Header list of 1cyz.pdb file
Complete list - 16 202 Bytes
HEADER DNA 31-AUG-99 1CYZ
TITLE NMR STRUCTURE OF THE GAACTGGTTC/TRI-IMIDAZOLE POLYAMIDE COMPLEX
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: 5'-D(*GP*AP*AP*CP*TP*GP*GP*TP*TP*C)-3';
COMPND 3 CHAIN: A, B;
COMPND 4 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 SYNTHETIC: YES
KEYWDS T:G RECOGNIZED BY IM/IM PAIR IN THE DNA MINOR GROOVE, DNA
EXPDTA SOLUTION NMR
AUTHOR X.-L.YANG,R.B.HUBBARD IV,M.LEE,Z.-F.TAO,H.SUGIYAMA,A.H.-J.WANG
REVDAT 4 16-FEB-22 1CYZ 1 COMPND REMARK HETNAM
REVDAT 3 24-FEB-09 1CYZ 1 VERSN
REVDAT 2 18-JAN-05 1CYZ 1 JRNL COMPND AUTHOR REMARK
REVDAT 1 14-SEP-99 1CYZ 0
JRNL AUTH X.-L.YANG,R.B.HUBBARD IV,M.LEE,Z.-F.TAO,H.SUGIYAMA,
JRNL AUTH 2 A.H.-J.WANG
JRNL TITL IMIDAZOLE-IMIDAZOLE PAIR AS A MINOR GROOVE RECOGNITION MOTIF
JRNL TITL 2 FOR T:G MISMATCHED BASE PAIRS
JRNL REF NUCLEIC ACIDS RES. V. 27 4183 1999
JRNL REFN ISSN 0305-1048
JRNL PMID 10518609
JRNL DOI 10.1093/NAR/27.21.4183
REMARK 1
REMARK 1 REFERENCE 1
REMARK 1 AUTH X.-L.YANG,C.KAENZIG,M.LEE,A.H.-J.WANG
REMARK 1 TITL BINDING OF AR-1-144, A TRI-IMIDAZOLE DNA MINOR GROOVE
REMARK 1 TITL 2 BINDER, TO CCGG SEQUENCE ANALYZED BY NMR SPECTROSCOPY
REMARK 1 REF EUR.J.BIOCHEM. V. 263 646 1999
REMARK 1 REFN ISSN 0014-2956
REMARK 1 DOI 10.1046/J.1432-1327.1999.00515.X
REMARK 2
REMARK 2 RESOLUTION. NOT APPLICABLE.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : FELIX 1.1 AND 98, X-PLOR 3.851
REMARK 3 AUTHORS : MSI (FELIX), BRUNGER (X-PLOR)
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 1CYZ COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 31-AUG-99.
REMARK 100 THE DEPOSITION ID IS D_1000009629.
REMARK 210
REMARK 210 EXPERIMENTAL DETAILS
REMARK 210 EXPERIMENT TYPE : NMR
REMARK 210 TEMPERATURE (KELVIN) : 275
REMARK 210 PH : 7
REMARK 210 IONIC STRENGTH : NO ADDITIONAL SALT
REMARK 210 PRESSURE : AMBIENT
REMARK 210 SAMPLE CONTENTS : 1.5 MM DNA DUPLEX; 20 MM
REMARK 210 PHOSPHATE BUFFER; 100% D2O OR 90%
REMARK 210 H2O, 10% D2O
REMARK 210
REMARK 210 NMR EXPERIMENTS CONDUCTED : 2D NOESY; TOCSY
REMARK 210 SPECTROMETER FIELD STRENGTH : 750 MHZ
REMARK 210 SPECTROMETER MODEL : INOVA
REMARK 210 SPECTROMETER MANUFACTURER : VARIAN
REMARK 210
REMARK 210 STRUCTURE DETERMINATION.
