HEADER ELECTRON TRANSPORT 10-FEB-98 1NEW
TITLE CYTOCHROME C551.5, NMR
CAVEAT 1NEW CHIRALITY ERROR AT CA ATOM OF ALA 1
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: CYTOCHROME C551.5;
COMPND 3 CHAIN: A;
COMPND 4 SYNONYM: CYTOCHROME C7, TRIHEME CYTOCHROME;
COMPND 5 OTHER_DETAILS: CLASS III OF C-TYPE CYTOCHROMES, FULLY OXIDIZED FORM
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: DESULFUROMONAS ACETOXIDANS;
SOURCE 3 ORGANISM_TAXID: 891
KEYWDS ELECTRON TRANSPORT, CYTOCHROME, MULTIHEME CYTOCHROME, CYTOCHROME C7
EXPDTA SOLUTION NMR
NUMMDL 35
AUTHOR M.ASSFALG,L.BANCI,I.BERTINI,M.BRUSCHI,P.TURANO
REVDAT 4 23-FEB-22 1NEW 1 REMARK LINK
REVDAT 3 26-JAN-10 1NEW 1 MODEL SPRSDE
REVDAT 2 24-FEB-09 1NEW 1 VERSN
REVDAT 1 29-APR-98 1NEW 0
SPRSDE 26-JAN-10 1NEW 2NEW
JRNL AUTH M.ASSFALG,L.BANCI,I.BERTINI,M.BRUSCHI,P.TURANO
JRNL TITL 800 MHZ 1H NMR SOLUTION STRUCTURE REFINEMENT OF OXIDIZED
JRNL TITL 2 CYTOCHROME C7 FROM DESULFUROMONAS ACETOXIDANS.
JRNL REF EUR.J.BIOCHEM. V. 256 261 1998
JRNL REFN ISSN 0014-2956
JRNL PMID 9760163
JRNL DOI 10.1046/J.1432-1327.1998.2560261.X
REMARK 1
REMARK 1 REFERENCE 1
REMARK 1 AUTH L.BANCI,I.BERTINI,M.BRUSCHI,P.SOMPORNPISUT,P.TURANO
REMARK 1 TITL NMR CHARACTERIZATION AND SOLUTION STRUCTURE DETERMINATION OF
REMARK 1 TITL 2 THE OXIDIZED CYTOCHROME C7 FROM DESULFUROMONAS ACETOXIDANS
REMARK 1 REF PROC.NATL.ACAD.SCI.USA V. 93 14396 1996
REMARK 1 REFN ISSN 0027-8424
REMARK 1 REFERENCE 2
REMARK 1 AUTH I.B.COUTINHO,D.L.TURNER,M.Y.LIU,J.LEGALL,A.V.XAVIER
REMARK 1 TITL STRUCTURE OF THE THREE-HAEM CORE OF CYTOCHROME C551.5
REMARK 1 TITL 2 DETERMINED BY 1H NMR
REMARK 1 REF J.BIOL.INORG.CHEM. V. 1 305 1996
REMARK 1 REFN ISSN 0949-8257
REMARK 1 REFERENCE 3
REMARK 1 AUTH J.G.MOURA,G.R.MOORE,R.J.WILLIAMS,I.PROBST,J.LEGALL,
REMARK 1 AUTH 2 A.V.XAVIER
REMARK 1 TITL NUCLEAR-MAGNETIC-RESONANCE STUDIES OF DESULFUROMONAS
REMARK 1 TITL 2 ACETOXIDANS CYTOCHROME C551.5 (C7)
REMARK 1 REF EUR.J.BIOCHEM. V. 144 433 1984
REMARK 1 REFN ISSN 0014-2956
REMARK 1 REFERENCE 4
REMARK 1 AUTH R.P.AMBLER
REMARK 1 TITL THE AMINO ACID RESEQUENCE OF CYTOCHROME C-551.5 (CYTOCHROME
REMARK 1 TITL 2 C7) FROM THE GREEN PHOTOSYNTHETIC BACTERIUM
REMARK 1 TITL 3 CHLOROPSEUDOMONAS ETHYLICA
REMARK 1 REF FEBS LETT. V. 18 351 1971
REMARK 1 REFN ISSN 0014-5793
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : AMBER
REMARK 3 AUTHORS : GUNTERT,WUTHRICH
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: ENERGY MINIMIZATION BY THE SANDER
REMARK 3 MODULE OF AMBER
REMARK 4
