GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fruF in Phaeacidiphilus oryzae TH49

Align Fructose import permease protein FruF (characterized)
to candidate WP_037568693.1 BS73_RS01760 substrate-binding domain-containing protein

Query= SwissProt::Q8G846
         (356 letters)



>NCBI__GCF_000744815.1:WP_037568693.1
          Length = 658

 Score =  168 bits (425), Expect = 4e-46
 Identities = 116/345 (33%), Positives = 190/345 (55%), Gaps = 29/345 (8%)

Query: 13  VKKLLSSNLTWSIVAFILLVIICTIFQHDFLALSWNSNTGGLAGPLITMLQESARYLMIA 72
           +++LL  N   ++VA +LLV++ ++    FL  S   N G           ++A   ++A
Sbjct: 20  LRRLLLEN--GALVALLLLVVVLSVLSGSFLTTSNLLNVG----------VQAAVDAVLA 67

Query: 73  TGMTLVISTAGIDLSVGSVMAVAGAA-AMQTLSNGMNVWLSILIALAVGLAIGCVNGALV 131
            G+T VI +AGIDLSVGS+ A++    A    S G+ VWL+++++L  G+A G +NG L+
Sbjct: 68  FGVTFVIVSAGIDLSVGSMAALSAIVLAWLASSGGLPVWLAVIVSLVTGVAGGLLNGVLI 127

Query: 132 SFLGLQPFITTLIMMLAGRGMAKVITSGENTDASAVAGNEPLKWFANGFILGIPANFVIA 191
           SF  L PFI TL M+  GRG+A VI+ G     S +A    +          +P   ++ 
Sbjct: 128 SFGKLPPFIATLAMLSVGRGLAMVISQG-----SPIAFPSSVSGLGETLGGWLPVPVLVM 182

Query: 192 VIIVILVGLLCRKTAMGMMIEAVGINQEASRMTGIKPKKILFLVYAISGFLAAIAGLFAT 251
           +++  +  ++  +T +G  + A+G N+EA+R++GI+ KK   ++Y +SG  AAIAG+   
Sbjct: 183 LVMGAVTAVILGRTYIGRTMYAIGGNEEAARLSGIRVKKQKLVIYGLSGLFAAIAGI-VL 241

Query: 252 ASVMRVDVVKTGQDLEMYAILAVVIGGTSLLGGKFSLAGSAVGAVIIAMIRKTIITLGVN 311
           AS +           E+ AI AVVIGG SL GGK   +G+ +GA+I+A++R      G+N
Sbjct: 242 ASRLASAQPDAANGYELDAIAAVVIGGASLSGGKGKASGTFIGALILAVLRN-----GLN 296

Query: 312 AEATPAFFAVVVIVICVMQAPKIHNLSANMKRKRALKAQAKAVAA 356
                +F+  VVI + +  A  +  L     R+R+ +A A   +A
Sbjct: 297 LLNVSSFWQQVVIGVVIALAVLLDTL-----RRRSARASAAGTSA 336


Lambda     K      H
   0.325    0.136    0.384 

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: 539
Number of extensions: 35
Number of successful extensions: 5
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: 356
Length of database: 658
Length adjustment: 34
Effective length of query: 322
Effective length of database: 624
Effective search space:   200928
Effective search space used:   200928
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: 40 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. 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