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: Occupancies atoms do not add up to 1.0.
In principle, the occupancy of all alternates of one atom should add up till
1.0. A valid exception is the missing atom (i.e. an atom not seen in the
electron density) that is allowed to have a 0.0 occupancy. Sometimes this
even happens when there are no alternate atoms given...
Atoms want to move. That is the direct result of the second law of thermodynamics, in a somewhat weird way of thinking. Any way, many atoms seem to have more than one position where they like to sit, and they jump between them. The population difference between those sites (which is related to their energy differences) is seen in the occupancy factors. As also for atoms it is 'to be or not to be', these occupancies should add up to 1.0. Obviously, it is possible that they add up to a number less than 1.0, in cases where there are yet more, but undetected' rotamers/positions in play, but also in those cases a warning is in place as the information shown in the PDB file is less certain than it could have been. The residues listed below contain atoms that have an occupancy greater than zero, but all their alternates do not add up to one.
WARNING. Presently WHAT CHECK only deals with a maximum of two alternate positions. A small number of atoms in the PDB has three alternates. In those cases the warning given here should obviously be neglected! In a next release we will try to fix this.
1 HIS ( 3-) A 0.50 2 HIS ( 4-) A 0.50 12 GLU ( 14-) A 0.30
Obviously, the temperature at which the X-ray data was collected has some importance too:
Crystal temperature (K) :300.000
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.
64 PHE ( 66-) 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.
65 ASN ( 67-) A C O 1.11 -5.9 65 ASN ( 67-) A CG ND2 1.10 -10.8
RMS Z-score for bond lengths: 0.332
RMS-deviation in bond distances: 0.007
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.
92 HIS ( 94-) A CG ND1 CE1 109.65 4.1 105 HIS ( 107-) A CG ND1 CE1 109.81 4.2 117 HIS ( 119-) A CG ND1 CE1 109.84 4.2 120 HIS ( 122-) A CG ND1 CE1 109.84 4.2 205 THR ( 208-) A N CA C 99.28 -4.3
204 VAL ( 207-) A 5.24 205 THR ( 208-) A 4.29 195 LEU ( 198-) A 4.27
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.
81 PRO ( 83-) A -2.6 173 PHE ( 176-) A -2.3 146 LYS ( 149-) A -2.1 90 GLN ( 92-) A -2.1 160 VAL ( 163-) A -2.1 148 GLY ( 151-) A -2.0 175 ASN ( 178-) A -2.0 249 LYS ( 252-) A -2.0
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.
27 SER ( 29-) A PRO omega poor 63 ALA ( 65-) A Poor phi/psi 109 LYS ( 111-) A Poor phi/psi 126 GLY ( 129-) A Poor phi/psi, omega poor 175 ASN ( 178-) A Poor phi/psi 198 PRO ( 201-) A PRO omega poor 200 LEU ( 203-) A Poor phi/psi 249 LYS ( 252-) A Poor phi/psi chi-1/chi-2 correlation Z-score : -0.166
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 TRP ( 5-) A 0 5 TYR ( 7-) A 0 8 HIS ( 10-) A 0 17 ASP ( 19-) A 0 18 PHE ( 20-) A 0 22 LYS ( 24-) A 0 25 ARG ( 27-) A 0 27 SER ( 29-) A 0 48 SER ( 50-) A 0 52 ALA ( 54-) A 0 60 ASP ( 62-) A 0 62 HIS ( 64-) A 0 64 PHE ( 66-) A 0 70 ASP ( 72-) A 0 71 SER ( 73-) A 0 73 ASP ( 75-) A 0 74 LYS ( 76-) A 0 75 ALA ( 77-) A 0 78 LYS ( 80-) A 0 81 PRO ( 83-) A 0 83 ASP ( 85-) A 0 90 GLN ( 92-) A 0 94 HIS ( 96-) A 0 101 GLN ( 103-) A 0 105 HIS ( 107-) A 0And so on for a total of 116 lines.
Standard deviation of omega values : 2.123
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.