REMARK 4 1NEW 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_1000175264.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 298
REMARK 210 PH : 6.5
REMARK 210 IONIC STRENGTH : NULL
REMARK 210 PRESSURE : NULL
REMARK 210 SAMPLE CONTENTS : NULL
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : NOESY
REMARK 210 SPECTROMETER FIELD STRENGTH : 800 MHZ
REMARK 210 SPECTROMETER MODEL : DMX800
REMARK 210 SPECTROMETER MANUFACTURER : BRUKER
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : DYANA
REMARK 210 METHOD USED : TORSION ANGLE MOLECULAR DYNAMICS
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 1000
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 35
REMARK 210 CONFORMERS, SELECTION CRITERIA : MINIMUM TARGET FUNCTION VALUE
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: 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
REMARK 500 REMARK: NULL
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 14 CYS A 49 CA - CB - SG ANGL. DEV. = 7.0 DEGREES
REMARK 500 18 CYS A 49 CB - CA - C ANGL. DEV. = 9.7 DEGREES
REMARK 500 22 CYS A 49 CA - CB - SG ANGL. DEV. = 6.9 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 CYS A 26 -69.89 66.67
REMARK 500 1 ALA A 28 -47.06 -157.50
REMARK 500 1 THR A 33 93.39 74.66
REMARK 500 1 LYS A 36 99.77 -60.83
REMARK 500 1 LYS A 41 31.58 -78.70
REMARK 500 1 LYS A 46 -135.18 -93.43
REMARK 500 1 LYS A 50 31.04 -63.07
REMARK 500 1 THR A 51 -60.60 -121.06
REMARK 500 1 CYS A 52 45.61 -78.70
REMARK 500 1 HIS A 53 -34.91 -139.47
REMARK 500 1 THR A 60 -43.06 -177.18
REMARK 500 1 LYS A 61 41.70 -73.41
REMARK 500 1 CYS A 62 -66.65 56.12
REMARK 500 2 ASP A 2 -28.73 79.78
REMARK 500 2 CYS A 26 -69.02 65.75
REMARK 500 2 THR A 33 95.84 116.14
REMARK 500 2 LYS A 46 -84.96 -114.50
REMARK 500 2 CYS A 49 -67.68 -109.11
REMARK 500 2 LYS A 50 60.68 -69.15
REMARK 500 2 THR A 51 -72.52 -147.06
REMARK 500 2 HIS A 53 -57.54 151.39
REMARK 500 2 LYS A 54 73.88 -65.83
REMARK 500 2 SER A 55 -52.48 179.82
REMARK 500 2 PRO A 59 -104.67 -73.33
REMARK 500 2 THR A 60 -57.78 71.60
REMARK 500 2 ILE A 67 84.22 -67.57
REMARK 500 3 ASP A 2 -75.71 -71.72
REMARK 500 3 HIS A 17 -53.22 -125.59
REMARK 500 3 CYS A 26 -66.76 68.04
REMARK 500 3 ALA A 28 -49.58 -153.33
REMARK 500 3 GLU A 31 -162.75 -124.85
REMARK 500 3 THR A 33 88.62 66.85
REMARK 500 3 ASP A 40 -67.86 178.22
REMARK 500 3 LYS A 42 -67.46 66.27
REMARK 500 3 LYS A 46 -116.53 -104.43
REMARK 500 3 ALA A 48 -76.19 -19.47
REMARK 500 3 HIS A 53 -68.74 72.71
REMARK 500 3 SER A 55 -44.85 -178.36
