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Table 2 The set of parameters describing the status of the chains in the dimer and the monomers in the PhoA-WT structure

From: Ab initio protein structure prediction: the necessary presence of external force field as it is delivered by Hsp40 chaperone

1EW8

Complex

Individual

PhoA-WT

PhoA-WT-A / PhoA-WT-B

PhoA-WT-A / PhoA-WT-B // PhoA-U

 

RD

K

RD

K

PhoA-AB

0.689

1.1

  

PhoA-A/PhoA-B

0.691 / 0.688

1.0 / 1.1

0.596 /0.596 // 0.778

0.6 / 0.6 // 1.7

CAT 102 ± 5

0.485 / 0.487

 

0.274 / 0.289 // 0.564

 

CAT 166 ± 5

0.610 / 0.605

 

0.539 / 0.537 // 0.518

 

SS 168–178

0.471 / 0.471

 

0.484 / 0.483 // 0.521

 

SS 286–336

0.572 / 0.597

 

0.480 /0.476 // 0.592

 

P-P

0.678

 

0.718 / 0.720

 

NO P-P

0.672

 

0.574 / 0.577

 
  1. Two values given in the COMPLEX column—the status of the chains A and B considered as components of PhoA-WT. The columns COMPLEX/ INDIVIDUAL—3D Gauss function stretched over a complex/chain. Values after the // sign—status in the form of PhoA-U. CAT ± 5 denotes the status of the catalytic residue along with a stretch of immediate surroundings ± 5 adjacent residues. SS—segments defined by Cyx positions building the appropriate disulfide bond. P-P—the status of the residues included in the interface, NoP-P—the status of the rest of the chain after elimination of the interface residues