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2loy-validation-full.cif
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2loy-validation-full.cif
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data_2LOY-validation-full
#
_entity.id 1
_entity.formula_weight 21642.564
_entity.pdbx_description
'Translationally-controlled tumor protein homolog'
_entity.pdbx_number_of_molecules 1
_entity.src_method man
_entity.type polymer
#
_entity_name_com.entity_id 1
_entity_name_com.name TCTP
#
_entity_poly.entity_id 1
_entity_poly.nstd_linkage no
_entity_poly.nstd_monomer no
_entity_poly.pdbx_seq_one_letter_code
;MLIYKDIFTDDELSSDSFPMKLVDDLVYEFKGKHVVRKEGEIVLAGSNPSAEEGAEDDGSDEHVERGIDIVLNHKLVEMN
CYEDASMFKAYIKKFMKNVIDHMEKNNRDKADVDAFKKKIQGWVVSLLAKDRFKNLAFFIGERAAEGAENGQVAIIEYRD
VDGTEVPTLMLVKEAIIEEKCLEHHHHHH
;
_entity_poly.pdbx_seq_one_letter_code_can
;MLIYKDIFTDDELSSDSFPMKLVDDLVYEFKGKHVVRKEGEIVLAGSNPSAEEGAEDDGSDEHVERGIDIVLNHKLVEMN
CYEDASMFKAYIKKFMKNVIDHMEKNNRDKADVDAFKKKIQGWVVSLLAKDRFKNLAFFIGERAAEGAENGQVAIIEYRD
VDGTEVPTLMLVKEAIIEEKCLEHHHHHH
;
_entity_poly.pdbx_strand_id A
_entity_poly.pdbx_target_identifier NESG-WR73
_entity_poly.type 'polypeptide(L)'
#
loop_
_entity_poly_seq.entity_id
_entity_poly_seq.mon_id
_entity_poly_seq.num
_entity_poly_seq.hetero
1 MET 1 n
1 LEU 2 n
1 ILE 3 n
1 TYR 4 n
1 LYS 5 n
1 ASP 6 n
1 ILE 7 n
1 PHE 8 n
1 THR 9 n
1 ASP 10 n
1 ASP 11 n
1 GLU 12 n
1 LEU 13 n
1 SER 14 n
1 SER 15 n
1 ASP 16 n
1 SER 17 n
1 PHE 18 n
1 PRO 19 n
1 MET 20 n
1 LYS 21 n
1 LEU 22 n
1 VAL 23 n
1 ASP 24 n
1 ASP 25 n
1 LEU 26 n
1 VAL 27 n
1 TYR 28 n
1 GLU 29 n
1 PHE 30 n
1 LYS 31 n
1 GLY 32 n
1 LYS 33 n
1 HIS 34 n
1 VAL 35 n
1 VAL 36 n
1 ARG 37 n
1 LYS 38 n
1 GLU 39 n
1 GLY 40 n
1 GLU 41 n
1 ILE 42 n
1 VAL 43 n
1 LEU 44 n
1 ALA 45 n
1 GLY 46 n
1 SER 47 n
1 ASN 48 n
1 PRO 49 n
1 SER 50 n
1 ALA 51 n
1 GLU 52 n
1 GLU 53 n
1 GLY 54 n
1 ALA 55 n
1 GLU 56 n
1 ASP 57 n
1 ASP 58 n
1 GLY 59 n
1 SER 60 n
1 ASP 61 n
1 GLU 62 n
1 HIS 63 n
1 VAL 64 n
1 GLU 65 n
1 ARG 66 n
1 GLY 67 n
1 ILE 68 n
1 ASP 69 n
1 ILE 70 n
1 VAL 71 n
1 LEU 72 n
1 ASN 73 n
1 HIS 74 n
1 LYS 75 n
1 LEU 76 n
1 VAL 77 n
1 GLU 78 n
1 MET 79 n
1 ASN 80 n
1 CYS 81 n
1 TYR 82 n
1 GLU 83 n
1 ASP 84 n
1 ALA 85 n
1 SER 86 n
1 MET 87 n
1 PHE 88 n
1 LYS 89 n
1 ALA 90 n
1 TYR 91 n
1 ILE 92 n
1 LYS 93 n
1 LYS 94 n
1 PHE 95 n
1 MET 96 n
1 LYS 97 n
1 ASN 98 n
1 VAL 99 n
1 ILE 100 n
1 ASP 101 n
1 HIS 102 n
1 MET 103 n
1 GLU 104 n
1 LYS 105 n
1 ASN 106 n
1 ASN 107 n
1 ARG 108 n
1 ASP 109 n
1 LYS 110 n
1 ALA 111 n
1 ASP 112 n
1 VAL 113 n
1 ASP 114 n
1 ALA 115 n
1 PHE 116 n
1 LYS 117 n
1 LYS 118 n
1 LYS 119 n
1 ILE 120 n
1 GLN 121 n
1 GLY 122 n
1 TRP 123 n
1 VAL 124 n
1 VAL 125 n
1 SER 126 n
1 LEU 127 n
1 LEU 128 n
1 ALA 129 n
1 LYS 130 n
1 ASP 131 n
1 ARG 132 n
1 PHE 133 n
1 LYS 134 n
1 ASN 135 n
1 LEU 136 n
1 ALA 137 n
1 PHE 138 n
1 PHE 139 n
1 ILE 140 n
1 GLY 141 n
1 GLU 142 n
1 ARG 143 n
1 ALA 144 n
1 ALA 145 n
1 GLU 146 n
1 GLY 147 n
1 ALA 148 n
1 GLU 149 n
1 ASN 150 n
1 GLY 151 n
1 GLN 152 n
1 VAL 153 n
1 ALA 154 n
1 ILE 155 n
1 ILE 156 n
1 GLU 157 n
1 TYR 158 n
1 ARG 159 n
1 ASP 160 n
1 VAL 161 n
1 ASP 162 n
1 GLY 163 n
1 THR 164 n
1 GLU 165 n
1 VAL 166 n
1 PRO 167 n
1 THR 168 n
1 LEU 169 n
1 MET 170 n
1 LEU 171 n
1 VAL 172 n
1 LYS 173 n
1 GLU 174 n
1 ALA 175 n
1 ILE 176 n
1 ILE 177 n
1 GLU 178 n
1 GLU 179 n
1 LYS 180 n
1 CYS 181 n
1 LEU 182 n
1 GLU 183 n
1 HIS 184 n
1 HIS 185 n
1 HIS 186 n
1 HIS 187 n
1 HIS 188 n
1 HIS 189 n
#
_entry.id 2LOY
#
_exptl.entry_id 2LOY
_exptl.method 'SOLUTION NMR'
_exptl.details
'Refinement of minimal constraint structure with residual dipolar couplings'
#
_pdbx_audit_revision_details.data_content_type 'Structure model'
_pdbx_audit_revision_details.ordinal 1
_pdbx_audit_revision_details.revision_ordinal 1
_pdbx_audit_revision_details.provider repository
_pdbx_audit_revision_details.type 'Initial release'
#
loop_
_pdbx_audit_revision_group.data_content_type
_pdbx_audit_revision_group.ordinal
_pdbx_audit_revision_group.revision_ordinal
_pdbx_audit_revision_group.group
'Structure model' 1 2 'Database references'
'Structure model' 2 3 'Database references'
#
loop_
_pdbx_audit_revision_history.data_content_type
_pdbx_audit_revision_history.ordinal
_pdbx_audit_revision_history.major_revision
_pdbx_audit_revision_history.minor_revision
_pdbx_audit_revision_history.revision_date
'Structure model' 1 1 0 2012-02-15
'Structure model' 2 1 1 2012-06-27
'Structure model' 3 1 2 2012-07-25
#
loop_
_pdbx_database_related.content_type
_pdbx_database_related.db_id
_pdbx_database_related.db_name
_pdbx_database_related.details
unspecified 2KWB PDB 'Original minimal constraint structure'
unspecified 16833 BMRB ?
