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. 2000 Mar 14;97(7):3765–3770. doi: 10.1073/pnas.040580797

Table 1.

Summary of MALDI-TOF MS and amino acid sequence data for SLR1-BP1 and SLR1-BP2

SLR1-BP1 SLR-BP2
Protein mass* (M + H)+ 6317.6 (6317.1) 6301.9 (6301.1)
N-terminal sequence (Q)KGGPVRKQCVEQYPDPNGKCVIDQCKAQCA (Q)KGGPVRKQCVEQYPDPNGKCVIDQCKAQCA
Internal fragments§ Peak 1 (28.8 min)  GHMQCRCDYHC Peak 1 (28.8 min)  GHMQCRCDYHC
Peak 2 (29.4 min)  CVIDQCK Peak 2 (29.4 min)  CVIDQCK
Peak 3 (30.3 min)  QCVEQYPDPNGK Peak 3 (30.3 min)  QCVEQYPDPNGK
Peak 4 (32.4 min)  GGLARCIDTGK Peak 4 (32.4 min)  GGLARCIDTGK
*

Experimental masses obtained by MALDI-TOF MS. Values in parentheses are the relative masses calculated from the deduced amino acid sequences shown in Fig. 3 and based on all eight cysteines forming intramolecular disulfide bridges. 

N-terminal sequences were obtained after pyroglutamate aminopeptidase treatment. 

The phenylthiohydantoin derivative of hydroxyproline was detected. 

§ Lysyl endopeptidase fragments were separated by reverse-phase HPLC and sequenced (see Materials and Methods). Values in parentheses indicate the retention time of each fragment.