WHAT IF Check report

This file was created 2011-12-21 from WHAT_CHECK output by a conversion script. If you are new to WHAT_CHECK, please study the pdbreport pages. There also exists a legend to the output.

Please note that you are looking at an abridged version of the output (all checks that gave normal results have been removed from this report). You can have a look at the Full report instead.

Verification log for pdb1cvh.ent

Non-validating, descriptive output paragraph

Note: Ramachandran plot

In this Ramachandran plot x-signs represent glycines, squares represent prolines, and plus-signs represent the other residues. If too many plus- signs fall outside the contoured areas then the molecule is poorly refined (or worse). Proline can only occur in the narrow region around phi=-60 that also falls within the other contour islands.

In a colour picture, the residues that are part of a helix are shown in blue, strand residues in red. Preferred regions for helical residues are drawn in blue, for strand residues in red, and for all other residues in green. A full explanation of the Ramachandran plot together with a series of examples can be found at the WHAT_CHECK website.

Chain identifier: A

Coordinate problems, unexpected atoms, B-factor and occupancy checks

Warning: What type of B-factor?

WHAT IF does not yet know well how to cope with B-factors in case TLS has been used. It simply assumes that the B-factor listed on the ATOM and HETATM cards are the total B-factors. When TLS refinement is used that assumption sometimes is not correct. TLS seems not mentioned in the header of the PDB file. But anyway, if WHAT IF complains about your B-factors, and you think that they are OK, then check for TLS related B-factor problems first.

Obviously, the temperature at which the X-ray data was collected has some importance too:

Temperature cannot be read from the PDB file. This most likely means that the temperature is listed as NULL (meaning unknown) in the PDB file.

Note: B-factor plot

The average atomic B-factor per residue is plotted as function of the residue number.

Chain identifier: A

Geometric checks

Warning: Unusual bond lengths

The bond lengths listed in the table below were found to deviate more than 4 sigma from standard bond lengths (both standard values and sigmas for amino acid residues have been taken from Engh and Huber [REF], for DNA they were taken from Parkinson et al [REF]). In the table below for each unusual bond the bond length and the number of standard deviations it differs from the normal value is given.

Atom names starting with "-" belong to the previous residue in the chain. If the second atom name is "-SG*", the disulphide bridge has a deviating length.

   3 TYR   (   7-)  A      N    CA    1.54    4.4
  83 THR   (  87-)  A      CB   OG1   1.53    5.9
  87 ILE   (  91-)  A      CB   CG1   1.65    4.4
 103 HIS   ( 107-)  A      CE1  NE2   1.26   -4.2
 113 GLU   ( 117-)  A      C    O     1.32    4.6
 114 LEU   ( 118-)  A      C    O     1.31    4.0
 133 PRO   ( 138-)  A      CD   N     1.42   -4.1
 164 THR   ( 169-)  A      CB   OG1   1.50    4.1
 171 PHE   ( 176-)  A      N    CA    1.54    4.4
 228 GLY   ( 233-)  A      CA   C     1.60    5.8
 234 GLU   ( 239-)  A      CD   OE2   1.35    5.1

Warning: Possible cell scaling problem

Comparison of bond distances with Engh and Huber [REF] standard values for protein residues and Parkinson et al [REF] values for DNA/RNA shows a significant systematic deviation. It could be that the unit cell used in refinement was not accurate enough. The deformation matrix given below gives the deviations found: the three numbers on the diagonal represent the relative corrections needed along the A, B and C cell axis. These values are 1.000 in a normal case, but have significant deviations here (significant at the 99.99 percent confidence level)

There are a number of different possible causes for the discrepancy. First the cell used in refinement can be different from the best cell calculated. Second, the value of the wavelength used for a synchrotron data set can be miscalibrated. Finally, the discrepancy can be caused by a dataset that has not been corrected for significant anisotropic thermal motion.

