GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Desulfovibrio vulgaris Hildenborough

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate 208681 DVU3161 ABC transporter, ATP-binding protein

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



>MicrobesOnline__882:208681
          Length = 349

 Score =  298 bits (763), Expect = 1e-85
 Identities = 164/345 (47%), Positives = 226/345 (65%), Gaps = 15/345 (4%)

Query: 1   MAGIKIDKINKFYGTTQALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEGVSSGRI 60
           M+ I +DK+++ +G  +A+ D++ ++E G+ +V +GPSGCGKST LR +AGLE V+SGRI
Sbjct: 1   MSTIVLDKVSRHWGDVRAVDDVSFEVEQGDMLVLLGPSGCGKSTTLRLIAGLESVTSGRI 60

Query: 61  EIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERIAEAARV 120
            IGGRDVT + PA R LAMVFQSYAL+PH+TVR+N+ FG+ V       R++R+  A  +
Sbjct: 61  LIGGRDVTNLPPAQRQLAMVFQSYALFPHLTVRDNILFGLVVRKVPAAERQKRLDRAVEI 120

Query: 121 LQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNPSVFLFDEPLSNLDAKLRVQMRVELEGLH 180
           L L   L+RKPG+LSGGQ+QRVA+GRA+V   +V L DEPLSNLDAKLR +MR E+  L 
Sbjct: 121 LGLGKLLERKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRQEMRREIRALQ 180

Query: 181 KQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEFIGSPAMN 240
           + LG TM+YVTHDQ EAM+MAD+I+++  GRI Q  +P ++Y +P + F   FIG+P MN
Sbjct: 181 QTLGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPTEMYSRPATAFAGSFIGTPPMN 240

Query: 241 VF---SSDVGLQ-------DISLDASA-AFVGCRPEHIEIVPDGDGHIAATVHVKERLGG 289
           +     +D G++        ++  A A   +G RPEHI IV DG     A V   E LG 
Sbjct: 241 LVRLQGNDDGIRVAGSRSGRVTCHAGADCMLGIRPEHIRIVDDG---WRAVVESVEYLGS 297

Query: 290 ESLLYLGLKGGGQIVARVGGDDETKVGAAVSLRFSRHRLHQFDEA 334
            S+L   + G  ++   V G  +T VGA + L      +H FD A
Sbjct: 298 NSVLSCRV-GSEELSVVVHGVTDTVVGAEIYLHCPEEHVHIFDAA 341


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: 320
Number of extensions: 13
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: 338
Length of database: 349
Length adjustment: 29
Effective length of query: 309
Effective length of database: 320
Effective search space:    98880
Effective search space used:    98880
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