GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Phaeobacter inhibens BS107

Align GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate GFF2690 PGA1_c27320 putative sugar ABC transporter, ATP-binding protein

Query= TCDB::G3LHY8
         (358 letters)



>FitnessBrowser__Phaeo:GFF2690
          Length = 349

 Score =  194 bits (492), Expect = 4e-54
 Identities = 118/344 (34%), Positives = 175/344 (50%), Gaps = 8/344 (2%)

Query: 2   LELRNAAKMVGADYHIYPTDLVLERGTLNVLLGPTLAGKTSLMRLMAGLDRPTGGSIHFD 61
           +ELRN +K  G+   +   DL +      VLLGP+  GKT+ MR++AGL+  + G I  D
Sbjct: 4   IELRNISKRWGSFVGVDNFDLTIADKEFLVLLGPSGCGKTTTMRMIAGLESASEGDILVD 63

Query: 62  GTDVTGMPVQKRNVAMVYQQFINYPALTVYNNIASPMRISGKDAATIDREVRKAAELLKL 121
           G  V  +  + R+VAMV+Q +  YP + VY NI  P+++ G DA T D +VR+A+ +++L
Sbjct: 64  GNRVNELEPKDRDVAMVFQSYALYPNMNVYENIRFPLKVRGVDAKTHDEKVRRASAMVEL 123

Query: 122 TPYLDRTPLNLSGGQQQRTALARALVKNASLVLMDEPLANLDYKLREELREELPKIFAQS 181
             +L R P  LSGGQ+QR ALARA+V+  ++ LMDEPL+NLD KLR   R ++  +  + 
Sbjct: 124 DEFLHRKPAELSGGQRQRVALARAIVREPNVFLMDEPLSNLDAKLRVSTRAQIKNLSHEL 183

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

Query: 242 VTKSGNVFTRPSGVTIPVPSHLAVVPDGPVTIAFHPHHLGLAPQTGDAARLQARTLVSEI 301
              SG  FT        +        DGPVT+ F      +    G   ++ A     E+
Sbjct: 244 GGLSGGRFTAQHTDIAGLSGQ-----DGPVTLGFRAEDASVVDSGG---QINAPIYTMEL 295

Query: 302 TGSESFVHLEYDGVRWVMLAHGIHDIDPDMEVEAFLDTRHLMAF 345
            G  + V +   GV   + A      + D  V   + T H   F
Sbjct: 296 LGDATMVTVRIGGVLVSVKADKTFRAEIDDMVSIHVPTDHCHLF 339


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: 305
Number of extensions: 11
Number of successful extensions: 1
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: 349
Length adjustment: 29
Effective length of query: 329
Effective length of database: 320
Effective search space:   105280
Effective search space used:   105280
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 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