GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruG in Collimonas arenae Ter10

Align Fructose import permease protein FruG (characterized)
to candidate WP_061533693.1 CAter10_RS12720 sugar ABC transporter permease YjfF

Query= SwissProt::Q8G845
         (340 letters)



>NCBI__GCF_001584165.1:WP_061533693.1
          Length = 334

 Score =  221 bits (563), Expect = 2e-62
 Identities = 127/316 (40%), Positives = 193/316 (61%), Gaps = 10/316 (3%)

Query: 25  TLAAVVIFILMIIMGQALFGTYIRLGFISSLFIDHAYLIILAVAMTLPILTGGIDLSVGA 84
           +LA V + +LM  MG   +  +  L  I +L ID+A+L+++A+ MT  IL+GGIDLSVG+
Sbjct: 15  SLATVALLVLMFGMGSFAYTGFFSLQVILNLLIDNAFLLVIAIGMTFVILSGGIDLSVGS 74

Query: 85  IVAITAVVGLKLANAGV-PAFLVMIIMLLIGAVFGLLAGTLIEEFNMQPFIATLSTMFLA 143
           ++A+T ++   L  +   P  LV+  +LLIG+ FG L G LI  F +Q FI TL+ MFLA
Sbjct: 75  VLALTTMISAYLLQSWHWPPLLVIACVLLIGSCFGALMGALIHFFKLQAFIVTLAGMFLA 134

Query: 144 RGLASIISTDSLTFPQGNDFSFISNVIKIIDNPKISNDLSFNVGVIIALVVVVFGYVFLH 203
           RGL  +IS +S+T  Q          + I+           +  V+IA++++       H
Sbjct: 135 RGLCYLISINSITIDQPLYVELSQARLGILG-------AFISPSVVIAMLMLALAIYLAH 187

Query: 204 HTRTGRTIYAIGGSRSSAELMGLPVKRTQYIIYLTSATLAALASIVYTANIGSAKNTVGV 263
           +TR GR +YAIGG+  SA LMGLPV RT+ ++Y  S   AALA ++++  + S       
Sbjct: 188 YTRFGRAVYAIGGNEQSALLMGLPVGRTKVLVYAFSGFCAALAGVLFSFYMLSGYGLHAQ 247

Query: 264 GWELDAVASVVIGGTIITGGFGYVLGSVLGSLVRSILDPLTS-DFGVPAEWTTIVIGLMI 322
           G ELDA+A+VVIGGT+++GG+GYV G++ G L+  ++  L + D  + + WT IVIG ++
Sbjct: 248 GTELDAIAAVVIGGTLLSGGYGYVAGTLTGVLILGVIQTLIAFDGSLSSWWTKIVIGALL 307

Query: 323 LVFVVLQRAV-MAVGG 337
            +F V QR + M+ GG
Sbjct: 308 FIFCVAQRLMSMSAGG 323


Lambda     K      H
   0.327    0.142    0.400 

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: 286
Number of extensions: 16
Number of successful extensions: 4
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: 340
Length of database: 334
Length adjustment: 28
Effective length of query: 312
Effective length of database: 306
Effective search space:    95472
Effective search space used:    95472
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 49 (23.5 bits)

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

Links

Downloads

Related tools

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