GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Marinobacter adhaerens HP15

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate GFF3011 HP15_2955 ATP-binding component of ABC transporter

Query= reanno::Dino:3607124
         (338 letters)



>FitnessBrowser__Marino:GFF3011
          Length = 372

 Score =  274 bits (700), Expect = 3e-78
 Identities = 152/363 (41%), Positives = 221/363 (60%), Gaps = 32/363 (8%)

Query: 1   MAGIKIDKINKFYG--TTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSG 58
           M+ +++  I K Y     + L  I++DI  GEF++ VGPSGCGKSTL+ T+AGLE ++ G
Sbjct: 1   MSQLELRSIRKTYPGVAEETLKGIDIDIASGEFLILVGPSGCGKSTLMNTIAGLETITDG 60

Query: 59  RIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAA 118
            I + G+D++T+EP DRD+AMVFQSYALYP M+VREN+ FG+K+ G       + +   A
Sbjct: 61  SIVLDGKDISTMEPKDRDIAMVFQSYALYPTMSVRENIAFGLKIRGLPKHEIDQEVERVA 120

Query: 119 RVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEG 178
            +LQ+   +++KP  LSGGQ+QRVA+GRA+ + P ++LFDEPLSNLDAKLRV+MR E++ 
Sbjct: 121 DLLQISPLMNKKPANLSGGQQQRVAMGRALARRPRIYLFDEPLSNLDAKLRVEMRTEIKK 180

Query: 179 LHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPA 238
           LH++L  T++YVTHDQ+EAMT+AD+I VL  G ++Q+G+P ++Y +P + FVA F+GSPA
Sbjct: 181 LHQRLKTTIVYVTHDQIEAMTLADRIAVLKDGELQQLGTPKEVYDRPENLFVAGFMGSPA 240

Query: 239 MN-----VFSSDVGLQ---------DISLD---------ASAAFVGCRPEHIEIVPD--G 273
           M+     V   + GLQ          + L               +G RPEHI    D   
Sbjct: 241 MSFVPVTVEQGEGGLQAEVRGNDGRSVKLPVPEFLADRVGKKVILGIRPEHITQPQDQKN 300

Query: 274 DGHIAA----TVHVKERLGGESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSRHRLH 329
           D  + A    T+ V E  G + +  + L     +  R+  +     G    L F   ++ 
Sbjct: 301 DQTLVAKGEFTIEVTEPTGPDVIALIQL-NDTNVHCRIDPEHPVTWGETAELMFDMKKVV 359

Query: 330 QFD 332
            FD
Sbjct: 360 FFD 362


Lambda     K      H
   0.320    0.139    0.396 

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: 393
Number of extensions: 20
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: 338
Length of database: 372
Length adjustment: 29
Effective length of query: 309
Effective length of database: 343
Effective search space:   105987
Effective search space used:   105987
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 (21.8 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