Header list of 1k45.pdb file
Complete list - 23 20 Bytes
HEADER HYDROLASE 05-OCT-01 1K45
TITLE THE SOLUTION STRUCTURE OF THE CBM4-2 CARBOHYDRATE BINDING MODULE FROM
TITLE 2 A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE.
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: XYLANASE;
COMPND 3 CHAIN: A;
COMPND 4 FRAGMENT: SECOND FAMILY 4 CARBOHYDRATE BINDING MODULE (CBM4-2)
COMPND 5 (RESIDUES 211-373);
COMPND 6 EC: 3.2.1.8;
COMPND 7 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: RHODOTHERMUS MARINUS;
SOURCE 3 ORGANISM_TAXID: 29549;
SOURCE 4 GENE: XYN10A;
SOURCE 5 EXPRESSION_SYSTEM: ESCHERICHIA COLI BL21(DE3);
SOURCE 6 EXPRESSION_SYSTEM_TAXID: 469008;
SOURCE 7 EXPRESSION_SYSTEM_STRAIN: BL21(DE3);
SOURCE 8 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 9 EXPRESSION_SYSTEM_PLASMID: PET-25B(+)
KEYWDS BETA-SANDWICH FORMED BY 11 STRANDS. BINDING-SITE CLEFT. SOLVENT
KEYWDS 2 EXPOSED AROMATICS (TRP69, PHE110) IN BINDING CLEFT. TWO HELICAL
KEYWDS 3 TWISTS. TWO CALCIUM BINDING SITES., HYDROLASE
EXPDTA SOLUTION NMR
MDLTYP MINIMIZED AVERAGE
AUTHOR P.J.SIMPSON,S.J.JAMIESON,M.ABOU-HACHEM,E.NORDBERG-KARLSSON,
AUTHOR 2 H.J.GILBERT,O.HOLST,M.P.WILLIAMSON
REVDAT 5 23-FEB-22 1K45 1 REMARK SEQADV
REVDAT 4 24-FEB-09 1K45 1 VERSN
REVDAT 3 01-APR-03 1K45 1 JRNL
REVDAT 2 19-JUN-02 1K45 1 JRNL
REVDAT 1 29-MAY-02 1K45 0
JRNL AUTH P.J.SIMPSON,S.J.JAMIESON,M.ABOU-HACHEM,E.N.KARLSSON,
JRNL AUTH 2 H.J.GILBERT,O.HOLST,M.P.WILLIAMSON
JRNL TITL THE SOLUTION STRUCTURE OF THE CBM4-2 CARBOHYDRATE BINDING
JRNL TITL 2 MODULE FROM A THERMOSTABLE RHODOTHERMUS MARINUS XYLANASE.
JRNL REF BIOCHEMISTRY V. 41 5712 2002
JRNL REFN ISSN 0006-2960
JRNL PMID 11980475
JRNL DOI 10.1021/BI012093I
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : FELIX 2000, X-PLOR 3.1
REMARK 3 AUTHORS : MOLECULAR SIMULATIONS INC. (FELIX), AXEL T.
REMARK 3 BRUNGER (X-PLOR)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: THE FINAL SET OF RESTRAINTS CONTAINED
REMARK 3 1654 NON-REDUNDANT UNAMBIGUOUS NOES AND 17 AMBIGUOUS NOES, 93
REMARK 3 DIHEDRAL ANGLE RESTRAINTS, 72 CHI1 AND 1 CHI2 RESTRAINT, AND 65
REMARK 3 PAIRS OF HYDROGEN BOND RESTRAINTS, PLUS 177 BACKBONE DIHEDRAL
REMARK 3 RESTRAINTS BASED ON 13C SHIFTS FROM TALOS.
REMARK 4
REMARK 4 1K45 COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 17-OCT-01.