REMARK 210 SOFTWARE USED : NULL
REMARK 210 METHOD USED : NOE-RESTRAINED CONJUGATE
REMARK 210 GRADIENT REFINEMENT IN X-PLOR;
REMARK 210 FULL MATRIX RELAXATION
REMARK 210
REMARK 210 CONFORMERS, NUMBER CALCULATED : 11
REMARK 210 CONFORMERS, NUMBER SUBMITTED : 1
REMARK 210 CONFORMERS, SELECTION CRITERIA : REFINED AVERAGE STRUCTURE
REMARK 210
REMARK 210 BEST REPRESENTATIVE CONFORMER IN THIS ENSEMBLE : 1
REMARK 210
REMARK 210 REMARK: THIS STRUCTURE WAS DETERMINED USING 2D HOMONUCLEAR
REMARK 210 TECHNIQUES WITH BACK NOE CALCULATION
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: DIMERIC
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A, B
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 LENGTHS
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,2(A3,1X,A1,I4,A1,1X,A4,3X),1X,F6.3)
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 RES CSSEQI ATM2 DEVIATION
REMARK 500 DG A 1 C5' DG A 1 C4' 0.043
REMARK 500 DT A 5 C5 DT A 5 C7 0.044
REMARK 500 DG B 16 C5' DG B 16 C4' 0.044
REMARK 500 DT B 20 C5 DT B 20 C7 0.044
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 DG A 1 O4' - C1' - N9 ANGL. DEV. = 6.7 DEGREES
REMARK 500 DA A 2 O4' - C1' - N9 ANGL. DEV. = 3.2 DEGREES
REMARK 500 DA A 3 O4' - C1' - C2' ANGL. DEV. = -5.0 DEGREES
REMARK 500 DT A 5 O4' - C1' - N1 ANGL. DEV. = 4.2 DEGREES
REMARK 500 DG A 7 O4' - C4' - C3' ANGL. DEV. = 4.6 DEGREES
REMARK 500 DG A 7 O4' - C1' - C2' ANGL. DEV. = -5.3 DEGREES
REMARK 500 DT A 8 O4' - C1' - N1 ANGL. DEV. = 9.2 DEGREES
REMARK 500 DT A 9 C6 - C5 - C7 ANGL. DEV. = -4.4 DEGREES
REMARK 500 DG B 16 O4' - C1' - N9 ANGL. DEV. = 6.7 DEGREES
REMARK 500 DA B 17 O4' - C1' - N9 ANGL. DEV. = 3.2 DEGREES
REMARK 500 DA B 18 O4' - C1' - C2' ANGL. DEV. = -5.0 DEGREES
REMARK 500 DT B 20 O4' - C1' - N1 ANGL. DEV. = 4.1 DEGREES
REMARK 500 DG B 22 O4' - C4' - C3' ANGL. DEV. = 4.7 DEGREES
REMARK 500 DG B 22 O4' - C1' - C2' ANGL. DEV. = -5.3 DEGREES
REMARK 500 DT B 23 O4' - C1' - N1 ANGL. DEV. = 9.2 DEGREES
REMARK 500 DT B 24 C6 - C5 - C7 ANGL. DEV. = -4.4 DEGREES
REMARK 500
REMARK 500 REMARK: NULL
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: AC1
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE AR1 A 12
REMARK 800
REMARK 800 SITE_IDENTIFIER: AC2
REMARK 800 EVIDENCE_CODE: SOFTWARE
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE AR1 B 26
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1B0S RELATED DB: PDB
REMARK 900 1B0S CONTAINS THE NMR STRUCTURE OF GAACCGGTTC/TRI-IMIDAZOLE
REMARK 900 POLYAMIDE COMPLEX
DBREF 1CYZ A 1 10 PDB 1CYZ 1CYZ 1 10
DBREF 1CYZ B 16 25 PDB 1CYZ 1CYZ 16 25
SEQRES 1 A 10 DG DA DA DC DT DG DG DT DT DC
SEQRES 1 B 10 DG DA DA DC DT DG DG DT DT DC
HET AR1 A 12 63
HET AR1 B 26 63
HETNAM AR1 (2-{[4-({4-[(4-FORMYLAMINO-1-METHYL-1H-IMIDAZOLE-2-
HETNAM 2 AR1 CARBONYL)-AMINO]-1-METHYL-1H-IMIDAZOLE-2-CARBONYL}-
HETNAM 3 AR1 AMINO)-1-METHYL-1 H-IMIDAZOLE-2-CARBONYL]-AMINO}-
HETNAM 4 AR1 ETHYL)-DIMETHYL-AMMONIUM
HETSYN AR1 TRI-IMIDAZOLE DNA MINOR GROOVE BINDER; AR-1-144
FORMUL 3 AR1 2(C20 H28 N11 O4 1+)
SITE 1 AC1 10 DC A 4 DT A 5 DG A 6 DG A 7
SITE 2 AC1 10 DT A 8 DT A 9 DC B 19 DG B 21
SITE 3 AC1 10 DG B 22 AR1 B 26
SITE 1 AC2 10 DC A 4 DG A 6 DG A 7 AR1 A 12
SITE 2 AC2 10 DC B 19 DT B 20 DG B 21 DG B 22
SITE 3 AC2 10 DT B 23 DT B 24
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 - 16 202 Bytes