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HEADER LYASE 06-FEB-08 3C6Y
TITLE HNL FROM HEVEA BRASILIENSIS TO ATOMIC RESOLUTION
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: HYDROXYNITRILASE;
COMPND 3 CHAIN: A;
COMPND 4 SYNONYM: (S)-ACETONE-CYANOHYDRIN LYASE, (S)-HYDROXYNITRILE
COMPND 5 LYASE, OXYNITRILASE;
COMPND 6 EC: 4.1.2.37;
COMPND 7 ENGINEERED: YES
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: HEVEA BRASILIENSIS;
SOURCE 3 ORGANISM_COMMON: PARA RUBBER TREE;
SOURCE 4 GENE: HNL;
SOURCE 5 EXPRESSION_SYSTEM: PICHIA PASTORIS;
SOURCE 6 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE 7 EXPRESSION_SYSTEM_PLASMID: BHIL-D2
KEYWDS ATOMIC RESOLUTION, HYDROXYNITRIL LYASE, CATALYSIS,
KEYWDS 2 PROTONATION STATE, AB INITIO CALCULATIONS, SUBSTRATE BINDING
EXPDTA X-RAY DIFFRACTION
AUTHOR A.SCHMIDT
REVDAT 1 03-JUN-08 3C6Y 0
JRNL AUTH A.SCHMIDT,K.GRUBER,C.KRATKY,V.S.LAMZIN
JRNL TITL ATOMIC RESOLUTION STRUCTURES AND QUANTUM CHEMISTRY
JRNL TITL 2 MEET TO REVEAL SUBTLETIES OF HYDROXYNITRILE LYASE
JRNL TITL 3 CATALYSIS
JRNL REF TO BE PUBLISHED
JRNL REFN
REMARK 1
REMARK 1 REFERENCE 1
REMARK 1 AUTH J.ZUEGG,K.GRUBER,M.GUGGANIG,U.G.WAGNER,C.KRATKY
REMARK 1 TITL THREE-DIMENSIONAL STRUCTURES OF ENZYME-SUBSTRATE
REMARK 1 TITL 2 COMPLEXES OF THE HYDROXYNITRILE LYASE FROM HEVEA
REMARK 1 TITL 3 BRASILIENSIS
REMARK 1 REF PROTEIN SCI. V. 8 1990 1999
REMARK 1 REFN ASTM PRCIEI US ISSN 0961-8368
REMARK 1 REFERENCE 2
REMARK 1 AUTH K.GRUBER,M.GUGGANIG,U.G.WAGNER,C.KRATKY
REMARK 1 TITL ATOMIC RESOLUTION CRYSTAL STRUCTURE OF
REMARK 1 TITL 2 HYDROXYNITRILE LYASE FROM HEVEA BRASILIENSIS
REMARK 1 REF BIOL.CHEM. V. 380 993 1999
REMARK 1 REFN GE ISSN 1431-6730
REMARK 2
REMARK 2 RESOLUTION. 1.25 ANGSTROMS.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : SHELXL-97
REMARK 3 AUTHORS : G.M.SHELDRICK
REMARK 3
REMARK 3 DATA USED IN REFINEMENT.
REMARK 3 RESOLUTION RANGE HIGH (ANGSTROMS) : 1.25
REMARK 3 RESOLUTION RANGE LOW (ANGSTROMS) : 15.00
REMARK 3 DATA CUTOFF (SIGMA(F)) : 0.000
REMARK 3 COMPLETENESS FOR RANGE (%) : 92.5
REMARK 3 CROSS-VALIDATION METHOD : FREE R INITIALLY, FINAL
REMARK 3 REFINEMENT AGAINST ALL
REMARK 3 ADATA
REMARK 3 FREE R VALUE TEST SET SELECTION : RANDOM
REMARK 3
REMARK 3 FIT TO DATA USED IN REFINEMENT (NO CUTOFF).
