Align Uronate isomerase; EC 5.3.1.12; Glucuronate isomerase; Uronic isomerase (uncharacterized)
to candidate SM_b21354 SM_b21354 glucuronate isomerase
Query= curated2:Q8YCQ2 (466 letters) >FitnessBrowser__Smeli:SM_b21354 Length = 469 Score = 614 bits (1583), Expect = e-180 Identities = 295/465 (63%), Positives = 361/465 (77%), Gaps = 1/465 (0%) Query: 3 LNPDRLFSAEPGTREIARRLFASVEKLPIISPHGHTEPIWYARNEAFPDPASLFVKPDHY 62 ++PD LF AE TR +ARRL+A V LPI+SPHGHTEP WYA +EAFPDPA L + PDHY Sbjct: 5 IDPDLLFPAEERTRALARRLYAEVSGLPIVSPHGHTEPRWYALDEAFPDPAQLLIVPDHY 64 Query: 63 ITRMLYSQGHSLESLGIASRDGRPSETDARKIWRLFATNWYLFRATPSRLWFEHAMETVF 122 + RML+SQG LE LG+ + DG P ETD R IWR F N++LFR TP+RLWF++ + +F Sbjct: 65 VFRMLFSQGIRLEELGVPALDGSPVETDGRAIWRRFCENYHLFRGTPTRLWFDYTLSELF 124 Query: 123 GITERLSQENADRIFDAIADQLTQPHMRPRALYDRFNIEAISTTDAATDPLIYHDEVIAS 182 GI E S ++D ++D +A+ LT+P RPRALY+RFNIE ISTTD+A D L +H +++ S Sbjct: 125 GIDELPSAASSDPLYDHVAECLTRPDYRPRALYERFNIEVISTTDSALDDLGWHAKILES 184 Query: 183 GWHGRIIPAYRPDAAVDAGRPDFASEVEKLVGVAGTPL-TWQGYLDAHRNRREYFKRRGA 241 GW GR++PAYRPDA VD F + ++KL + G TW GYLDAHR RR YFK GA Sbjct: 185 GWKGRVVPAYRPDAVVDPDFQGFPTNLDKLGDITGADTGTWSGYLDAHRTRRAYFKDFGA 244 Query: 242 TSSDHGHPTAQTADLSAGDASRLFDRVIKGNASTSDAEMFRAQMLTEMARMSIDDGLVMQ 301 TS+DHGH TA TA+L +A+ LFD+V G A+ + +FRAQMLTEMA+MS+DDGLVMQ Sbjct: 245 TSTDHGHATADTANLPQAEAAALFDKVRLGKANADERRLFRAQMLTEMAKMSLDDGLVMQ 304 Query: 302 IHPGSFRNHNPTVFERFGLDKGADIPRQTGFVDQLKPLLDAFGNDPRLTVILFTLDETAL 361 IHPGSFRNH+P + +FG DKG DIP +T +V LKPLLDA G + LTVILFTLDET+ Sbjct: 305 IHPGSFRNHSPAILAKFGRDKGFDIPTRTDYVTALKPLLDAVGLERDLTVILFTLDETSY 364 Query: 362 SRELAPLAGHYPALKLGPAWWFFDSPEGILRYRKLTTETAGFYNTVGFNDDTRAYLSIPA 421 +RELAPLAG YPALKLGPAWWF DS EG+ R+R++TTETAGFYNTVGFNDDTRA+ SIPA Sbjct: 365 ARELAPLAGVYPALKLGPAWWFHDSAEGMRRFREMTTETAGFYNTVGFNDDTRAFPSIPA 424 Query: 422 RHDMARRVDCAYLAGLVADHRLEEDEAYEVAHDLAYRLAKQTYKL 466 RHD+ARRVDCA+LA LVA+HRL EDEAYE+A DLAY LAK+ Y+L Sbjct: 425 RHDIARRVDCAFLARLVAEHRLREDEAYELARDLAYGLAKEAYRL 469 Lambda K H 0.321 0.136 0.418 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: 819 Number of extensions: 31 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: 466 Length of database: 469 Length adjustment: 33 Effective length of query: 433 Effective length of database: 436 Effective search space: 188788 Effective search space used: 188788 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 Sep 17 2021. 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