Xrn1 5′-phosphate recognition is the selective interaction between Xrn1 and the monophosphate at an RNA chain's end. The enzyme recognizes the terminal nucleotide in context; free inorganic phosphate elsewhere in the sample is not the same substrate feature.
In a structural study of a defined Xrn1 construct, a pocket containing Lys93, Gln97, Arg100 and Arg101 contacted the terminal phosphate, while His41 stacked with the terminal base. Mutating phosphate-pocket residues impaired cleavage and processivity, linking a structural contact to enzyme function.[ref]
For a matched-substrate example, compare two RNAs with the same sequence but a monophosphate on one and a hydroxyl on the other. A difference in reaction progress can then test terminal chemistry while sequence is held fixed. Concentration and turnover regime must also be controlled: the study found that ordinary Xrn1 could degrade hydroxylated RNA under its single-turnover conditions, so monophosphate preference should not be rewritten as an absolute prohibition under every assay condition.[ref]
Recognition also matters after an initial cleavage. The newly exposed end must adopt a productive configuration for the next step. Thus a change at a binding pocket can alter repeated action as well as initial substrate selection; a binding signal alone does not establish productive hydrolysis.

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