REMARK 500 3 ASN A 56 -68.32 -101.54
REMARK 500 3 ASN A 57 176.56 167.08
REMARK 500 3 THR A 60 19.30 -154.90
REMARK 500 3 LYS A 61 33.94 -142.80
REMARK 500 3 CYS A 62 -176.49 48.90
REMARK 500 4 ALA A 28 -48.00 -159.13
REMARK 500 4 THR A 33 105.43 95.59
REMARK 500 4 ASP A 40 -155.23 59.97
REMARK 500 4 LYS A 41 77.21 37.50
REMARK 500 4 SER A 43 -72.37 -122.18
REMARK 500 4 LYS A 46 -92.80 -118.60
REMARK 500 4 CYS A 49 -74.24 -107.76
REMARK 500
REMARK 500 THIS ENTRY HAS 529 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 ASP A 40 LYS A 41 4 147.38
REMARK 500 ALA A 1 ASP A 2 5 -148.88
REMARK 500 ALA A 1 ASP A 2 18 128.82
REMARK 500 ALA A 1 ASP A 2 21 130.98
REMARK 500 ALA A 1 ASP A 2 30 -148.21
REMARK 500 LYS A 61 CYS A 62 32 143.86
REMARK 500 ALA A 1 ASP A 2 34 -148.23
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 HIS A 20 0.08 SIDE CHAIN
REMARK 500 2 HIS A 66 0.10 SIDE CHAIN
REMARK 500 3 HIS A 20 0.08 SIDE CHAIN
REMARK 500 5 PHE A 15 0.12 SIDE CHAIN
REMARK 500 6 PHE A 15 0.11 SIDE CHAIN
REMARK 500 7 PHE A 15 0.08 SIDE CHAIN
REMARK 500 8 PHE A 15 0.13 SIDE CHAIN
REMARK 500 13 TYR A 6 0.10 SIDE CHAIN
REMARK 500 13 PHE A 15 0.12 SIDE CHAIN
REMARK 500 14 PHE A 15 0.09 SIDE CHAIN
REMARK 500 14 HIS A 53 0.09 SIDE CHAIN
REMARK 500 15 PHE A 15 0.14 SIDE CHAIN
REMARK 500 16 PHE A 15 0.09 SIDE CHAIN
REMARK 500 17 PHE A 15 0.07 SIDE CHAIN
REMARK 500 18 PHE A 15 0.13 SIDE CHAIN
REMARK 500 19 TYR A 6 0.09 SIDE CHAIN
REMARK 500 20 PHE A 15 0.08 SIDE CHAIN
REMARK 500 21 TYR A 6 0.07 SIDE CHAIN
REMARK 500 21 PHE A 15 0.14 SIDE CHAIN
REMARK 500 25 PHE A 15 0.09 SIDE CHAIN
REMARK 500 29 PHE A 15 0.10 SIDE CHAIN
REMARK 500 29 HIS A 20 0.08 SIDE CHAIN
REMARK 500 29 HIS A 45 0.09 SIDE CHAIN
REMARK 500 30 PHE A 15 0.11 SIDE CHAIN
REMARK 500 31 TYR A 6 0.20 SIDE CHAIN
REMARK 500 32 TYR A 6 0.20 SIDE CHAIN
REMARK 500 33 TYR A 6 0.06 SIDE CHAIN
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 HEC A 69 FE
REMARK 620 N RES CSSEQI ATOM
REMARK 620 1 HIS A 17 NE2
REMARK 620 2 HEC A 69 NA 93.1
REMARK 620 3 HEC A 69 NB 88.6 91.4
REMARK 620 4 HEC A 69 NC 87.8 177.4 91.1
REMARK 620 5 HEC A 69 ND 91.9 88.9 179.4 88.7
REMARK 620 6 HIS A 30 NE2 175.6 91.3 90.9 87.8 88.5
REMARK 620 N 1 2 3 4 5
REMARK 620
REMARK 620 COORDINATION ANGLES FOR: M RES CSSEQI METAL
REMARK 620 HEC A 70 FE
REMARK 620 N RES CSSEQI ATOM
REMARK 620 1 HIS A 20 NE2
REMARK 620 2 HEC A 70 NA 91.6
REMARK 620 3 HEC A 70 NB 93.0 89.2
REMARK 620 4 HEC A 70 NC 88.0 179.4 90.3
REMARK 620 5 HEC A 70 ND 88.3 89.4 178.2 91.1