Please note that the proposed scale matrix has NOT been restrained to obey the space group symmetry. This is done on purpose. The distortions can give you an indication of the accuracy of the determination.

If you intend to use the result of this check to change the cell dimension of your crystal, please read the extensive literature on this topic first. This check depends on the wavelength, the cell dimensions, and on the standard bond lengths and bond angles used by your refinement software.

Unit Cell deformation matrix

 |  0.997028  0.001479 -0.000273|
 |  0.001479  0.992690 -0.000423|
 | -0.000273 -0.000423  0.996483|
Proposed new scale matrix

 |  0.023491 -0.000032  0.006128|
 | -0.000036  0.024158  0.000010|
 |  0.000004  0.000006  0.014206|
With corresponding cell

    A    =  42.573  B   =  41.395  C    =  72.754
    Alpha=  90.090  Beta= 104.637  Gamma=  89.830

The CRYST1 cell dimensions

    A    =  42.700  B   =  41.700  C    =  73.000
    Alpha=  90.000  Beta= 104.600  Gamma=  90.000

Variance: 204.575
(Under-)estimated Z-score: 10.541

Warning: Unusual bond angles

The bond angles listed in the table below were found to deviate more than 4 sigma from standard bond angles (both standard values and sigma for protein residues have been taken from Engh and Huber [REF], for DNA/RNA from Parkinson et al [REF]). In the table below for each strange angle the bond angle and the number of standard deviations it differs from the standard values is given. Please note that disulphide bridges are neglected. Atoms starting with "-" belong to the previous residue in the sequence.

   6 HIS   (  10-)  A      CA   CB   CG  106.56   -7.2
   6 HIS   (  10-)  A      CG   ND1  CE1 110.39    4.8
   6 HIS   (  10-)  A      CE1  NE2  CD2 112.34    4.2
   7 ASN   (  11-)  A      CA   CB   CG  107.42   -5.2
  10 GLU   (  14-)  A      CA   CB   CG  122.87    4.4
  10 GLU   (  14-)  A      CB   CG   CD  123.09    6.2
  11 HIS   (  15-)  A      C    CA   CB  100.77   -4.9
  11 HIS   (  15-)  A      CE1  NE2  CD2 112.36    4.2
  20 LYS   (  24-)  A      CA   CB   CG  133.20    9.6
  20 LYS   (  24-)  A      CB   CG   CD   99.73   -5.0
  22 GLU   (  26-)  A      CA   C    O   111.34   -5.6
  23 ARG   (  27-)  A     -CA  -C    N   124.37    4.1
  23 ARG   (  27-)  A     -C    N    CA  114.06   -4.2
  23 ARG   (  27-)  A      CG   CD   NE  118.41    4.7
  28 ASP   (  32-)  A      CA   CB   CG  108.35   -4.2
  30 ASP   (  34-)  A      C    CA   CB  118.23    4.3
  30 ASP   (  34-)  A      CA   CB   CG  117.27    4.7
  32 HIS   (  36-)  A      CA   CB   CG  107.94   -5.9
  33 THR   (  37-)  A      CA   CB   CG2 120.95    6.1
  33 THR   (  37-)  A      CA   CB   OG1 101.90   -5.1
  36 TYR   (  40-)  A      N    CA   CB  118.96    5.0
  37 ASP   (  41-)  A      CA   CB   CG  108.56   -4.0
  40 LEU   (  44-)  A      N    CA   CB  117.66    4.2
  42 PRO   (  46-)  A      CA   C    O   113.40   -4.4
  46 SER   (  50-)  A     -O   -C    N   130.88    4.9
And so on for a total of 145 lines.

Warning: Chirality deviations detected

The atoms listed in the table below have an improper dihedral value that is deviating from expected values. As the improper dihedral values are all getting very close to ideal values in recent X-ray structures, and as we actually do not know how big the spread around these values should be, this check only warns for 6 sigma deviations.