unspecified NESG-WR73 TargetTrack ?
#
_pdbx_database_status.entry_id 2LOY
_pdbx_database_status.SG_entry Y
_pdbx_database_status.deposit_site BMRB
_pdbx_database_status.pdb_format_compatible Y
_pdbx_database_status.process_site RCSB
_pdbx_database_status.recvd_initial_deposition_date 2012-01-27
_pdbx_database_status.status_code REL
_pdbx_database_status.status_code_cs REL
_pdbx_database_status.status_code_mr REL
_pdbx_database_status.validation_created_date 2021-01-26
#
_pdbx_nmr_constraints.entry_id 2LOY
_pdbx_nmr_constraints.NOE_constraints_total 970
#
_pdbx_nmr_details.entry_id 2LOY
_pdbx_nmr_details.text
;THE PROTEIN IS MONOMERIC AT 298 K BY 15N T1/T2 RELAXATION AND STATIC LIGHT SCATTERING. THE STRUCTURE IS A MINIMAL CONSTRAINT STRUCTURE DETERMINED USING TRIPLE RESONANCE NMR SPECTROSCOPY. ALL NOESY DATA WERE ACQUIRED AT 800 MHZ USING A 5-MM CRYOPROBE. BACKBONE ASSIGNMENTS WERE MADE USING PINE, AND THE SIDE CHAIN METHYL ASSIGNMENTS WERE COMPLETED MANUALLY. AUTOMATIC NOESY ASSIGNMENTS WERE DETERMINED USING CYANA 3.0. BACKBONE (PHI/PSI) DIHEDRAL ANGLE CONSTRAINTS WERE OBTAINED FROM TALOSplus. FINAL STRUCTURE QUALITY FACTORS (FOR RESIDUE NUMBERS 1 TO 183, PSVS 1.4), WHERE ORDERED RESIDUES [S(PHI) + S(PSI) > 1.8] COMPRISE: 2-12,18-38,66-106,111-146,152-162,164-181: (A) RMSD (ORDERED RESIDUES): BB, 1.0, HEAVY ATOM, 1.6. (B) MOLPROBITY RAMACHANDRAN STATISTICS FOR ORDERED RESIDUES: MOST FAVORED, 96.8%, ALLOWED, 2.9%, DISALLOWED, 0.2%. (C) PROCHECK SCORES FOR ORDERED RESIDUES (RAW/Z-): PHI-PSI, -0.28/-0.79, ALL, -0.26/-1.54. (D) MOLPROBITY CLASH SCORE (RAW/Z-): 15.30/-1.10 (E) NUMBER OF CLOSE CONTACTS PER 20 MODELS: 40. (F) AGREEMENT WITH N-H RESIDUAL DIPOLAR COUPLINGS: CORRELATION COEFFICIENT (R): 0.985; Qrms: 0.171. THE C-TERMINAL HIS TAG RESIDUES OF THE PROTEIN (HHHHHH) WERE NOT INCLUDED IN THE STRUCTURE CALCULATIONS AND HAVE BEEN OMITTED FROM THIS DEPOSITION. COORDINATES FOR THE FOLLOWING RESIDUES ARE NOT WELL DETERMINED [S(PHI) + S(PSI) < 1.8]: 1,13-17,39-65,107-110,147-151,163,182-183.
;
#
_pdbx_nmr_ensemble.entry_id 2LOY
_pdbx_nmr_ensemble.conformer_selection_criteria
'structures with the lowest energy'
_pdbx_nmr_ensemble.conformers_calculated_total_number 100
_pdbx_nmr_ensemble.conformers_submitted_total_number 20
_pdbx_nmr_ensemble.atom_consistency_flag Y
#
loop_
_pdbx_nmr_exptl.conditions_id
_pdbx_nmr_exptl.experiment_id
_pdbx_nmr_exptl.solution_id
_pdbx_nmr_exptl.type
1 1 1 '2D 1H-15N HSQC'
1 2 1 '2D 1H-15N TROSY-HSQC'
1 3 1 '2D 1H-13C HSQC aliphatic'
1 4 1 '3D HNCO'
1 5 1 '3D HN(CA)CO'
1 6 1 '3D TROSY-HNCACB'
1 7 1 '3D TROSY-HN(CO)CACB'
1 8 1 '3D 1H-15N NOESY'
1 9 1 '3D 1H-13C NOESY aliphatic'
1 10 1 '3D 15N-15N-1H NOESY'
1 11 1 '3D 13C-13C-1H NOESY'
1 12 1 '3D 15N-13C-1H NOESY'
1 13 1 '3D 13C-15N-1H NOESY'
1 14 1 '3D C(CO)NH TOCSY'
1 15 2 '2D 1H-13C HSQC high resolution'
1 16 3 'NH J-MODULATION (RDC)'
#
loop_
_pdbx_nmr_exptl_sample.component
_pdbx_nmr_exptl_sample.solution_id
_pdbx_nmr_exptl_sample.concentration
_pdbx_nmr_exptl_sample.concentration_units
_pdbx_nmr_exptl_sample.isotopic_labeling
WR73.009-1 1 0.822 mM
'[U-100% 13C; U-100% 15N; U-100% 2H; ILVFY-1H]'
NaN3-2 1 0.02 % ?
DTT-3 1 10 mM ?
CaCL2-4 1 5 mM ?
NaCL-5 1 100 mM ?
'Proteinase Inhibitors-6' 1 1 % ?
'MES pH 6.5-7' 1 20 mM ?
