Residue-by-residue listing for refined_1 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 ASP 1 - - 184.8 - - - - - - - - 175.9 - 35.5 - 2 PRO 2 - - - - - -55.5 - - - - - 180.6 - 38.6 - * * 3 ASN 3 A - 182.1 - - - - - - - - 183.3 - 34.6 - 4 ALA 4 l - - - - - - - - - - 182.4 - 31.0 - 5 GLU 5 a - 181.8 - 173.8 - - - - - - 175.8 - 32.4 - 6 PHE 6 B - 183.8 - - - - - - - - 175.2 - 32.4 - 7 ASP 7 B - 183.3 - - - - - - - - 181.9 -1.5 34.7 - 8 PRO 8 S - - - - - -84.6 - - - - - 180.2 - 37.5 - +* * +* 9 ASP 9 S A - 183.9 - - - - - - - - 175.2 - 33.0 - 10 LEU 10 t B - - -73.2 - - - - - - - 189.9 - 33.3 - +* +* 11 PRO 11 T - - - - - -51.3 - - - - - 177.8 - 36.4 - * * 12 GLY 12 T - - - - - - - - - - - 183.2 - - - 13 GLY 13 T - - - - - - - - - - - 186.5 -.5 - - * ** ** 14 GLY 14 T - - - - - - - - - - - 186.9 -1.5 - - * * 15 LEU 15 T A - 176.1 - - - - - - - - 186.1 -1.2 36.5 - * * * 16 HIS 16 t B - - -47.6 - - - - - - - 182.4 -3.0 33.5 - * * * 17 ARG 17 B B 46.3 - - 193.0 - - - - - - 177.1 -1.2 33.6 - * * * 18 CYS 18 t B - 174.7 - - - - - - - - 184.3 -1.5 34.5 - Residue-by-residue listing for refined_1 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 LEU 19 T A - - -59.6 176.8 - - - - - - 181.1 -.7 34.1 - +* +* 20 ALA 20 T A - - - - - - - - - - 182.9 - 33.7 - 21 CYS 21 T A - - -60.7 - - - - - - - 178.5 -1.3 30.7 - 22 ALA 22 t l - - - - - - - - - - 181.9 -2.7 32.3 - 23 ARG 23 B - - -59.9 180.5 - - - - - - 185.5 - 33.4 - 24 TYR 24 B B - - -55.2 - - - - - - - 182.9 - 36.4 - 25 PHE 25 B - - -57.4 - - - - - - - 186.6 -2.1 34.9 - * * 26 ILE 26 S A - - -54.1 - - - - - - - 182.8 - 34.9 - 27 ASP 27 h B - 175.5 - - - - - - - - 181.5 - 34.1 - 28 SER 28 H A 57.3 - - - - -61.0 -32.1 - - - 178.0 - 34.7 - 29 THR 29 H A - - -51.5 - - -60.9 -47.1 - - - 180.0 - 34.9 - * * 30 ASN 30 H A - - -68.0 - - -62.7 -45.9 - - - 176.6 - 34.2 - 31 LEU 31 H A - 172.2 - - - -55.6 -49.8 - - - 176.9 -2.2 32.5 - 32 LYS 32 H A - - -65.3 181.2 - -68.9 -31.6 - - - 174.7 -2.8 29.9 - * * 33 THR 33 H A - - -59.6 - - -62.3 -33.3 - - - 175.8 -2.6 34.4 - 34 HIS 34 H A - 159.7 - - - -61.2 -33.6 - - - 183.0 -2.0 33.3 - * * 35 PHE 35 h A - - -49.2 - - - - - - - 179.1 -.7 33.1 - * +* +* 36 ARG 36 T A - - -64.5 176.3 - - - - - - 169.1 -1.2 31.4 - +* * +* 37 SER 37 h b 51.4 - - - - - - - - - 184.0 -.9 33.2 - +* +* 38 LYS 38 H A 56.8 - - 179.6 - -54.9 -31.0 - - - 177.2 -1.3 33.4 - 39 ASP 39 H A - 173.1 - - - -56.6 -39.3 - - - 181.1 - 35.9 - 40 HIS 40 H A - 180.8 - - - -68.1 -47.5 - - - 183.3 -1.4 35.9 - 41 LYS 41 H A - - -55.7 183.8 - -69.8 -29.4 - - - 172.8 -1.3 32.0 - * * 42 LYS 42 H A - 172.7 - 179.2 - -64.1 -39.2 - - - 179.1 -2.3 33.8 - 43 ARG 43 H A - 204.7 - - - -70.3 -29.2 - - - 179.7 -1.7 35.4 - * * 44 LEU 44 H A - - -64.4 