REMARK 620 6 HIS A 53 NE2 173.1 94.6 90.0 85.8 88.9
REMARK 620 N 1 2 3 4 5
REMARK 620
REMARK 620 COORDINATION ANGLES FOR: M RES CSSEQI METAL
REMARK 620 HEC A 71 FE
REMARK 620 N RES CSSEQI ATOM
REMARK 620 1 HIS A 45 NE2
REMARK 620 2 HEC A 71 NA 88.1
REMARK 620 3 HEC A 71 NB 89.7 90.3
REMARK 620 4 HEC A 71 NC 92.8 178.6 90.8
REMARK 620 5 HEC A 71 ND 91.9 91.7 177.5 87.2
REMARK 620 6 HIS A 66 NE2 179.4 91.5 89.8 87.5 88.6
REMARK 620 N 1 2 3 4 5
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: AC1
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE HEC A 69
REMARK 800
REMARK 800 SITE_IDENTIFIER: AC2
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE HEC A 70
REMARK 800
REMARK 800 SITE_IDENTIFIER: AC3
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE HEC A 71
DBREF 1NEW A 1 68 UNP P00137 CYC3_DESAC 1 68
SEQRES 1 A 68 ALA ASP VAL VAL THR TYR GLU ASN LYS LYS GLY ASN VAL
SEQRES 2 A 68 THR PHE ASP HIS LYS ALA HIS ALA GLU LYS LEU GLY CYS
SEQRES 3 A 68 ASP ALA CYS HIS GLU GLY THR PRO ALA LYS ILE ALA ILE
SEQRES 4 A 68 ASP LYS LYS SER ALA HIS LYS ASP ALA CYS LYS THR CYS
SEQRES 5 A 68 HIS LYS SER ASN ASN GLY PRO THR LYS CYS GLY GLY CYS
SEQRES 6 A 68 HIS ILE LYS
HET HEC A 69 75
HET HEC A 70 75
HET HEC A 71 75
HETNAM HEC HEME C
FORMUL 2 HEC 3(C34 H34 FE N4 O4)
HELIX 1 1 LYS A 18 LEU A 24 1 7
SHEET 1 A 2 VAL A 3 TYR A 6 0
SHEET 2 A 2 VAL A 13 ASP A 16 -1 N PHE A 15 O VAL A 4
LINK SG CYS A 26 CAB HEC A 69 1555 1555 1.81
LINK SG CYS A 29 CAC HEC A 69 1555 1555 1.81
LINK SG CYS A 49 CAB HEC A 70 1555 1555 1.83
LINK SG CYS A 52 CAC HEC A 70 1555 1555 1.82
LINK SG CYS A 62 CAB HEC A 71 1555 1555 1.82
LINK SG CYS A 65 CAC HEC A 71 1555 1555 1.82
LINK NE2 HIS A 17 FE HEC A 69 1555 1555 1.96
LINK NE2 HIS A 20 FE HEC A 70 1555 1555 1.98
LINK NE2 HIS A 30 FE HEC A 69 1555 1555 1.95
LINK NE2 HIS A 45 FE HEC A 71 1555 1555 2.00
LINK NE2 HIS A 53 FE HEC A 70 1555 1555 1.98
LINK NE2 HIS A 66 FE HEC A 71 1555 1555 1.96
SITE 1 AC1 12 TYR A 6 HIS A 17 HIS A 20 ALA A 21
SITE 2 AC1 12 LEU A 24 CYS A 26 CYS A 29 HIS A 30
SITE 3 AC1 12 PRO A 34 ALA A 35 ILE A 37 ILE A 39
SITE 1 AC2 13 THR A 14 PHE A 15 HIS A 20 LYS A 23
SITE 2 AC2 13 LEU A 24 CYS A 29 ALA A 48 CYS A 49
SITE 3 AC2 13 CYS A 52 HIS A 53 ASN A 56 ASN A 57
SITE 4 AC2 13 CYS A 65
SITE 1 AC3 13 ASN A 8 LYS A 9 LYS A 10 PHE A 15
SITE 2 AC3 13 LYS A 41 ALA A 44 HIS A 45 CYS A 49
SITE 3 AC3 13 LYS A 50 HIS A 53 CYS A 62 CYS A 65
SITE 4 AC3 13 HIS A 66
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
(ATOM LINES ARE NOT SHOWN.)
END