D2O-8 1 10 % ?
DSS-9 1 50 uM ?
WR73.004-10 2 0.85 mM '[U-5% 13C; U-100% 15N]'
NaN3-11 2 0.02 % ?
DTT-12 2 10 mM ?
CaCL2-13 2 5 mM ?
NaCL-14 2 100 mM ?
'Proteinase Inhibitors-15' 2 1 % ?
'MES pH 6.5-16' 2 20 mM ?
D2O-17 2 10 % ?
DSS-18 2 50 uM ?
#
_pdbx_nmr_exptl_sample_conditions.conditions_id 1
_pdbx_nmr_exptl_sample_conditions.pH 6.5
_pdbx_nmr_exptl_sample_conditions.pressure ambient
_pdbx_nmr_exptl_sample_conditions.temperature 298
_pdbx_nmr_exptl_sample_conditions.temperature_units K
#
_pdbx_nmr_refine.entry_id 2LOY
_pdbx_nmr_refine.software_ordinal 1
_pdbx_nmr_refine.details
;THE FINAL RDC-REFINED MINIMAL CONSTRAINT STRUCTURES ARE BASED ON A TOTAL OF 970 CONFORMATIONALLY-RESTRICTING DISTANCE CONSTRAINTS, 293 DIHEDRAL ANGLE CONSTRAINTS, 126 HYDROGEN BOND CONSTRAINTS, and 99 N-H RESIDUAL DIPOLAR COUPLINGS FROM A SINGLE ALIGNMENT IN PHAGE. (7.7 CONSTRAINTS PER RESIDUE, 2.3 LONG RANGE CONSTRAINTS PER RESIDUE, COMPUTED FOR RESIDUES 1 TO 183 BY PSVS 1.4). STRUCTURE DETERMINATION WAS PERFORMED ITERATIVELY USING CYANA 3.0. THE 20 FINAL STRUCTURES OUT OF 100 WITH THE LOWEST TARGET FUNCTION WERE FURTHER REFINED BY RESTRAINED MOLECULAR DYNAMICS/ENERGY MINIMIZATION IN EXPLICIT WATER (CNS) WITH PARAM19.
;
_pdbx_nmr_refine.method 'simulated annealing'
#
_pdbx_nmr_representative.entry_id 2LOY
_pdbx_nmr_representative.conformer_id 1
_pdbx_nmr_representative.selection_criteria 'lowest energy'
#
loop_
_pdbx_nmr_software.ordinal
_pdbx_nmr_software.authors
_pdbx_nmr_software.classification
_pdbx_nmr_software.name
_pdbx_nmr_software.version
1 'Brunger, Adams, Clore, Gros, Nilges and Read' refinement CNS
1.3
2 'Brunger, Adams, Clore, Gros, Nilges and Read' 'structure solution'
CNS 1.3
3 'Brunger, Adams, Clore, Gros, Nilges and Read' 'geometry optimization'
CNS 1.3
4 'Guntert, Mumenthaler and Wuthrich' 'structure solution'
CYANA 3.0
5 'Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax' processing NMRPipe
2.3
6 'Bruker Biospin' 'data collection'
TOPSPIN 2.1
7 Varian 'data collection' VNMRJ
?
8 'Bahrami, Markley, Assadi, and Eghbalnia'
'chemical shift assignment' PINE 1.0
9 Goddard 'data analysis' SPARKY
3
10 Goddard 'peak picking' SPARKY 3
11 'Shen, Cornilescu, Delaglio and Bax'
'dihedral angle constraints' TALOS+ ?
12 'PALES (Zweckstetter, Bax)' 'rdc analysis' PALES ?
13 'Bhattacharya, Montelione' 'structure validation'
PSVS 1.4
14 'Bhattacharya, Montelione' 'quality assessment'
PSVS 1.4
15 'Tejero, Montelione' 'data analysis' PdbStat
5.5
16 Richardson 'structure validation'
MolProbity 3.19
17 Richardson 'quality assessment'
MolProbity 3.19
#
loop_
_pdbx_nmr_spectrometer.spectrometer_id
_pdbx_nmr_spectrometer.field_strength
_pdbx_nmr_spectrometer.manufacturer
_pdbx_nmr_spectrometer.model
_pdbx_nmr_spectrometer.type
1 800 Bruker Avance 'Bruker Avance'
2 600 Varian INOVA 'Varian INOVA'
#
loop_
_pdbx_poly_seq_scheme.asym_id
_pdbx_poly_seq_scheme.entity_id
_pdbx_poly_seq_scheme.mon_id
_pdbx_poly_seq_scheme.seq_id
_pdbx_poly_seq_scheme.auth_mon_id
_pdbx_poly_seq_scheme.auth_seq_num
_pdbx_poly_seq_scheme.hetero
_pdbx_poly_seq_scheme.ndb_seq_num
_pdbx_poly_seq_scheme.pdb_ins_code
_pdbx_poly_seq_scheme.pdb_mon_id
_pdbx_poly_seq_scheme.pdb_seq_num
_pdbx_poly_seq_scheme.pdb_strand_id
A 1 MET 1 MET 1 n 1 ? MET 1 A
A 1 LEU 2 LEU 2 n 2 ? LEU 2 A
A 1 ILE 3 ILE 3 n 3 ? ILE 3 A
A 1 TYR 4 TYR 4 n 4 ? TYR 4 A
A 1 LYS 5 LYS 5 n 5 ? LYS 5 A
A 1 ASP 6 ASP 6 n 6 ? ASP 6 A
A 1 ILE 7 ILE 7 n 7 ? ILE 7 A
A 1 PHE 8 PHE 8 n 8 ? PHE 8 A
A 1 THR 9 THR 9 n 9 ? THR 9 A
A 1 ASP 10 ASP 10 n 10 ? ASP 10 A
A 1 ASP 11 ASP 11 n 11 ? ASP 11 A
A 1 GLU 12 GLU 12 n 12 ? GLU 12 A
A 1 LEU 13 LEU 13 n 13 ? LEU 13 A
A 1 SER 14 SER 14 n 14 ? SER 14 A
A 1 SER 15 SER 15 n 15 ? SER 15 A
