8 8 A D >< - 0 0 57 -4,-2.9 3,-1.4 3,-0.1 -1,-0.2 -0.852 61.5-167.8-144.3 106.0 3.6 13.0 49.9]]>
</pre>
</pre>
<p>Below is a brief description of the data columns. More details are described in the Kabsch and Sander paper.</p>
<p>Below is a brief description of the data columns. More details are described in the Kabsch and Sander
paper.</p>
<h3>RESIDUE</h3>
<h3>RESIDUE</h3>
<p>Two columns of residue numbers. First column is DSSP's sequential residue number, starting at the first residue actually in the model set
<p>Two columns of residue numbers. First column is DSSP's sequential residue number, starting at the first
and including chain breaks; this number is used to refer to residues throughout. The second column gives the numbering as is used in the
residue actually in the model set
structure model 'residue number','insertion code' and 'chain identifier'; these are given for reference only.</p>
and including chain breaks; this number is used to refer to residues throughout. The second column gives
the numbering as is used in the
structure model 'residue number','insertion code' and 'chain identifier'; these are given for reference
only.</p>
<h3>AA</h3>
<h3>AA</h3>
<p>One letter amino acid code, non standard residues are marked as <em>X</em>. CYS in an SS-bridge are marked by a lower case letter. So when cysteines
<p>One letter amino acid code, non standard residues are marked as <em>X</em>. CYS in an SS-bridge are
are bridged, then the first bridged cysteine in the sequence and its partner elsewhere in the sequence are marked <em>a</em>. The next bridged cysteine,
marked by a lower case letter. So when cysteines
that is not yet marked, and its partner are both marked <em>b</em>, etcetera. Unbridged cysteines remain marked as <em>C</em>.</p>
are bridged, then the first bridged cysteine in the sequence and its partner elsewhere in the sequence
are marked <em>a</em>. The next bridged cysteine,
that is not yet marked, and its partner are both marked <em>b</em>, etcetera. Unbridged cysteines remain
marked as <em>C</em>.</p>
<h3>S (first column in STRUCTURE block)</h3>
<h3>S (first column in STRUCTURE block)</h3>
<p>The one-letter summary of secondary structure, intended to approximate crystallographers' intuition, based on columns 19-38, which are the principal
<p>The one-letter summary of secondary structure, intended to approximate crystallographers' intuition,
based on columns 19-38, which are the principal
result of DSSP analysis of the atomic coordinates. More details in the Kabsch and Sander paper.</p>
result of DSSP analysis of the atomic coordinates. More details in the Kabsch and Sander paper.</p>
<h3>BP1 and BP2</h3>
<h3>BP1 and BP2</h3>
<p>Residue numbers of the first and (if available) second beta bridge partner. The letter marked the B-sheet that contains the bridges.</p>
<p>Residue numbers of the first and (if available) second beta bridge partner. The letter marked the B-sheet
that contains the bridges.</p>
<h3>ACC</h3>
<h3>ACC</h3>
<p>Water exposed surface in Angstrom**2. <em>Note:</em>The values for solvent exposure may not mean what you think:
<p>Water exposed surface in Angstrom**2. <em>Note:</em>The values for solvent exposure may not mean what you
think:
<ul>
<ul>
<li>Effects leading to larger than expected values: solvent exposure calculation ignores unusual residues, like ACE, or residues with incomplete backbone.
<li>Effects leading to larger than expected values: solvent exposure calculation ignores unusual
it also ignores HETATOMS, like a heme or metal ligands. Also, side chains may not have all atoms explicitly modeled.</li>
residues, like ACE, or residues with incomplete backbone.
<li>Effects leading to smaller than expected values: in complexes, e.g. a dimer, solvent exposure is for the entire assembly, not for the monomer.
it also ignores HETATOMS, like a heme or metal ligands. Also, side chains may not have all atoms
Also, atom OXT of c-terminal residues is treated like a side chain atom if it is listed as part of the last residue.</li>
explicitly modeled.</li>
<li>Unknown or non-standard residues are named X on output and are not checked for the expected number of sidechain atoms.</li>
<li>Effects leading to smaller than expected values: in complexes, e.g. a dimer, solvent exposure is for
the entire assembly, not for the monomer.
