Residue-by-residue listing for refined_19 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 MET 1 - - - -72.9 - - - - - - - 181.9 - 34.0 - 2 GLY 2 - - - - - - - - - - - 180.8 - - - 3 HIS 3 B - 181.2 - - - - - - - - 176.8 - 33.7 - 4 HIS 4 b - - -70.4 - - - - - - - 181.4 -.9 33.0 - +* +* 5 HIS 5 B 63.7 - - - - - - - - - 173.7 - 32.8 - * * 6 HIS 6 B - - -71.4 - - - - - - - 182.3 - 33.5 - 7 HIS 7 B 65.1 - - - - - - - - - 180.0 -.6 32.8 - +* +* 8 HIS 8 b 56.1 - - - - - - - - - 178.1 - 31.4 - 9 LEU 9 S a - 187.2 - 172.7 - - - - - - 176.1 -1.1 34.5 - * * 10 GLU 10 S B - 185.3 - 179.7 - - - - - - 183.8 - 34.0 - 11 MET 11 B 61.2 - - 181.6 - - - - - - 179.2 -.5 34.5 - ** ** 12 ALA 12 b - - - - - - - - - - 179.0 - 32.7 - 13 SER 13 b - 187.4 - - - - - - - - 176.9 -1.8 31.9 - 14 GLU 14 b - 181.8 - 176.5 - - - - - - 192.4 -.8 35.0 - ** +* ** 15 GLU 15 B 58.5 - - 191.6 - - - - - - 176.6 - 37.6 - * * 16 GLY 16 S - - - - - - - - - - - 183.8 -2.7 - - 17 GLN 17 e B 48.6 - - 179.4 - - - - - - 175.0 -.5 31.0 - ** ** 18 VAL 18 E B - 180.4 - - - - - - - - 182.8 -.6 35.2 - +* +* Residue-by-residue listing for refined_19 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 ----------------------------------------------------------------------------------------------------------------------------------- 19 ILE 19 E B - - -58.1 179.8 - - - - - - 178.5 -3.1 33.4 - * * 20 ALA 20 E B - - - - - - - - - - 178.9 -.8 34.0 - +* +* 21 CYS 21 e B - - -52.4 - - - - - - - 179.2 -1.0 36.0 - * * 22 HIS 22 S A - - -66.4 - - - - - - - 180.8 -.8 33.3 - +* +* 23 THR 23 h B 54.7 - - - - - - - - - 176.4 - 35.8 - 24 VAL 24 H A 61.7 - - - - -73.2 -22.1 - - - 178.8 - 32.3 - +* +* 25 GLU 25 H A - 191.5 - - - -57.5 -51.9 - - - 178.3 - 36.2 - * * 26 THR 26 H A - - -55.7 - - -67.3 -41.5 - - - 181.2 - 35.5 - 27 TRP 27 H A - 173.9 - - - -53.4 -55.1 - - - 181.5 -1.7 34.7 - * * * 28 ASN 28 H A - 179.3 - - - -64.3 -40.8 - - - 180.9 -3.1 34.1 - * * 29 GLU 29 H A - 178.8 - 182.4 - -61.6 -47.8 - - - 183.8 -1.6 35.1 - 30 GLN 30 H A - - -66.0 - - -73.2 -35.1 - - - 174.9 -2.9 32.6 - * * 31 LEU 31 H A - - -70.8 180.9 - -63.7 -41.4 - - - 176.8 -2.1 34.6 - 32 GLN 32 H A - 179.0 - 179.2 - -62.1 -36.1 - - - 177.0 -2.0 33.4 - 33 LYS 33 H A - 181.1 - 181.1 - -61.4 -37.3 - - - 177.8 -1.6 33.8 - 34 ALA 34 H A - - - - - -75.9 -43.5 - - - 182.1 -1.5 33.8 - 35 ASN 35 H A - 183.4 - - - -57.4 -55.9 - - - 184.6 -3.2 38.1 - * +* * +* 36 GLU 36 H A - - -57.1 183.7 - -67.8 -25.6 - - - 182.8 -3.1 33.4 - * * * 37 SER 37 h A - - -53.2 - - - - - - - 180.0 -.8 35.1 - +* +* 38 LYS 38 T L - 188.4 - 186.6 - - - - - - 182.5 -1.6 33.6 - 39 THR 39 t B - - -47.1 - - - - - - - 178.7 -2.8 35.9 - * * * 40 LEU 40 E B - 186.6 - 170.9 - - - - - - 184.5 -1.0 35.2 - * * 41 VAL 41 E B 60.0 - - - - - - - - - 178.6 - 33.0 - 42 VAL 42 E B - 180.8 - - - - - - - - 182.6 -2.9 34.4 - * * 43 VAL 43 E B - 184.3 - - - - - - - - 176.5 -3.1 34.2 - * * 44 ASP 44 E B - 171.1 - - - - - - - - 177.3 -2.9 35.4 - * * 45 PHE 45 E B - - -62.3 - - - - - - - 178.2 -3.0 36.9 - * * 46 THR 46 E B - 190.1 - - - - - - - - 176.5 -2.6 33.3 - 47 ALA 47 t B - - - - - - - - - - 184.5 - 33.6 - 48 SER 48 T A - 186.2 - - - - - - - - 178.9 - 33.2 - 49 TRP 49 T A 54.2 - - - - - - - - - 182.0 - 32.0 - 50 CYS 50 h B - 174.0 - 223.1 - - - 54.8 - 2.0 182.5 -2.0 34.2 - ** +** +** 51 GLY 51 H - - - - - - -62.0 -62.7 - - - 178.9 -.6 - - ** +* ** 52 PRO 52 H - - - - - -57.2 -57.2 -30.6 - - - 179.8 - 39.0 - * * 53 CYS 53 H A - - -54.3 - - -70.5 -40.0 54.8 - 2.0 178.6 - 35.2 - +** +** Residue-by-residue listing for refined_19 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 ----------------------------------------------------------------------------------------------------------------------------------- 54 ARG 54 H A - 192.3 - - - -65.1 -31.6 - - - 180.4 -2.0 35.3 - 55 PHE 55 H A - 183.0 - - - -72.7 -38.5 - - - 184.1 -1.7 34.6 - 56 ILE 56 H A - 192.7 - - - -87.6 -13.3 - - - 179.3 -1.8 33.8 - +* ** ** 57 ALA 57 H A - - - - - -57.7 -51.0 - - - 178.3 -1.5 31.1 - * * 58 PRO 58 H - - - - - -64.0 -64.0 -27.6 - - - 179.7 - 38.7 - * * * 59 PHE 59 H A - 187.9 - - - -67.6 -44.8 - - - 177.9 - 34.8 - 60 PHE 60 H A - 182.9 - - - -66.7 -35.5 - - - 177.7 -2.2 34.3 - 61 ALA 61 H A - - - - - -66.1 -31.3 - - - 178.6 -2.1 33.9 - 62 ASP 62 H A - 183.4 - - - -73.1 -43.0 - - - 176.2 -1.5 35.6 - 63 LEU 63 H A - - -66.2 181.9 - -53.7 -39.5 - - - 178.6 -2.1 35.2 - 64 ALA 64 H A - - - - - -63.4 -32.8 - - - 181.5 -1.7 34.2 - 65 LYS 65 H A - 187.8 - 179.9 - -79.5 -27.8 - - - 180.9 -.8 33.8 - * * +* +* 66 LYS 66 H A - - -59.8 187.1 - -77.1 -40.2 - - - 179.4 -1.6 33.0 - 67 LEU 67 h B - - -69.1 173.1 - - - - - - 182.5 -2.3 32.3 - 68 PRO 68 S - - - - - -73.1 - - - - - 186.7 - 38.0 - * * * 69 ASN 69 e a - 195.1 - - - - - - - - 175.9 - 33.1 - 70 VAL 70 E B - 178.4 - - - - - - - - 182.6 - 33.9 - 71 LEU 71 E B - 185.1 - - - - - - - - 180.2 -2.9 34.4 - * * 72 PHE 72 E B - - -60.2 - - - - - - - 179.4 -1.1 34.4 - * * 73 LEU 73 E B - - -74.2 - - - - - - - 181.8 -2.6 32.5 - 74 LYS 74 E B - 188.8 - - - - - - - - 179.3 -2.6 36.5 - 75 VAL 75 E B - 178.2 - - - - - - - - 176.3 -3.4 33.5 - +* +* 76 ASP 76 E B - 188.0 - - - - - - - - 185.6 -.6 34.3 - +* +* 77 THR 77 e A 55.0 - - - - - - - - - 179.5 -2.1 32.9 - 78 ASP 78 T A - 187.5 - - - - - - - - 176.0 - 35.1 - 79 GLU 79 T a - 190.3 - - - - - - - - 180.8 - 37.3 - 80 LEU 80 h b - - -69.6 - - - - - - - 180.6 -3.6 33.8 - ** ** 81 LYS 81 H A - - -57.7 174.4 - -69.8 -46.4 - - - 183.0 -1.4 35.1 - 82 SER 82 H A - - -57.2 - - -64.8 -41.7 - - - 178.2 - 33.4 - 83 VAL 83 H A - 179.9 - - - -63.5 -41.8 - - - 179.9 - 33.5 - 84 ALA 84 H A - - - - - -62.7 -41.8 - - - 180.8 -1.6 34.3 - 85 SER 85 H A - 189.6 - - - -75.7 -31.6 - - - 181.9 -2.4 33.5 - 86 ASP 86 H A - 179.2 - - - -71.5 -36.3 - - - 178.2 -2.5 33.9 - 87 TRP 87 h A - - -65.2 - - - - - - - 178.1 -2.2 32.3 - 88 ALA 88 T l - - - - - - - - - - 176.6 - 30.7 - 89 ILE 89 t b - - -53.8 - - - - - - - 182.1 -2.3 34.6 - 90 GLN 90 A - - -71.5 - - - - - - - 182.0 -.7 34.3 - +* +* 91 ALA 91 S B - - - - - - - - - - 182.9 - 33.6 - 92 MET 92 S B - - -62.0 167.7 - - - - - - -2.7 - 35.5 - 93 PRO 93 e cis - - - - - -90.5 - - - - - 176.8 - 39.7 - ** +* ** 94 THR 94 E B - - -63.0 - - - - - - - 177.9 -2.4 33.4 - 95 PHE 95 E B - - -62.2 - - - - - - - 181.5 -3.1 36.5 - * * 96 MET 96 E B - 182.2 - 179.7 - - - - - - 181.2 -3.3 33.7 - +* +* Residue-by-residue listing for refined_19 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 ----------------------------------------------------------------------------------------------------------------------------------- 97 PHE 97 E B - - -64.4 - - - - - - - 178.4 -2.8 36.7 - * * 98 LEU 98 E B - - -55.6 - - - - - - - 175.5 -2.9 34.6 - * * 99 LYS 99 E B - 177.5 - 171.5 - - - - - - 179.8 -3.4 33.2 - +* +* 100 GLU 100 T l - - -56.7 177.8 - - - - - - 180.5 - 33.4 - 101 GLY 101 T - - - - - - - - - - - 175.3 - - - 102 LYS 102 E B - 179.9 - 179.9 - - - - - - 183.7 -1.9 34.1 - 103 ILE 103 E B - - -55.9 175.0 - - - - - - 181.5 - 35.0 - 104 LEU 104 E a - 183.6 - - - - - - - - 184.0 -3.1 36.0 - * * 105 ASP 105 E B - - -61.2 - - - - - - - 178.9 -2.7 35.3 - 106 LYS 106 E B - 192.4 - 186.8 - - - - - - 179.7 - 36.0 - 107 VAL 107 E B - 179.2 - - - - - - - - 180.8 -3.3 34.3 - +* +* 108 VAL 108 E B 60.7 - - - - - - - - - 181.2 - 33.0 - 109 GLY 109 e - - - - - - - - - - - 181.2 -3.1 - - * * 110 ALA 110 B - - - - - - - - - - 177.6 - 34.2 - 111 LYS 111 h B - - -68.9 172.4 - - - - - - 186.0 -1.1 34.7 - * * * 112 LYS 112 H A - - -63.8 178.2 - -62.4 -50.5 - - - 184.0 - 35.0 - 113 ASP 113 H A 72.1 - - - - -69.0 -39.2 - - - 181.5 - 32.6 - 114 GLU 114 H A - 187.2 - 183.6 - -69.9 -36.0 - - - 178.1 - 33.9 - 115 LEU 115 H A - 187.1 - - - -62.1 -47.5 - - - 175.6 -2.2 35.4 - 116 GLN 116 H A - - -71.3 - - -55.9 -39.6 - - - 180.8 -2.3 33.8 - 117 SER 117 H A - - -56.9 - - -69.7 -30.9 - - - 177.1 -2.0 33.1 - 118 THR 118 H A - - -54.7 - - -74.3 -35.8 - - - 177.9 -1.9 34.8 - 119 ILE 119 H A - - -60.9 - - -64.2 -50.0 - - - 180.4 -2.3 33.5 - 120 ALA 120 H A - - - - - -63.8 -31.8 - - - 177.6 -2.8 33.1 - * * 121 LYS 121 H A - 192.3 - 183.3 - -59.3 -43.7 - - - 179.2 -1.4 36.5 - 122 HIS 122 H A - - -75.6 - - -80.3 -29.1 - - - 184.1 -1.6 34.8 - * * 123 LEU 123 h b - 198.9 - 170.2 - - - - - - 180.5 -2.2 34.5 - 124 ALA 124 - - - - - - - - - - - - -.7 34.0 - +* +* ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: * ** ** +* ** +** ** ** +* +** ----------------------------------------------------------------------------------------------------------------------------------- Mean values: 59.3 184.5 -62.4 180.4 -71.2 -66.6 -39.1 54.8 - 2.0 180.0 -2.0 34.3 +** +** Standard deviations: 5.9 5.8 7.0 9.5 14.4 7.3 9.4 .0 - .0 2.9 .9 1.6 Numbers of values: 13 49 40 32 4 46 46 2 0 2 122 83 119 0 Number of cis-peptides (labelled cis): 1 Residue-by-residue listing for refined_19 Page 5 ---------------------------------------- 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 refined_19 Page 6 ---------------------------------------- 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 MET 1 - 1.232 1.513 1.535 1.467 - 116.94 120.17 110.48 109.15 110.96 122.89 2 GLY 2 1.307 1.231 1.506 - 1.438 120.92 116.35 120.71 - 111.81 - 122.94 +* +* 3 HIS 3 1.313 1.233 1.526 1.541 1.450 121.45 115.69 121.06 110.45 110.78 111.11 123.23 * * 4 HIS 4 1.305 1.230 1.518 1.542 1.457 123.36 118.12 119.60 111.33 108.88 111.80 122.27 +* +* 5 HIS 5 1.322 1.231 1.520 1.562 1.457 119.93 116.00 120.87 110.64 112.28 111.84 123.11 +* +* 6 HIS 6 1.304 1.230 1.499 1.543 1.455 122.55 116.66 120.42 109.59 108.17 113.18 122.91 +* * * +* +* 7 HIS 7 1.301 1.236 1.500 1.548 1.446 120.35 115.77 120.67 110.77 110.44 112.40 123.56 +* * * +* 8 HIS 8 1.299 1.228 1.523 1.560 1.441 121.87 115.51 121.48 112.28 111.26 112.51 122.94 ** +* * * ** 9 LEU 9 1.306 1.233 1.512 1.557 1.446 121.85 115.45 121.24 112.32 106.83 109.47 123.31 +* * * +* +* 10 GLU 10 1.306 1.232 1.512 1.537 1.428 122.20 115.66 121.17 111.37 107.18 111.08 123.06 +* +* * +* 11 MET 11 1.300 1.242 1.506 1.535 1.445 121.70 116.50 120.67 110.13 110.12 110.58 122.84 ** ** Residue-by-residue listing for refined_19 Page 7 ---------------------------------------- ................................................................................................................................... 