Improper dihedrals are a measure of the chirality/planarity of the structure at a specific atom. Values around -35 or +35 are expected for chiral atoms, and values around 0 for planar atoms. Planar side chains are left out of the calculations, these are better handled by the planarity checks.

Three numbers are given for each atom in the table. The first is the Z-score for the improper dihedral. The second number is the measured improper dihedral. The third number is the expected value for this atom type. A final column contains an extra warning if the chirality for an atom is opposite to the expected value.

 192 SER   ( 197-)  A      CA     7.6    48.51    34.32
The average deviation= 1.727

Error: Tau angle problems

The side chains of the residues listed in the table below contain a tau angle (N-Calpha-C) that was found to deviate from te expected value by more than 4.0 times the expected standard deviation. The number in the table is the number of standard deviations this RMS value deviates from the expected value.

 202 VAL   ( 207-)  A    5.37
 161 SER   ( 166-)  A    4.71
  64 VAL   (  68-)  A    4.52
 187 TRP   ( 192-)  A    4.16
 193 LEU   ( 198-)  A    4.02

Warning: High tau angle deviations

The RMS Z-score for the tau angles (N-Calpha-C) in the structure is too high. For well refined structures this number is expected to be near 1.0. The fact that it is higher than 1.5 worries us. However, we determined the tau normal distributions from 500 high-resolution X-ray structures, rather than from CSD data, so we cannot be 100 percent certain about these numbers.

Tau angle RMS Z-score : 1.752

Error: Side chain planarity problems

The side chains of the residues listed in the table below contain a planar group that was found to deviate from planarity by more than 4.0 times the expected value. For an amino acid residue that has a side chain with a planar group, the RMS deviation of the atoms to a least squares plane was determined. The number in the table is the number of standard deviations this RMS value deviates from the expected value. Not knowing better yet, we assume that planarity of the groups analyzed should be perfect.

 102 GLU   ( 106-)  A    4.28
  90 HIS   (  94-)  A    4.23

Torsion-related checks

Warning: Torsion angle evaluation shows unusual residues

The residues listed in the table below contain bad or abnormal torsion angles.

These scores give an impression of how `normal' the torsion angles in protein residues are. All torsion angles except omega are used for calculating a `normality' score. Average values and standard deviations were obtained from the residues in the WHAT IF database. These are used to calculate Z-scores. A residue with a Z-score of below -2.0 is poor, and a score of less than -3.0 is worrying. For such residues more than one torsion angle is in a highly unlikely position.

  54 ARG   (  58-)  A    -2.8
 162 ILE   ( 167-)  A    -2.4
  56 LEU   (  60-)  A    -2.3
  49 GLN   (  53-)  A    -2.2
 158 VAL   ( 163-)  A    -2.2
  96 LEU   ( 100-)  A    -2.2
  76 LYS   (  80-)  A    -2.2
  79 PRO   (  83-)  A    -2.2
 150 PRO   ( 155-)  A    -2.2
 188 THR   ( 193-)  A    -2.1
  75 LEU   (  79-)  A    -2.1
 107 LYS   ( 111-)  A    -2.0
 190 PRO   ( 195-)  A    -2.0
  88 GLN   (  92-)  A    -2.0
 146 GLY   ( 151-)  A    -2.0
  27 VAL   (  31-)  A    -2.0

Warning: Backbone evaluation reveals unusual conformations

The residues listed in the table below have abnormal backbone torsion angles.

Residues with `forbidden' phi-psi combinations are listed, as well as residues with unusual omega angles (deviating by more than 3 sigma from the normal value). Please note that it is normal if about 5 percent of the residues is listed here as having unusual phi-psi combinations.