A 1 ASP 16 ASP 16 n 16 ? ASP 16 A
A 1 SER 17 SER 17 n 17 ? SER 17 A
A 1 PHE 18 PHE 18 n 18 ? PHE 18 A
A 1 PRO 19 PRO 19 n 19 ? PRO 19 A
A 1 MET 20 MET 20 n 20 ? MET 20 A
A 1 LYS 21 LYS 21 n 21 ? LYS 21 A
A 1 LEU 22 LEU 22 n 22 ? LEU 22 A
A 1 VAL 23 VAL 23 n 23 ? VAL 23 A
A 1 ASP 24 ASP 24 n 24 ? ASP 24 A
A 1 ASP 25 ASP 25 n 25 ? ASP 25 A
A 1 LEU 26 LEU 26 n 26 ? LEU 26 A
A 1 VAL 27 VAL 27 n 27 ? VAL 27 A
A 1 TYR 28 TYR 28 n 28 ? TYR 28 A
A 1 GLU 29 GLU 29 n 29 ? GLU 29 A
A 1 PHE 30 PHE 30 n 30 ? PHE 30 A
A 1 LYS 31 LYS 31 n 31 ? LYS 31 A
A 1 GLY 32 GLY 32 n 32 ? GLY 32 A
A 1 LYS 33 LYS 33 n 33 ? LYS 33 A
A 1 HIS 34 HIS 34 n 34 ? HIS 34 A
A 1 VAL 35 VAL 35 n 35 ? VAL 35 A
A 1 VAL 36 VAL 36 n 36 ? VAL 36 A
A 1 ARG 37 ARG 37 n 37 ? ARG 37 A
A 1 LYS 38 LYS 38 n 38 ? LYS 38 A
A 1 GLU 39 GLU 39 n 39 ? GLU 39 A
A 1 GLY 40 GLY 40 n 40 ? GLY 40 A
A 1 GLU 41 GLU 41 n 41 ? GLU 41 A
A 1 ILE 42 ILE 42 n 42 ? ILE 42 A
A 1 VAL 43 VAL 43 n 43 ? VAL 43 A
A 1 LEU 44 LEU 44 n 44 ? LEU 44 A
A 1 ALA 45 ALA 45 n 45 ? ALA 45 A
A 1 GLY 46 GLY 46 n 46 ? GLY 46 A
A 1 SER 47 SER 47 n 47 ? SER 47 A
A 1 ASN 48 ASN 48 n 48 ? ASN 48 A
A 1 PRO 49 PRO 49 n 49 ? PRO 49 A
A 1 SER 50 SER 50 n 50 ? SER 50 A
A 1 ALA 51 ALA 51 n 51 ? ALA 51 A
A 1 GLU 52 GLU 52 n 52 ? GLU 52 A
A 1 GLU 53 GLU 53 n 53 ? GLU 53 A
A 1 GLY 54 GLY 54 n 54 ? GLY 54 A
A 1 ALA 55 ALA 55 n 55 ? ALA 55 A
A 1 GLU 56 GLU 56 n 56 ? GLU 56 A
A 1 ASP 57 ASP 57 n 57 ? ASP 57 A
A 1 ASP 58 ASP 58 n 58 ? ASP 58 A
A 1 GLY 59 GLY 59 n 59 ? GLY 59 A
A 1 SER 60 SER 60 n 60 ? SER 60 A
A 1 ASP 61 ASP 61 n 61 ? ASP 61 A
A 1 GLU 62 GLU 62 n 62 ? GLU 62 A
A 1 HIS 63 HIS 63 n 63 ? HIS 63 A
A 1 VAL 64 VAL 64 n 64 ? VAL 64 A
A 1 GLU 65 GLU 65 n 65 ? GLU 65 A
A 1 ARG 66 ARG 66 n 66 ? ARG 66 A
A 1 GLY 67 GLY 67 n 67 ? GLY 67 A
A 1 ILE 68 ILE 68 n 68 ? ILE 68 A
A 1 ASP 69 ASP 69 n 69 ? ASP 69 A
A 1 ILE 70 ILE 70 n 70 ? ILE 70 A
A 1 VAL 71 VAL 71 n 71 ? VAL 71 A
A 1 LEU 72 LEU 72 n 72 ? LEU 72 A
A 1 ASN 73 ASN 73 n 73 ? ASN 73 A
A 1 HIS 74 HIS 74 n 74 ? HIS 74 A
A 1 LYS 75 LYS 75 n 75 ? LYS 75 A
A 1 LEU 76 LEU 76 n 76 ? LEU 76 A
A 1 VAL 77 VAL 77 n 77 ? VAL 77 A
A 1 GLU 78 GLU 78 n 78 ? GLU 78 A
A 1 MET 79 MET 79 n 79 ? MET 79 A
A 1 ASN 80 ASN 80 n 80 ? ASN 80 A
A 1 CYS 81 CYS 81 n 81 ? CYS 81 A
A 1 TYR 82 TYR 82 n 82 ? TYR 82 A
A 1 GLU 83 GLU 83 n 83 ? GLU 83 A
A 1 ASP 84 ASP 84 n 84 ? ASP 84 A
A 1 ALA 85 ALA 85 n 85 ? ALA 85 A
A 1 SER 86 SER 86 n 86 ? SER 86 A
A 1 MET 87 MET 87 n 87 ? MET 87 A
A 1 PHE 88 PHE 88 n 88 ? PHE 88 A
A 1 LYS 89 LYS 89 n 89 ? LYS 89 A
A 1 ALA 90 ALA 90 n 90 ? ALA 90 A
A 1 TYR 91 TYR 91 n 91 ? TYR 91 A
A 1 ILE 92 ILE 92 n 92 ? ILE 92 A
A 1 LYS 93 LYS 93 n 93 ? LYS 93 A
A 1 LYS 94 LYS 94 n 94 ? LYS 94 A
A 1 PHE 95 PHE 95 n 95 ? PHE 95 A
A 1 MET 96 MET 96 n 96 ? MET 96 A
A 1 LYS 97 LYS 97 n 97 ? LYS 97 A
A 1 ASN 98 ASN 98 n 98 ? ASN 98 A
A 1 VAL 99 VAL 99 n 99 ? VAL 99 A
A 1 ILE 100 ILE 100 n 100 ? ILE 100 A
A 1 ASP 101 ASP 101 n 101 ? ASP 101 A
A 1 HIS 102 HIS 102 n 102 ? HIS 102 A
A 1 MET 103 MET 103 n 103 ? MET 103 A
A 1 GLU 104 GLU 104 n 104 ? GLU 104 A
A 1 LYS 105 LYS 105 n 105 ? LYS 105 A
A 1 ASN 106 ASN 106 n 106 ? ASN 106 A
A 1 ASN 107 ASN 107 n 107 ? ASN 107 A
A 1 ARG 108 ARG 108 n 108 ? ARG 108 A
A 1 ASP 109 ASP 109 n 109 ? ASP 109 A
A 1 LYS 110 LYS 110 n 110 ? LYS 110 A
A 1 ALA 111 ALA 111 n 111 ? ALA 111 A
A 1 ASP 112 ASP 112 n 112 ? ASP 112 A
A 1 VAL 113 VAL 113 n 113 ? VAL 113 A
A 1 ASP 114 ASP 114 n 114 ? ASP 114 A
A 1 ALA 115 ALA 115 n 115 ? ALA 115 A
A 1 PHE 116 PHE 116 n 116 ? PHE 116 A
A 1 LYS 117 LYS 117 n 117 ? LYS 117 A
A 1 LYS 118 LYS 118 n 118 ? LYS 118 A
A 1 LYS 119 LYS 119 n 119 ? LYS 119 A
A 1 ILE 120 ILE 120 n 120 ? ILE 120 A
A 1 GLN 121 GLN 121 n 121 ? GLN 121 A
