Header list of 1tus.pdb file
Complete list - 29 20 Bytes
HEADER SERINE PROTEINASE INHIBITOR 06-JUL-94 1TUS
TITLE SOLUTION STRUCTURE OF REACTIVE-SITE HYDROLYZED TURKEY OVOMUCOID THIRD
TITLE 2 DOMAIN BY NUCLEAR MAGNETIC RESONANCE AND DISTANCE GEOMETRY METHODS
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: OVOMUCOID;
COMPND 3 CHAIN: A;
COMPND 4 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: MELEAGRIS GALLOPAVO;
SOURCE 3 ORGANISM_COMMON: TURKEY;
SOURCE 4 ORGANISM_TAXID: 9103
KEYWDS SERINE PROTEINASE INHIBITOR
EXPDTA SOLUTION NMR
NUMMDL 12
AUTHOR W.F.WALKENHORST,A.M.KREZEL,G.I.RHYU,J.L.MARKLEY
REVDAT 4 29-NOV-17 1TUS 1 REMARK HELIX
REVDAT 3 24-FEB-09 1TUS 1 VERSN
REVDAT 2 15-JAN-95 1TUS 1 SOURCE
REVDAT 1 15-OCT-94 1TUS 0
JRNL AUTH W.F.WALKENHORST,A.M.KREZEL,G.I.RHYU,J.L.MARKLEY
JRNL TITL SOLUTION STRUCTURE OF REACTIVE-SITE HYDROLYZED TURKEY
JRNL TITL 2 OVOMUCOID THIRD DOMAIN BY NUCLEAR MAGNETIC RESONANCE AND
JRNL TITL 3 DISTANCE GEOMETRY METHODS.
JRNL REF J.MOL.BIOL. V. 242 215 1994
JRNL REFN ISSN 0022-2836
JRNL PMID 8089843
JRNL DOI 10.1006/JMBI.1994.1574
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : DSPACE 4.0
REMARK 3 AUTHORS : NULL
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 1TUS COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY BNL.
REMARK 100 THE DEPOSITION ID IS D_1000176864.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : NULL
REMARK 210 PH : NULL
REMARK 210 IONIC STRENGTH : NULL
REMARK 210 PRESSURE : NULL
REMARK 210 SAMPLE CONTENTS : NULL
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : NULL
REMARK 210 SPECTROMETER FIELD STRENGTH : NULL
REMARK 210 SPECTROMETER MODEL : NULL
REMARK 210 SPECTROMETER MANUFACTURER : NULL
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NULL
REMARK 210 METHOD USED : NULL
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : NULL
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 12
REMARK 210 CONFORMERS, SELECTION CRITERIA : NULL
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : NULL
REMARK 210
REMARK 210 REMARK: NULL
REMARK 215
REMARK 215 NMR STUDY
REMARK 215 THE COORDINATES IN THIS ENTRY WERE GENERATED FROM SOLUTION
REMARK 215 NMR DATA. PROTEIN DATA BANK CONVENTIONS REQUIRE THAT
REMARK 215 CRYST1 AND SCALE RECORDS BE INCLUDED, BUT THE VALUES ON
REMARK 215 THESE RECORDS ARE MEANINGLESS.
REMARK 300
REMARK 300 BIOMOLECULE: 1
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON
REMARK 300 BURIED SURFACE AREA.
REMARK 350
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS
REMARK 350 GIVEN BELOW. BOTH NON-CRYSTALLOGRAPHIC AND
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.
