Header list of 1fjc.pdb file
Complete list - b 23 2 Bytes
HEADER STRUCTURAL PROTEIN 07-AUG-00 1FJC
TITLE SOLUTION STRUCTURE OF NUCLEOLIN RBD2
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: NUCLEOLIN RBD2;
COMPND 3 CHAIN: A;
COMPND 4 SYNONYM: PROTEIN C23;
COMPND 5 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: MESOCRICETUS AURATUS;
SOURCE 3 ORGANISM_COMMON: GOLDEN HAMSTER;
SOURCE 4 ORGANISM_TAXID: 10036;
SOURCE 5 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE 6 EXPRESSION_SYSTEM_TAXID: 562;
SOURCE 7 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 8 EXPRESSION_SYSTEM_PLASMID: BL21(DE3)
KEYWDS RNP, RBD, RRM, RNA BINDING DOMAIN, NUCLEOLUS, STRUCTURAL PROTEIN
EXPDTA SOLUTION NMR
NUMMDL 33
AUTHOR F.H.-T.ALLAIN,D.E.GILBERT,P.BOUVET,J.FEIGON
REVDAT 4 23-FEB-22 1FJC 1 REMARK SEQADV
REVDAT 3 24-FEB-09 1FJC 1 VERSN
REVDAT 2 01-APR-03 1FJC 1 JRNL
REVDAT 1 16-OCT-00 1FJC 0
JRNL AUTH F.H.ALLAIN,D.E.GILBERT,P.BOUVET,J.FEIGON
JRNL TITL SOLUTION STRUCTURE OF THE TWO N-TERMINAL RNA-BINDING DOMAINS
JRNL TITL 2 OF NUCLEOLIN AND NMR STUDY OF THE INTERACTION WITH ITS RNA
JRNL TITL 3 TARGET.
JRNL REF J.MOL.BIOL. V. 303 227 2000
JRNL REFN ISSN 0022-2836
JRNL PMID 11023788
JRNL DOI 10.1006/JMBI.2000.4118
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : X-PLOR 3.841
REMARK 3 AUTHORS : BRUNGER
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: STRUCTURES ARE BASED ON 1279
REMARK 3 RESTRAINTS, 1209 ARE NOE-DERIVED AND 70 ARE FROM HYDROGEN BONDS
REMARK 4
REMARK 4 1FJC COMPLIES WITH FORMAT V. 3.15, 01-DEC-08
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 14-AUG-00.
REMARK 100 THE DEPOSITION ID IS D_1000011636.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 293; 293
REMARK 210 PH : 6.2; 6.2
REMARK 210 IONIC STRENGTH : 150; 150
REMARK 210 PRESSURE : AMBIENT; AMBIENT
REMARK 210 SAMPLE CONTENTS : 1MM U-15N,13C; 50MM POTASSIUM
REMARK 210 PHOSPHATE BUFFER; 100 MM KCL,
REMARK 210 5MM DEUTERATED DTT, PH 6.2; 1MM
REMARK 210 U-15N,13C; 50MM POTASSIUM
REMARK 210 PHOSPHATE BUFFER; 100 MM KCL,
REMARK 210 5MM DEUTERATED DTT, PH 6.2
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 3D_13C-SEPARATED_NOESY; 3D_15N
REMARK 210 -SEPARATED_NOESY; 2D NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 600 MHZ; 500 MHZ
REMARK 210 SPECTROMETER MODEL : DRX
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : X-PLOR 3.841, DYANA 1
REMARK 210 METHOD USED : SIMULATED ANNEALING USING XPLOR
REMARK 210 3.841
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 50
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 33
REMARK 210 CONFORMERS, SELECTION CRITERIA : ALL CALCULATED STRUCTURES
REMARK 210 SUBMITTED
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 1
REMARK 210
REMARK 210 REMARK: THE STRUCTURE WAS DETERMINED USING TRIPLE-RESONANCE NMR
REMARK 210 SPECTROSCOPY
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 H LEU A 20 O TYR A 86 1.44
REMARK 500 O ILE A 78 H ARG A 81 1.46
REMARK 500 H ALA A 21 O ALA A 56 1.47
REMARK 500 H ARG A 44 O TYR A 57 1.48
REMARK 500 O LEU A 20 H TYR A 86 1.49
REMARK 500 H LEU A 19 O ILE A 58 1.50
REMARK 500 O LYS A 22 H SER A 84 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 MET A 3 175.39 52.10
REMARK 500 1 GLU A 5 96.79 -177.71
REMARK 500 1 ASP A 6 62.44 -179.51
REMARK 500 1 LEU A 24 -144.05 -67.89
REMARK 500 1 GLU A 38 27.45 40.40
REMARK 500 1 ASP A 39 14.46 -151.98
REMARK 500 1 LYS A 51 118.95 -171.03
REMARK 500 1 SER A 52 127.83 -37.64
REMARK 500 1 GLN A 74 86.07 39.63
REMARK 500 1 ALA A 76 15.87 57.84
