Align uronate isomerase (characterized)
to candidate WP_086510918.1 BZY95_RS16135 glucuronate isomerase
Query= CharProtDB::CH_024902 (470 letters) >NCBI__GCF_002151265.1:WP_086510918.1 Length = 473 Score = 518 bits (1333), Expect = e-151 Identities = 249/462 (53%), Positives = 325/462 (70%), Gaps = 2/462 (0%) Query: 4 FMTEDFLLDTEFARRLYHDYAKDQPIFDYHCHLPPQQIAEDYRFKNLYDIWLKGDHYKWR 63 FM DFLL+ E ARRLYH++A PI DYH HL PQ+IA D RF NL ++WLKGDHYKWR Sbjct: 9 FMGPDFLLENEPARRLYHEHAAAMPICDYHSHLSPQEIAGDVRFDNLTELWLKGDHYKWR 68 Query: 64 AMRTNGVAERLCTGDASDREKFDAWAATVPHTIGNPLYHWTHLELRRPFGITGKLLSPST 123 AMR G+ ER TG+ASDRE+F AWA TVPH +GNPLYHWTHLELR P GI LLSP+T Sbjct: 69 AMRIAGIDERRITGEASDRERFQAWAETVPHCLGNPLYHWTHLELRHPLGIDNMLLSPAT 128 Query: 124 ADEIWNECNELLAQDNFSARGIMQQMNVKMVGTTDDPIDSLEHHAEIAKDGSFTIKVLPS 183 A+EIW E LA SA+GI+++ V+ V TTDDP+D L H + G+ + +LP+ Sbjct: 129 AEEIWATARERLATPQLSAQGILERFAVRTVCTTDDPVDDLALHRRHVESGA-SPAMLPT 187 Query: 184 WRPDKAFNIEQATFNDYMAKLGEVSDTDIRRFADLQTALTKRLDHFAAHGCKVSDHALDV 243 +R D IEQA F DY+ +L S IR + DL AL +RL+HFAAHGC +SDH+L+ Sbjct: 188 FRADTVLKIEQAGFVDYLGELERASGVTIRGYDDLLAALYQRLEHFAAHGCCLSDHSLEK 247 Query: 244 VMF-AEANEAELDSILARRLAGETLSEHEVAQFKTAVLVFLGAEYARRGWVQQYHIGALR 302 F A + AELD ++ RR G L E A F TAVL++LG EYARRGWV Q H+GALR Sbjct: 248 PAFVAPPSTAELDRLIERRRQGRALGSDESASFTTAVLLWLGREYARRGWVMQLHLGALR 307 Query: 303 NNNLRQFKLLGPDVGFDSINDRPMAEELSKLLSKQNEENLLPKTILYCLNPRDNEVLGTM 362 + + R +G + GFD+I D AE L+ +L + E LP+T++Y LNPRDNE+L ++ Sbjct: 308 SLSQRGLAEIGANSGFDAIGDVTYAEPLAAILDALDRERALPRTVVYNLNPRDNEMLASL 367 Query: 363 IGNFQGEGMPGKMQFGSGWWFNDQKDGMERQMTQLAQLGLLSRFVGMLTDSRSFLSYTRH 422 +G+F +G+PGK+QFG+ WWFNDQ+DG+ERQ+ GLL FVGMLTDSRS LS++RH Sbjct: 368 VGSFASDGIPGKLQFGAAWWFNDQRDGIERQLVTQMNFGLLRHFVGMLTDSRSLLSFSRH 427 Query: 423 EYFRRILCQMIGRWVEAGEAPADINLLGEMVKNICFNNARDY 464 +YFRRI CQM+G ++ GE P D++ +GE+V+ +C++N + Y Sbjct: 428 DYFRRIFCQMLGAQIQRGELPGDLDRIGELVRAVCYDNVQRY 469 Lambda K H 0.322 0.137 0.425 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: 669 Number of extensions: 27 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: 470 Length of database: 473 Length adjustment: 33 Effective length of query: 437 Effective length of database: 440 Effective search space: 192280 Effective search space used: 192280 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 (21.9 bits) S2: 51 (24.3 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