Align Putative PTS system glucosamine-specific EIICBA component; EC 2.7.1.193 (characterized)
to candidate BWI76_RS16295 BWI76_RS16295 bifunctional PTS system maltose and glucose-specific transporter subunits IICB
Query= SwissProt::P39816 (631 letters) >FitnessBrowser__Koxy:BWI76_RS16295 Length = 530 Score = 284 bits (727), Expect = 6e-81 Identities = 180/515 (34%), Positives = 280/515 (54%), Gaps = 49/515 (9%) Query: 6 FQILQQLGRALMTPVAVLPAAGLLLRFGDK----------DLLNIPIIK-------DAGG 48 ++ QQLG+ M PVA+L G++L G L++P+++ G Sbjct: 12 WEFFQQLGKTFMLPVALLSFCGIMLGIGSSLSSHDVLTLLPWLDVPLLQAVFIWMGKVGS 71 Query: 49 VVFDNLPLIFAVGVAIGLAG-GEGVAGLAAVIGYLILTVTLDNMGKLLGLQPPYEGAE-- 105 F LP++F + + +GLA +GVA A +GY ++ + ++ G+ P + A Sbjct: 72 FAFSFLPVMFCIAIPLGLARENKGVAAFAGFVGYAVMNLAVNFWLTAKGILPTTDAAVLK 131 Query: 106 ----------HLIDMGVFGGIIIGLLAAYLYKRFSSIELHPVLGFFSGKRFVPIITSVSS 155 ID G+ G +I G++ L++RF +I L L FF G RFVPIIT+V Sbjct: 132 ANNIQNIIGIQSIDTGILGAVIAGIIVWMLHERFHNIRLPDALAFFGGTRFVPIITTVVL 191 Query: 156 LVIGVIFSFVWPLIQNGINAASSLIADS-TVGLFFYATIYRLLIPFGLHHIFYTPFYFMM 214 ++G++ +WP+ GINA +I + G + T RLL+PFGLHHI F Sbjct: 192 GLVGLVIPLIWPVFAMGINALGQVINSAGDFGPMIFGTGERLLLPFGLHHILVALIRFTE 251 Query: 215 GEYTDPSTGNTVTGDLTRFFAG---------DPTAGRFM-MGDFPYMIFCLPAVALAIIH 264 T G++V+G LT F A +A RF+ G P + LP ALA+ H Sbjct: 252 AGGTMDVCGHSVSGALTIFQAQLSCPTTHGFSESATRFLSQGKMPAFLGGLPGAALAMYH 311 Query: 265 TARPEKKKMISGVMISAALTSMLTGITEPVEFSFLFVAPVLYLINSILAGVIFVVCDLFH 324 ARPE + I G++IS + ++ G TEP+EF FLFVAPVLY+I+++L G+ F + + Sbjct: 312 CARPENRHKIKGLLISGVIACVVGGTTEPLEFLFLFVAPVLYVIHALLTGLGFTMMAILG 371 Query: 325 VRHGYTFSGGGIDYV---LNYGLSTNGWVVIPVGIVFAFIYYYLFRFAILKWNLKTPGRE 381 V G T G ID+V + +GLST ++V V ++ +YY +FRFAI ++NLKTPGR+ Sbjct: 372 VTIGNT-DGNVIDFVVFGILHGLSTKWYLVPVVAAIWFAVYYGIFRFAITRFNLKTPGRD 430 Query: 382 TDEDGQNEEKAPVAKDQLAFHV---LQALGGQQNIANLDACITRLRVTVHQPSQVCKDEL 438 + + E+ + ++V L ALGG +NI +LD CITRLR++V+ S+V L Sbjct: 431 IETNSAFEKAVTGVTGKSGYNVPAILAALGGAENIVSLDNCITRLRLSVNDMSKVDSAAL 490 Query: 439 KRLGAVGVLEVN-NNFQAIFGTKSDALKDDIKTIM 472 K A+GV+++N +N Q + G + ++KD++ +M Sbjct: 491 KANRAIGVVQLNQHNLQVVIGPQVQSVKDEMAVLM 525 Lambda K H 0.324 0.142 0.421 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: 901 Number of extensions: 45 Number of successful extensions: 6 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: 631 Length of database: 530 Length adjustment: 36 Effective length of query: 595 Effective length of database: 494 Effective search space: 293930 Effective search space used: 293930 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (22.0 bits) S2: 53 (25.0 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