O N T A C T S L I S T I N G ....................................................................... Residue Residue ----------- ----------- No. Type No. Type Contact Distance Chain Atom Chain Atom type (Angstroms) ----------------------------------------------------------------------- 1. 19 ASN OD1 --> 112 ALA O Side-Main 2.6 2. 36 LEU O --> 37 ASP OD2 Main-Side 2.6 3. 83 GLU O --> 86 ASN OD1 Main-Side 2.6 4. 91 GLU O --> 95 TYR O Main-Main 2.5 5. 102 ILE O --> 111 MET O Main-Main 2.6 6. 120 ASN O --> 121 LYS C Main-Main 2.6 7. 167 HIS O --> 168 VAL O Main-Main 2.6 Residue-by-residue listing for analyzed_6 Page 14 ---------------------------------------- R A M A C H A N D R A N P L O T S T A T I S T I C S Residues in most favoured regions [A,B,L] 126 82.4% Residues in additional allowed regions [a,b,l,p] 23 15.0% Residues in generously allowed regions [~a,~b,~l,~p] 3 2.0% Residues in disallowed regions [XX] 1 .7% ---- ------ Number of non-glycine and non-proline residues 153 100.0% Number of end-residues (excl. Gly and Pro) 1 Number of glycine residues 12 Number of proline residues 7 ---- Total number of residues 173 Based on the analysis of 118 structures of resolution of at least 2.0 Angstroms and R-factor no greater than 20%, a good quality model would be expected to have over 90% in the most favoured regions [E,H,L]. S T E R E O C H E M I S T R Y O F M A I N - C H A I N Comparison values No. of No. of Parameter Typical Band band widths Stereochemical parameter data pts value value width from mean ------------------------ -------- ----- ----- ----- --------- a. %-tage residues in A, B, L 153 82.4 83.8 10.0 -.1 Inside b. Omega angle st dev 172 .1 6.0 3.0 -2.0 BETTER c. Bad contacts / 100 residues 7 4.0 4.2 10.0 .0 Inside d. Zeta angle st dev 161 .9 3.1 1.6 -1.4 BETTER e. H-bond energy st dev 89 .8 .8 .2 .1 Inside f. Overall G-factor 173 .1 -.4 .3 1.7 BETTER S T E R E O C H E M I S T R Y O F S I D E - C H A I N Comparison values No. of No. of Parameter Typical Band band widths Stereochemical parameter data pts value value width from mean ------------------------ -------- ----- ----- ----- --------- a. Chi-1 gauche minus st dev 24 23.6 18.1 6.5 .8 Inside b. Chi-1 trans st dev 54 20.2 19.0 5.3 .2 Inside c. Chi-1 gauche plus st dev 72 25.9 17.5 4.9 1.7 WORSE d. Chi-1 pooled st dev 150 24.7 18.2 4.8 1.3 WORSE e. Chi-2 trans st dev 41 27.9 20.4 5.0 1.5 WORSE M O R R I S E T A L . C L A S S I F I C A T I O N Mean St.dev Classification Parameter m s 1 2 3 4 Value Class --------- ---- --- ------------------------------------ ----- ----- Phi-psi distribution - - >75.0% >65.0% >55.0% <55.0% 82.4 1 Chi-1 st.dev. 18.2 6.2 <12.0 <18.2 <24.4 >24.4 27.3 4 H-bond energy st dev .87 .24 < .63 < .87 <1.11 >1.11 .91 3 Residue-by-residue listing for analyzed_6 Page 15 ---------------------------------------- G - F A C T O R S Average Parameter Score Score --------- ----- ----- Dihedral angles:- Phi-psi distribution -.58 Chi1-chi2 distribution -1.36 Chi1 only -.42 Chi3 & chi4 .17 Omega .74 ------ -.23 ===== Main-chain covalent forces:- Main-chain bond lengths .71 Main-chain bond angles .70 ------ .70 ===== OVERALL AVERAGE .12 ===== Ideally, scores should be above -0.5. Values below -1.0 may need investigation.