A 1 GLY 122 GLY 122 n 122 ? GLY 122 A
A 1 TRP 123 TRP 123 n 123 ? TRP 123 A
A 1 VAL 124 VAL 124 n 124 ? VAL 124 A
A 1 VAL 125 VAL 125 n 125 ? VAL 125 A
A 1 SER 126 SER 126 n 126 ? SER 126 A
A 1 LEU 127 LEU 127 n 127 ? LEU 127 A
A 1 LEU 128 LEU 128 n 128 ? LEU 128 A
A 1 ALA 129 ALA 129 n 129 ? ALA 129 A
A 1 LYS 130 LYS 130 n 130 ? LYS 130 A
A 1 ASP 131 ASP 131 n 131 ? ASP 131 A
A 1 ARG 132 ARG 132 n 132 ? ARG 132 A
A 1 PHE 133 PHE 133 n 133 ? PHE 133 A
A 1 LYS 134 LYS 134 n 134 ? LYS 134 A
A 1 ASN 135 ASN 135 n 135 ? ASN 135 A
A 1 LEU 136 LEU 136 n 136 ? LEU 136 A
A 1 ALA 137 ALA 137 n 137 ? ALA 137 A
A 1 PHE 138 PHE 138 n 138 ? PHE 138 A
A 1 PHE 139 PHE 139 n 139 ? PHE 139 A
A 1 ILE 140 ILE 140 n 140 ? ILE 140 A
A 1 GLY 141 GLY 141 n 141 ? GLY 141 A
A 1 GLU 142 GLU 142 n 142 ? GLU 142 A
A 1 ARG 143 ARG 143 n 143 ? ARG 143 A
A 1 ALA 144 ALA 144 n 144 ? ALA 144 A
A 1 ALA 145 ALA 145 n 145 ? ALA 145 A
A 1 GLU 146 GLU 146 n 146 ? GLU 146 A
A 1 GLY 147 GLY 147 n 147 ? GLY 147 A
A 1 ALA 148 ALA 148 n 148 ? ALA 148 A
A 1 GLU 149 GLU 149 n 149 ? GLU 149 A
A 1 ASN 150 ASN 150 n 150 ? ASN 150 A
A 1 GLY 151 GLY 151 n 151 ? GLY 151 A
A 1 GLN 152 GLN 152 n 152 ? GLN 152 A
A 1 VAL 153 VAL 153 n 153 ? VAL 153 A
A 1 ALA 154 ALA 154 n 154 ? ALA 154 A
A 1 ILE 155 ILE 155 n 155 ? ILE 155 A
A 1 ILE 156 ILE 156 n 156 ? ILE 156 A
A 1 GLU 157 GLU 157 n 157 ? GLU 157 A
A 1 TYR 158 TYR 158 n 158 ? TYR 158 A
A 1 ARG 159 ARG 159 n 159 ? ARG 159 A
A 1 ASP 160 ASP 160 n 160 ? ASP 160 A
A 1 VAL 161 VAL 161 n 161 ? VAL 161 A
A 1 ASP 162 ASP 162 n 162 ? ASP 162 A
A 1 GLY 163 GLY 163 n 163 ? GLY 163 A
A 1 THR 164 THR 164 n 164 ? THR 164 A
A 1 GLU 165 GLU 165 n 165 ? GLU 165 A
A 1 VAL 166 VAL 166 n 166 ? VAL 166 A
A 1 PRO 167 PRO 167 n 167 ? PRO 167 A
A 1 THR 168 THR 168 n 168 ? THR 168 A
A 1 LEU 169 LEU 169 n 169 ? LEU 169 A
A 1 MET 170 MET 170 n 170 ? MET 170 A
A 1 LEU 171 LEU 171 n 171 ? LEU 171 A
A 1 VAL 172 VAL 172 n 172 ? VAL 172 A
A 1 LYS 173 LYS 173 n 173 ? LYS 173 A
A 1 GLU 174 GLU 174 n 174 ? GLU 174 A
A 1 ALA 175 ALA 175 n 175 ? ALA 175 A
A 1 ILE 176 ILE 176 n 176 ? ILE 176 A
A 1 ILE 177 ILE 177 n 177 ? ILE 177 A
A 1 GLU 178 GLU 178 n 178 ? GLU 178 A
A 1 GLU 179 GLU 179 n 179 ? GLU 179 A
A 1 LYS 180 LYS 180 n 180 ? LYS 180 A
A 1 CYS 181 CYS 181 n 181 ? CYS 181 A
A 1 LEU 182 LEU 182 n 182 ? LEU 182 A
A 1 GLU 183 GLU 183 n 183 ? GLU 183 A
A 1 HIS 184 ? ? n 184 ? ? 184 A
A 1 HIS 185 ? ? n 185 ? ? 185 A
A 1 HIS 186 ? ? n 186 ? ? 186 A
A 1 HIS 187 ? ? n 187 ? ? 187 A
A 1 HIS 188 ? ? n 188 ? ? 188 A
A 1 HIS 189 ? ? n 189 ? ? 189 A
#
_pdbx_struct_assembly.id 1
_pdbx_struct_assembly.details author_defined_assembly
_pdbx_struct_assembly.oligomeric_count 1
_pdbx_struct_assembly.oligomeric_details monomeric
#
_pdbx_struct_assembly_gen.assembly_id 1
_pdbx_struct_assembly_gen.asym_id_list A
_pdbx_struct_assembly_gen.oper_expression 1
#
_pdbx_struct_oper_list.id 1
_pdbx_struct_oper_list.matrix[1][1] 1.0000000000
_pdbx_struct_oper_list.matrix[1][2] 0.0000000000
_pdbx_struct_oper_list.matrix[1][3] 0.0000000000
_pdbx_struct_oper_list.matrix[2][1] 0.0000000000
_pdbx_struct_oper_list.matrix[2][2] 1.0000000000
_pdbx_struct_oper_list.matrix[2][3] 0.0000000000
_pdbx_struct_oper_list.matrix[3][1] 0.0000000000
_pdbx_struct_oper_list.matrix[3][2] 0.0000000000
_pdbx_struct_oper_list.matrix[3][3] 1.0000000000
_pdbx_struct_oper_list.name 1_555
_pdbx_struct_oper_list.symmetry_operation x,y,z
_pdbx_struct_oper_list.type 'identity operation'
_pdbx_struct_oper_list.vector[1] 0.0000000000
_pdbx_struct_oper_list.vector[2] 0.0000000000
_pdbx_struct_oper_list.vector[3] 0.0000000000
#
loop_
_pdbx_struct_sheet_hbond.range_id_1
_pdbx_struct_sheet_hbond.range_id_2