REMARK 3 R VALUE (WORKING + TEST SET, NO CUTOFF) : 0.127
REMARK 3 R VALUE (WORKING SET, NO CUTOFF) : 0.127
REMARK 3 FREE R VALUE (NO CUTOFF) : NULL
REMARK 3 FREE R VALUE TEST SET SIZE (%, NO CUTOFF) : NULL
REMARK 3 FREE R VALUE TEST SET COUNT (NO CUTOFF) : NULL
REMARK 3 TOTAL NUMBER OF REFLECTIONS (NO CUTOFF) : 83123
REMARK 3
REMARK 3 FIT/AGREEMENT OF MODEL FOR DATA WITH F>4SIG(F).
REMARK 3 R VALUE (WORKING + TEST SET, F>4SIG(F)) : 0.106
REMARK 3 R VALUE (WORKING SET, F>4SIG(F)) : NULL
REMARK 3 FREE R VALUE (F>4SIG(F)) : NULL
REMARK 3 FREE R VALUE TEST SET SIZE (%, F>4SIG(F)) : NULL
REMARK 3 FREE R VALUE TEST SET COUNT (F>4SIG(F)) : NULL
REMARK 3 TOTAL NUMBER OF REFLECTIONS (F>4SIG(F)) : 64103
REMARK 3
REMARK 3 NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.
REMARK 3 PROTEIN ATOMS : 4328
REMARK 3 NUCLEIC ACID ATOMS : 0
REMARK 3 HETEROGEN ATOMS : 24
REMARK 3 SOLVENT ATOMS : 550
REMARK 3
REMARK 3 MODEL REFINEMENT.
REMARK 3 OCCUPANCY SUM OF NON-HYDROGEN ATOMS : 2552.60
REMARK 3 OCCUPANCY SUM OF HYDROGEN ATOMS : 2013.38
REMARK 3 NUMBER OF DISCRETELY DISORDERED RESIDUES : 34
REMARK 3 NUMBER OF LEAST-SQUARES PARAMETERS : 24616
REMARK 3 NUMBER OF RESTRAINTS : 30456
REMARK 3
REMARK 3 RMS DEVIATIONS FROM RESTRAINT TARGET VALUES.
REMARK 3 BOND LENGTHS (A) : 0.012
REMARK 3 ANGLE DISTANCES (A) : 0.028
REMARK 3 SIMILAR DISTANCES (NO TARGET VALUES) (A) : 0.000
REMARK 3 DISTANCES FROM RESTRAINT PLANES (A) : 0.028
REMARK 3 ZERO CHIRAL VOLUMES (A**3) : 0.072
REMARK 3 NON-ZERO CHIRAL VOLUMES (A**3) : 0.079
REMARK 3 ANTI-BUMPING DISTANCE RESTRAINTS (A) : 0.060
REMARK 3 RIGID-BOND ADP COMPONENTS (A**2) : 0.004
REMARK 3 SIMILAR ADP COMPONENTS (A**2) : 0.040
REMARK 3 APPROXIMATELY ISOTROPIC ADPS (A**2) : 0.093
REMARK 3
REMARK 3 BULK SOLVENT MODELING.
REMARK 3 METHOD USED: NULL
REMARK 3
REMARK 3 STEREOCHEMISTRY TARGET VALUES : ENGH AND HUBER
REMARK 3 SPECIAL CASE: NULL
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: FULL ANISOTROPIC REFINEMENT APPLIED
REMARK 4
REMARK 4 3C6Y COMPLIES WITH FORMAT V. 3.1, 01-AUG-2007
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ.
REMARK 100 THE RCSB ID CODE IS RCSB046418.
