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 GFF1302 PGA1_c13180 ABC transporter, ATP binding protein

Query= TCDB::G3LHY8
         (358 letters)



>FitnessBrowser__Phaeo:GFF1302
          Length = 334

 Score =  201 bits (510), Expect = 3e-56
 Identities = 128/354 (36%), Positives = 181/354 (51%), Gaps = 27/354 (7%)

Query: 2   LELRNAAKMVGADYHIYPTDLVLERGTLNVLLGPTLAGKTSLMRLMAGLDRPTGGSIHFD 61
           ++L +  K  G    I P DL +E G   V +GP+  GK++L+RL+AGL+  T G+I  D
Sbjct: 4   IKLESVTKNFGPVEVIPPLDLTIEDGEFTVFVGPSGCGKSTLLRLIAGLEDITSGTIRID 63

Query: 62  GTDVTGMPVQKRNVAMVYQQFINYPALTVYNNIASPMRISGKDAATIDREVRKAAELLKL 121
           G D T +P  KR +AMV+Q +  YP ++V  NIA PM+++G  A    R +  AA  L L
Sbjct: 64  GEDATNIPPAKRGLAMVFQSYALYPHMSVRKNIAFPMKMAGIPADEQKRRIDNAAAALNL 123

Query: 122 TPYLDRTPLNLSGGQQQRTALARALVKNASLVLMDEPLANLDYKLREELREELPKIFAQS 181
           T YLDR P  LSGGQ+QR A+ RA+V+  +  L DEPL+NLD  LR  +R E+ ++  + 
Sbjct: 124 TDYLDRRPGQLSGGQRQRVAIGRAIVREPAAFLFDEPLSNLDAALRVGMRLEISELHKRL 183

Query: 182 GAIFVYATTEPSEALLLGGNTATLNQGRVTQFGPTIEVYRRPVNLATAGIFADPPLNTLD 241
               +Y T +  EA+ +      L  G + Q G  +E+YR P N+  AG    P +N L 
Sbjct: 184 ATTMIYVTHDQVEAMTMADKIVVLQAGVIEQVGSPMELYRAPRNVFVAGFIGSPKMNLL- 242

Query: 242 VTKSGNVFTRPSGVTIPVPSHLAVVPDGPVTIAFHPHHLGLAPQTGDAARLQARTL-VSE 300
                   T P         H A       TI   P HL ++   G    + A T+ VSE
Sbjct: 243 --------TGPQAA-----QHNA------ATIGIRPEHLSISETEG----MWAGTIGVSE 279

Query: 301 ITGSESFVHLEYDGVRWVMLAHGIHDIDPDMEVEAFL--DTRHLMAFGSDGRAI 352
             GS++F H++ D     +      ++D       FL  D  HL  FGSDG  I
Sbjct: 280 HLGSDTFFHVQCDAFDDPLTVRASGELDLGYGERVFLTPDMTHLHRFGSDGLRI 333


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: 325
Number of extensions: 14
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: 358
Length of database: 334
Length adjustment: 29
Effective length of query: 329
Effective length of database: 305
Effective search space:   100345
Effective search space used:   100345
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