182.5 - -72.4 -30.0 - - - 175.9 -1.8 34.2 - 45 LYS 45 H A - - -54.6 - - -60.6 -31.1 - - - 179.9 -1.5 35.5 - 46 GLN 46 H A - - -56.5 174.5 - -74.3 -31.7 - - - 175.6 -.8 34.9 - +* +* 47 LEU 47 H A - - -84.1 - - -78.4 -27.2 - - - 181.5 -.8 34.6 - * * * +* +* 48 SER 48 h b - - -54.3 - - - - - - - 177.8 -2.0 33.1 - 49 VAL 49 S A - 182.4 - - - - - - - - 176.2 -1.8 34.9 - 50 GLU 50 S B - - -60.3 177.3 - - - - - - 181.3 - 35.0 - 51 PRO 51 - - - - - -70.2 - - - - - 177.6 - 37.4 - * * 52 TYR 52 b - 188.7 - - - - - - - - 186.6 -1.7 34.6 - * * 53 SER 53 t b - 183.5 - - - - - - - - 183.0 - 35.6 - 54 GLN 54 T a - 184.1 - 172.8 - - - - - - 172.9 - 33.8 - * * 55 GLU 55 T A - - -72.2 - - - - - - - 177.3 - 32.1 - 56 GLU 56 T A - - -68.7 - - - - - - - 179.4 -.5 34.1 - ** ** 57 ALA 57 t b - - - - - - - - - - 178.4 -.8 34.9 - +* +* Residue-by-residue listing for refined_1 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 ----------------------------------------------------------------------------------------------------------------------------------- 58 GLU 58 ~l - - -66.0 175.6 - - - - - - 176.3 - 31.4 - ** ** 59 ARG 59 a - - -63.2 - - - - - - - 175.6 - 33.7 - 60 ALA 60 S ~l - - - - - - - - - - 180.4 - 31.4 - ** ** 61 ALA 61 b - - - - - - - - - - 177.1 - 33.3 - 62 GLY 62 - - - - - - - - - - - 181.4 - - - 63 MET 63 B - - -57.7 177.7 - - - - - - 182.5 - 34.4 - 64 GLY 64 - - - - - - - - - - - 178.4 -.5 - - +* +* 65 SER 65 b 53.0 - - - - - - - - - 182.7 - 33.0 - 66 TYR 66 B - 180.7 - - - - - - - - 178.7 -.8 33.3 - +* +* 67 VAL 67 - - 183.1 - - - - - - - - - -.6 34.8 - +* +* ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: ** * * * +* * * +* ** * ** ----------------------------------------------------------------------------------------------------------------------------------- Mean values: 53.0 180.6 -60.9 179.0 -65.4 -64.8 -35.8 - - - 179.9 -1.5 34.0 Standard deviations: 4.5 8.5 8.1 5.0 15.1 6.8 7.4 - - - 3.9 .7 1.7 Numbers of values: 5 21 26 15 4 17 17 0 0 0 66 35 62 0 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_1 Page 4 ---------------------------------------- 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 ASP 1 - 1.235 1.502 1.547 1.462 - 118.85 119.23 109.54 107.76 110.40 121.86 * * * * 2 PRO 2 1.347 1.234 1.542 1.534 1.469 122.43 115.80 121.73 110.12 112.52 103.66 122.47 3 ASN 3 1.300 1.239 1.524 1.537 1.465 122.72 115.29 120.71 110.39 111.14 109.56 123.98 ** ** 4 ALA 4 1.332 1.232 1.509 1.543 1.449 124.21 114.94 121.62 112.71 109.77 113.03 123.25 * * +* +* 5 GLU 5 1.313 1.207 1.507 1.524 1.417 121.81 117.75 119.94 112.54 110.39 111.03 122.31 * * ** * ** 6 PHE 6 1.314 1.243 1.509 1.520 1.418 119.11 115.07 121.28 110.81 111.09 112.41 123.64 * ** * * ** 7 ASP 7 1.298 1.222 