Also, atom OXT of c-terminal residues is treated like a side chain atom if it is listed as part of
the last residue.</li>
<li>Unknown or non-standard residues are named X on output and are not checked for the expected number
of sidechain atoms.</li>
<li>All explicit water molecules, like other hetatoms, are ignored.</li>
<li>All explicit water molecules, like other hetatoms, are ignored.</li>
</ul>
</ul>
</p>
</p>
<h3>N-H-->O etc.</h3>
<h3>N-H-->O etc.</h3>
<p>Hydrogen bonds; e.g. -3,-1.4 means that this residue (i) has its HN atom H-bonded to O of residue i-3 with an electrostatic H-bond energy of -1.4 kcal/mol.
<p>Hydrogen bonds; e.g. -3,-1.4 means that this residue (i) has its HN atom H-bonded to O of residue i-3
There are two columns for each type of H-bond, to allow for bifurcated H-bonds. <em>Note:</em>The marked H-bonds are the best and second best candidate. The second best
with an electrostatic H-bond energy of -1.4 kcal/mol.
There are two columns for each type of H-bond, to allow for bifurcated H-bonds. <em>Note:</em>The marked
H-bonds are the best and second best candidate. The second best
and even the best (in rare occasions) may be unrealistically por H-bonds.</p>
and even the best (in rare occasions) may be unrealistically por H-bonds.</p>
<h3>TCO</h3>
<h3>TCO</h3>
<p>The cosine of angle between C=O of residue i and C=O of residue i-1. For α-helices, TCO is near +1, for β-sheets TCO is near -1.
<p>The cosine of angle between C=O of residue i and C=O of residue i-1. For α-helices, TCO is near +1,
for β-sheets TCO is near -1.
These values are descriptive and not used for structure definition.</p>
These values are descriptive and not used for structure definition.</p>
<h3>KAPPA</h3>
<h3>KAPPA</h3>
<p>Virtual bond angle (bend angle) defined by the three Cα atoms of residues i-2, i, and i+2. Used to define bends (structure code <em>S</em>).</p>
<p>Virtual bond angle (bend angle) defined by the three Cα atoms of residues i-2, i, and i+2. Used to
define bends (structure code <em>S</em>).</p>
<h3>ALPHA</h3>
<h3>ALPHA</h3>
<p>Virtual torsion angle (dihedral angle) defined by the four Cα atoms of residues i-1, i, i+1, and i+2. Used to define chirality (structure code <em>+</em> or <em>-</em>).
<p>Virtual torsion angle (dihedral angle) defined by the four Cα atoms of residues i-1, i, i+1, and
i+2. Used to define chirality (structure code <em>+</em> or <em>-</em>).</p>
<h3>PHI and PSI</h3>
<h3>PHI and PSI</h3>
<p>The peptide backbone torsion angles as described in the IUPAC standard</p>
<p>The peptide backbone torsion angles as described in the IUPAC standard</p>
<p>The mmCIF-formatted DSSP output caries the same information as the DSSP format but in a more scalable way and with a formal description caputered in
<p>The mmCIF-formatted DSSP output caries the same information as the DSSP format but in a more scalable way
an mmCIF dictionary. It is designed to be machine readable. Developers who create software to read these annotations can use our
and with a formal description caputered in
<ahref="https://github.com/PDB-REDO/dssp/blob/trunk/mmcif_pdbx/dssp-extension.dic"target="_BLANK">extension to the mmCIF dictionary</a> on GitHub.
an mmCIF dictionary. It is designed to be machine readable. Developers who create software to read these
<em>Note:</em> For sake of speed the solvent accessibility is not calculated by default when using mmCIF output. The command-line switch