REMARK 200
REMARK 200 EXPERIMENTAL DETAILS
REMARK 200 EXPERIMENT TYPE : X-RAY DIFFRACTION
REMARK 200 DATE OF DATA COLLECTION : 06-MAR-2005
REMARK 200 TEMPERATURE (KELVIN) : 100.0
REMARK 200 PH : 7.50
REMARK 200 NUMBER OF CRYSTALS USED : 1
REMARK 200
REMARK 200 SYNCHROTRON (Y/N) : Y
REMARK 200 RADIATION SOURCE : EMBL/DESY, HAMBURG
REMARK 200 BEAMLINE : X11
REMARK 200 X-RAY GENERATOR MODEL : NULL
REMARK 200 MONOCHROMATIC OR LAUE (M/L) : M
REMARK 200 WAVELENGTH OR RANGE (A) : 0.8162
REMARK 200 MONOCHROMATOR : SI
REMARK 200 OPTICS : MIRROR
REMARK 200
REMARK 200 DETECTOR TYPE : CCD
REMARK 200 DETECTOR MANUFACTURER : MAR CCD 165 MM
REMARK 200 INTENSITY-INTEGRATION SOFTWARE : DENZO
REMARK 200 DATA SCALING SOFTWARE : SCALEPACK
REMARK 200
REMARK 200 NUMBER OF UNIQUE REFLECTIONS : 83123
REMARK 200 RESOLUTION RANGE HIGH (A) : 1.250
REMARK 200 RESOLUTION RANGE LOW (A) : 15.000
REMARK 200 REJECTION CRITERIA (SIGMA(I)) : -3.000
REMARK 200
REMARK 200 OVERALL.
REMARK 200 COMPLETENESS FOR RANGE (%) : 100.0
REMARK 200 DATA REDUNDANCY : 3.500
REMARK 200 R MERGE (I) : 0.05700
REMARK 200 R SYM (I) : NULL
REMARK 200 FOR THE DATA SET : 19.0000
REMARK 200
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.
REMARK 200 HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 1.25
REMARK 200 HIGHEST RESOLUTION SHELL, RANGE LOW (A) : 1.26
REMARK 200 COMPLETENESS FOR SHELL (%) : 60.0
REMARK 200 DATA REDUNDANCY IN SHELL : 3.50
REMARK 200 R MERGE FOR SHELL (I) : 0.54000
REMARK 200 R SYM FOR SHELL (I) : NULL
REMARK 200 FOR SHELL : 1.500
REMARK 200
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MR/RIGID BODY PLACEMENT
REMARK 200 SOFTWARE USED: REFMAC (RIGID BODY)
REMARK 200 STARTING MODEL: PDB ENTRY 1QJ4
REMARK 200
REMARK 200 REMARK: NULL
REMARK 280
REMARK 280 CRYSTAL
REMARK 280 SOLVENT CONTENT, VS (%): 55.20
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.75
REMARK 280
REMARK 280 CRYSTALLIZATION CONDITIONS: 2% PEG400, 2M AMMONIUM SULPHATE,
REMARK 280 0.1M HEPES-NA, PH7.5, VAPOR DIFFUSION, HANGING DROP,
REMARK 280 TEMPERATURE 293K
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: C 2 2 21
REMARK 290
REMARK 290 SYMOP SYMMETRY
REMARK 290 NNNMMM OPERATOR
REMARK 290 1555 X,Y,Z
REMARK 290 2555 -X,-Y,1/2+Z
REMARK 290 3555 -X,Y,1/2-Z
REMARK 290 4555 X,-Y,-Z
REMARK 290 5555 1/2+X,1/2+Y,Z
REMARK 290 6555 1/2-X,1/2-Y,1/2+Z
REMARK 290 7555 1/2-X,1/2+Y,1/2-Z
REMARK 290 8555 1/2+X,1/2-Y,-Z
REMARK 290
REMARK 290 WHERE NNN -> OPERATOR NUMBER
REMARK 290 MMM -> TRANSLATION VECTOR
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY TRANSFORMATIONS
REMARK 290 THE FOLLOWING TRANSFORMATIONS OPERATE ON THE ATOM/HETATM
REMARK 290 RECORDS IN THIS ENTRY TO PRODUCE CRYSTALLOGRAPHICALLY
REMARK 290 RELATED MOLECULES.
