GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Halomonas desiderata SP1

Align GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate WP_086511129.1 BZY95_RS17245 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::G3LHY8
         (358 letters)



>NCBI__GCF_002151265.1:WP_086511129.1
          Length = 380

 Score =  179 bits (454), Expect = 1e-49
 Identities = 105/306 (34%), Positives = 164/306 (53%), Gaps = 5/306 (1%)

Query: 2   LELRNAAKMVGADYHIYPTDLVLERGTLNVLLGPTLAGKTSLMRLMAGLDRPTGGSIHFD 61
           L+L +  K       I   DL +      V +GP+  GK++L+R++AGL+  T G I  D
Sbjct: 4   LQLHDIVKRFDDTEVIKGVDLEVNDREFVVFVGPSGCGKSTLLRMIAGLESATSGDILID 63

Query: 62  GTDVTGMPVQKRNVAMVYQQFINYPALTVYNNIASPMRISGKDAATIDREVRKAAELLKL 121
           G  +  +   +R +AMV+Q +  YP +TV +N+   ++++G       R+VR+AA +L+L
Sbjct: 64  GVRMNEVGPAERGLAMVFQSYALYPHMTVEDNMGFSLKLAGVPKEERRRKVREAASILQL 123

Query: 122 TPYLDRTPLNLSGGQQQRTALARALVKNASLVLMDEPLANLDYKLREELREELPKIFAQS 181
            P L+R P  LSGGQ+QR A+ RA+V+N S+ L DEPL+NLD  LR ++R EL ++  + 
Sbjct: 124 EPLLERKPKALSGGQRQRVAIGRAIVRNPSIFLFDEPLSNLDAALRVQMRIELARLHEEL 183

Query: 182 GAIFVYATTEPSEALLLGGNTATLNQGRVTQFGPTIEVYRRPVNLATAGIFADPPLNTLD 241
            A  +Y T +  EA+ +      L  G V Q G  +E+Y  P N   AG    P +N L+
Sbjct: 184 DATMIYVTHDQIEAMTMADKIVVLQGGVVEQVGSPMELYHHPRNRFVAGFIGSPKMNFLE 243

Query: 242 VTK-----SGNVFTRPSGVTIPVPSHLAVVPDGPVTIAFHPHHLGLAPQTGDAARLQART 296
           V +     +G     P G T  VP   + + D  +T+   P HL L PQ   + R++   
Sbjct: 244 VERVSAAATGVEVRLPDGDTCTVPVDGSGLDDDALTLGIRPEHLQLDPQGPLSGRIEVIE 303

Query: 297 LVSEIT 302
            +  +T
Sbjct: 304 RLGGVT 309


Lambda     K      H
   0.319    0.136    0.392 

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: 14
Number of successful extensions: 2
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: 358
Length of database: 380
Length adjustment: 30
Effective length of query: 328
Effective length of database: 350
Effective search space:   114800
Effective search space used:   114800
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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 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