127 ASP ( 130-) A CG <-> 260 HOH ( 534 ) A O 0.36 2.44 INTRA 174 THR ( 177-) A C <-> 175 ASN ( 178-) A ND2 0.25 2.75 INTRA 127 ASP ( 130-) A CA <-> 260 HOH ( 534 ) A O 0.24 2.56 INTRA 174 THR ( 177-) A CB <-> 175 ASN ( 178-) A ND2 0.22 2.78 INTRA 125 TYR ( 128-) A O <-> 127 ASP ( 130-) A N 0.21 2.49 INTRA 73 ASP ( 75-) A OD1 <-> 87 ARG ( 89-) A NE 0.20 2.50 INTRA 127 ASP ( 130-) A OD1 <-> 129 GLY ( 132-) A N 0.19 2.51 INTRA 133 GLN ( 136-) A CG <-> 260 HOH ( 494 ) A O 0.18 2.62 INTRA BF 78 LYS ( 80-) A NZ <-> 260 HOH ( 433 ) A O 0.17 2.53 INTRA 249 LYS ( 252-) A NZ <-> 260 HOH ( 391 ) A O 0.16 2.54 INTRA 115 GLU ( 117-) A OE2 <-> 117 HIS ( 119-) A NE2 0.11 2.59 INTRA BL 258 LYS ( 261-) A C <-> 260 HOH ( 435 ) A O 0.10 2.70 INTRA BF 13 HIS ( 15-) A ND1 <-> 16 LYS ( 18-) A NZ 0.09 2.91 INTRA BL 34 HIS ( 36-) A CD2 <-> 260 HOH ( 477 ) A O 0.08 2.72 INTRA 105 HIS ( 107-) A NE2 <-> 191 TYR ( 194-) A OH 0.08 2.62 INTRA BL 23 GLY ( 25-) A O <-> 249 LYS ( 252-) A NZ 0.07 2.63 INTRA 127 ASP ( 130-) A CB <-> 130 LYS ( 133-) A CG 0.06 3.14 INTRA 134 GLN ( 137-) A NE2 <-> 260 HOH ( 472 ) A O 0.05 2.65 INTRA 125 TYR ( 128-) A C <-> 127 ASP ( 130-) A N 0.05 2.85 INTRA 158 VAL ( 161-) A CG1 <-> 222 LYS ( 225-) A CD 0.04 3.16 INTRA 249 LYS ( 252-) A CB <-> 250 ASN ( 253-) A N 0.03 2.67 INTRA B3 2 HIS ( 4-) A ND1 <-> 3 TRP ( 5-) A N 0.03 2.87 INTRA 177 ASP ( 180-) A OD2 <-> 179 ARG ( 182-) A NH2 0.03 2.67 INTRA 39 ASP ( 41-) A OD1 <-> 41 SER ( 43-) A CB 0.03 2.77 INTRA 175 ASN ( 178-) A CG <-> 260 HOH ( 306 ) A O 0.02 2.78 INTRA 39 ASP ( 41-) A OD1 <-> 41 SER ( 43-) A N 0.01 2.69 INTRA 108 ASP ( 110-) A OD2 <-> 260 HOH ( 315 ) A O 0.01 2.39 INTRA 174 THR ( 177-) A C <-> 175 ASN ( 178-) A CG 0.01 3.09 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.
8 HIS ( 10-) A -5.97 2 HIS ( 4-) A -5.39 98 LEU ( 100-) A -5.07 7 LYS ( 9-) A -5.01
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.
260 HOH ( 452 ) A O -0.92 -8.37 33.28 260 HOH ( 479 ) A O -15.66 -10.31 37.76 260 HOH ( 481 ) A O -5.74 0.63 40.60 260 HOH ( 518 ) A O -12.43 16.64 8.80 260 HOH ( 527 ) A O -18.16 -9.82 37.50
1 HIS ( 3-) A 65 ASN ( 67-) A 133 GLN ( 136-) 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.
29 VAL ( 31-) A N 56 ARG ( 58-) A NH2 72 GLN ( 74-) A N 98 LEU ( 100-) A N 122 ASN ( 124-) A ND2 127 ASP ( 130-) A N 197 THR ( 200-) A N 201 LEU ( 204-) A N 218 GLU ( 221-) A N 227 ASN ( 230-) A ND2 241 ASN ( 244-) A ND2 242 TRP ( 245-) A N 257 PHE ( 260-) A N Only metal coordination for 94 HIS ( 96-) A NE2 Only metal coordination for 117 HIS ( 119-) A ND1
60 ASP ( 62-) A H-bonding suggests Asn
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 : -0.297 2nd generation packing quality : 0.640 Ramachandran plot appearance : -1.118 chi-1/chi-2 rotamer normality : -0.166 Backbone conformation : -0.662
Bond lengths : 0.332 (tight) Bond angles : 0.702 Omega angle restraints : 0.386 (tight) Side chain planarity : 0.259 (tight) Improper dihedral distribution : 0.582 B-factor distribution : 0.537 Inside/Outside distribution : 0.948
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 : 1.60
Structure Z-scores, positive is better than average:
1st generation packing quality : -0.0 2nd generation packing quality : -0.4 Ramachandran plot appearance : -1.5 chi-1/chi-2 rotamer normality : -0.5 Backbone conformation : -1.0
Bond lengths : 0.332 (tight) Bond angles : 0.702 Omega angle restraints : 0.386 (tight) Side chain planarity : 0.259 (tight) Improper dihedral distribution : 0.582 B-factor distribution : 0.537 Inside/Outside distribution : 0.948 ==============
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.