REMARK 290 SMTRY1 1 1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 1 0.000000 1.000000 0.000000 0.00000
REMARK 290 SMTRY3 1 0.000000 0.000000 1.000000 0.00000
REMARK 290 SMTRY1 2 -1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 2 0.000000 -1.000000 0.000000 0.00000
REMARK 290 SMTRY3 2 0.000000 0.000000 1.000000 64.10300
REMARK 290 SMTRY1 3 -1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 3 0.000000 1.000000 0.000000 0.00000
REMARK 290 SMTRY3 3 0.000000 0.000000 -1.000000 64.10300
REMARK 290 SMTRY1 4 1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 4 0.000000 -1.000000 0.000000 0.00000
REMARK 290 SMTRY3 4 0.000000 0.000000 -1.000000 0.00000
REMARK 290 SMTRY1 5 1.000000 0.000000 0.000000 23.62450
REMARK 290 SMTRY2 5 0.000000 1.000000 0.000000 53.05200
REMARK 290 SMTRY3 5 0.000000 0.000000 1.000000 0.00000
REMARK 290 SMTRY1 6 -1.000000 0.000000 0.000000 23.62450
REMARK 290 SMTRY2 6 0.000000 -1.000000 0.000000 53.05200
REMARK 290 SMTRY3 6 0.000000 0.000000 1.000000 64.10300
REMARK 290 SMTRY1 7 -1.000000 0.000000 0.000000 23.62450
REMARK 290 SMTRY2 7 0.000000 1.000000 0.000000 53.05200
REMARK 290 SMTRY3 7 0.000000 0.000000 -1.000000 64.10300
REMARK 290 SMTRY1 8 1.000000 0.000000 0.000000 23.62450
REMARK 290 SMTRY2 8 0.000000 -1.000000 0.000000 53.05200
REMARK 290 SMTRY3 8 0.000000 0.000000 -1.000000 0.00000
REMARK 290
REMARK 290 REMARK: NULL
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 SOFTWARE DETERMINED QUATERNARY STRUCTURE: DIMERIC
REMARK 350 SOFTWARE USED: PISA
REMARK 350 TOTAL BURIED SURFACE AREA: 4550 ANGSTROM**2
REMARK 350 TOTAL SURFACE AREA FOR THE COMPLEX: 19020 ANGSTROM**2
REMARK 350 GAIN IN SOLVENT FREE ENERGY: -98 KCAL/MOL
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 350 BIOMT1 2 1.000000 0.000000 0.000000 0.00000
REMARK 350 BIOMT2 2 0.000000 -1.000000 0.000000 106.10400
REMARK 350 BIOMT3 2 0.000000 0.000000 -1.000000 0.00000
REMARK 375
REMARK 375 SPECIAL POSITION
REMARK 375 THE FOLLOWING ATOMS ARE FOUND TO BE WITHIN 0.15 ANGSTROMS
REMARK 375 OF A SYMMETRY RELATED ATOM AND ARE ASSUMED TO BE ON SPECIAL
REMARK 375 POSITIONS.
REMARK 375
REMARK 375 ATOM RES CSSEQI
REMARK 375 HOH A3006 LIES ON A SPECIAL POSITION.
REMARK 375 HOH A3068 LIES ON A SPECIAL POSITION.
REMARK 375 HOH A3138 LIES ON A SPECIAL POSITION.
REMARK 375 HOH A3352 LIES ON A SPECIAL POSITION.
REMARK 375 HOH A3578 LIES ON A SPECIAL POSITION.
REMARK 465
REMARK 465 MISSING RESIDUES
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE
REMARK 465 EXPERIMENT. (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 465 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)
REMARK 465
REMARK 465 M RES C SSEQI
REMARK 465 MET A 1
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: CLOSE CONTACTS IN SAME ASYMMETRIC UNIT
REMARK 500
REMARK 500 THE FOLLOWING ATOMS ARE IN CLOSE CONTACT.