1.521 1.525 1.440 123.06 119.19 119.70 109.41 107.91 111.37 121.09 ** * * * ** 8 PRO 8 1.339 1.236 1.538 1.532 1.451 121.77 117.79 120.25 110.92 114.52 104.10 121.96 * * 9 ASP 9 1.317 1.234 1.503 1.534 1.457 120.43 115.35 121.07 110.83 108.65 112.45 123.54 * * * 10 LEU 10 1.312 1.224 1.534 1.557 1.449 122.54 117.40 120.40 111.53 107.73 111.72 122.20 * * * * 11 PRO 11 1.355 1.231 1.528 1.520 1.492 124.33 118.10 119.91 110.95 117.36 104.40 121.99 +* ** * ** Residue-by-residue listing for refined_1 Page 5 ---------------------------------------- ................................................................................................................................... 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 GLY 12 1.296 1.230 1.482 - 1.441 119.07 115.56 120.56 - 111.32 - 123.85 ** +* ** 13 GLY 13 1.323 1.204 1.496 - 1.441 121.95 115.94 120.51 - 111.29 - 123.54 * * * 14 GLY 14 1.331 1.232 1.533 - 1.462 121.98 116.58 120.60 - 113.65 - 122.77 15 LEU 15 1.313 1.233 1.536 1.516 1.406 123.33 116.77 121.13 110.57 112.75 106.36 122.09 * +** ** +** 16 HIS 16 1.304 1.242 1.497 1.525 1.458 120.92 114.75 121.43 109.84 110.08 112.08 123.77 +* * +* 17 ARG 17 1.288 1.230 1.511 1.526 1.433 122.71 115.07 121.32 112.22 112.33 108.94 123.60 +** * * +** 18 CYS 18 1.310 1.229 1.501 1.567 1.459 122.16 116.71 119.77 110.37 107.00 111.46 123.52 * * +* * +* 19 LEU 19 1.313 1.222 1.516 1.525 1.463 122.75 116.22 120.86 110.25 111.83 110.15 122.90 * * 20 ALA 20 1.310 1.224 1.527 1.509 1.452 121.80 117.40 120.45 110.20 112.50 110.34 122.15 * * 21 CYS 21 1.322 1.227 1.504 1.545 1.444 119.90 115.37 120.84 113.60 112.27 111.53 123.79 * +* +* 22 ALA 22 1.329 1.228 1.533 1.532 1.460 124.47 115.85 121.28 111.55 111.71 111.33 122.83 +* +* 23 ARG 23 1.313 1.250 1.496 1.528 1.434 121.89 115.14 120.73 111.16 109.58 111.24 124.13 * * * * 24 TYR 24 1.294 1.230 1.505 1.513 1.397 123.43 116.06 120.92 110.97 109.43 107.13 123.02 +** *** +* *** 25 PHE 25 1.294 1.216 1.490 1.518 1.442 121.66 115.95 119.44 110.16 109.17 110.09 124.55 ** +* ** 26 ILE 26 1.324 1.236 1.534 1.545 1.477 124.19 115.64 121.18 108.60 112.54 110.46 123.14 * * 27 ASP 27 1.304 1.242 1.514 1.545 1.451 122.42 116.71 119.83 111.32 109.41 110.16 123.46 +* +* 28 SER 28 1.326 1.231 1.523 1.536 1.451 123.35 115.81 120.70 111.65 110.45 108.56 123.45 * * 29 THR 29 1.332 1.215 1.532 1.530 1.439 122.16 116.65 120.40 109.51 109.91 110.47 122.91 * * 30 ASN 30 1.338 1.229 1.512 1.524 1.448 122.87 115.73 120.71 110.13 110.92 110.52 123.55 31 LEU 31 1.322 1.232 1.534 1.566 1.449 122.88 116.52 120.76 114.05 111.01 109.20 122.72 +* ** ** 32 LYS 32 1.300 1.228 1.543 1.523 1.457 120.91 117.42 120.17 113.50 113.31 111.81 122.38 ** +* ** 33 THR 33 1.339 