REMARK 500 1 GLU A 77 90.60 32.20
REMARK 500 1 TYR A 87 -171.34 -52.02
REMARK 500 1 THR A 88 34.89 -173.22
REMARK 500 1 GLU A 90 29.92 -179.11
REMARK 500 1 LYS A 91 -65.77 -134.34
REMARK 500 1 ARG A 95 109.02 -39.82
REMARK 500 2 HIS A 2 -40.08 -159.31
REMARK 500 2 LEU A 4 140.39 -174.97
REMARK 500 2 GLU A 5 80.48 -176.99
REMARK 500 2 ASP A 6 101.73 56.10
REMARK 500 2 THR A 9 -73.25 -173.12
REMARK 500 2 ASN A 23 17.61 55.45
REMARK 500 2 LEU A 24 -156.82 -70.66
REMARK 500 2 ILE A 28 161.90 -42.26
REMARK 500 2 GLU A 38 30.51 38.28
REMARK 500 2 ASP A 39 -35.99 -152.94
REMARK 500 2 ALA A 40 -168.54 -62.66
REMARK 500 2 SER A 47 -147.04 -123.65
REMARK 500 2 GLN A 48 -145.33 -105.09
REMARK 500 2 LYS A 51 117.55 -163.04
REMARK 500 2 SER A 52 130.43 -38.29
REMARK 500 2 GLN A 74 91.58 -37.95
REMARK 500 2 ALA A 76 93.99 37.22
REMARK 500 2 GLU A 77 88.50 -56.71
REMARK 500 2 TYR A 87 -170.37 -52.31
REMARK 500 2 THR A 88 35.26 179.56
REMARK 500 2 GLU A 90 -135.91 -155.94
REMARK 500 2 THR A 94 26.65 -149.75
REMARK 500 2 ARG A 95 -161.34 45.47
REMARK 500 3 HIS A 2 -58.38 -147.10
REMARK 500 3 MET A 3 -156.44 -157.02
REMARK 500 3 GLU A 5 -95.98 42.38
REMARK 500 3 SER A 10 49.89 -77.31
REMARK 500 3 LEU A 24 -160.80 -57.03
REMARK 500 3 ILE A 28 170.24 -46.66
REMARK 500 3 PHE A 37 47.93 -101.74
REMARK 500 3 SER A 47 -151.20 -125.24
REMARK 500 3 GLN A 48 -155.60 -98.98
REMARK 500 3 LYS A 51 119.51 -176.27
REMARK 500 3 SER A 52 131.93 -37.20
REMARK 500
REMARK 500 THIS ENTRY HAS 586 RAMACHANDRAN OUTLIERS.
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 ARG A 14 0.23 SIDE CHAIN
REMARK 500 1 ARG A 17 0.24 SIDE CHAIN
REMARK 500 1 ARG A 44 0.08 SIDE CHAIN
REMARK 500 1 ARG A 81 0.12 SIDE CHAIN
REMARK 500 1 ARG A 95 0.24 SIDE CHAIN
REMARK 500 2 ARG A 14 0.32 SIDE CHAIN
REMARK 500 2 ARG A 17 0.27 SIDE CHAIN
REMARK 500 2 ARG A 44 0.25 SIDE CHAIN
REMARK 500 2 ARG A 81 0.29 SIDE CHAIN
REMARK 500 2 ARG A 95 0.22 SIDE CHAIN
REMARK 500 3 ARG A 14 0.31 SIDE CHAIN
REMARK 500 3 ARG A 17 0.17 SIDE CHAIN
REMARK 500 3 ARG A 44 0.27 SIDE CHAIN
REMARK 500 3 ARG A 81 0.30 SIDE CHAIN
REMARK 500 3 ARG A 95 0.14 SIDE CHAIN
REMARK 500 4 ARG A 14 0.16 SIDE CHAIN
REMARK 500 4 ARG A 17 0.19 SIDE CHAIN
REMARK 500 4 ARG A 44 0.32 SIDE CHAIN
REMARK 500 4 ARG A 81 0.16 SIDE CHAIN
REMARK 500 4 ARG A 95 0.15 SIDE CHAIN
REMARK 500 5 ARG A 14 0.25 SIDE CHAIN
REMARK 500 5 ARG A 17 0.18 SIDE CHAIN
REMARK 500 5 ARG A 44 0.30 SIDE CHAIN
REMARK 500 5 ARG A 81 0.23 SIDE CHAIN
REMARK 500 5 ARG A 95 0.31 SIDE CHAIN
REMARK 500 6 ARG A 14 0.21 SIDE CHAIN
REMARK 500 6 ARG A 17 0.22 SIDE CHAIN
REMARK 500 6 ARG A 44 0.31 SIDE CHAIN
REMARK 500 6 ARG A 95 0.23 SIDE CHAIN
REMARK 500 7 ARG A 14 0.15 SIDE CHAIN
REMARK 500 7 ARG A 17 0.32 SIDE CHAIN
REMARK 500 7 ARG A 44 0.19 SIDE CHAIN
REMARK 500 7 ARG A 81 0.22 SIDE CHAIN
REMARK 500 7 ARG A 95 0.31 SIDE CHAIN
REMARK 500 8 ARG A 14 0.30 SIDE CHAIN
REMARK 500 8 ARG A 17 0.09 SIDE CHAIN
REMARK 500 8 ARG A 44 0.29 SIDE CHAIN
REMARK 500 8 ARG A 81 0.27 SIDE CHAIN
REMARK 500 8 ARG A 95 0.29 SIDE CHAIN
REMARK 500 9 ARG A 14 0.31 SIDE CHAIN
REMARK 500 9 ARG A 17 0.19 SIDE CHAIN
REMARK 500 9 ARG A 44 0.24 SIDE CHAIN
REMARK 500 9 ARG A 81 0.32 SIDE CHAIN
REMARK 500 9 ARG A 95 0.30 SIDE CHAIN
REMARK 500 10 ARG A 14 0.28 SIDE CHAIN
REMARK 500 10 ARG A 44 0.20 SIDE CHAIN
REMARK 500 10 ARG A 81 0.21 SIDE CHAIN
REMARK 500 10 ARG A 95 0.32 SIDE CHAIN
REMARK 500 11 ARG A 14 0.28 SIDE CHAIN
REMARK 500 11 ARG A 17 0.29 SIDE CHAIN
REMARK 500
REMARK 500 THIS ENTRY HAS 158 PLANE DEVIATIONS.