  25 SER   (  29-)  A  PRO omega poor
  71 ASP   (  75-)  A  Poor phi/psi
 107 LYS   ( 111-)  A  Poor phi/psi
 124 GLY   ( 129-)  A  Poor phi/psi
 196 PRO   ( 201-)  A  PRO omega poor
 200 GLU   ( 205-)  A  Poor phi/psi
 248 ASN   ( 253-)  A  Poor phi/psi
 chi-1/chi-2 correlation Z-score : -2.597

Warning: Unusual backbone conformations

For the residues listed in the table below, the backbone formed by itself and two neighbouring residues on either side is in a conformation that is not seen very often in the database of solved protein structures. The number given in the table is the number of similar backbone conformations in the database with the same amino acid in the centre.

For this check, backbone conformations are compared with database structures using C-alpha superpositions with some restraints on the backbone oxygen positions.

A residue mentioned in the table can be part of a strange loop, or there might be something wrong with it or its directly surrounding residues. There are a few of these in every protein, but in any case it is worth looking at!

   3 TYR   (   7-)  A      0
   6 HIS   (  10-)  A      0
  16 PHE   (  20-)  A      0
  20 LYS   (  24-)  A      0
  23 ARG   (  27-)  A      0
  24 GLN   (  28-)  A      0
  25 SER   (  29-)  A      0
  46 SER   (  50-)  A      0
  48 ASP   (  52-)  A      0
  50 ALA   (  54-)  A      0
  54 ARG   (  58-)  A      0
  58 ASN   (  62-)  A      0
  60 HIS   (  64-)  A      0
  68 ASP   (  72-)  A      0
  69 SER   (  73-)  A      0
  71 ASP   (  75-)  A      0
  72 LYS   (  76-)  A      0
  73 ALA   (  77-)  A      0
  75 LEU   (  79-)  A      0
  76 LYS   (  80-)  A      0
  79 PRO   (  83-)  A      0
  81 ASP   (  85-)  A      0
  88 GLN   (  92-)  A      0
  99 GLN   ( 103-)  A      0
 103 HIS   ( 107-)  A      0
And so on for a total of 114 lines.

Warning: Omega angles too tightly restrained

The omega angles for trans-peptide bonds in a structure are expected to give a gaussian distribution with the average around +178 degrees and a standard deviation around 5.5 degrees. These expected values were obtained from very accurately determined structures. Many protein structures are too tightly restrained. This seems to be the case with the current structure too, as the observed standard deviation is below 4.0 degrees.

Standard deviation of omega values : 1.660

Warning: Unusual PRO puckering amplitudes

The proline residues listed in the table below have a puckering amplitude that is outside of normal ranges. Puckering parameters were calculated by the method of Cremer and Pople [REF]. Normal PRO rings have a puckering amplitude Q between 0.20 and 0.45 Angstrom. If Q is lower than 0.20 Angstrom for a PRO residue, this could indicate disorder between the two different normal ring forms (with C-gamma below and above the ring, respectively). If Q is higher than 0.45 Angstrom something could have gone wrong during the refinement. Be aware that this is a warning with a low confidence level. See: Who checks the checkers? Four validation tools applied to eight atomic resolution structures [REF]

 181 PRO   ( 186-)  A    0.13 LOW
 210 PRO   ( 215-)  A    0.17 LOW

Warning: Unusual PRO puckering phases

The proline residues listed in the table below have a puckering phase that is not expected to occur in protein structures. Puckering parameters were calculated by the method of Cremer and Pople [REF]. Normal PRO rings approximately show a so-called envelope conformation with the C-gamma atom above the plane of the ring (phi=+72 degrees), or a half-chair conformation with C-gamma below and C-beta above the plane of the ring (phi=-90 degrees). If phi deviates strongly from these values, this is indicative of a very strange conformation for a PRO residue, and definitely requires a manual check of the data. Be aware that this is a warning with a low confidence level. See: Who checks the checkers? Four validation tools applied to eight atomic resolution structures [REF].