_pdbx_struct_sheet_hbond.sheet_id
_pdbx_struct_sheet_hbond.range_1_auth_asym_id
_pdbx_struct_sheet_hbond.range_1_auth_atom_id
_pdbx_struct_sheet_hbond.range_1_auth_comp_id
_pdbx_struct_sheet_hbond.range_1_auth_seq_id
_pdbx_struct_sheet_hbond.range_1_label_asym_id
_pdbx_struct_sheet_hbond.range_1_label_atom_id
_pdbx_struct_sheet_hbond.range_1_label_comp_id
_pdbx_struct_sheet_hbond.range_1_label_seq_id
_pdbx_struct_sheet_hbond.range_2_auth_asym_id
_pdbx_struct_sheet_hbond.range_2_auth_atom_id
_pdbx_struct_sheet_hbond.range_2_auth_comp_id
_pdbx_struct_sheet_hbond.range_2_auth_seq_id
_pdbx_struct_sheet_hbond.range_2_label_asym_id
_pdbx_struct_sheet_hbond.range_2_label_atom_id
_pdbx_struct_sheet_hbond.range_2_label_comp_id
_pdbx_struct_sheet_hbond.range_2_label_seq_id
1 2 A A O ASP 16 A O ASP 16 A N LEU 2 A N LEU 2
2 3 A A N ILE 3 A N ILE 3 A O GLU 179 A O GLU 179
1 2 B A N VAL 23 A N VAL 23 A O VAL 27 A O VAL 27
2 3 B A N PHE 30 A N PHE 30 A O LEU 169 A O LEU 169
3 4 B A O VAL 166 A O VAL 166 A N ARG 159 A N ARG 159
4 5 B A O ALA 154 A O ALA 154 A N PHE 139 A N PHE 139
5 6 B A O PHE 138 A O PHE 138 A N MET 79 A N MET 79
1 2 C A N ARG 37 A N ARG 37 A O GLU 65 A O GLU 65
#
loop_
_pdbx_unobs_or_zero_occ_residues.id
_pdbx_unobs_or_zero_occ_residues.PDB_model_num
_pdbx_unobs_or_zero_occ_residues.auth_asym_id
_pdbx_unobs_or_zero_occ_residues.auth_comp_id
_pdbx_unobs_or_zero_occ_residues.auth_seq_id
_pdbx_unobs_or_zero_occ_residues.label_asym_id
_pdbx_unobs_or_zero_occ_residues.label_comp_id
_pdbx_unobs_or_zero_occ_residues.label_seq_id
_pdbx_unobs_or_zero_occ_residues.occupancy_flag
_pdbx_unobs_or_zero_occ_residues.polymer_flag
1 1 A HIS 184 A HIS 184 1 Y
2 1 A HIS 185 A HIS 185 1 Y
3 1 A HIS 186 A HIS 186 1 Y
4 1 A HIS 187 A HIS 187 1 Y
5 1 A HIS 188 A HIS 188 1 Y
6 1 A HIS 189 A HIS 189 1 Y
7 2 A HIS 184 A HIS 184 1 Y
8 2 A HIS 185 A HIS 185 1 Y
9 2 A HIS 186 A HIS 186 1 Y
10 2 A HIS 187 A HIS 187 1 Y
11 2 A HIS 188 A HIS 188 1 Y
12 2 A HIS 189 A HIS 189 1 Y
13 3 A HIS 184 A HIS 184 1 Y
14 3 A HIS 185 A HIS 185 1 Y
15 3 A HIS 186 A HIS 186 1 Y
16 3 A HIS 187 A HIS 187 1 Y
17 3 A HIS 188 A HIS 188 1 Y
18 3 A HIS 189 A HIS 189 1 Y
19 4 A HIS 184 A HIS 184 1 Y
20 4 A HIS 185 A HIS 185 1 Y
21 4 A HIS 186 A HIS 186 1 Y
22 4 A HIS 187 A HIS 187 1 Y
23 4 A HIS 188 A HIS 188 1 Y
24 4 A HIS 189 A HIS 189 1 Y
25 5 A HIS 184 A HIS 184 1 Y
26 5 A HIS 185 A HIS 185 1 Y
27 5 A HIS 186 A HIS 186 1 Y
28 5 A HIS 187 A HIS 187 1 Y
29 5 A HIS 188 A HIS 188 1 Y
30 5 A HIS 189 A HIS 189 1 Y
31 6 A HIS 184 A HIS 184 1 Y
32 6 A HIS 185 A HIS 185 1 Y
33 6 A HIS 186 A HIS 186 1 Y
34 6 A HIS 187 A HIS 187 1 Y
35 6 A HIS 188 A HIS 188 1 Y
36 6 A HIS 189 A HIS 189 1 Y
37 7 A HIS 184 A HIS 184 1 Y
38 7 A HIS 185 A HIS 185 1 Y
39 7 A HIS 186 A HIS 186 1 Y
40 7 A HIS 187 A HIS 187 1 Y
41 7 A HIS 188 A HIS 188 1 Y
42 7 A HIS 189 A HIS 189 1 Y
43 8 A HIS 184 A HIS 184 1 Y
44 8 A HIS 185 A HIS 185 1 Y
45 8 A HIS 186 A HIS 186 1 Y
46 8 A HIS 187 A HIS 187 1 Y
47 8 A HIS 188 A HIS 188 1 Y
48 8 A HIS 189 A HIS 189 1 Y
49 9 A HIS 184 A HIS 184 1 Y
50 9 A HIS 185 A HIS 185 1 Y
51 9 A HIS 186 A HIS 186 1 Y
52 9 A HIS 187 A HIS 187 1 Y
53 9 A HIS 188 A HIS 188 1 Y
54 9 A HIS 189 A HIS 189 1 Y
55 10 A HIS 184 A HIS 184 1 Y
56 10 A HIS 185 A HIS 185 1 Y
57 10 A HIS 186 A HIS 186 1 Y
58 10 A HIS 187 A HIS 187 1 Y
59 10 A HIS 188 A HIS 188 1 Y
60 10 A HIS 189 A HIS 189 1 Y
61 11 A HIS 184 A HIS 184 1 Y
62 11 A HIS 185 A HIS 185 1 Y
63 11 A HIS 186 A HIS 186 1 Y
64 11 A HIS 187 A HIS 187 1 Y
65 11 A HIS 188 A HIS 188 1 Y
66 11 A HIS 189 A HIS 189 1 Y
67 12 A HIS 184 A HIS 184 1 Y
68 12 A HIS 185 A HIS 185 1 Y
69 12 A HIS 186 A HIS 186 1 Y
70 12 A HIS 187 A HIS 187 1 Y
71 12 A HIS 188 A HIS 188 1 Y