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 ----------------------------------------------------------------------------------------------------------------------------------- 12 ALA 12 1.303 1.243 1.507 1.525 1.430 120.96 115.54 121.22 111.32 109.99 111.92 123.08 +* * * +* 13 SER 13 1.312 1.249 1.511 1.541 1.420 120.81 113.38 122.31 112.12 109.38 112.73 124.15 * +* * * * +* 14 GLU 14 1.280 1.206 1.488 1.531 1.419 125.30 115.21 120.91 112.24 103.12 109.72 123.56 +*** * +* ** ** * +** +*** 15 GLU 15 1.297 1.246 1.509 1.535 1.437 121.72 116.70 119.99 109.70 109.64 106.61 123.31 ** * ** ** 16 GLY 16 1.319 1.227 1.492 - 1.440 120.88 116.51 120.61 - 112.22 - 122.87 * * 17 GLN 17 1.304 1.233 1.476 1.507 1.420 120.13 112.74 122.63 111.40 114.50 112.28 124.63 +* ** * +* +* * * * * ** 18 VAL 18 1.273 1.236 1.505 1.554 1.427 123.64 117.39 119.93 109.16 105.94 111.99 122.68 +*** +* * +* +*** 19 ILE 19 1.296 1.228 1.514 1.545 1.432 120.36 115.93 121.17 110.54 110.80 111.54 122.89 ** * ** 20 ALA 20 1.301 1.235 1.502 1.517 1.427 121.57 116.03 120.93 110.59 109.42 110.93 123.01 ** * +* ** 21 CYS 21 1.295 1.224 1.507 1.509 1.415 121.47 116.69 120.37 109.79 108.40 108.95 122.91 ** * ** ** 22 HIS 22 1.305 1.229 1.516 1.544 1.456 121.53 115.87 120.98 110.45 110.32 111.80 123.15 +* +* 23 THR 23 1.321 1.247 1.517 1.546 1.448 122.83 116.71 120.25 107.73 109.30 111.33 123.04 24 VAL 24 1.324 1.237 1.540 1.567 1.451 121.05 115.52 121.18 111.34 109.47 112.78 123.28 * * * 25 GLU 25 1.337 1.241 1.530 1.529 1.454 123.12 115.27 121.07 109.31 109.23 108.83 123.60 26 THR 26 1.324 1.227 1.536 1.541 1.444 122.59 115.30 121.14 109.80 110.00 109.28 123.53 * * 27 TRP 27 1.321 1.233 1.534 1.533 1.456 123.94 116.31 120.59 111.49 112.15 108.04 123.07 * * * 28 ASN 28 1.317 1.243 1.518 1.533 1.464 122.07 115.08 120.93 110.57 111.35 110.01 123.98 29 GLU 29 1.311 1.241 1.536 1.531 1.459 123.22 116.16 120.97 109.72 111.60 109.37 122.86 * * 30 GLN 30 1.314 1.231 1.515 1.483 1.416 122.30 117.34 120.25 112.17 113.85 109.41 122.41 * ** ** * ** 31 LEU 31 1.318 1.226 1.502 1.486 1.422 121.22 115.78 120.83 109.90 110.54 110.03 123.39 * ** +* ** 32 GLN 32 1.314 1.227 1.530 1.524 1.437 121.84 116.15 120.61 111.72 109.99 110.30 123.20 * * * 33 LYS 33 1.328 1.237 1.529 1.533 1.454 122.18 116.66 120.67 110.27 110.40 111.01 122.68 34 ALA 34 1.323 1.231 1.527 1.521 1.444 120.70 115.48 120.82 110.62 110.18 110.74 123.68 35 ASN 35 1.325 1.232 1.508 1.526 1.471 123.64 114.87 121.37 106.40 111.15 108.43 123.70 * +* * +* 36 GLU 36 1.311 1.222 1.521 1.525 1.468 122.32 117.17 120.45 109.51 113.06 111.37 122.37 * * 37 SER 37 1.302 1.234 1.532 1.508 1.434 120.80 116.29 120.32 110.45 111.35 108.62 123.40 +* * * * +* 38 LYS 38 1.358 1.245 1.554 1.514 1.443 124.10 114.81 122.87 112.31 109.82 109.26 122.25 ** * * * * ** 39 THR 39 1.300 1.239 1.520 1.523 1.419 122.51 115.37 121.40 108.90 109.17 109.89 123.21 ** ** ** 40 LEU 40 1.275 1.237 1.536 1.559 1.432 122.67 117.33 120.11 112.89 106.13 108.06 122.55 +*** * * * +* * +*** 41 VAL 41 1.309 1.230 1.535 1.567 1.439 120.98 116.03 121.08 111.79 111.57 110.77 122.86 * * * * Residue-by-residue listing for refined_19 Page 8 ---------------------------------------- ................................................................................................................................... 