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.
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: Missing atoms
The atoms listed in the table below are missing from the entry. If many atoms
are missing, the other checks can become less sensitive. Be aware that it
often happens that groups at the termini of DNA or RNA are really missing,
so that the absence of these atoms normally is neither an error nor the
result of poor electron density. Some of the atoms listed here might also be
listed by other checks, most noticeably by the options in the previous
section that list missing atoms in several categories. The plausible atoms
with zero occupancy are not listed here, as they already got assigned a
non-zero occupancy, and thus are no longer 'missing'.
9 LYS ( 147-) A CE 12 ASN ( 150-) A ND2 149 LYS ( 287-) A CE
Obviously, the temperature at which the X-ray data was collected has some importance too:
Number of TLS groups mentione in PDB file header: 0
Crystal temperature (K) :100.000
Note: B-factor plot
The average atomic B-factor per residue is plotted as function of the residue
Chain identifier: A
Nomenclature related problems
Warning: Phenylalanine convention problem
The phenylalanine residues listed in the table below have their chi-2 not
between -90.0 and 90.0.
51 PHE ( 189-) A 81 PHE ( 219-) A 111 PHE ( 249-) A 127 PHE ( 265-) A
41 GLU ( 179-) A
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.
8 ILE ( 146-) A CA CB 1.61 4.2 136 VAL ( 274-) A CA CB 1.61 4.2 155 ILE ( 293-) A CA CB 1.62 4.6
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
| 0.992722 0.001052 0.000723| | 0.001052 0.991502 0.002476| | 0.000723 0.002476 0.990687|Proposed new scale matrix
| 0.015123 -0.000016 -0.000011| | -0.000016 0.015142 -0.000038| | -0.000010 -0.000033 0.013148|With corresponding cell
A = 66.124 B = 66.043 C = 76.061 Alpha= 89.714 Beta= 89.916 Gamma= 89.878
The CRYST1 cell dimensions
A = 66.610 B = 66.610 C = 76.780 Alpha= 90.000 Beta= 90.000 Gamma= 90.000
(Under-)estimated Z-score: 14.388
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.
12 ASN ( 150-) A -C N CA 111.56 -5.6 13 LYS ( 151-) A N CA CB 103.22 -4.3 24 SER ( 162-) A CA CB OG 101.62 -4.7
41 GLU ( 179-) A
41 GLU ( 179-) A 4.12
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.
27 VAL ( 165-) A -2.3 59 MET ( 197-) A -2.3 58 PHE ( 196-) A -2.2 107 GLY ( 245-) A -2.1
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.
12 ASN ( 150-) A omega poor 40 HIS ( 178-) A Poor phi/psi 45 GLY ( 183-) A omega poor 50 SER ( 188-) A omega poor 57 GLN ( 195-) A Poor phi/psi 68 HIS ( 206-) A Poor phi/psi 69 ASN ( 207-) A Poor phi/psi 82 ASP ( 220-) A omega poor 90 HIS ( 228-) A omega poor 98 MET ( 236-) A omega poor 104 ASN ( 242-) A Poor phi/psi chi-1/chi-2 correlation Z-score : -0.060
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!
10 ILE ( 148-) A 0 12 ASN ( 150-) A 0 15 ALA ( 153-) A 0 23 ARG ( 161-) A 0 26 VAL ( 164-) A 0 41 GLU ( 179-) A 0 42 LYS ( 180-) A 0 44 PHE ( 182-) A 0 46 PHE ( 184-) A 0 47 LYS ( 185-) A 0 49 SER ( 187-) A 0 51 PHE ( 189-) A 0 52 HIS ( 190-) A 0 53 ARG ( 191-) A 0 56 PRO ( 194-) A 0 57 GLN ( 195-) A 0 58 PHE ( 196-) A 0 59 MET ( 197-) A 0 66 THR ( 204-) A 0 68 HIS ( 206-) A 0 69 ASN ( 207-) A 0 71 THR ( 209-) A 0 77 TYR ( 215-) A 0 80 LYS ( 218-) A 0 84 GLU ( 222-) A 0And so on for a total of 77 lines.
For each of the residues in the structure, a search was performed to find 5-residue stretches in the WHAT IF database with superposable C-alpha coordinates, and some restraining on the neighbouring backbone oxygens.