REMARK 350
REMARK 350 BIOMOLECULE: 1
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: MONOMERIC
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A
REMARK 350 BIOMT1 1 1.000000 0.000000 0.000000 0.00000
REMARK 350 BIOMT2 1 0.000000 1.000000 0.000000 0.00000
REMARK 350 BIOMT3 1 0.000000 0.000000 1.000000 0.00000
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: COVALENT BOND ANGLES
REMARK 500
REMARK 500 THE STEREOCHEMICAL PARAMETERS OF THE FOLLOWING RESIDUES
REMARK 500 HAVE VALUES WHICH DEVIATE FROM EXPECTED VALUES BY MORE
REMARK 500 THAN 6*RMSD (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 500 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT: (10X,I3,1X,A3,1X,A1,I4,A1,3(1X,A4,2X),12X,F5.1)
REMARK 500
REMARK 500 EXPECTED VALUES PROTEIN: ENGH AND HUBER, 1999
REMARK 500 EXPECTED VALUES NUCLEIC ACID: CLOWNEY ET AL 1996
REMARK 500
REMARK 500 M RES CSSEQI ATM1 ATM2 ATM3
REMARK 500 3 PRO A 22 N - CA - CB ANGL. DEV. = -7.9 DEGREES
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: TORSION ANGLES
REMARK 500
REMARK 500 TORSION ANGLES OUTSIDE THE EXPECTED RAMACHANDRAN REGIONS:
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT:(10X,I3,1X,A3,1X,A1,I4,A1,4X,F7.2,3X,F7.2)
REMARK 500
REMARK 500 EXPECTED VALUES: GJ KLEYWEGT AND TA JONES (1996). PHI/PSI-
REMARK 500 CHOLOGY: RAMACHANDRAN REVISITED. STRUCTURE 4, 1395 - 1400
REMARK 500
REMARK 500 M RES CSSEQI PSI PHI
REMARK 500 1 GLU A 10 -24.44 -173.01
REMARK 500 1 THR A 17 44.24 -100.26
REMARK 500 1 SER A 26 40.57 -98.07
REMARK 500 1 THR A 47 -35.12 -169.99
REMARK 500 1 LEU A 48 -83.19 -61.47
REMARK 500 1 THR A 49 171.69 61.85
REMARK 500 1 HIS A 52 146.17 174.25
REMARK 500 2 GLU A 10 -25.56 -173.43
REMARK 500 2 THR A 17 -40.20 -158.34
REMARK 500 2 LEU A 23 -166.88 -119.46
REMARK 500 2 SER A 26 39.73 -98.38
REMARK 500 2 ASN A 28 -26.82 -176.34
REMARK 500 2 LEU A 48 -86.99 -62.14
REMARK 500 2 THR A 49 164.13 67.17
REMARK 500 2 LYS A 55 -179.00 -63.22
REMARK 500 3 ALA A 2 -79.77 -69.24
REMARK 500 3 ALA A 3 -164.49 61.69
REMARK 500 3 VAL A 4 63.69 -113.16
REMARK 500 3 SER A 9 55.69 -96.13
REMARK 500 3 GLU A 10 -23.76 -173.20
REMARK 500 3 SER A 26 34.43 -97.74
REMARK 500 3 THR A 47 -36.67 -151.77
REMARK 500 4 ALA A 3 19.95 -141.51
REMARK 500 4 SER A 9 58.56 -92.66
REMARK 500 4 GLU A 10 -24.33 -172.81
REMARK 500 4 ALA A 15 116.07 -163.59
REMARK 500 4 ARG A 21 133.77 177.36
REMARK 500 4 LEU A 23 -163.84 -121.92
REMARK 500 4 THR A 47 -87.84 -96.12
REMARK 500 4 HIS A 52 157.49 174.73
REMARK 500 4 LYS A 55 171.44 60.73
REMARK 500 5 GLU A 10 -23.75 -172.38
REMARK 500 5 ARG A 21 154.98 176.72
REMARK 500 5 SER A 26 39.13 -98.26
REMARK 500 5 LEU A 48 -82.61 -74.21
REMARK 500 5 THR A 49 161.84 61.96
REMARK 500 6 ALA A 2 -82.90 -100.47
REMARK 500 6 ALA A 3 74.20 61.58
REMARK 500 6 GLU A 10 -25.17 -173.81
REMARK 500 6 CYS A 16 139.65 64.46
REMARK 500 6 THR A 17 23.77 -172.12
REMARK 500 6 ARG A 21 134.86 177.73
REMARK 500 6 SER A 26 43.73 -98.09
REMARK 500 6 ASN A 33 -169.40 -126.17
REMARK 500 6 THR A 47 -39.89 -171.47
REMARK 500 6 LEU A 48 -83.02 -75.82
REMARK 500 6 THR A 49 163.47 59.09
REMARK 500 7 ALA A 3 74.40 -108.09
REMARK 500 7 GLU A 10 -24.81 -173.03
REMARK 500 7 ARG A 21 131.91 177.37
REMARK 500
REMARK 500 THIS ENTRY HAS 103 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: NON-CIS, NON-TRANS
REMARK 500
REMARK 500 THE FOLLOWING PEPTIDE BONDS DEVIATE SIGNIFICANTLY FROM BOTH
REMARK 500 CIS AND TRANS CONFORMATION. CIS BONDS, IF ANY, ARE LISTED
REMARK 500 ON CISPEP RECORDS. TRANS IS DEFINED AS 180 +/- 30 AND
REMARK 500 CIS IS DEFINED AS 0 +/- 30 DEGREES.