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 ----------------------------------------------------------------------------------------------------------------------------------- 42 VAL 42 1.309 1.231 1.511 1.538 1.444 122.47 116.77 120.57 109.17 108.80 112.00 122.65 * * 43 VAL 43 1.297 1.235 1.520 1.548 1.433 120.93 115.48 120.92 109.15 110.64 111.84 123.60 ** * ** 44 ASP 44 1.299 1.240 1.512 1.529 1.452 123.24 116.92 120.23 109.61 109.53 109.72 122.81 ** ** 45 PHE 45 1.316 1.252 1.525 1.526 1.423 121.16 116.60 120.66 108.14 109.16 109.20 122.73 * +* * +* 46 THR 46 1.309 1.209 1.536 1.543 1.433 121.61 117.36 120.27 110.77 109.99 111.57 122.37 * * * * 47 ALA 47 1.312 1.240 1.513 1.512 1.445 121.93 116.33 120.33 110.71 108.81 111.40 123.33 * * 48 SER 48 1.312 1.239 1.560 1.548 1.459 122.85 117.22 120.81 112.14 112.40 109.34 121.96 * +* * +* 49 TRP 49 1.328 1.225 1.529 1.552 1.464 121.31 116.90 120.78 111.13 112.49 112.03 122.31 * * 50 CYS 50 1.305 1.233 1.531 1.532 1.446 121.26 115.61 120.78 111.25 110.88 109.46 123.59 +* +* 51 GLY 51 1.331 1.239 1.525 - 1.462 123.17 119.19 119.58 - 114.33 - 121.23 +* * * +* 52 PRO 52 1.360 1.234 1.525 1.533 1.482 122.53 114.97 121.79 110.07 111.12 103.36 123.23 * * * * 53 CYS 53 1.301 1.218 1.531 1.497 1.433 123.10 116.55 120.73 110.40 110.84 108.45 122.70 ** +* * * ** 54 ARG 54 1.330 1.225 1.539 1.567 1.465 122.53 115.35 121.45 111.47 107.97 108.70 123.18 +* * * +* 55 PHE 55 1.319 1.229 1.536 1.540 1.453 122.77 116.77 120.77 110.23 111.14 109.84 122.44 56 ILE 56 1.319 1.236 1.551 1.572 1.460 121.20 115.83 121.40 110.86 110.41 110.74 122.76 * * * 57 ALA 57 1.328 1.239 1.556 1.533 1.463 122.58 120.12 119.28 112.29 113.35 111.48 120.59 * +* * +* +* 58 PRO 58 1.381 1.232 1.519 1.537 1.472 121.99 115.66 121.16 110.11 111.39 103.92 123.17 ** ** 59 PHE 59 1.313 1.225 1.534 1.535 1.441 122.29 115.60 121.24 111.44 108.45 109.10 123.12 * * 60 PHE 60 1.324 1.234 1.536 1.541 1.464 122.78 115.97 121.13 111.45 110.02 109.24 122.88 61 ALA 61 1.321 1.237 1.533 1.519 1.461 121.95 115.74 121.06 110.56 110.74 110.33 123.20 62 ASP 62 1.324 1.230 1.498 1.514 1.467 122.87 114.53 121.44 109.22 109.17 109.78 124.03 * * 63 LEU 63 1.316 1.239 1.527 1.525 1.439 123.89 115.66 120.76 110.28 111.18 108.88 123.56 * * * 64 ALA 64 1.325 1.225 1.519 1.514 1.449 122.49 116.52 120.95 110.08 111.53 110.19 122.53 65 LYS 65 1.316 1.232 1.524 1.534 1.443 120.90 116.32 120.97 111.10 110.30 110.46 122.71 66 LYS 66 1.323 1.237 1.518 1.522 1.447 120.65 116.58 120.35 110.00 111.57 111.98 123.07 67 LEU 67 1.319 1.232 1.521 1.515 1.437 121.51 116.18 121.24 111.97 111.72 110.96 122.57 * * 68 PRO 68 1.334 1.218 1.538 1.534 1.453 123.03 117.91 120.55 110.93 114.31 103.47 121.50 * * 69 ASN 69 1.322 1.235 1.535 1.544 1.465 120.69 114.85 122.47 112.56 109.91 110.05 122.65 * * 70 VAL 70 1.307 1.235 1.516 1.554 1.426 123.29 116.28 120.73 110.30 107.48 112.27 122.96 +* +* * +* 71 LEU 71 1.300 1.231 1.515 1.535 1.428 121.17 116.52 120.68 110.96 109.51 110.09 122.78 ** +* ** Residue-by-residue