REMARK 500
REMARK 500 ATM1 RES C SSEQI ATM2 RES C SSEQI
REMARK 500 O HOH A 3318 O HOH A 3401 1.74
REMARK 500 O HOH A 3304 O HOH A 3481 2.07
REMARK 500 O HOH A 3469 O HOH A 3471 2.07
REMARK 500 O HOH A 3273 O HOH A 3315 2.08
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 NUCELIC ACID: CLOWNEY ET AL 1996
REMARK 500
REMARK 500 M RES CSSEQI ATM1 ATM2 ATM3
REMARK 500 HIS A 31 CG - ND1 - CE1 ANGL. DEV. = 11.9 DEGREES
REMARK 500 HIS A 31 ND1 - CE1 - NE2 ANGL. DEV. = -7.7 DEGREES
REMARK 500 GLU A 123 OE1 - CD - OE2 ANGL. DEV. = 9.2 DEGREES
REMARK 500 ARG A 154 NE - CZ - NH1 ANGL. DEV. = 4.6 DEGREES
REMARK 500 ARG A 154 NE - CZ - NH2 ANGL. DEV. = -7.4 DEGREES
REMARK 500 LEU A 178 O - C - N ANGL. DEV. = -11.2 DEGREES
REMARK 500 ASP A 225 CB - CG - OD1 ANGL. DEV. = -5.8 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 SER A 80 -114.23 50.31
REMARK 500 LYS A 129 -121.15 62.43
REMARK 500
REMARK 500 REMARK: NULL
REMARK 525
REMARK 525 SOLVENT
REMARK 525
REMARK 525 THE SOLVENT MOLECULES HAVE CHAIN IDENTIFIERS THAT
REMARK 525 INDICATE THE POLYMER CHAIN WITH WHICH THEY ARE MOST
REMARK 525 CLOSELY ASSOCIATED. THE REMARK LISTS ALL THE SOLVENT
REMARK 525 MOLECULES WHICH ARE MORE THAN 5A AWAY FROM THE
REMARK 525 NEAREST POLYMER CHAIN (M=MODEL NUMBER;
REMARK 525 RES=RESIDUE NAME; C=CHAIN IDENTIFIER; SSEQ=SEQUENCE
REMARK 525 NUMBER; I=INSERTION CODE):
REMARK 525
REMARK 525 M RES CSSEQI
REMARK 525 HOH A3196 DISTANCE = 5.10 ANGSTROMS
REMARK 525 HOH A3254 DISTANCE = 5.52 ANGSTROMS
REMARK 525 HOH A3267 DISTANCE = 5.35 ANGSTROMS
REMARK 525 HOH A3495 DISTANCE = 7.10 ANGSTROMS
REMARK 525 HOH A3537 DISTANCE = 6.63 ANGSTROMS
REMARK 525 HOH A3608 DISTANCE = 7.26 ANGSTROMS
REMARK 800
REMARK 800 SITE
REMARK 800 SITE_IDENTIFIER: AC1
REMARK 800 SITE_DESCRIPTION: SO4 BINDING SITE FOR RESIDUE A 2001
REMARK 800 SITE_IDENTIFIER: AC2
REMARK 800 SITE_DESCRIPTION: SO4 BINDING SITE FOR RESIDUE A 2002
REMARK 800 SITE_IDENTIFIER: AC3
REMARK 800 SITE_DESCRIPTION: SO4 BINDING SITE FOR RESIDUE A 2003
REMARK 800 SITE_IDENTIFIER: AC4
REMARK 800 SITE_DESCRIPTION: SO4 BINDING SITE FOR RESIDUE A 2004
REMARK 800 SITE_IDENTIFIER: AC5
REMARK 800 SITE_DESCRIPTION: BME BINDING SITE FOR RESIDUE A 2005
REMARK 800 SITE_IDENTIFIER: AC6
