Header list of 1ixa.pdb file
Complete list - 23 202 Bytes
HEADER HUMAN FACTOR IX 14-NOV-91 1IXA
TITLE THE THREE-DIMENSIONAL STRUCTURE OF THE FIRST EGF-LIKE MODULE OF HUMAN
TITLE 2 FACTOR IX: COMPARISON WITH EGF AND TGF-A
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: EGF-LIKE MODULE OF HUMAN FACTOR IX;
COMPND 3 CHAIN: A;
COMPND 4 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: HOMO SAPIENS;
SOURCE 3 ORGANISM_COMMON: HUMAN;
SOURCE 4 ORGANISM_TAXID: 9606
KEYWDS HUMAN FACTOR IX
EXPDTA SOLUTION NMR
AUTHOR M.BARON,D.G.NORMAN,T.S.HARVEY,P.A.HANFORD,M.MAYHEW,A.G.D.TSE,
AUTHOR 2 G.G.BROWNLEE,I.D.C.CAMPBELL
REVDAT 4 23-FEB-22 1IXA 1 REMARK
REVDAT 3 24-FEB-09 1IXA 1 VERSN
REVDAT 2 01-APR-03 1IXA 1 JRNL
REVDAT 1 31-OCT-93 1IXA 0
JRNL AUTH M.BARON,D.G.NORMAN,T.S.HARVEY,P.A.HANDFORD,M.MAYHEW,A.G.TSE,
JRNL AUTH 2 G.G.BROWNLEE,I.D.CAMPBELL
JRNL TITL THE THREE-DIMENSIONAL STRUCTURE OF THE FIRST EGF-LIKE MODULE
JRNL TITL 2 OF HUMAN FACTOR IX: COMPARISON WITH EGF AND TGF-ALPHA.
JRNL REF PROTEIN SCI. V. 1 81 1992
JRNL REFN ISSN 0961-8368
JRNL PMID 1304885
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : X-PLOR
REMARK 3 AUTHORS : BRUNGER
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 1IXA COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY BNL.
REMARK 100 THE DEPOSITION ID IS D_1000174286.
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 : 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: 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 TRP A 72 CG - CD1 - NE1 ANGL. DEV. = -7.2 DEGREES
REMARK 500 TRP A 72 CD1 - NE1 - CE2 ANGL. DEV. = 7.9 DEGREES
REMARK 500 TRP A 72 NE1 - CE2 - CZ2 ANGL. DEV. = 8.5 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 ASP A 49 70.54 -112.70
REMARK 500 CYS A 51 69.90 -113.50
REMARK 500 ASN A 54 71.92 24.03
REMARK 500 ASN A 58 -36.49 88.45
REMARK 500 ASP A 65 -82.01 -118.31
REMARK 500 ILE A 66 -64.56 -131.41
REMARK 500 CYS A 82 77.42 38.65
REMARK 500
REMARK 500 REMARK: NULL
DBREF 1IXA A 46 84 UNP P00740 FA9_HUMAN 92 130
SEQRES 1 A 39 VAL ASP GLY ASP GLN CYS GLU SER ASN PRO CYS LEU ASN
SEQRES 2 A 39 GLY GLY SER CYS LYS ASP ASP ILE ASN SER TYR GLU CYS
SEQRES 3 A 39 TRP CYS PRO PHE GLY PHE GLU GLY LYS ASN CYS GLU LEU
SHEET 1 A 2 SER A 61 ASP A 64 0
SHEET 2 A 2 TYR A 69 TRP A 72 -1 N GLU A 70 O LYS A 63
SSBOND 1 CYS A 51 CYS A 62 1555 1555 2.02
SSBOND 2 CYS A 56 CYS A 71 1555 1555 2.02
SSBOND 3 CYS A 73 CYS A 82 1555 1555 2.02
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 - 23 202 Bytes