listing for refined_19 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 ----------------------------------------------------------------------------------------------------------------------------------- 72 PHE 72 1.308 1.236 1.508 1.524 1.441 121.34 115.64 121.04 109.47 109.92 111.29 123.32 +* +* 73 LEU 73 1.291 1.232 1.508 1.551 1.443 123.15 115.49 120.99 110.14 110.71 113.29 123.52 +** * +* +** 74 LYS 74 1.301 1.244 1.521 1.535 1.436 122.80 116.87 120.53 109.44 108.20 108.78 122.58 +* * * * +* 75 VAL 75 1.298 1.233 1.501 1.553 1.439 121.08 115.69 120.99 109.77 110.25 112.54 123.30 ** * ** 76 ASP 76 1.302 1.216 1.505 1.512 1.427 121.02 116.71 120.35 110.35 107.34 111.30 122.91 +* +* * +* 77 THR 77 1.299 1.233 1.527 1.536 1.451 122.41 116.96 120.52 110.58 113.65 110.97 122.52 ** ** 78 ASP 78 1.314 1.239 1.509 1.522 1.457 120.70 113.88 121.89 109.91 107.54 110.35 124.23 * * * * 79 GLU 79 1.317 1.240 1.523 1.523 1.443 124.05 114.90 121.54 108.22 108.66 108.36 123.56 * * * 80 LEU 80 1.317 1.237 1.524 1.533 1.423 123.38 115.40 121.24 109.79 111.26 111.45 123.29 +* +* 81 LYS 81 1.302 1.239 1.522 1.510 1.457 122.87 115.64 121.21 109.31 111.37 109.70 123.15 +* +* 82 SER 82 1.321 1.221 1.515 1.514 1.439 122.07 116.74 120.23 111.33 111.15 110.30 123.01 * * 83 VAL 83 1.328 1.234 1.537 1.558 1.458 121.42 116.27 120.89 110.15 109.99 112.02 122.78 84 ALA 84 1.331 1.230 1.524 1.517 1.456 121.82 116.07 121.08 110.01 110.94 110.29 122.85 85 SER 85 1.309 1.231 1.553 1.538 1.437 121.47 116.60 120.90 111.79 111.21 109.78 122.48 * * * * 86 ASP 86 1.324 1.237 1.528 1.540 1.476 122.68 116.52 121.10 110.93 111.65 109.80 122.38 87 TRP 87 1.313 1.224 1.514 1.516 1.453 121.54 115.08 120.94 111.62 111.63 111.24 123.98 * * 88 ALA 88 1.324 1.248 1.526 1.522 1.453 124.44 115.03 121.85 111.96 113.57 112.26 123.05 +* * +* 89 ILE 89 1.306 1.239 1.520 1.558 1.440 122.15 115.97 120.92 109.75 107.91 111.65 123.00 +* * +* 90 GLN 90 1.306 1.237 1.507 1.537 1.450 122.01 115.96 120.97 109.01 110.78 111.62 123.07 +* +* 91 ALA 91 1.305 1.228 1.507 1.516 1.439 121.57 116.39 121.06 111.13 109.95 110.64 122.54 +* * +* 92 MET 92 1.292 1.227 1.521 1.522 1.435 121.59 118.41 120.00 110.69 109.98 108.43 121.56 +** * * * +** 93 PRO 93 1.342 1.235 1.540 1.527 1.459 123.95 116.90 120.68 109.88 111.76 102.42 122.39 94 THR 94 1.301 1.233 1.522 1.532 1.435 120.97 116.04 120.72 109.88 110.70 112.09 123.24 +* * +* 95 PHE 95 1.308 1.240 1.506 1.528 1.417 122.70 116.61 120.69 108.94 107.29 109.58 122.68 * ** * ** 96 MET 96 1.287 1.230 1.502 1.518 1.429 120.76 115.33 121.28 111.08 109.96 110.69 123.38 +** * +* +** 97 PHE 97 1.289 1.233 1.474 1.496 1.399 122.85 116.37 120.60 108.61 109.14 109.08 123.03 +** ** +* *** *** 98 LEU 98 1.268 1.220 1.507 1.555 1.403 120.27 116.39 120.78 108.79 107.62 112.90 122.83 **** * +** * * **** 99 LYS 99 1.270 1.234 1.477 1.525 1.411 121.98 114.63 120.56 111.73 107.85 111.75 124.66 **** ** ** * * **** 100 GLU 100 1.323 1.232 1.553 1.520 1.451 123.99 115.73 121.47 111.25 111.10 110.14 122.71 * * * Residue-by-residue listing for refined_19 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 ----------------------------------------------------------------------------------------------------------------------------------- 101 GLY 101 1.329 1.235 1.535 - 1.453 121.67 117.67 120.14 - 114.38 - 