REMARK 500 MODEL OMEGA
REMARK 500 TYR A 20 ARG A 21 1 -145.82
REMARK 500 TYR A 20 ARG A 21 2 -144.67
REMARK 500 TYR A 20 ARG A 21 3 -146.96
REMARK 500 ARG A 21 PRO A 22 3 -142.68
REMARK 500 TYR A 20 ARG A 21 8 -145.53
REMARK 500 ARG A 21 PRO A 22 8 -148.93
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: PLANAR GROUPS
REMARK 500
REMARK 500 PLANAR GROUPS IN THE FOLLOWING RESIDUES HAVE A TOTAL
REMARK 500 RMS DISTANCE OF ALL ATOMS FROM THE BEST-FIT PLANE
REMARK 500 BY MORE THAN AN EXPECTED VALUE OF 6*RMSD, WITH AN
REMARK 500 RMSD 0.02 ANGSTROMS, OR AT LEAST ONE ATOM HAS
REMARK 500 AN RMSD GREATER THAN THIS VALUE
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 M RES CSSEQI RMS TYPE
REMARK 500 1 TYR A 20 0.09 SIDE CHAIN
REMARK 500 2 TYR A 20 0.08 SIDE CHAIN
REMARK 500 3 TYR A 20 0.08 SIDE CHAIN
REMARK 500 8 TYR A 20 0.09 SIDE CHAIN
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: MAIN CHAIN PLANARITY
REMARK 500
REMARK 500 THE FOLLOWING RESIDUES HAVE A PSEUDO PLANARITY
REMARK 500 TORSION ANGLE, C(I) - CA(I) - N(I+1) - O(I), GREATER
REMARK 500 10.0 DEGREES. (M=MODEL NUMBER; RES=RESIDUE NAME;
REMARK 500 C=CHAIN IDENTIFIER; SSEQ=SEQUENCE NUMBER;
REMARK 500 I=INSERTION CODE).
REMARK 500
REMARK 500 M RES CSSEQI ANGLE
REMARK 500 1 GLU A 10 -12.43
REMARK 500 1 TYR A 20 15.35
REMARK 500 1 ARG A 21 11.56
REMARK 500 1 VAL A 42 -10.83
REMARK 500 2 GLU A 10 -11.91
REMARK 500 2 TYR A 20 15.46
REMARK 500 2 VAL A 42 -10.29
REMARK 500 3 GLU A 10 -11.14
REMARK 500 3 PRO A 14 10.26
REMARK 500 3 TYR A 20 13.92
REMARK 500 3 ARG A 21 10.11
REMARK 500 3 GLY A 32 -10.10
REMARK 500 3 LYS A 55 -11.09
REMARK 500 4 GLU A 10 -10.79
REMARK 500 4 TYR A 20 -11.22
REMARK 500 4 CYS A 38 10.45
REMARK 500 5 VAL A 6 10.09
REMARK 500 5 GLU A 10 -11.16
REMARK 500 5 TYR A 20 -10.74
REMARK 500 5 ARG A 21 11.23
REMARK 500 5 LYS A 55 -11.68
REMARK 500 6 GLU A 10 -12.83
REMARK 500 6 TYR A 20 -12.13
REMARK 500 6 ASN A 33 -11.29
REMARK 500 6 VAL A 42 -11.51
REMARK 500 7 ALA A 3 11.49
REMARK 500 7 GLU A 10 -12.78
REMARK 500 7 TYR A 20 -11.60
REMARK 500 7 SER A 44 -10.48
REMARK 500 8 GLU A 10 -12.03
REMARK 500 8 TYR A 20 15.38
REMARK 500 8 VAL A 42 -10.31
REMARK 500 9 GLU A 10 -12.56
REMARK 500 9 TYR A 20 -11.95
REMARK 500 9 VAL A 42 -11.77
REMARK 500 10 CYS A 8 -11.29
REMARK 500 10 TYR A 20 -11.40
REMARK 500 10 VAL A 42 -11.64
REMARK 500 11 GLU A 10 -12.19
REMARK 500 11 TYR A 20 -11.97
REMARK 500 11 ARG A 21 10.70
REMARK 500 11 CYS A 24 11.12
REMARK 500 11 LEU A 50 -10.98
REMARK 500 12 GLU A 10 -12.76
REMARK 500 12 TYR A 20 -11.33
REMARK 500 12 THR A 47 10.59
REMARK 500
REMARK 500 REMARK: NULL
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: REA
REMARK 800 EVIDENCE_CODE: UNKNOWN
REMARK 800 SITE_DESCRIPTION: NULL
DBREF 1TUS A 1 56 UNP P68390 IOVO_MELGA 130 185
SEQRES 1 A 56 LEU ALA ALA VAL SER VAL ASP CYS SER GLU TYR PRO LYS
SEQRES 2 A 56 PRO ALA CYS THR LEU GLU TYR ARG PRO LEU CYS GLY SER
SEQRES 3 A 56 ASP ASN LYS THR TYR GLY ASN LYS CYS ASN PHE CYS ASN
SEQRES 4 A 56 ALA VAL VAL GLU SER ASN GLY THR LEU THR LEU SER HIS
SEQRES 5 A 56 PHE GLY LYS CYS
HELIX 1 AHE ASN A 33 SER A 44 1 12
SHEET 1 BSH 3 ASN A 28 GLY A 32 0
SHEET 2 BSH 3 ARG A 21 SER A 26 -1
SHEET 3 BSH 3 THR A 49 GLY A 54 -1
SSBOND 1 CYS A 8 CYS A 38 1555 1555 2.03
SSBOND 2 CYS A 16 CYS A 35 1555 1555 2.03
SSBOND 3 CYS A 24 CYS A 56 1555 1555 2.03
CISPEP 1 TYR A 11 PRO A 12 1 10.69
CISPEP 2 TYR A 11 PRO A 12 2 4.58
CISPEP 3 TYR A 11 PRO A 12 3 -0.17
CISPEP 4 TYR A 11 PRO A 12 4 5.39
CISPEP 5 TYR A 11 PRO A 12 5 1.11
CISPEP 6 TYR A 11 PRO A 12 6 1.05
CISPEP 7 TYR A 11 PRO A 12 7 9.81
CISPEP 8 TYR A 11 PRO A 12 8 0.08
CISPEP 9 TYR A 11 PRO A 12 9 8.87
CISPEP 10 TYR A 11 PRO A 12 10 -7.15
CISPEP 11 TYR A 11 PRO A 12 11 3.93
CISPEP 12 TYR A 11 PRO A 12 12 6.02
SITE 1 REA 2 LEU A 18 GLU A 19
CRYST1 1.000 1.000 1.000 90.00 90.00 90.00 P 1 1
ORIGX1 1.000000 0.000000 0.000000 0.00000
ORIGX2 0.000000 1.000000 0.000000 0.00000
ORIGX3 0.000000 0.000000 1.000000 0.00000
SCALE1 1.000000 0.000000 0.000000 0.00000
SCALE2 0.000000 1.000000 0.000000 0.00000
SCALE3 0.000000 0.000000 1.000000 0.00000
MODEL 1
Complete list - 29 20 Bytes