72 12 A HIS 189 A HIS 189 1 Y
73 13 A HIS 184 A HIS 184 1 Y
74 13 A HIS 185 A HIS 185 1 Y
75 13 A HIS 186 A HIS 186 1 Y
76 13 A HIS 187 A HIS 187 1 Y
77 13 A HIS 188 A HIS 188 1 Y
78 13 A HIS 189 A HIS 189 1 Y
79 14 A HIS 184 A HIS 184 1 Y
80 14 A HIS 185 A HIS 185 1 Y
81 14 A HIS 186 A HIS 186 1 Y
82 14 A HIS 187 A HIS 187 1 Y
83 14 A HIS 188 A HIS 188 1 Y
84 14 A HIS 189 A HIS 189 1 Y
85 15 A HIS 184 A HIS 184 1 Y
86 15 A HIS 185 A HIS 185 1 Y
87 15 A HIS 186 A HIS 186 1 Y
88 15 A HIS 187 A HIS 187 1 Y
89 15 A HIS 188 A HIS 188 1 Y
90 15 A HIS 189 A HIS 189 1 Y
91 16 A HIS 184 A HIS 184 1 Y
92 16 A HIS 185 A HIS 185 1 Y
93 16 A HIS 186 A HIS 186 1 Y
94 16 A HIS 187 A HIS 187 1 Y
95 16 A HIS 188 A HIS 188 1 Y
96 16 A HIS 189 A HIS 189 1 Y
97 17 A HIS 184 A HIS 184 1 Y
98 17 A HIS 185 A HIS 185 1 Y
99 17 A HIS 186 A HIS 186 1 Y
100 17 A HIS 187 A HIS 187 1 Y
101 17 A HIS 188 A HIS 188 1 Y
102 17 A HIS 189 A HIS 189 1 Y
103 18 A HIS 184 A HIS 184 1 Y
104 18 A HIS 185 A HIS 185 1 Y
105 18 A HIS 186 A HIS 186 1 Y
106 18 A HIS 187 A HIS 187 1 Y
107 18 A HIS 188 A HIS 188 1 Y
108 18 A HIS 189 A HIS 189 1 Y
109 19 A HIS 184 A HIS 184 1 Y
110 19 A HIS 185 A HIS 185 1 Y
111 19 A HIS 186 A HIS 186 1 Y
112 19 A HIS 187 A HIS 187 1 Y
113 19 A HIS 188 A HIS 188 1 Y
114 19 A HIS 189 A HIS 189 1 Y
115 20 A HIS 184 A HIS 184 1 Y
116 20 A HIS 185 A HIS 185 1 Y
117 20 A HIS 186 A HIS 186 1 Y
118 20 A HIS 187 A HIS 187 1 Y
119 20 A HIS 188 A HIS 188 1 Y
120 20 A HIS 189 A HIS 189 1 Y
#
loop_
_pdbx_validate_torsion.id
_pdbx_validate_torsion.PDB_model_num
_pdbx_validate_torsion.auth_asym_id
_pdbx_validate_torsion.auth_comp_id
_pdbx_validate_torsion.auth_seq_id
_pdbx_validate_torsion.phi
_pdbx_validate_torsion.psi
1 1 A SER 15 172.88 89.96
2 1 A SER 17 -68.88 65.11
3 1 A LEU 26 -134.74 -50.21
4 1 A GLU 41 -174.90 105.00
5 1 A PRO 49 -67.57 92.49
6 1 A GLU 52 -99.20 -70.32
7 1 A ALA 55 -90.89 39.18
8 1 A GLU 62 -106.27 54.10
9 1 A GLU 65 -69.62 74.52
10 1 A LYS 75 66.71 70.14
11 1 A ARG 108 74.86 -30.49
12 1 A LYS 110 79.99 -2.55
13 1 A LYS 134 -50.56 -9.48
14 2 A SER 15 172.30 81.87
15 2 A SER 17 -67.80 88.35
16 2 A ASP 25 59.47 11.68
17 2 A GLU 39 50.73 -76.11
18 2 A LEU 44 -56.54 86.30
19 2 A ASN 48 -155.07 -50.77
20 2 A SER 50 -66.50 97.37
21 2 A ALA 55 77.19 -52.90
22 2 A SER 60 -117.40 51.94
23 2 A HIS 63 60.59 83.98
24 2 A VAL 64 -74.14 -96.89
25 2 A GLU 65 65.15 -36.08
26 2 A LYS 75 60.07 69.97
27 2 A ASN 107 -129.11 -83.43
28 2 A LYS 110 86.53 -35.22
29 2 A LYS 134 -47.64 -10.85
30 3 A LEU 13 -59.43 -73.58
31 3 A ASP 16 51.88 -90.07
32 3 A SER 17 -60.71 5.85
33 3 A ASP 25 68.15 -9.29
34 3 A ILE 42 -163.56 87.39
35 3 A LEU 44 58.03 75.51
36 3 A ASN 48 -161.35 111.54
37 3 A ALA 51 -69.27 92.68
38 3 A GLU 52 -169.07 -167.94
39 3 A SER 60 71.41 -23.36
40 3 A GLU 62 -175.07 -52.79
41 3 A LYS 75 63.11 66.97
42 3 A ASP 162 67.83 -67.64
43 4 A ASP 11 -50.81 -2.29
44 4 A LEU 13 36.51 -88.67
45 4 A ASP 16 -166.52 -90.64
46 4 A SER 17 -170.20 78.72
47 4 A ASP 24 59.92 14.65
48 4 A ASP 25 58.23 10.36
49 4 A ILE 42 -161.25 104.01
50 4 A ALA 45 -67.29 94.18
51 4 A GLU 62 68.54 -72.02
52 4 A HIS 63 -161.99 36.89
53 4 A LYS 75 64.37 61.12
54 4 A ARG 108 77.82 -17.17
55 5 A LEU 13 -57.42 -83.21
56 5 A ASP 16 -172.67 -176.35
57 5 A ASP 25 55.59 11.17
58 5 A ILE 42 -140.32 35.84
59 5 A PRO 49 -62.72 94.78
60 5 A ALA 55 -47.61 98.78
61 5 A GLU 56 -60.54 94.21
62 5 A SER 60 -144.88 -40.52
63 5 A ASP 61 -162.58 74.14
64 5 A LYS 75 65.67 71.13
65 5 A LYS 134 -45.95 -14.60
66 6 A LEU 13 -78.23 -135.00
67 6 A ASP 16 -160.64 -100.89
68 6 A ASP 24 59.39 8.23
69 6 A LEU 26 -134.99 -51.74
70 6 A GLU 39 -62.80 89.02
71 6 A PRO 49 -82.61 42.89
72 6 A ALA 51 68.34 81.93