REMARK 100 THE DEPOSITION ID IS D_1000014537.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 310
REMARK 210 PH : 6.0
REMARK 210 IONIC STRENGTH : 0.2 M
REMARK 210 PRESSURE : AMBIENT
REMARK 210 SAMPLE CONTENTS : 1.5 MM CBM4-2 15N-LABELLED, AND
REMARK 210 13C,15N DOUBLE LABELLED PROTEIN;
REMARK 210 50 MM CACL2, 50 MM SODIUM
REMARK 210 ACETATE-D3, PH 6.0, 10% D2O, 10
REMARK 210 MM SODIUM AZIDE, 0.1 MM SODIUM
REMARK 210 TRIMETHYLSILYLPROPIONATE (TSP)
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_13C-SEPARATED_NOESY; 3D_15N
REMARK 210 -SEPARATED_NOESY; HNHA
REMARK 210 SPECTROMETER FIELD STRENGTH : 500 MHZ; 600 MHZ
REMARK 210 SPECTROMETER MODEL : DRX
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : X-PLOR 3.1
REMARK 210 METHOD USED : HYBRID DISTANCE
REMARK 210 GEOMETRY/SIMULATED ANNEALING
REMARK 210 USING XPLOR
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : NULL
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 1
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: 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 LEU A 2 -171.39 -66.79
REMARK 500 ALA A 15 169.21 -43.45
REMARK 500 VAL A 36 93.11 -66.32
REMARK 500 ASN A 54 23.33 -159.12
REMARK 500 ASN A 62 61.58 -160.08
REMARK 500 PHE A 76 169.32 175.84
REMARK 500 TYR A 113 -69.87 -107.97
REMARK 500 GLU A 118 57.12 77.36
REMARK 500 GLU A 124 -169.06 -112.60
REMARK 500 PHE A 130 -174.71 -170.43
REMARK 500 VAL A 134 110.39 -38.63
REMARK 500 ASP A 136 -95.30 -103.12
REMARK 500 GLN A 137 52.96 -157.14
REMARK 500 ASP A 160 136.64 -173.71
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 ARG A 81 0.14 SIDE CHAIN
REMARK 500 ARG A 93 0.20 SIDE CHAIN
REMARK 500 ARG A 115 0.31 SIDE CHAIN
REMARK 500 ARG A 142 0.23 SIDE CHAIN
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1K42 RELATED DB: PDB
REMARK 900 1K42 CONTAINS THE NMR ENSEMBLE STRUCTURE FOR THIS PROTEIN
DBREF 1K45 A 2 164 UNP P96988 P96988_RHOMR 211 373
SEQADV 1K45 MET A 1 UNP P96988 INITIATING METHIONINE
SEQADV 1K45 ALA A 165 UNP P96988 CLONING ARTIFACT
SEQADV 1K45 SER A 166 UNP P96988 CLONING ARTIFACT
SEQADV 1K45 GLN A 167 UNP P96988 CLONING ARTIFACT
SEQADV 1K45 PRO A 168 UNP P96988 CLONING ARTIFACT
SEQRES 1 A 168 MET LEU VAL ALA ASN ILE ASN GLY GLY PHE GLU SER THR
SEQRES 2 A 168 PRO ALA GLY VAL VAL THR ASP LEU ALA GLU GLY VAL GLU
SEQRES 3 A 168 GLY TRP ASP LEU ASN VAL GLY SER SER VAL THR ASN PRO
SEQRES 4 A 168 PRO VAL PHE GLU VAL LEU GLU THR SER ASP ALA PRO GLU
SEQRES 5 A 168 GLY ASN LYS VAL LEU ALA VAL THR VAL ASN GLY VAL GLY
SEQRES 6 A 168 ASN ASN PRO TRP ASP ILE GLU ALA THR ALA PHE PRO VAL
SEQRES 7 A 168 ASN VAL ARG PRO GLY VAL THR TYR THR TYR THR ILE TRP
SEQRES 8 A 168 ALA ARG ALA GLU GLN ASP GLY ALA VAL VAL SER PHE THR
SEQRES 9 A 168 VAL GLY ASN GLN SER PHE GLN GLU TYR GLY ARG LEU HIS
SEQRES 10 A 168 GLU GLN GLN ILE THR THR GLU TRP GLN PRO PHE THR PHE
SEQRES 11 A 168 GLU PHE THR VAL SER ASP GLN GLU THR VAL ILE ARG ALA
SEQRES 12 A 168 PRO ILE HIS PHE GLY TYR ALA ALA ASN VAL GLY ASN THR
SEQRES 13 A 168 ILE TYR ILE ASP GLY LEU ALA ILE ALA SER GLN PRO
HELIX 1 1 ASP A 20 GLY A 24 5 5
HELIX 2 2 TYR A 149 VAL A 153 5 5
SHEET 1 A 6 GLY A 16 VAL A 17 0
SHEET 2 A 6 VAL A 41 GLU A 46 -1 O VAL A 44 N GLY A 16
SHEET 3 A 6 LYS A 55 VAL A 61 -1 O VAL A 56 N LEU A 45
SHEET 4 A 6 ASN A 155 ILE A 164 -1 O ILE A 159 N LEU A 57
SHEET 5 A 6 THR A 85 ALA A 94 -1 N THR A 89 O ALA A 163
SHEET 6 A 6 GLN A 126 THR A 133 -1 O PHE A 128 N ILE A 90
SHEET 1 B 5 TRP A 28 VAL A 32 0
SHEET 2 B 5 ILE A 71 ASN A 79 -1 O THR A 74 N ASP A 29
SHEET 3 B 5 VAL A 140 PHE A 147 -1 O ILE A 145 N ALA A 73
SHEET 4 B 5 ALA A 99 THR A 104 -1 N SER A 102 O HIS A 146
SHEET 5 B 5 ARG A 115 ILE A 121 -1 O LEU A 116 N PHE A 103
CISPEP 1 PHE A 76 PRO A 77 0 -0.31
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
Complete list - 23 20 Bytes