  26 PRO   (  30-)  A   -57.5 half-chair C-beta/C-alpha (-54 degrees)
  38 PRO   (  42-)  A    51.8 half-chair C-delta/C-gamma (54 degrees)
 150 PRO   ( 155-)  A  -114.1 envelop C-gamma (-108 degrees)
 190 PRO   ( 195-)  A    31.8 envelop C-delta (36 degrees)

Bump checks

Error: Abnormally short interatomic distances

The pairs of atoms listed in the table below have an unusually short interactomic distance; each bump is listed in only one direction.

The contact distances of all atom pairs have been checked. Two atoms are said to `bump' if they are closer than the sum of their Van der Waals radii minus 0.40 Angstrom. For hydrogen bonded pairs a tolerance of 0.55 Angstrom is used. The first number in the table tells you how much shorter that specific contact is than the acceptable limit. The second distance is the distance between the centres of the two atoms. Although we believe that two water atoms at 2.4 A distance are too close, we only report water pairs that are closer than this rather short distance.

The last text-item on each line represents the status of the atom pair. If the final column contains the text 'HB', the bump criterion was relaxed because there could be a hydrogen bond. Similarly relaxed criteria are used for 1-3 and 1-4 interactions (listed as 'B2' and 'B3', respectively). BL indicates that the B-factors of the clashing atoms have a low B-factor thereby making this clash even more worrisome. INTRA and INTER indicate whether the clashes are between atoms in the same asymmetric unit, or atoms in symmetry related asymmetric units, respectively.

  54 ARG   (  58-)  A      CD  <->   65 GLU   (  69-)  A      OE1    0.40    2.40  INTRA BL
   1 TRP   (   5-)  A      N   <->  257 HOH   ( 272 )  A      O      0.39    2.31  INTRA
  41 LYS   (  45-)  A      NZ  <->  257 HOH   ( 290 )  A      O      0.39    2.31  INTRA
 244 GLN   ( 249-)  A      NE2 <->  257 HOH   ( 273 )  A      O      0.35    2.35  INTRA
  60 HIS   (  64-)  A      ND1 <->  257 HOH   ( 321 )  A      O      0.28    2.42  INTRA
  25 SER   (  29-)  A      O   <->  241 ARG   ( 246-)  A      NH1    0.27    2.43  INTRA BL
  92 CYS   (  96-)  A      SG  <->  102 GLU   ( 106-)  A      CG     0.26    3.14  INTRA BL
  71 ASP   (  75-)  A      OD1 <->   85 ARG   (  89-)  A      NE     0.25    2.45  INTRA BL
  21 GLY   (  25-)  A      O   <->  247 LYS   ( 252-)  A      NZ     0.24    2.46  INTRA BL
  11 HIS   (  15-)  A      ND1 <->   14 LYS   (  18-)  A      NZ     0.23    2.77  INTRA BL
 103 HIS   ( 107-)  A      NE2 <->  189 TYR   ( 194-)  A      OH     0.23    2.47  INTRA BL
  37 ASP   (  41-)  A      CG  <->   40 LEU   (  44-)  A      CD1    0.23    2.97  INTRA
 202 VAL   ( 207-)  A      CG1 <->  203 THR   ( 208-)  A      N      0.22    2.78  INTRA BL
 242 PRO   ( 247-)  A      O   <->  244 GLN   ( 249-)  A      NE2    0.21    2.49  INTRA BL
 257 HOH   ( 264 )  A      O   <->  257 HOH   ( 265 )  A      O      0.19    2.01  INTRA
 163 LYS   ( 168-)  A      NZ  <->  257 HOH   ( 358 )  A      O      0.19    2.51  INTRA
  36 TYR   (  40-)  A      CD1 <->  255 PHE   ( 260-)  A      C      0.19    3.01  INTRA
 248 ASN   ( 253-)  A      ND2 <->  249 ARG   ( 254-)  A      N      0.18    2.57  INTRA BL
  36 TYR   (  40-)  A      N   <->  257 HOH   ( 314 )  A      O      0.18    2.52  INTRA
 109 LYS   ( 113-)  A      NZ  <->  257 HOH   ( 361 )  A      O      0.18    2.52  INTRA BL
 102 GLU   ( 106-)  A      OE1 <->  115 HIS   ( 119-)  A      CE1    0.17    2.63  INTRA BL
 247 LYS   ( 252-)  A      O   <->  248 ASN   ( 253-)  A      CG     0.16    2.54  INTRA BL
  88 GLN   (  92-)  A      OE1 <->   90 HIS   (  94-)  A      ND1    0.16    2.54  INTRA BL
  47 TYR   (  51-)  A      OH  <->  118 HIS   ( 122-)  A      NE2    0.16    2.54  INTRA BL
 225 ASN   ( 230-)  A      ND2 <->  233 GLU   ( 238-)  A      OE2    0.15    2.55  INTRA
And so on for a total of 66 lines.

