GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Desulfovibrio vulgaris Miyazaki F

Align GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate 8499890 DvMF_0655 ABC transporter related (RefSeq)

Query= TCDB::G3LHY8
         (358 letters)



>FitnessBrowser__Miya:8499890
          Length = 350

 Score =  167 bits (423), Expect = 4e-46
 Identities = 111/347 (31%), Positives = 170/347 (48%), Gaps = 15/347 (4%)

Query: 2   LELRNAAKMVGADYHIYPTDLVLERGTLNVLLGPTLAGKTSLMRLMAGLDRPTGGSIHFD 61
           ++L N ++  G    +      +E+GT+ VLLGP+  GK++ +RL+AGL+  T G I   
Sbjct: 4   IQLLNVSRHWGDVRAVDDVSFEVEQGTMLVLLGPSGCGKSTTLRLIAGLESVTSGRIMIG 63

Query: 62  GTDVTGMPVQKRNVAMVYQQFINYPALTVYNNIASPMRISGKDAATIDREVRKAAELLKL 121
             DVT +P  +R +AMV+Q +  +P LTV  NI   + +     A  ++ + +A ++L L
Sbjct: 64  ERDVTHLPPAQRQLAMVFQSYALFPHLTVRENILFGLTVRKVPEAEREKRLTRAVDILGL 123

Query: 122 TPYLDRTPLNLSGGQQQRTALARALVKNASLVLMDEPLANLDYKLREELREELPKIFAQS 181
           +  L R P  LSGGQQQR AL RALV  A++ LMDEPL+NLD KLR E+R E+  +    
Sbjct: 124 SALLQRKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRHEMRREIRALQQTL 183

Query: 182 GAIFVYATTEPSEALLLGGNTATLNQGRVTQFGPTIEVYRRPVNLATAGIFADPPLNTL- 240
           G   VY T + +EA+ +      +  GR+ Q     E+Y RP           PP+N + 
Sbjct: 184 GMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPSELYSRPATTFAGNFIGTPPMNLVR 243

Query: 241 --DVTKSGNVFTRPSGVTIPVPSHLAVVPDGPVTIAFHPHHLGLAPQTGDAARLQARTLV 298
             D   S  V    SG        ++VV      +   P H+ + P+ G  A +++    
Sbjct: 244 LDDARGSVCVAGSRSGT-------VSVVDSADYVLGIRPEHIRIVPE-GWRAVVES---- 291

Query: 299 SEITGSESFVHLEYDGVRWVMLAHGIHDIDPDMEVEAFLDTRHLMAF 345
            E  GS S +     G    ++  G+  I    E+       H+  F
Sbjct: 292 VEYLGSGSVLGCRVGGEELSVVVDGVPTIAVGAEIYLHCPDEHIHIF 338


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: 291
Number of extensions: 15
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: 350
Length adjustment: 29
Effective length of query: 329
Effective length of database: 321
Effective search space:   105609
Effective search space used:   105609
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