Align purine-nucleoside phosphorylase (EC 2.4.2.1) (characterized)
to candidate WP_015944769.1 DHAF_RS18800 S-methyl-5'-thioadenosine phosphorylase
Query= BRENDA::Q8U2I1 (265 letters) >NCBI__GCF_000021925.1:WP_015944769.1 Length = 258 Score = 261 bits (666), Expect = 1e-74 Identities = 128/256 (50%), Positives = 172/256 (67%), Gaps = 7/256 (2%) Query: 6 IVGGSGVYDFPAENKREETVKTPYGEVKITVG--VVGDEEVAFLARHGKGHSIPPHKINY 63 ++GG+G+ + R E++ TPYG+V + +G DE + F++RHGKGH++PPH +NY Sbjct: 1 MIGGTGLETVALLDLRTESIATPYGKVTVEIGRFEAHDEPIVFMSRHGKGHTVPPHLVNY 60 Query: 64 RANIWALYELGVERIIATSAVGSMNPEMKPGDFVILDQIIDFTVSRPRTFYDGEESPHER 123 RANIWAL ELGV +IIAT+AVGS++ ++ GD V+LDQ +DFT SRP+TFY+G Sbjct: 61 RANIWALKELGVRKIIATAAVGSLSSRLQLGDIVLLDQFLDFTKSRPQTFYEGGGQG--- 117 Query: 124 KFVAHVDFTEPYCPEIRKALITAARNLGLPYHPRGTYVCTEGPRFETAAEIRAYRILGGD 183 V HVD TEPYC ++ + A ++G+P YVCTEGPRFET AEIR Y+ILGG+ Sbjct: 118 --VLHVDMTEPYCRSVQAVIREAGESIGVPLQGGAAYVCTEGPRFETPAEIRMYQILGGE 175 Query: 184 VVGMTQCPEAILARELEMCYATVAIVTNYAAGMSGKKLTHSEVVELMQKKSEDIVKLILA 243 VGMT PE +LARE MCYAT+A+VTN AAG++ LTH EVVE +Q LI Sbjct: 176 CVGMTSVPEVVLARECGMCYATIAMVTNEAAGIADHPLTHQEVVESLQAAGNKAAGLIQE 235 Query: 244 AIPLIPKERRCGCKDA 259 ++ E+ C C+ A Sbjct: 236 TFRILRHEQDCRCQMA 251 Lambda K H 0.320 0.138 0.412 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 229 Number of extensions: 9 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 265 Length of database: 258 Length adjustment: 25 Effective length of query: 240 Effective length of database: 233 Effective search space: 55920 Effective search space used: 55920 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 47 (22.7 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory