Header list of 1nku.pdb file
Complete list - b 23 2 Bytes
HEADER HYDROLASE 03-JAN-03 1NKU
TITLE NMR SOLUTION STRUCTURE OF ZINC-BINDING PROTEIN 3-METHYLADENINE DNA
TITLE 2 GLYCOSYLASE I (TAG)
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: 3-METHYLADENINE DNA GLYCOSYLASE I (TAG);
COMPND 3 CHAIN: A;
COMPND 4 EC: 3.2.2.20;
COMPND 5 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: ESCHERICHIA COLI;
SOURCE 3 ORGANISM_TAXID: 562;
SOURCE 4 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE 5 EXPRESSION_SYSTEM_TAXID: 562
KEYWDS HYDROLASE
EXPDTA SOLUTION NMR
NUMMDL 25
AUTHOR K.KWON,C.CAO,J.T.STIVERS
REVDAT 3 23-FEB-22 1NKU 1 REMARK LINK
REVDAT 2 24-FEB-09 1NKU 1 VERSN
REVDAT 1 03-JUN-03 1NKU 0
JRNL AUTH K.KWON,C.CAO,J.T.STIVERS
JRNL TITL A NOVEL ZINC SNAP MOTIF CONVEYS STRUCTURAL STABILITY TO
JRNL TITL 2 3-METHYLADENINE DNA GLYCOSYLASE I
JRNL REF J.BIOL.CHEM. V. 278 19442 2003
JRNL REFN ISSN 0021-9258
JRNL PMID 12654914
JRNL DOI 10.1074/JBC.M300934200
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : CNS 1.1, X-PLOR NIH 2.2
REMARK 3 AUTHORS : BRUNGER,ADAMS,CLORE,DELANO,GROS,GROSSE
REMARK 3 -KUNSTLEVE,JIANG,KUSZEWSKI,NILGES, PANNU,READ,RICE,
REMARK 3 SIMONSON,WARREN (CNS), G.M CLORE (X-PLOR)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 1NKU COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 13-JAN-03.
REMARK 100 THE DEPOSITION ID IS D_1000017959.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 293
REMARK 210 PH : 6.6
REMARK 210 IONIC STRENGTH : NULL
REMARK 210 PRESSURE : AMBIENT
REMARK 210 SAMPLE CONTENTS : 0.5-1MM 3-METHYLADENINE DNA
REMARK 210 GLYCOSYLASE I (TAG), 10MM
REMARK 210 PHOSPHATE BUFFER, PH 6.6, 100MM
REMARK 210 NACL, 3MM DTT, 0.34 MM NAN3
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_13C-SEPARATED_NOESY; 3D_15N
REMARK 210 -SEPARATED_NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 500 MHZ; 600 MHZ; 750 MHZ
REMARK 210 SPECTROMETER MODEL : DMX; UNITYPLUS
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER; VARIAN
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NULL
REMARK 210 METHOD USED : TORSION ANGLE DYNAMICS
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 100
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 25
REMARK 210 CONFORMERS, SELECTION CRITERIA : STRUCTURES WITH ACCEPTABLE
REMARK 210 COVALENT GEOMETRY, STRUCTURES
REMARK 210 WITH FAVORABLE NON-BOND ENERGY,
REMARK 210 STRUCTURES WITH THE LEAST
REMARK 210 RESTRAINT VIOLATIONS, STRUCTURES
REMARK 210 WITH THE LOWEST ENERGY
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 17
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: CLOSE CONTACTS
REMARK 500
REMARK 500 THE FOLLOWING ATOMS ARE IN CLOSE CONTACT.
REMARK 500
REMARK 500 ATM1 RES C SSEQI ATM2 RES C SSEQI DISTANCE
REMARK 500 O CYS A 179 H CYS A 181 1.53
REMARK 500 O LYS A 52 H TYR A 56 1.59
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 GLN A 9 -139.71 -168.05
REMARK 500 1 ASP A 10 89.44 46.14
REMARK 500 1 GLU A 20 -114.49 -157.14
REMARK 500 1 TRP A 21 100.58 49.62
REMARK 500 1 ASP A 64 172.13 68.85
REMARK 500 1 HIS A 88 90.44 -179.92
REMARK 500 1 HIS A 122 13.55 44.54
REMARK 500 1 VAL A 176 -163.09 38.19
REMARK 500 1 CYS A 180 -63.75 62.17
REMARK 500 1 ASN A 185 27.64 -173.35
REMARK 500 2 SER A 8 119.82 -169.57
REMARK 500 2 GLN A 9 -152.27 38.69
REMARK 500 2 ASP A 10 74.66 44.75
REMARK 500 2 ASN A 19 -73.69 -80.16
REMARK 500 2 TRP A 21 99.10 -175.74
REMARK 500 2 PHE A 63 18.24 -54.72
REMARK 500 2 MET A 71 171.39 -52.39
REMARK 500 2 ILE A 86 91.96 -59.87
REMARK 500 2 HIS A 88 34.06 -148.25
REMARK 500 2 ARG A 89 -65.70 59.20
REMARK 500 2 HIS A 175 -117.76 -133.38
REMARK 500 3 ASN A 19 -71.23 -72.26