122.20 * * 102 LYS 102 1.321 1.221 1.525 1.534 1.466 121.28 117.50 119.51 110.45 109.07 110.80 122.99 103 ILE 103 1.330 1.245 1.525 1.554 1.476 122.27 116.53 120.42 108.64 110.02 111.15 123.05 104 LEU 104 1.322 1.226 1.521 1.512 1.367 122.05 116.76 120.60 110.40 109.66 108.45 122.58 *4.8* * *4.8* 105 ASP 105 1.330 1.237 1.469 1.532 1.442 121.62 115.87 120.58 106.90 108.84 113.12 123.54 +** +* +* +** 106 LYS 106 1.277 1.231 1.519 1.524 1.412 121.20 117.10 120.21 110.15 107.77 108.98 122.68 +*** ** * +*** 107 VAL 107 1.304 1.234 1.514 1.563 1.456 122.25 116.47 120.48 109.68 109.04 111.81 123.03 +* +* 108 VAL 108 1.305 1.245 1.534 1.559 1.436 121.49 116.08 121.12 111.61 110.48 111.25 122.79 +* * * +* 109 GLY 109 1.314 1.238 1.506 - 1.438 121.00 117.64 120.17 - 110.40 - 122.19 * * 110 ALA 110 1.314 1.242 1.508 1.520 1.431 118.66 114.55 121.55 110.58 109.71 110.49 123.90 * * +* +* 111 LYS 111 1.298 1.226 1.499 1.512 1.421 124.38 116.69 119.94 111.81 108.63 108.93 123.37 ** * +* * ** 112 LYS 112 1.303 1.237 1.528 1.499 1.421 123.00 116.68 120.39 110.32 113.08 108.39 122.90 +* +* +* * +* 113 ASP 113 1.325 1.222 1.520 1.550 1.466 121.07 117.00 120.25 110.02 111.36 112.77 122.72 * * 114 GLU 114 1.329 1.240 1.518 1.527 1.455 120.89 115.57 121.14 110.11 109.68 111.27 123.28 115 LEU 115 1.324 1.220 1.508 1.512 1.441 121.91 115.02 121.19 109.65 108.60 109.84 123.78 116 GLN 116 1.318 1.232 1.513 1.528 1.472 122.64 116.13 120.72 109.71 111.87 111.13 123.12 117 SER 117 1.305 1.234 1.529 1.522 1.442 121.01 115.79 121.11 112.27 110.41 110.05 123.06 +* * +* 118 THR 118 1.316 1.239 1.542 1.541 1.434 122.01 115.91 121.30 110.10 109.24 110.39 122.77 * * 119 ILE 119 1.327 1.225 1.520 1.561 1.450 122.02 116.39 120.44 109.75 110.09 112.44 123.14 120 ALA 120 1.327 1.228 1.522 1.519 1.460 122.02 115.74 120.63 111.08 111.06 110.84 123.63 121 LYS 121 1.324 1.239 1.532 1.509 1.458 123.28 115.06 121.39 109.08 109.37 108.19 123.54 * * * 122 HIS 122 1.327 1.232 1.519 1.531 1.452 123.22 116.71 120.13 108.24 112.62 111.04 123.15 123 LEU 123 1.319 1.245 1.540 1.531 1.440 122.94 115.57 121.13 112.46 110.53 107.83 123.28 * +* +* 124 ALA 124 1.319 - 1.519 1.528 1.441 123.09 - - 110.84 109.24 110.67 - ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: **** * +** ** *4.8* ** +* * +* +** ** +* *4.8* ----------------------------------------------------------------------------------------------------------------------------------- Residue-by-residue listing for refined_19 Page 11 ---------------------------------------- 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 .014 119 1.268 1.358 1.311 .014 **** ** * C-N (Pro) 1.341 .016 4 1.334 1.381 1.354 .018 ** C-O C-O 1.231 .020 123 1.206 1.252 1.233 .008 * * CA-C CH1E-C (except Gly) 1.525 .021 119 1.469 1.560 1.520 .016 +** +* CH2G*-C (Gly) 1.516 .018 5 1.492 1.535 1.513 .015 * * CA-CB CH1E-CH3E (Ala) 1.521 .033 13 1.512 1.533 1.520 .005 CH1E-CH1E (Ile,Thr,Val) 1.540 .027 22 1.523 1.572 1.551 .012 * CH1E-CH2E (the rest) 1.530 .020 84 1.483 1.567 1.529 .016 ** +* N-CA NH1-CH1E (except Gly,Pro)1.458 .019 115 1.367 1.476 1.443 .017 *4.8* NH1-CH2G* (Gly) 1.451 .016 5 1.438 1.462 1.446 .010 N-CH1E (Pro) 1.466 .015 4 1.453 1.482 1.467 .011 * ------------------------------------------------------------------------------------------------------------- Residue-by-residue