REMARK 800 SITE_DESCRIPTION: ACN BINDING SITE FOR RESIDUE A 1001
REMARK 800 SITE_IDENTIFIER: AC7
REMARK 800 SITE_DESCRIPTION: PEG BINDING SITE FOR RESIDUE A 1501
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1QJ4 RELATED DB: PDB
REMARK 900 HNL AT ATOMIC RESOLUTION
REMARK 900 RELATED ID: 7YAS RELATED DB: PDB
REMARK 900 HNL LOW TEMPERATURE NATIVE STRUCTURE
REMARK 900 RELATED ID: 3C6X RELATED DB: PDB
REMARK 900 HNL FROM HEVEA BRASILIENSIS TO ATOMIC RESOLUTION, NATIVE
REMARK 900 WITH PEG200
REMARK 900 RELATED ID: 3C6Z RELATED DB: PDB
REMARK 900 HNL FROM HEVEA BRASILIENSIS TO ATOMIC RESOLUTION, COMPLEX
REMARK 900 WITH ISOPROPANOL
REMARK 900 RELATED ID: 3C70 RELATED DB: PDB
REMARK 900 HNL FROM HEVEA BRASILIENSIS TO ATOMIC RESOLUTION, COMPLEX
REMARK 900 WITH RHODANIDE (SCN)
DBREF 3C6Y A 1 257 UNP P52704 HNL_HEVBR 1 257
SEQRES 1 A 257 MET ALA PHE ALA HIS PHE VAL LEU ILE HIS THR ILE CYS
SEQRES 2 A 257 HIS GLY ALA TRP ILE TRP HIS LYS LEU LYS PRO LEU LEU
SEQRES 3 A 257 GLU ALA LEU GLY HIS LYS VAL THR ALA LEU ASP LEU ALA
SEQRES 4 A 257 ALA SER GLY VAL ASP PRO ARG GLN ILE GLU GLU ILE GLY
SEQRES 5 A 257 SER PHE ASP GLU TYR SER GLU PRO LEU LEU THR PHE LEU
SEQRES 6 A 257 GLU ALA LEU PRO PRO GLY GLU LYS VAL ILE LEU VAL GLY
SEQRES 7 A 257 GLU SER CYS GLY GLY LEU ASN ILE ALA ILE ALA ALA ASP
SEQRES 8 A 257 LYS TYR CYS GLU LYS ILE ALA ALA ALA VAL PHE HIS ASN
SEQRES 9 A 257 SER VAL LEU PRO ASP THR GLU HIS CYS PRO SER TYR VAL
SEQRES 10 A 257 VAL ASP LYS LEU MET GLU VAL PHE PRO ASP TRP LYS ASP
SEQRES 11 A 257 THR THR TYR PHE THR TYR THR LYS ASP GLY LYS GLU ILE
SEQRES 12 A 257 THR GLY LEU LYS LEU GLY PHE THR LEU LEU ARG GLU ASN
SEQRES 13 A 257 LEU TYR THR LEU CYS GLY PRO GLU GLU TYR GLU LEU ALA
SEQRES 14 A 257 LYS MET LEU THR ARG LYS GLY SER LEU PHE GLN ASN ILE
SEQRES 15 A 257 LEU ALA LYS ARG PRO PHE PHE THR LYS GLU GLY TYR GLY
SEQRES 16 A 257 SER ILE LYS LYS ILE TYR VAL TRP THR ASP GLN ASP GLU
SEQRES 17 A 257 ILE PHE LEU PRO GLU PHE GLN LEU TRP GLN ILE GLU ASN
SEQRES 18 A 257 TYR LYS PRO ASP LYS VAL TYR LYS VAL GLU GLY GLY ASP
SEQRES 19 A 257 HIS LYS LEU GLN LEU THR LYS THR LYS GLU ILE ALA GLU
SEQRES 20 A 257 ILE LEU GLN GLU VAL ALA ASP THR TYR ASN
HET SO4 A2001 5
HET SO4 A2002 5
HET SO4 A2003 5