1.237 1.537 1.544 1.468 121.93 114.62 121.85 109.69 109.14 111.10 123.52 34 HIS 34 1.312 1.232 1.542 1.555 1.442 123.95 117.92 120.30 112.19 112.40 109.42 121.77 * * * * * 35 PHE 35 1.326 1.204 1.516 1.526 1.454 119.18 117.40 120.23 108.28 111.03 113.78 122.35 * * +* +* 36 ARG 36 1.329 1.244 1.530 1.521 1.473 121.29 115.12 121.69 112.62 111.12 111.55 123.18 * * 37 SER 37 1.314 1.237 1.545 1.549 1.403 122.14 115.29 121.57 113.25 107.36 110.42 123.01 * +** +* * +** 38 LYS 38 1.332 1.237 1.523 1.527 1.471 123.77 115.45 120.68 110.88 112.47 110.27 123.86 * * 39 ASP 39 1.325 1.233 1.522 1.525 1.467 123.91 115.02 121.59 109.36 110.88 108.73 123.36 * * * 40 HIS 40 1.306 1.214 1.467 1.515 1.449 122.99 115.28 120.96 108.76 110.29 109.77 123.76 +* +** +** Residue-by-residue listing for refined_1 Page 6 ---------------------------------------- ................................................................................................................................... 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 ----------------------------------------------------------------------------------------------------------------------------------- 41 LYS 41 1.281 1.214 1.511 1.492 1.411 120.88 116.28 120.66 113.15 110.48 110.59 123.04 *** +* ** +* *** 42 LYS 42 1.321 1.245 1.528 1.530 1.444 121.70 116.04 120.98 109.95 110.04 111.61 122.97 43 ARG 43 1.326 1.222 1.551 1.550 1.447 121.41 115.81 121.42 111.40 107.03 108.65 122.71 * * * * * 44 LEU 44 1.332 1.223 1.511 1.518 1.445 123.35 116.41 120.48 109.74 111.20 110.77 123.10 45 LYS 45 1.321 1.222 1.532 1.541 1.468 122.39 115.16 121.37 108.49 108.69 110.82 123.45 46 GLN 46 1.328 1.224 1.531 1.523 1.454 123.33 116.02 121.10 110.53 109.98 109.24 122.87 47 LEU 47 1.326 1.230 1.508 1.531 1.442 122.59 115.82 121.19 109.57 110.53 110.82 122.98 48 SER 48 1.304 1.241 1.528 1.528 1.419 121.63 115.04 121.66 111.94 110.71 110.46 123.21 +* ** ** 49 VAL 49 1.319 1.241 1.523 1.556 1.451 122.60 114.14 122.19 110.03 107.62 110.89 123.66 * * * 50 GLU 50 1.306 1.241 1.515 1.518 1.425 123.99 117.39 120.37 110.61 107.56 109.99 122.11 +* +* * * +* 51 PRO 51 1.340 1.241 1.533 1.536 1.451 122.72 115.12 121.46 110.86 113.16 104.60 123.31 * * * 52 TYR 52 1.308 1.245 1.515 1.530 1.442 123.79 116.05 120.73 110.98 106.97 110.38 123.19 * * +* +* 53 SER 53 1.285 1.244 1.537 1.553 1.416 122.57 115.07 121.54 111.24 110.47 108.01 123.36 *** * ** * *** 54 GLN 54 1.306 1.225 1.560 1.552 1.448 124.49 115.79 122.08 113.18 110.27 108.26 122.13 +* +* * +* +* * +* 55 GLU 55 1.319 1.237 1.521 1.532 1.462 121.66 115.96 120.99 110.88 110.56 112.83 123.05 * * 56 GLU 56 1.327 1.231 1.521 1.547 1.465 122.17 114.98 121.80 109.66 109.49 111.67 123.19 57 ALA 57 1.300 1.226 1.505 