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Solution structure of the C-terminal domain of ERCC1 complexed with the C-terminal domain of XPF
Authors
Tripsianes, K., Folkers, G., Odijk, H., Jaspers, N.G., Hoeijmakers, J.H., Kaptein, R., Boelens, R.
Assembly
DNA excision repair protein ERCC-1, DNA repair endonuclease XPF (E.C.3.1.-.-)
Entity
1. ERCC-1 (polymer, Thiol state: all free), 89 monomers, 9984.341 Da Detail

MADLLMEKLE QDFVSRVTEC LTTVKSVNKT DSQTLLTTFG SLEQLIAASR EDLALCPGLG PQKARRLFDV LHEPFLKVPG GLEHHHHHH


2. XPF (polymer, Thiol state: all free), 84 monomers, 9217.408 Da Detail

MDSETLPESE KYNPGPQDFL LKMPGVNAKN CRSLMHHVKN IAELAALSQD ELTSILGNAA NAKQLYDFIH TSFAEVVSKG KGKK


Total weight
19201.75 Da
Max. entity weight
9984.341 Da
Source organism
Homo sapiens
Exptl. method
NMR
Refine. method
water refinment in CNS
Data set
assigned_chemical_shifts
Chem. Shift Complete1
Sequence coverage: 56.6 %, Completeness: 48.3 %, Completeness (bb): 45.2 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All48.3 % (968 of 2005)52.4 % (546 of 1042)42.5 % (333 of 784)49.7 % (89 of 179)
Backbone45.2 % (462 of 1022)52.9 % (184 of 348)38.1 % (194 of 509)50.9 % (84 of 165)
Sidechain51.6 % (591 of 1146)52.2 % (362 of 694)51.1 % (224 of 438)35.7 % (5 of 14)
Aromatic34.1 % (43 of 126)34.9 % (22 of 63)33.3 % (21 of 63)
Methyl59.6 % (118 of 198)59.6 % (59 of 99)59.6 % (59 of 99)

1. ERCC-1

MADLLMEKLE QDFVSRVTEC LTTVKSVNKT DSQTLLTTFG SLEQLIAASR EDLALCPGLG PQKARRLFDV LHEPFLKVPG GLEHHHHHH

2. XPF

MDSETLPESE KYNPGPQDFL LKMPGVNAKN CRSLMHHVKN IAELAALSQD ELTSILGNAA NAKQLYDFIH TSFAEVVSKG KGKK

Sample

Pressure 1 atm, Temperature 295.5 K, pH 7.0


#NameIsotope labelingTypeConcentration
1ERCC-1[U-15N; U-13C]1.5 mM
2XPF[U-15N; U-13C]1.5 mM
3phosphate50 mM
4NaCl100 mM
5D2O8 %
6H2O92 %

Chem. Shift Complete2
Sequence coverage: 59.0 %, Completeness: 48.4 %, Completeness (bb): 45.9 % Detail

Polymer type: polypeptide(L)

Total1H13C15N
All48.4 % (1941 of 4010)52.4 % (1092 of 2084)41.9 % (657 of 1568)53.6 % (192 of 358)
Backbone45.9 % (939 of 2044)53.9 % (375 of 696)38.0 % (387 of 1018)53.6 % (177 of 330)
Sidechain50.7 % (1162 of 2292)51.2 % (710 of 1388)50.0 % (438 of 876)50.0 % (14 of 28)
Aromatic34.5 % (87 of 252)35.7 % (45 of 126)33.3 % (42 of 126)
Methyl54.5 % (216 of 396)55.6 % (110 of 198)53.5 % (106 of 198)

1. ERCC-1

MADLLMEKLE QDFVSRVTEC LTTVKSVNKT DSQTLLTTFG SLEQLIAASR EDLALCPGLG PQKARRLFDV LHEPFLKVPG GLEHHHHHH

2. XPF

MDSETLPESE KYNPGPQDFL LKMPGVNAKN CRSLMHHVKN IAELAALSQD ELTSILGNAA NAKQLYDFIH TSFAEVVSKG KGKK

Sample

Pressure 1 atm, Temperature 295.5 K, pH 7.0


#NameIsotope labelingTypeConcentration
1ERCC-1[U-15N; U-13C]1.5 mM
2XPF[U-15N; U-13C]1.5 mM
3phosphate50 mM
4NaCl100 mM
5D2O8 %
6H2O92 %

LACS Plot; CA
Referencing offset: -0.36 ppm, Outliers: 1 Detail
LACS Plot; CB
Referencing offset: -0.36 ppm, Outliers: 1 Detail
LACS Plot; HA
Referencing offset: 0.09 ppm, Outliers: 1 Detail
Protein Blocks Logo
Calculated from 20 models in PDB: 1Z00, Strand ID: A, B Detail


Release date
2005-12-13
Citation
The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair
Tripsianes, K., Folkers, G., AB, E., Das, D., Odijk, H., Jaspers, N.G.J., Hoeijmakers, J.H.J., Kaptein, R., Boelens, R.
Structure (2005), 13, 1849-1858, PubMed 16338413 , DOI 10.1016/j.str.2005.08.014 ,
Related entities 1. ERCC-1, : 1 : 4 : 14 entities Detail
Related entities 2. XPF, : 1 : 2 : 2 : 13 entities Detail
Interaction partners 1. ERCC-1, : 21 : 1 interactors Detail
Interaction partners 2. XPF, : 24 : 1 interactors Detail
Experiments performed 6 experiments Detail
nullKeywords helix-hairpin-helix