Packing, accessibility and threading

Note: Inside/Outside RMS Z-score plot

The Inside/Outside distribution normality RMS Z-score over a 15 residue window is plotted as function of the residue number. High areas in the plot (above 1.5) indicate unusual inside/outside patterns.

Chain identifier: A

Warning: Abnormal packing environment for some residues

The residues listed in the table below have an unusual packing environment.

The packing environment of the residues is compared with the average packing environment for all residues of the same type in good PDB files. A low packing score can indicate one of several things: Poor packing, misthreading of the sequence through the density, crystal contacts, contacts with a co-factor, or the residue is part of the active site. It is not uncommon to see a few of these, but in any case this requires further inspection of the residue.

   6 HIS   (  10-)  A      -6.06
 131 GLN   ( 136-)  A      -5.20
  96 LEU   ( 100-)  A      -5.14

Note: Quality value plot

The quality value smoothed over a 10 residue window is plotted as function of the residue number. Low areas in the plot (below -2.0) indicate unusual packing.

Chain identifier: A

Note: Second generation quality Z-score plot

The second generation quality Z-score smoothed over a 10 residue window is plotted as function of the residue number. Low areas in the plot (below -1.3) indicate unusual packing.

Chain identifier: A

Water, ion, and hydrogenbond related checks

Warning: Water molecules need moving

The water molecules listed in the table below were found to be significantly closer to a symmetry related non-water molecule than to the ones given in the coordinate file. For optimal viewing convenience revised coordinates for these water molecules should be given.

The number in brackets is the identifier of the water molecule in the input file. Suggested coordinates are also given in the table. Please note that alternative conformations for protein residues are not taken into account for this calculation. If you are using WHAT IF / WHAT-CHECK interactively, then the moved waters can be found in PDB format in the file: MOVEDH2O.pdb.

 257 HOH   ( 320 )  A      O    -20.34   -7.30   -1.77

Error: Water molecules without hydrogen bonds

The water molecules listed in the table below do not form any hydrogen bonds, neither with the protein or DNA/RNA, nor with other water molecules. This is a strong indication of a refinement problem. The last number on each line is the identifier of the water molecule in the input file.

 257 HOH   ( 276 )  A      O
 257 HOH   ( 309 )  A      O
 257 HOH   ( 325 )  A      O
 257 HOH   ( 328 )  A      O
 257 HOH   ( 333 )  A      O
 257 HOH   ( 348 )  A      O
 257 HOH   ( 351 )  A      O
 257 HOH   ( 365 )  A      O
Metal-coordinating Histidine residue  90 fixed to   1
Metal-coordinating Histidine residue 115 fixed to   1

Error: HIS, ASN, GLN side chain flips

Listed here are Histidine, Asparagine or Glutamine residues for which the orientation determined from hydrogen bonding analysis are different from the assignment given in the input. Either they could form energetically more favourable hydrogen bonds if the terminal group was rotated by 180 degrees, or there is no assignment in the input file (atom type 'A') but an assignment could be made. Be aware, though, that if the topology could not be determined for one or more ligands, then this option will make errors.