In the following table the RMS distance between the backbone oxygen positions of these matching structures in the database and the position of the backbone oxygen atom in the current residue is given. If this number is larger than 1.5 a significant number of structures in the database show an alternative position for the backbone oxygen. If the number is larger than 2.0 most matching backbone fragments in the database have the peptide plane flipped. A manual check needs to be performed to assess whether the experimental data can support that alternative as well. The number in the last column is the number of database hits (maximum 80) used in the calculation. It is "normal" that some glycine residues show up in this list, but they are still worth checking!
11 GLY ( 149-) A 1.86 13
2 PRO ( 140-) A 0.05 LOW 14 PRO ( 152-) A 0.18 LOW
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.
162 TYR ( 300-) A C <-> 163 HOH ( 398 ) A O 0.48 2.22 INTRA 146 LYS ( 284-) A CG <-> 163 HOH ( 438 ) A O 0.41 2.39 INTRA 153 LYS ( 291-) A NZ <-> 163 HOH ( 426 ) A O 0.39 2.31 INTRA 146 LYS ( 284-) A CD <-> 163 HOH ( 438 ) A O 0.27 2.53 INTRA 124 HIS ( 262-) A CE1 <-> 163 HOH ( 440 ) A O 0.27 2.53 INTRA 79 LYS ( 217-) A NZ <-> 163 HOH ( 341 ) A O 0.24 2.46 INTRA 40 HIS ( 178-) A CE1 <-> 47 LYS ( 185-) A N 0.22 2.88 INTRA BL 86 PHE ( 224-) A O <-> 89 LYS ( 227-) A NZ 0.20 2.50 INTRA 42 LYS ( 180-) A NZ <-> 163 HOH ( 409 ) A O 0.10 2.60 INTRA 98 MET ( 236-) A SD <-> 127 PHE ( 265-) A CE1 0.10 3.30 INTRA BL 57 GLN ( 195-) A N <-> 141 GLU ( 279-) A OE2 0.06 2.64 INTRA BL 83 ASP ( 221-) A N <-> 104 ASN ( 242-) A ND2 0.03 2.82 INTRA BL 48 GLY ( 186-) A N <-> 156 ILE ( 294-) A O 0.03 2.67 INTRA BL 129 GLU ( 267-) A OE2 <-> 163 HOH ( 429 ) A O 0.02 2.38 INTRA 98 MET ( 236-) A O <-> 124 HIS ( 262-) A CD2 0.02 2.78 INTRA BL 161 GLU ( 299-) A OE1 <-> 163 HOH ( 381 ) A O 0.01 2.39 INTRA
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.
146 LYS ( 284-) A -5.95 151 LYS ( 289-) A -5.48 57 GLN ( 195-) A -5.23
Chain identifier: A
Warning: Low packing Z-score for some residues
The residues listed in the table below have an unusual packing
environment according to the 2nd generation packing check. The score
listed in the table is a packing normality Z-score: positive means
better than average, negative means worse than average. Only residues
scoring less than -2.50 are listed here. These are the unusual
residues in the structure, so it will be interesting to take a
special look at them.
79 LYS ( 217-) A -3.11
Chain identifier: A
Water, ion, and hydrogenbond related checks
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.
163 HOH ( 405 ) A O
1 ASN ( 139-) A 40 HIS ( 178-) A 104 ASN ( 242-) A 124 HIS ( 262-) A
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.
44 PHE ( 182-) A N 85 ASN ( 223-) A N 115 ASP ( 253-) A N
84 GLU ( 222-) A H-bonding suggests Gln
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 : -0.684 2nd generation packing quality : -1.484 Ramachandran plot appearance : -0.272 chi-1/chi-2 rotamer normality : -0.060 Backbone conformation : -0.475
Bond lengths : 1.205 Bond angles : 1.027 Omega angle restraints : 1.238 Side chain planarity : 1.839 Improper dihedral distribution : 1.309 B-factor distribution : 0.833 Inside/Outside distribution : 0.913
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 : 1.88
Structure Z-scores, positive is better than average:
1st generation packing quality : -0.2 2nd generation packing quality : -1.2 Ramachandran plot appearance : 0.1 chi-1/chi-2 rotamer normality : 0.4 Backbone conformation : -0.8
Bond lengths : 1.205 Bond angles : 1.027 Omega angle restraints : 1.238 Side chain planarity : 1.839 Improper dihedral distribution : 1.309 B-factor distribution : 0.833 Inside/Outside distribution : 0.913 ==============
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.