1.523 1.436 123.30 116.76 118.96 110.54 107.51 110.14 124.28 ** * * * ** 58 GLU 58 1.328 1.227 1.527 1.534 1.466 123.40 115.51 121.66 111.06 112.96 112.55 122.78 * * 59 ARG 59 1.311 1.230 1.513 1.534 1.450 122.16 115.56 120.65 109.87 109.08 112.14 123.76 * * 60 ALA 60 1.344 1.232 1.542 1.531 1.483 124.76 117.41 120.02 111.25 114.28 111.69 122.57 * * +* * +* 61 ALA 61 1.320 1.239 1.507 1.526 1.437 122.63 115.43 121.07 110.36 109.80 112.02 123.35 * * * 62 GLY 62 1.295 1.233 1.511 - 1.443 121.44 116.34 120.72 - 111.62 - 122.93 ** ** 63 MET 63 1.316 1.242 1.522 1.532 1.459 121.81 116.40 120.59 110.29 109.97 110.37 123.02 64 GLY 64 1.311 1.234 1.505 - 1.442 120.43 116.10 120.87 - 112.48 - 123.02 * * 65 SER 65 1.302 1.240 1.525 1.537 1.438 121.71 116.45 121.04 112.23 110.42 110.42 122.49 +* * * +* 66 TYR 66 1.314 1.238 1.507 1.515 1.441 121.00 114.49 121.68 110.96 111.75 110.68 123.82 * * 67 VAL 67 1.287 - 1.516 1.567 1.445 123.94 - - 108.83 107.29 112.51 - *** * * * *** ----------------------------------------------------------------------------------------------------------------------------------- Max deviations: *** * +** +* *** +* * * ** ** ** * *** ----------------------------------------------------------------------------------------------------------------------------------- Residue-by-residue listing for refined_1 Page 7 ---------------------------------------- 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 62 1.281 1.344 1.314 .014 *** * * C-N (Pro) 1.341 .016 4 1.339 1.355 1.345 .007 C-O C-O 1.231 .020 66 1.204 1.250 1.231 .010 * CA-C CH1E-C (except Gly) 1.525 .021 62 1.467 1.560 1.521 .016 +** +* CH2G*-C (Gly) 1.516 .018 5 1.482 1.533 1.506 .017 +* CA-CB CH1E-CH3E (Ala) 1.521 .033 6 1.509 1.543 1.527 .010 CH1E-CH1E (Ile,Thr,Val) 1.540 .027 5 1.530 1.567 1.548 .013 * CH1E-CH2E (the rest) 1.530 .020 51 1.492 1.567 1.532 .014 +* +* N-CA NH1-CH1E (except Gly,Pro)1.458 .019 58 1.397 1.483 1.446 .018 *** * NH1-CH2G* (Gly) 1.451 .016 5 1.441 1.462 1.446 .008 N-CH1E (Pro) 1.466 .015 4 1.451 1.492 1.466 .017 +* ------------------------------------------------------------------------------------------------------------- Residue-by-residue listing for refined_1 Page 8 ---------------------------------------- +-----------------+ | 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 57 114.14 119.19 116.03 1.04 * * CH2G*-C-NH1 (Gly) 116.4 2.1 5 115.56 116.58 116.10 .35 CH1E-C-N (Pro) 116.9 1.5 4 115.12 118.10 116.70 1.27 * O-C-N O-C-NH1 (except Pro) 123.0 1.6 62 121.09 124.55 123.09 .65 * O-C-N (Pro) 122.0 1.4 4 121.96 123.31 122.43 .55 C-N-CA C-NH1-CH1E (except Gly,Pro)121.7 1.8 57 119.11 124.76 122.46 1.25 * +* C-NH1-CH2G* (Gly) 120.6 1.7 5 119.07 121.98 120.97 1.10 C-N-CH1E (Pro) 122.6 5.0 4 121.77 124.33 122.81 .94 CA-C-O CH1E-C-O (except Gly) 120.8 1.7 61 118.96 122.19 120.86 .70 * CH2G*-C-O (Gly) 120.8 2.1 5 120.51 120.87 120.65 .13 CB-CA-C CH3E-CH1E-C (Ala) 110.5 1.5 6 110.20 112.71 111.10 .86 * CH1E-CH1E-C (Ile,Thr,Val) 109.1 2.2 5 108.60 110.03 109.33 .54 CH2E-CH1E-C (the rest) 110.1 1.9 51 108.28 114.05 110.96 1.31 ** N-CA-C NH1-CH1E-C (except Gly,Pro)111.2 2.8 58 106.97 114.28 110.17 1.76 +* * NH1-CH2G*-C (Gly) 112.5 2.9 5 111.29 113.65 112.07 .90 N-CH1E-C (Pro) 111.8 2.5 4 112.52 117.36 114.39 1.86 ** * N-CA-CB NH1-CH1E-CH3E (Ala) 110.4 1.5 6 110.14 113.03 111.43 .99 +* NH1-CH1E-CH1E (Ile,Thr,Val) 111.5 1.7 5 110.46 112.51 111.08 .76 N-CH1E-CH2E (Pro) 103.0 1.1 4 103.66 104.60 104.19 .36 * * NH1-CH1E-CH2E (the rest) 110.5 1.7 47 106.36 113.78 110.48 1.48 ** +* ------------------------------------------------------------------------------------------------------------- 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_1 Page 9 ---------------------------------------- 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] 42 75.0% Residues in additional allowed regions [a,b,l,p] 12 21.4% Residues in generously allowed regions [~a,~b,~l,~p] 2 3.6% Residues in disallowed regions [XX] 0 .0% ---- ------ Number of non-glycine and non-proline residues 56 100.0% Number of end-residues (excl. Gly and Pro) 2 Number of glycine residues 5 Number of proline residues 4 ---- Total number of residues 67 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 56 75.0 83.8 10.0 -.9 Inside b. Omega angle st dev 66 3.9 6.0 3.0 -.7 Inside c. Bad contacts / 100 residues 0 .0 4.2 10.0 -.4 Inside d. Zeta angle st dev 62 1.7 3.1 1.6 -.9 Inside e. H-bond energy st dev 35 .7 .8 .2 -.6 Inside f. Overall G-factor 67 -.1 -.4 .3 1.1 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 5 4.5 18.1 6.5 -2.1 BETTER b. Chi-1 trans st dev 21 8.5 19.0 5.3 -2.0 BETTER c. Chi-1 gauche plus st dev 26 8.1 17.5 4.9 -1.9 BETTER d. Chi-1 pooled st dev 52 9.9 18.2 4.8 -1.7 BETTER e. Chi-2 trans st dev 15 5.0 20.4 5.0 -3.1 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% 75.0 2 Chi-1 st.dev. 18.2 6.2 <12.0 <18.2 <24.4 >24.4 10.0 1 H-bond energy st dev .87 .24 < .63 < .87 <1.11 >1.11 .90 3 Residue-by-residue listing for refined_1 Page 10 ---------------------------------------- G - F A C T O R S Average Parameter Score Score --------- ----- ----- Dihedral angles:- Phi-psi distribution -.76 Chi1-chi2 distribution -.06 Chi1 only .24 Chi3 & chi4 .37 Omega -.17 ------ -.24 ===== Main-chain covalent forces:- Main-chain bond lengths .06 Main-chain bond angles .39 ------ .25 ===== OVERALL AVERAGE -.06 ===== Ideally, scores should be above -0.5. Values below -1.0 may need investigation.