   6 HIS   (  10-)  A
  49 GLN   (  53-)  A
 173 ASN   ( 178-)  A

Warning: Buried unsatisfied hydrogen bond donors

The buried hydrogen bond donors listed in the table below have a hydrogen atom that is not involved in a hydrogen bond in the optimized hydrogen bond network.

Hydrogen bond donors that are buried inside the protein normally use all of their hydrogens to form hydrogen bonds within the protein. If there are any non hydrogen bonded buried hydrogen bond donors in the structure they will be listed here. In very good structures the number of listed atoms will tend to zero.

Waters are not listed by this option.

  27 VAL   (  31-)  A      N
  49 GLN   (  53-)  A      N
  62 PHE   (  66-)  A      N
 125 ASP   ( 130-)  A      N
 195 THR   ( 200-)  A      N
 199 LEU   ( 204-)  A      N
 239 ASN   ( 244-)  A      ND2
 240 TRP   ( 245-)  A      N
 255 PHE   ( 260-)  A      N
Only metal coordination for  115 HIS  ( 119-) A      ND1

Warning: No crystallisation information

No, or very inadequate, crystallisation information was observed upon reading the PDB file header records. This information should be available in the form of a series of REMARK 280 lines. Without this information a few things, such as checking ions in the structure, cannot be performed optimally.

Warning: Possible wrong residue type

The residues listed in the table below have a weird environment that cannot be improved by rotamer flips. This can mean one of three things, non of which WHAT CHECK really can do much about. 1) The side chain has actually another rotamer than is present in the PDB file; 2) A counter ion is present in the structure but is not given in the PDB file; 3) The residue actually is another amino acid type. The annotation 'Alt-rotamer' indicates that WHAT CHECK thinks you might want to find an alternate rotamer for this residue. The annotation 'Sym-induced' indicates that WHAT CHECK believes that symmetry contacts might have something to do with the difficulties of this residue's side chain. Determination of these two annotations is difficult, so their absence is less meaningful than their presence. The annotation Ligand-bound indicates that a ligand seems involved with this residue. In nine of ten of these cases this indicates that the ligand is causing the weird situation rather than the residue.

  28 ASP   (  32-)  A   H-bonding suggests Asn

Final summary

Note: Summary report for users of a structure

This is an overall summary of the quality of the structure as compared with current reliable structures. This summary is most useful for biologists seeking a good structure to use for modelling calculations.

The second part of the table mostly gives an impression of how well the model conforms to common refinement restraint values. The first part of the table shows a number of global quality indicators.


Structure Z-scores, positive is better than average:

  1st generation packing quality :  -0.357
  2nd generation packing quality :   0.136
  Ramachandran plot appearance   :  -1.973
  chi-1/chi-2 rotamer normality  :  -2.597
  Backbone conformation          :  -0.994

RMS Z-scores, should be close to 1.0:
  Bond lengths                   :   1.370
  Bond angles                    :   1.995
  Omega angle restraints         :   0.302 (tight)
  Side chain planarity           :   1.487
  Improper dihedral distribution :   1.417
  B-factor distribution          :   0.356
  Inside/Outside distribution    :   0.945

Note: Summary report for depositors of a structure

This is an overall summary of the quality of the X-ray structure as compared with structures solved at similar resolutions. This summary can be useful for a crystallographer to see if the structure makes the best possible use of the data. Warning. This table works well for structures solved in the resolution range of the structures in the WHAT IF database, which is presently (summer 2008) mainly 1.1 - 1.3 Angstrom. The further the resolution of your file deviates from this range the more meaningless this table becomes.

The second part of the table mostly gives an impression of how well the model conforms to common refinement restraint values. The first part of the table shows a number of global quality indicators, which have been calibrated against structures of similar resolution.

