WALLEN et al. V. WALLEN et al. V. SRIVASTAVA - Page 8


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            Interference No. 104,761 Paper`108                                                      
            Univ. of New Mexico v. Fordham Univ. Page 8                                             

                  biochemical traits, i.e. the ability to bind adenine nucleotides (ATP and         
                  ADP), and peptides or other proteins. In fact, the Board has concluded            
                  that "at the time of UNM' s invention, the state of the art pointed to both       
                  protein-binding and ATP-binding for hspl 10" (Decision, at page 42, first         
                  full paragraph, last sentence). Fordham submits that in rendering the             
                  Decision the Board has overlooked Fordham's arguments that, in view of            
                  e.g. DnaK-ADP-peptide ternary complexes of Count 3, it is obvious that            
                  hspl 10, which is known to be able to bind ADP and a peptide separately,          
                  can also bind both simultaneously to provide the ternary complexes of             
                  UNM716 claims 7-12 (see e.g. Fordharn Preliminary Motion 4 at page 9;             
                  Fordharn Reply Motion 4 at page 5, last two paragraphs extending onto             
                  page 6; and Fordham Reply Motion 4, at page 8, third full paragraph).             

      [14] While the first paragraph of the cited portion of the Board decision does suggest that   

            the obviousness of hspl 10 in view of hsp70 is the issue under consideration, the       

            second paragraph clarifies that in fact the Board considered the motivation for         

            substituting hspl 10 for hsp70 in the hsp70-ADP-peptide complex of count 3.             

                  Fordharn focuses on the fact that hspl 10-peptide complexes can be formed in      

            the same way that hsp70-pepbde complexes are formed. The Board decision does not        

            question the similarity of the process for forming such hsp-peptide complexes. Rather   

            the decision focuses on the motivation for substituting hspl 10 for hsp70 in the process.

            "The mere fact that the prior art could be so modified would not have made the          

            modification obvious unless the prior art suggested the desirability of the modification."

            In re Gordon, 733 F.2d 900, 902, 221 USPQ 1125, 1127 (Fed. Cir. 1984). The Board        

            decision found no such motivation and based its decision to deny on that lack of        

            motivation. Moreover, there is no per se rule that similar complexes made the same      

            way are thereby obvious in view of each other, thus side-stepping the question of       

            motivation. Cf. TorPharm, Inc. v. Ranbaxy Pharm., Inc., 336 F.3d 1322, 1327,            

            67 USPQ2d 1511, 1514 (Fed. Cir. 2003) (confirming the absence of a per se rule of       









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