73 6 A GLU 52 -151.46 -40.95
74 6 A GLU 53 -172.65 -70.31
75 6 A LYS 75 68.42 66.32
76 6 A ARG 108 57.37 8.37
77 6 A GLU 149 -172.95 -173.01
78 6 A ASN 150 79.21 -20.82
79 7 A THR 9 -131.33 -33.82
80 7 A LEU 13 -45.28 -76.06
81 7 A ASP 24 58.44 10.46
82 7 A ILE 42 -155.04 -43.61
83 7 A LEU 44 -103.18 -162.89
84 7 A ASN 48 63.37 74.13
85 7 A GLU 53 69.34 77.42
86 7 A ASP 61 -136.79 -63.53
87 7 A GLU 65 -67.36 80.86
88 7 A TYR 82 -94.13 -60.24
89 7 A ARG 108 81.38 -21.45
90 7 A ALA 129 -59.67 108.38
91 7 A LYS 134 -52.57 2.53
92 7 A ALA 148 -90.95 -67.48
93 8 A PHE 8 -107.76 -60.21
94 8 A LEU 13 -62.99 -92.30
95 8 A ASP 24 72.78 -85.53
96 8 A ASP 25 172.14 28.48
97 8 A LEU 26 -135.15 -52.16
98 8 A GLU 39 39.95 -77.75
99 8 A PRO 49 -54.15 104.88
100 8 A GLU 56 -164.26 56.66
101 8 A SER 60 -86.12 45.14
102 8 A ASP 61 -152.85 66.85
103 8 A ASN 107 47.02 77.29
104 8 A ASP 109 152.06 147.44
105 9 A THR 9 -132.30 -34.73
106 9 A LEU 13 -44.93 -93.95
107 9 A SER 17 -68.33 92.82
108 9 A LEU 26 -130.74 -52.83
109 9 A LEU 44 60.67 88.36
110 9 A PRO 49 -63.60 84.90
111 9 A GLU 53 -152.01 22.91
112 9 A SER 60 -145.53 -57.12
113 9 A LYS 75 62.21 69.88
114 9 A ARG 108 73.29 -13.30
115 9 A ALA 129 -58.97 99.75
116 9 A ALA 148 -169.96 98.53
117 9 A TYR 158 -69.86 88.54
118 9 A ASP 162 71.68 -66.91
119 10 A LEU 13 -84.96 -154.45
120 10 A ASP 16 -166.03 -105.73
121 10 A SER 17 -177.91 84.67
122 10 A ASP 25 59.56 18.35
123 10 A LEU 26 -129.54 -50.03
124 10 A GLU 39 60.02 -66.36
125 10 A ASN 48 64.16 65.74
126 10 A GLU 53 -89.59 -136.90
127 10 A ALA 55 -158.98 70.51
128 10 A GLU 56 -90.48 34.56
129 10 A LYS 75 54.63 70.32
130 10 A ASN 107 -129.85 -50.30
131 10 A ARG 108 49.28 21.67
132 10 A LYS 134 -46.25 -7.44
133 10 A GLU 149 -68.01 1.56
134 10 A LEU 182 -139.28 -35.35
135 11 A LEU 13 -77.19 -81.88
136 11 A SER 15 177.30 -177.22
137 11 A ASP 16 85.91 -109.86
138 11 A SER 17 -144.04 42.39
139 11 A ASP 25 53.11 16.02
140 11 A PRO 49 -58.88 97.32
141 11 A SER 50 -58.64 93.47
142 11 A GLU 65 73.53 -57.71
143 11 A ALA 154 -66.43 97.16
144 11 A LYS 180 -69.84 98.04
145 12 A LEU 13 -66.91 -95.90
146 12 A SER 15 163.32 104.43
147 12 A SER 17 -68.87 83.77
148 12 A LEU 26 -135.10 -51.17
149 12 A ALA 45 -159.12 -43.01
150 12 A LYS 75 69.28 70.36
151 12 A ASN 107 -140.05 -59.64
152 12 A ALA 154 -63.79 97.51
153 13 A PHE 8 -106.70 -64.02
154 13 A LEU 13 28.55 -87.89
155 13 A SER 15 -113.70 67.46
156 13 A ASP 25 59.81 12.38
157 13 A GLU 39 -64.45 84.39
158 13 A ALA 51 -164.05 78.71
159 13 A GLU 53 -59.98 78.34
160 13 A GLU 56 -166.17 100.24
161 13 A ASP 57 77.72 -30.28
162 13 A HIS 63 76.41 -57.34
163 13 A VAL 64 72.26 -78.09
164 13 A GLU 65 51.39 -70.56
165 13 A LYS 75 62.82 61.66
166 13 A ASN 107 -92.69 -78.66
167 13 A ARG 108 -153.47 13.43
168 13 A ASP 109 68.94 -74.13
169 13 A LYS 110 -99.04 -66.42
170 13 A ALA 129 -62.12 88.31
171 13 A GLU 149 49.29 89.66
172 14 A LEU 13 -64.63 -79.68
173 14 A ASP 16 -61.94 95.65
174 14 A ASP 24 58.82 16.23
175 14 A ASP 25 47.25 26.56
176 14 A LEU 44 51.38 81.44
177 14 A ALA 55 179.32 -76.23
178 14 A GLU 56 59.44 -82.66
179 14 A ASP 57 -168.94 -90.72
180 14 A ASN 107 -130.42 -53.43
181 14 A ASP 109 -120.48 -89.00
182 14 A LYS 110 173.13 -42.21
183 14 A LEU 182 -170.08 0.24
184 15 A PHE 8 -94.15 -64.68
185 15 A THR 9 -132.08 -37.68
186 15 A LEU 13 -54.63 -73.69
187 15 A ASP 24 56.09 18.98
188 15 A ASP 25 55.62 14.71
189 15 A GLU 39 -59.43 88.34
190 15 A PRO 49 -81.01 -155.89
191 15 A ASP 57 -59.04 105.36
192 15 A ASN 107 -120.02 -74.11
193 15 A ARG 108 50.08 18.78
194 15 A LYS 110 84.15 -38.76
195 15 A ALA 154 -64.81 97.09
196 16 A LEU 13 42.90 -80.02
197 16 A SER 15 -163.16 96.35
198 16 A PHE 18 43.07 108.29