GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcB in Tistlia consotensis USBA 355

Align Fructose import binding protein FrcB (characterized)
to candidate WP_089229763.1 B9O00_RS13770 sugar ABC transporter substrate-binding protein

Query= SwissProt::Q9F9B2
         (341 letters)



>NCBI__GCF_900177295.1:WP_089229763.1
          Length = 333

 Score =  431 bits (1109), Expect = e-125
 Identities = 219/341 (64%), Positives = 262/341 (76%), Gaps = 8/341 (2%)

Query: 1   MKKTVLSAAFGALAMGVAFASPSQAAEVSACLITKTDTNPFFVKMKEGAAAKAKELGVTL 60
           M  TVL+A   A         P+ AA+    L+TKT+TNPFFVKM+EGA AKAKELGV L
Sbjct: 1   MASTVLAACLAA--------GPAAAADTIVGLVTKTNTNPFFVKMREGAEAKAKELGVEL 52

Query: 61  KSYAGKIDGDSESQVAAIETCIADGAKGILIAASDTQGIVPQVQKARDAGLLVIALDTPL 120
           +SYAGK DGD ESQV AIE+ IA GAKGILI  SD+  +VP + +AR AGLLVIALDTPL
Sbjct: 53  RSYAGKYDGDVESQVEAIESLIAAGAKGILITPSDSAAVVPALARARKAGLLVIALDTPL 112

Query: 121 EPLDAADATFATDNLLAGKLIGQWAAATLGDAAKEAKVAFLDLTPSQPSVDVLRDQGFMI 180
           +P  AADATFATDN  AG+LIG+WA A LGD A++AK+A LDL  +Q SVDV RDQGF+ 
Sbjct: 113 DPASAADATFATDNFKAGQLIGEWAKARLGDKAEDAKIAMLDLNANQISVDVARDQGFLE 172

Query: 181 GFGIDPKDPNKIGDEDDPRIVGHDITNGNEEGGRTAMENLLQKDPTINVVHTINEPAAAG 240
           GFGID  +P +IGDE D RIVGHDIT G EEGGR AMENL+Q++P++N+V+TINEPAAAG
Sbjct: 173 GFGIDIGNPKQIGDEKDGRIVGHDITQGAEEGGRRAMENLMQRNPSLNLVYTINEPAAAG 232

Query: 241 AYEALKSVGREKDVLIVSVDGGCPGVKNVAEGVIGATSQQYPLMMAALGIEAIKKFADTG 300
           AYEAL+S G +    IVS+DGGCPGVKNV  GVIGATS Q+PL MA+LGIEA+  +A TG
Sbjct: 233 AYEALRSFGLDSQATIVSIDGGCPGVKNVKAGVIGATSMQFPLRMASLGIEAVVDYARTG 292

Query: 301 EKPTPTEGKDFVDTGVSLVADKPVSGVESIDTKTGMEKCWG 341
            +P PT G DF DTGV LV DKP+ G+ SI ++ G++ CWG
Sbjct: 293 ARPKPTPGLDFTDTGVQLVTDKPIDGIPSITSEEGLKLCWG 333


Lambda     K      H
   0.313    0.132    0.372 

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: 424
Number of extensions: 11
Number of successful extensions: 1
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: 341
Length of database: 333
Length adjustment: 28
Effective length of query: 313
Effective length of database: 305
Effective search space:    95465
Effective search space used:    95465
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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