Align L-rhamnose isomerase (EC 5.3.1.14) (characterized)
to candidate CA265_RS02635 CA265_RS02635 sugar isomerase
Query= reanno::Cola:Echvi_1573 (427 letters) >lcl|FitnessBrowser__Pedo557:CA265_RS02635 CA265_RS02635 sugar isomerase Length = 426 Score = 557 bits (1436), Expect = e-163 Identities = 277/429 (64%), Positives = 341/429 (79%), Gaps = 5/429 (1%) Query: 1 MRIDKQKIKEVNDQALSEHRESFGHLSSVLGKKGIDVNVLVEKLKEFQVAVPSWALGTGG 60 M I++ +I++ ND L+ H+ L +D+ +++KL +FQ+A+PSWALGTGG Sbjct: 1 MNIEQNQIEKHNDSLLTSHQRKLSFLKEDWAH--VDLESVIQKLVDFQIAIPSWALGTGG 58 Query: 61 TRFGRFS-GGGEPGTLEDKISDVGLLHQLSQSAGAISLHIPWDIPNDVQAIKELAASHGL 119 TRFGRF+ GGEP T+E+KI DVGLLH L+ ++GAISLHIPWDIP + +A+K LAA +GL Sbjct: 59 TRFGRFAITGGEPRTIEEKIEDVGLLHALNGASGAISLHIPWDIPQNAEALKTLAAGYGL 118 Query: 120 IFDAVNSNTFQDQPDQELSYKFGSLCHADKKVRDQAVKHNLEVIKYGDALGSKSLTVWLA 179 FDA+NSNTFQDQ SYKFGSL + +K +R QA++HN+EVIK+G ALGS +LTVWLA Sbjct: 119 KFDAMNSNTFQDQKGAAHSYKFGSLQNVNKDIRKQAIEHNIEVIKHGIALGSDALTVWLA 178 Query: 180 DGSSFPGQLNFKKAFQRTLESLQEIYAGMPEDWKLFVEYKPYEPNFYSTVIQDWGTSHML 239 DGS FPGQLNF+KAF+ TLESLQEIY+ +PEDWK+FVEYK +EPNFYST + DWG S + Sbjct: 179 DGSCFPGQLNFRKAFENTLESLQEIYSALPEDWKMFVEYKAFEPNFYSTTVGDWGQSLLY 238 Query: 240 ADKLGDRAYSLVDLGHHLPNTNIEQIVATLMMVGKLGGFHFNDSKYGDDDVTVGSLKPYQ 299 A KLG +AY+LVDLGHHLPN NIEQIVA L+M GKLGGFHFNDSKYGDDD+T GS+KPYQ Sbjct: 239 ASKLGKKAYTLVDLGHHLPNANIEQIVALLLMEGKLGGFHFNDSKYGDDDLTAGSIKPYQ 298 Query: 300 LFLIFNELVDGMEDPSSNNPYP-AWMIDASHNLKDPLEDLLQSLEAIKLAYAQALLVDRD 358 LFLIFNELV+GM+ N+ WMIDASHN+KDPLEDLLQS+EAI +AYAQALLVDR Sbjct: 299 LFLIFNELVEGMDAKGMNHAKDLGWMIDASHNVKDPLEDLLQSVEAIMIAYAQALLVDRK 358 Query: 359 ALEEARENNDPALAQEILQAAYRTDVRSLLAEARLQADGALDPIAAYRKLNVRKELIAQR 418 AL EA+ NND A AQEILQ +R+D+R+L+AEARL+A AL PIA YR L VR +L+ R Sbjct: 359 ALNEAQNNNDVAKAQEILQHTFRSDLRALVAEARLRAGAALSPIALYRGLEVRNQLVNHR 418 Query: 419 GEKVISTGL 427 G ++TGL Sbjct: 419 G-NTVATGL 426 Lambda K H 0.316 0.135 0.391 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: 573 Number of extensions: 24 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: 427 Length of database: 426 Length adjustment: 32 Effective length of query: 395 Effective length of database: 394 Effective search space: 155630 Effective search space used: 155630 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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