REMARK 500 3 TRP A 21 103.24 -175.32
REMARK 500 3 ALA A 42 109.89 -47.72
REMARK 500 3 LEU A 44 -165.38 -77.94
REMARK 500 3 PHE A 63 68.24 -101.37
REMARK 500 3 ASP A 64 162.25 -36.11
REMARK 500 3 ALA A 83 82.50 164.09
REMARK 500 3 ILE A 85 -147.08 -58.14
REMARK 500 3 HIS A 88 101.54 -178.34
REMARK 500 3 HIS A 122 11.82 51.97
REMARK 500 3 HIS A 175 -119.49 123.67
REMARK 500 3 CYS A 179 61.25 -69.90
REMARK 500 3 CYS A 180 -87.64 34.31
REMARK 500 3 PRO A 183 -102.34 -82.26
REMARK 500 4 TRP A 6 16.01 44.42
REMARK 500 4 GLN A 9 69.20 -175.40
REMARK 500 4 GLU A 20 -124.58 -153.78
REMARK 500 4 TRP A 21 93.43 57.56
REMARK 500 4 LEU A 44 -141.25 -111.23
REMARK 500 4 ASP A 64 148.33 62.80
REMARK 500 4 ALA A 83 -31.29 92.29
REMARK 500 4 HIS A 88 14.77 -164.25
REMARK 500 4 ARG A 89 -70.43 53.30
REMARK 500 4 HIS A 122 18.28 42.95
REMARK 500 4 THR A 137 -2.03 52.24
REMARK 500 4 HIS A 175 -67.45 -122.52
REMARK 500 4 VAL A 176 -89.89 -159.57
REMARK 500 4 VAL A 177 -35.36 -150.52
REMARK 500 4 CYS A 179 79.71 -64.74
REMARK 500
REMARK 500 THIS ENTRY HAS 343 RAMACHANDRAN OUTLIERS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 620
REMARK 620 METAL COORDINATION
REMARK 620 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 620 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE):
REMARK 620
REMARK 620 COORDINATION ANGLES FOR: M RES CSSEQI METAL
REMARK 620 ZN A 188 ZN
REMARK 620 N RES CSSEQI ATOM
REMARK 620 1 CYS A 4 SG
REMARK 620 2 HIS A 17 NE2 106.8
REMARK 620 3 HIS A 175 ND1 113.3 108.5
REMARK 620 4 CYS A 179 SG 107.4 111.3 109.5
REMARK 620 N 1 2 3
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: AC1
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE ZN A 188
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1LMZ RELATED DB: PDB
REMARK 900 THE SOLUTION STRUCTURE OF TAG WITHOUT ZINC
DBREF 1NKU A 1 187 UNP P05100 3MG1_ECOLI 1 187
SEQRES 1 A 187 MET GLU ARG CYS GLY TRP VAL SER GLN ASP PRO LEU TYR
SEQRES 2 A 187 ILE ALA TYR HIS ASP ASN GLU TRP GLY VAL PRO GLU THR
SEQRES 3 A 187 ASP SER LYS LYS LEU PHE GLU MET ILE CYS LEU GLU GLY
SEQRES 4 A 187 GLN GLN ALA GLY LEU SER TRP ILE THR VAL LEU LYS LYS
SEQRES 5 A 187 ARG GLU ASN TYR ARG ALA CYS PHE HIS GLN PHE ASP PRO
SEQRES 6 A 187 VAL LYS VAL ALA ALA MET GLN GLU GLU ASP VAL GLU ARG
SEQRES 7 A 187 LEU VAL GLN ASP ALA GLY ILE ILE ARG HIS ARG GLY LYS
SEQRES 8 A 187 ILE GLN ALA ILE ILE GLY ASN ALA ARG ALA TYR LEU GLN
SEQRES 9 A 187 MET GLU GLN ASN GLY GLU PRO PHE ALA ASP PHE VAL TRP
SEQRES 10 A 187 SER PHE VAL ASN HIS GLN PRO GLN MET THR GLN ALA THR
SEQRES 11 A 187 THR LEU SER GLU ILE PRO THR SER THR PRO ALA SER ASP
SEQRES 12 A 187 ALA LEU SER LYS ALA LEU LYS LYS ARG GLY PHE LYS PHE
SEQRES 13 A 187 VAL GLY THR THR ILE CYS TYR SER PHE MET GLN ALA CYS
SEQRES 14 A 187 GLY LEU VAL ASN ASP HIS VAL VAL GLY CYS CYS CYS TYR
SEQRES 15 A 187 PRO GLY ASN LYS PRO
HET ZN A 188 1
HETNAM ZN ZINC ION
FORMUL 2 ZN ZN 2+
HELIX 1 1 ASP A 10 GLU A 20 1 11
HELIX 2 2 ASP A 27 ALA A 42 1 16
HELIX 3 3 SER A 45 HIS A 61 1 17
HELIX 4 4 ASP A 64 ALA A 70 1 7
HELIX 5 5 GLN A 72 GLN A 81 1 10
HELIX 6 6 HIS A 88 ASN A 108 1 21
HELIX 7 7 PRO A 111 VAL A 120 1 10
HELIX 8 8 THR A 131 ILE A 135 5 5
HELIX 9 9 THR A 139 GLY A 153 1 15
HELIX 10 10 GLY A 158 GLY A 170 1 13
SHEET 1 A 2 GLN A 125 MET A 126 0
SHEET 2 A 2 VAL A 172 ASN A 173 1 O ASN A 173 N GLN A 125
LINK SG CYS A 4 ZN ZN A 188 1555 1555 2.30
LINK NE2 HIS A 17 ZN ZN A 188 1555 1555 2.01
LINK ND1 HIS A 175 ZN ZN A 188 1555 1555 2.00
LINK SG CYS A 179 ZN ZN A 188 1555 1555 2.30
SITE 1 AC1 5 CYS A 4 HIS A 17 TRP A 21 HIS A 175
SITE 2 AC1 5 CYS A 179
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 - b 23 2 Bytes