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Role of backbone dynamics and structure in controlling the hydrolysis constants of serine proteinase inhibitors
Authors
Song, J., Markley, J.L.
Assembly
Turkey Ovomucoid Third Domain
Entity
1. Turkey Ovomucoid Third Domain (polymer, Thiol state: all disulfide bound), 56 monomers, 6020.759 Da Detail

LAAVSVDCSE YPKPACTLEY RPLCGSDNKT YGNKCNFCNA VVESNGTLTL SHFGKC


Formula weight
6020.759 Da
Entity Connection
disulfide 3 Detail

IDTypeValue orderAtom ID 1Atom ID 2
1disulfidesing1:CYS8:SG1:CYS38:SG
2disulfidesing1:CYS16:SG1:CYS35:SG
3disulfidesing1:CYS24:SG1:CYS56:SG

Source organism
Meleagris gallopavo
Exptl. method
NMR
Data set
assigned_chemical_shifts, heteronucl_NOEs, heteronucl_T1_relaxation, heteronucl_T2_relaxation
Chem. Shift Complete
Sequence coverage: 98.2 %, Completeness: 25.5 %, Completeness (bb): 47.0 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All25.5 % (155 of 609)16.6 % (52 of 313)21.4 % (51 of 238)89.7 % (52 of 58)
Backbone47.0 % (155 of 330)46.0 % (52 of 113)31.1 % (51 of 164)98.1 % (52 of 53)
Sidechain 0.0 % (0 of 331) 0.0 % (0 of 200) 0.0 % (0 of 126) 0.0 % (0 of 5)
Aromatic 0.0 % (0 of 48) 0.0 % (0 of 24) 0.0 % (0 of 24)
Methyl 0.0 % (0 of 52) 0.0 % (0 of 26) 0.0 % (0 of 26)

1. Ovomucoid Third Domain from Turkey

LAAVSVDCSE YPKPACTLEY RPLCGSDNKT YGNKCNFCNA VVESNGTLTL SHFGKC

Sample

Temperature 298 (±1) K, pH 6.0 (±0.2)


#NameIsotope labelingTypeConcentration
1Ovomucoid Third Domain from Turkey[U-13C; U-15N]2 mM

Heteronucl. T1
154 T1 values in 3 lists
Coherence Sz, Field strength (1H) 750 MHz, 500 MHz, 600 MHz, Temperature 298 (±1) K, pH 6.0 (±0.2) Detail
Heteronucl. T2
153 T2 values in 3 lists
Coherence S(+,-), Field strength (1H) 750 MHz, 500 MHz, 600 MHz, Temperature 298 (±1) K, pH 6.0 (±0.2) Detail
Heteronucl. NOE
155 NOE values in 3 lists
Value type relative intensities, Field strength (1H) 750 MHz, 500 MHz, 600 MHz, Temperature 298 (±1) K, pH 6.0 (±0.2) Detail
Heteronucl. T1/T2
153 T1/T2 values in 3 lists
Field strength (1H) 750 MHz, 500 MHz, 600 MHz, Temperature 298 (±1) K, pH 6.0 (±0.2) Detail
Release date
2002-09-11
Citation
Protein inhibitors of serine proteinases: role of backbone structure and dynamics in controlling the hydrolysis constant
Song, J., Markley, J.L.
Biochemistry (2003), 42, 5186-5194, PubMed 12731859 , DOI 10.1021/bi034041u ,
Entries sharing articles BMRB: 3 entries Detail
  BMRB: 5520 released on 2003-07-29
    Title Role of backbone dynamics and structure in controlling the hydrolysis constants of serine proteinase inhibitors
  BMRB: 5519 released on 2002-09-11
    Title Role of backbone dynamics and structure in controlling the hydrolysis constants of serine proteinase inhibitors
  BMRB: 5521 released on 2002-09-11
    Title Role of backbone dynamics and structure in controlling the hydrolysis constants of serine proteinase inhibitors
Related entities 1. Turkey Ovomucoid Third Domain, : 3 : 9 : 6 : 35 : 170 entities Detail
Interaction partners 1. Turkey Ovomucoid Third Domain, : 3 interactors Detail
Experiments performed 3 experiments Detail
Chemical shift validation 3 contents Detail