listing for refined_19 Page 12 ---------------------------------------- +-----------------+ | 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 2.0 114 112.74 120.12 116.07 .94 +* +* CH2G*-C-NH1 (Gly) 116.4 2.1 5 116.35 119.19 117.47 1.02 * CH1E-C-N (Pro) 116.9 1.5 4 114.97 117.91 116.36 1.13 * O-C-N O-C-NH1 (except Pro) 123.0 1.6 119 120.59 124.66 123.02 .57 +* * O-C-N (Pro) 122.0 1.4 4 121.50 123.23 122.57 .70 C-N-CA C-NH1-CH1E (except Gly,Pro)121.7 1.8 114 118.66 125.30 122.05 1.09 +* ** C-NH1-CH2G* (Gly) 120.6 1.7 5 120.88 123.17 121.53 .87 +* C-N-CH1E (Pro) 122.6 5.0 4 121.99 123.95 122.87 .72 CA-C-O CH1E-C-O (except Gly) 120.8 1.7 118 119.28 122.87 120.86 .57 * CH2G*-C-O (Gly) 120.8 2.1 5 119.58 120.71 120.24 .40 CB-CA-C CH3E-CH1E-C (Ala) 110.5 1.5 13 110.01 112.29 110.91 .63 * CH1E-CH1E-C (Ile,Thr,Val) 109.1 2.2 22 107.73 111.79 109.97 .96 * CH2E-CH1E-C (the rest) 110.1 1.9 84 106.40 112.89 110.48 1.25 +* * N-CA-C NH1-CH1E-C (except Gly,Pro)111.2 2.8 115 103.12 114.50 110.06 1.74 +** * NH1-CH2G*-C (Gly) 112.5 2.9 5 110.40 114.38 112.63 1.54 N-CH1E-C (Pro) 111.8 2.5 4 111.12 114.31 112.15 1.27 * N-CA-CB NH1-CH1E-CH3E (Ala) 110.4 1.5 13 110.19 112.26 110.94 .62 * NH1-CH1E-CH1E (Ile,Thr,Val) 111.5 1.7 22 109.28 112.78 111.47 .85 * N-CH1E-CH2E (Pro) 103.0 1.1 4 102.42 103.92 103.29 .54 NH1-CH1E-CH2E (the rest) 110.5 1.7 80 106.61 113.29 110.22 1.46 ** +* ------------------------------------------------------------------------------------------------------------- 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 refined_19 Page 13 ---------------------------------------- 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] 99 87.6% Residues in additional allowed regions [a,b,l,p] 14 12.4% Residues in generously allowed regions [~a,~b,~l,~p] 0 .0% Residues in disallowed regions [XX] 0 .0% ---- ------ Number of non-glycine and non-proline residues 113 100.0% Number of end-residues (excl. Gly and Pro) 2 Number of glycine residues 5 Number of proline residues 4 ---- Total number of residues 124 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 113 87.6 83.8 10.0 .4 Inside b. Omega angle st dev 122 2.9 6.0 3.0 -1.0 BETTER c. Bad contacts / 100 residues 0 .0 4.2 10.0 -.4 Inside d. Zeta angle st dev 119 1.6 3.1 1.6 -1.0 Inside e. H-bond energy st dev 83 .9 .8 .2 .3 Inside f. Overall G-factor 124 .1 -.4 .3 1.6 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 13 5.9 18.1 6.5 -1.9 BETTER b. Chi-1 trans st dev 49 5.8 19.0 5.3 -2.5 BETTER c. Chi-1 gauche plus st dev 40 7.0 17.5 4.9 -2.1 BETTER d. Chi-1 pooled st dev 102 7.1 18.2 4.8 -2.3 BETTER e. Chi-2 trans st dev 32 9.5 20.4 5.0 -2.2 BETTER 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% 87.6 1 Chi-1 st.dev. 18.2 6.2 <12.0 <18.2 <24.4 >24.4 8.3 1 H-bond energy st dev .87 .24 < .63 < .87 <1.11 >1.11 .87 2 Residue-by-residue listing for refined_19 Page 14 ---------------------------------------- G - F A C T O R S Average Parameter Score Score --------- ----- ----- Dihedral angles:- Phi-psi distribution -.20 Chi1-chi2 distribution -.10 Chi1 only .01 Chi3 & chi4 .53 Omega .11 ------ .02 ===== Main-chain covalent forces:- Main-chain bond lengths -.05 Main-chain bond angles .46 ------ .25 ===== OVERALL AVERAGE .09 ===== Ideally, scores should be above -0.5. Values below -1.0 may need investigation.