GapMind for catabolism of small carbon sources

 

Alignments for a candidate for frcC in Cupriavidus basilensis 4G11

Align Fructose import permease protein FrcC (characterized)
to candidate RR42_RS32895 RR42_RS32895 ABC transporter permease

Query= SwissProt::Q9F9B1
         (360 letters)



>FitnessBrowser__Cup4G11:RR42_RS32895
          Length = 318

 Score =  136 bits (343), Expect = 7e-37
 Identities = 96/309 (31%), Positives = 151/309 (48%), Gaps = 16/309 (5%)

Query: 50  VPLIVLVLSLIAFGV-ILGGKFFSAFTMTLILQQVAIVGIVGAAQTLVILTAGIDLSVGA 108
           VP  V VL L++ G  + G  F S   +  I  Q  I+ ++    TL+I+T G+DLS+GA
Sbjct: 18  VPGSVWVLLLLSLGFSVTGPGFLSVENLLNIGAQSTILLLIALPMTLIIMTEGLDLSMGA 77

Query: 109 IMVLSSVIMGQFTFRYGFPPALSVICGLGVGALCGYINGTLVARMKLPPFIVTLGMWQIV 168
           ++ L  V++          P L++   L  G   G +NG LV+ +++PPF+ TLG   + 
Sbjct: 78  VLTLCGVVLAMVMVATESLP-LALGAALLTGLAFGLLNGALVSWLEIPPFVATLGT--LG 134

Query: 169 LASNFLYSANETIRAQDISANASIL---QFFGQNFRIGNAVFTYGVVVMVLLVCLLWYVL 225
           +A      A +      I     ++   Q  G    I  A   YG         L  ++L
Sbjct: 135 VAQGLALVATDGQSVTGIGEAIPLIYAGQLLGVPLPIWIAAVFYG---------LFHWLL 185

Query: 226 NRTAWGRYVYAVGDDPEAAKLAGVNVTRMLISIYTLSGLICALAGWALIGRIGSVSPTAG 285
             T +G YV+A+G + EA K +GV +   LI++Y L GL+  +A   L  R+ +  PTA 
Sbjct: 186 YHTRFGAYVFALGGNREALKFSGVRINVYLIAVYALGGLMAGVAALLLTARMNAGHPTAA 245

Query: 286 QFANIESITAVVIGGISLFGGRGSIMGMLFGALIVGVFSLGLRLMGTDPQWTYLLIGLLI 345
                ++I AV +GG +   G G + G + G L VGV   GL L+G         IGLL+
Sbjct: 246 IGLEFDAIAAVAVGGTTFDRGNGWLPGTVLGVLAVGVLRNGLNLVGVPSSVQVAAIGLLV 305

Query: 346 IIAVAIDQW 354
           ++ + I+ +
Sbjct: 306 LVVLLIESF 314


Lambda     K      H
   0.327    0.141    0.420 

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: 331
Number of extensions: 17
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: 360
Length of database: 318
Length adjustment: 28
Effective length of query: 332
Effective length of database: 290
Effective search space:    96280
Effective search space used:    96280
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 17 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