GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natF in Methylocystis bryophila S285

Align NatF, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized)
to candidate WP_085770149.1 B1812_RS02245 transporter substrate-binding domain-containing protein

Query= TCDB::Q8YPM9
         (369 letters)



>NCBI__GCF_002117405.1:WP_085770149.1
          Length = 335

 Score =  175 bits (444), Expect = 1e-48
 Identities = 108/318 (33%), Positives = 162/318 (50%), Gaps = 6/318 (1%)

Query: 54  ANRWNTIKNRGQLICGVSGEVPGFSFVGTDGEYSGIDVDVCRAIAAALFDNPDAVEFRNL 113
           A    +I++   + CGV   V  ++     G  S ++ +VCRA+A AL  +  AV  +N 
Sbjct: 22  AQTLESIRSAKHMECGVVTGVDDWNGEDLHGNLSALEAEVCRAVAVALLGDASAVTIQNF 81

Query: 114 SAK-ERFTALQTGEVDILSRNTTWTLSRATSVGLEFAPVVFYDGQAIMVRKNSAIKSLAD 172
            A+ E   AL+ G++  L+   T + S A   G+ F P VFYD Q +MV K S +  +A 
Sbjct: 82  PAELEALNALKAGKIQ-LAIGVTPSASTAARFGVGFGPPVFYDSQRLMVAKGSGVTDIAG 140

Query: 173 LKDKAICVQTGTTTEQNLADQMRKRNITYKPVVFEDVNVTFATYAEGRCDAITADRSALV 232
           L+DK +C    T  E+ L +++  R I Y  +   +     A  A  RC+A TA  S L 
Sbjct: 141 LRDKLVCALDMTPPERILREELTARGIPYGLMAHSEQGEMDAAVAVSRCEAATAMESRLA 200

Query: 233 SRRTTLPTPEDNV-VLDEVISSEPLAPAVARGDAKWSNTVNWVVYALIKGEELGINAQNL 291
             R     P  N   L E     P+ PA   GD  +  TV+W + ALI+ E LGI   N+
Sbjct: 201 QSRAGFHAPTSNFSFLPERFGINPVVPAYRYGDQIFGLTVDWTIGALIEAEALGITRDNV 260

Query: 292 GQFTTSNDPDVKRFLGTEGDLGQGLGLTNDFAARIIKHVGNYAEVYDRNLGPKTKLNLAR 351
              +   D   ++ LG +    Q LGL +D+AA++I   GNY E++ R +G     +L R
Sbjct: 261 AA-SKREDLRAEQLLGRDFATAQALGLAHDWAAKVIAATGNYGEIFQRTVG--GPYHLDR 317

Query: 352 GQNQLWSKGGLLYSPPFR 369
           G N LW++GGL++ PP +
Sbjct: 318 GLNALWTEGGLMHPPPMK 335


Lambda     K      H
   0.317    0.133    0.387 

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: 258
Number of extensions: 10
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: 369
Length of database: 335
Length adjustment: 29
Effective length of query: 340
Effective length of database: 306
Effective search space:   104040
Effective search space used:   104040
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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