Resolution found in PDB file : 2.30


Structure Z-scores, positive is better than average:

  1st generation packing quality :   0.3
  2nd generation packing quality :   0.7
  Ramachandran plot appearance   :  -0.4
  chi-1/chi-2 rotamer normality  :  -1.0
  Backbone conformation          :  -0.9

RMS Z-scores, should be close to 1.0:
  Bond lengths                   :   1.370
  Bond angles                    :   1.995
  Omega angle restraints         :   0.302 (tight)
  Side chain planarity           :   1.487
  Improper dihedral distribution :   1.417
  B-factor distribution          :   0.356
  Inside/Outside distribution    :   0.945
==============

WHAT IF
    G.Vriend,
      WHAT IF: a molecular modelling and drug design program,
    J. Mol. Graph. 8, 52--56 (1990).

WHAT_CHECK (verification routines from WHAT IF)
    R.W.W.Hooft, G.Vriend, C.Sander and E.E.Abola,
      Errors in protein structures
    Nature 381, 272 (1996).
    (see also http://swift.cmbi.ru.nl/gv/whatcheck for a course and extra inform

Bond lengths and angles, protein residues
    R.Engh and R.Huber,
      Accurate bond and angle parameters for X-ray protein structure
      refinement,
    Acta Crystallogr. A47, 392--400 (1991).

Bond lengths and angles, DNA/RNA
    G.Parkinson, J.Voitechovsky, L.Clowney, A.T.Bruenger and H.Berman,
      New parameters for the refinement of nucleic acid-containing structures
    Acta Crystallogr. D52, 57--64 (1996).

DSSP
    W.Kabsch and C.Sander,
      Dictionary of protein secondary structure: pattern
      recognition of hydrogen bond and geometrical features
    Biopolymers 22, 2577--2637 (1983).

Hydrogen bond networks
    R.W.W.Hooft, C.Sander and G.Vriend,
      Positioning hydrogen atoms by optimizing hydrogen bond networks in
      protein structures
    PROTEINS, 26, 363--376 (1996).

Matthews' Coefficient
    B.W.Matthews
      Solvent content of Protein Crystals
    J. Mol. Biol. 33, 491--497 (1968).

Protein side chain planarity
    R.W.W. Hooft, C. Sander and G. Vriend,
      Verification of protein structures: side-chain planarity
    J. Appl. Cryst. 29, 714--716 (1996).

Puckering parameters
    D.Cremer and J.A.Pople,
      A general definition of ring puckering coordinates
    J. Am. Chem. Soc. 97, 1354--1358 (1975).

Quality Control
    G.Vriend and C.Sander,
      Quality control of protein models: directional atomic
      contact analysis,
    J. Appl. Cryst. 26, 47--60 (1993).

Ramachandran plot
    G.N.Ramachandran, C.Ramakrishnan and V.Sasisekharan,
      Stereochemistry of Polypeptide Chain Conformations
    J. Mol. Biol. 7, 95--99 (1963).

Symmetry Checks
    R.W.W.Hooft, C.Sander and G.Vriend,
      Reconstruction of symmetry related molecules from protein
      data bank (PDB) files
    J. Appl. Cryst. 27, 1006--1009 (1994).

Ion Checks
    I.D.Brown and K.K.Wu,
      Empirical Parameters for Calculating Cation-Oxygen Bond Valences
    Acta Cryst. B32, 1957--1959 (1975).

    M.Nayal and E.Di Cera,
      Valence Screening of Water in Protein Crystals Reveals Potential Na+
      Binding Sites
    J.Mol.Biol. 256 228--234 (1996).

    P.Mueller, S.Koepke and G.M.Sheldrick,
      Is the bond-valence method able to identify metal atoms in protein
      structures?
    Acta Cryst. D 59 32--37 (2003).

Checking checks
    K.Wilson, C.Sander, R.W.W.Hooft, G.Vriend, et al.
      Who checks the checkers
    J.Mol.Biol. (1998) 276,417-436.