HET SO4 A2004 5
HET BME A2005 4
HET ACN A1001 8
HET PEG A1501 7
HETNAM SO4 SULFATE ION
HETNAM BME BETA-MERCAPTOETHANOL
HETNAM ACN ACETONE
HETNAM PEG DI(HYDROXYETHYL)ETHER
FORMUL 2 SO4 4(O4 S 2-)
FORMUL 6 BME C2 H6 O S
FORMUL 7 ACN C3 H6 O
FORMUL 8 PEG C4 H10 O3
FORMUL 9 HOH *534(H2 O)
HELIX 1 1 GLY A 15 HIS A 20 5 6
HELIX 2 2 LYS A 21 LEU A 29 1 9
HELIX 3 3 GLN A 47 ILE A 51 5 5
HELIX 4 4 SER A 53 SER A 58 1 6
HELIX 5 5 SER A 58 ALA A 67 1 10
HELIX 6 6 CYS A 81 CYS A 94 1 14
HELIX 7 7 SER A 115 PHE A 125 1 11
HELIX 8 8 GLY A 149 LEU A 157 1 9
HELIX 9 9 GLY A 162 THR A 173 1 12
HELIX 10 10 PHE A 179 ARG A 186 1 8
HELIX 11 11 GLY A 193 ILE A 197 5 5
HELIX 12 12 LEU A 211 TYR A 222 1 12
HELIX 13 13 LYS A 236 LYS A 241 1 6
HELIX 14 14 LYS A 241 TYR A 256 1 16
SHEET 1 A 6 LYS A 32 LEU A 36 0
SHEET 2 A 6 HIS A 5 ILE A 9 1 N LEU A 8 O THR A 34
SHEET 3 A 6 VAL A 74 SER A 80 1 O VAL A 77 N ILE A 9
SHEET 4 A 6 ILE A 97 SER A 105 1 O VAL A 101 N LEU A 76
SHEET 5 A 6 LYS A 199 TRP A 203 1 O VAL A 202 N PHE A 102
SHEET 6 A 6 LYS A 226 LYS A 229 1 O LYS A 226 N TYR A 201
SHEET 1 B 3 THR A 132 LYS A 138 0
SHEET 2 B 3 LYS A 141 LYS A 147 -1 O ILE A 143 N TYR A 136
SHEET 3 B 3 GLY A 176 SER A 177 -1 O GLY A 176 N LEU A 146
LINK SG BCYS A 94 S2 BBME A2005 1555 1555 2.11
SITE 1 AC1 9 LYS A 23 LYS A 170 HOH A3019 HOH A3134
SITE 2 AC1 9 HOH A3172 HOH A3249 HOH A3444 HOH A3495
SITE 3 AC1 9 HOH A3530
SITE 1 AC2 11 THR A 137 LYS A 138 ASP A 139 GLY A 140
SITE 2 AC2 11 GLY A 232 GLY A 233 LYS A 241 HOH A3224
SITE 3 AC2 11 HOH A3236 HOH A3340 HOH A3380
SITE 1 AC3 8 LYS A 141 ASN A 181 LYS A 185 HOH A3115
SITE 2 AC3 8 HOH A3128 HOH A3142 HOH A3421 HOH A3488
SITE 1 AC4 5 THR A 110 GLY A 195 TYR A 222 HOH A3257
SITE 2 AC4 5 HOH A3471
SITE 1 AC5 4 CYS A 94 GLU A 95 GLU A 192 HOH A3356
SITE 1 AC6 8 THR A 11 ILE A 12 SER A 80 TRP A 128
SITE 2 AC6 8 LEU A 148 LEU A 157 HIS A 235 HOH A3050
SITE 1 AC7 7 GLN A 47 LYS A 147 ARG A 174 LYS A 175
SITE 2 AC7 7 HOH A3149 HOH A3324 HOH A3455
CRYST1 47.249 106.104 128.206 90.00 90.00 90.00 C 2 2 21 8
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 0.021164 0.000000 0.000000 0.00000
SCALE2 0.000000 0.009425 0.000000 0.00000
SCALE3 0.000000 0.000000 0.007800 0.00000
END |