REMARK 500
REMARK 500 REMARK: NULL
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1FJ7 RELATED DB: PDB
REMARK 900 SOLUTION STRUCTURE OF NUCLEOLIN RBD1
DBREF 1FJC A 1 96 UNP P08199 NUCL_MESAU 378 473
SEQADV 1FJC SER A 1 UNP P08199 LYS 378 CONFLICT
SEQADV 1FJC HIS A 2 UNP P08199 LEU 379 CONFLICT
SEQADV 1FJC MET A 3 UNP P08199 GLU 380 CONFLICT
SEQADV 1FJC LEU A 4 UNP P08199 LYS 381 CONFLICT
SEQADV 1FJC GLU A 5 UNP P08199 PRO 382 CONFLICT
SEQADV 1FJC ASP A 6 UNP P08199 LYS 383 CONFLICT
SEQADV 1FJC PRO A 7 UNP P08199 GLY 384 CONFLICT
SEQADV 1FJC CYS A 8 UNP P08199 ARG 385 CONFLICT
SEQADV 1FJC THR A 9 UNP P08199 ASP 386 CONFLICT
SEQADV 1FJC GLY A 93 UNP P08199 GLN 470 CONFLICT
SEQADV 1FJC THR A 94 UNP P08199 ARG 471 CONFLICT
SEQADV 1FJC ARG A 95 UNP P08199 GLN 472 CONFLICT
SEQADV 1FJC GLY A 96 UNP P08199 GLU 473 CONFLICT
SEQRES 1 A 96 SER HIS MET LEU GLU ASP PRO CYS THR SER LYS LYS VAL
SEQRES 2 A 96 ARG ALA ALA ARG THR LEU LEU ALA LYS ASN LEU SER PHE
SEQRES 3 A 96 ASN ILE THR GLU ASP GLU LEU LYS GLU VAL PHE GLU ASP
SEQRES 4 A 96 ALA LEU GLU ILE ARG LEU VAL SER GLN ASP GLY LYS SER
SEQRES 5 A 96 LYS GLY ILE ALA TYR ILE GLU PHE LYS SER GLU ALA ASP
SEQRES 6 A 96 ALA GLU LYS ASN LEU GLU GLU LYS GLN GLY ALA GLU ILE
SEQRES 7 A 96 ASP GLY ARG SER VAL SER LEU TYR TYR THR GLY GLU LYS
SEQRES 8 A 96 GLY GLY THR ARG GLY
HELIX 1 1 ARG A 14 ALA A 16 5 3
HELIX 2 2 THR A 29 GLU A 38 1 10
HELIX 3 3 SER A 62 LYS A 73 1 12
SHEET 1 A 5 GLY A 75 ILE A 78 0
SHEET 2 A 5 ARG A 81 TYR A 87 -1 N ARG A 81 O ILE A 78
SHEET 3 A 5 THR A 18 LYS A 22 -1 N LEU A 20 O TYR A 86
SHEET 4 A 5 LYS A 51 PHE A 60 -1 O ALA A 56 N ALA A 21
SHEET 5 A 5 ALA A 40 ILE A 43 -1 N LEU A 41 O GLU A 59
SHEET 1 B 5 GLY A 75 ILE A 78 0
SHEET 2 B 5 ARG A 81 TYR A 87 -1 N ARG A 81 O ILE A 78
SHEET 3 B 5 THR A 18 LYS A 22 -1 N LEU A 20 O TYR A 86
SHEET 4 B 5 LYS A 51 PHE A 60 -1 O ALA A 56 N ALA A 21
SHEET 5 B 5 VAL A 46 GLN A 48 -1 N VAL A 46 O ILE A 55
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