GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_0546 in Desulfovibrio oxyclinae DSM 11498

Align ABC transporter for Xylitol, ATPase component (characterized)
to candidate WP_018125624.1 B149_RS0113115 ABC transporter ATP-binding protein

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



>NCBI__GCF_000375485.1:WP_018125624.1
          Length = 362

 Score =  188 bits (477), Expect = 2e-52
 Identities = 124/339 (36%), Positives = 185/339 (54%), Gaps = 29/339 (8%)

Query: 1   MAGIKIDKINKFYGTTQ------ALFDINLDIEDGEFVVFVGPSGCGKSTLLRTLAGLEG 54
           MA I++D++   Y          AL  I+   +DG     +GPSGCGK+T+L  ++GL  
Sbjct: 1   MARIELDELAHSYMANPKGPDDYALKRIHTTWDDGGAYALLGPSGCGKTTMLNIISGLLV 60

Query: 55  VSSGRIEIGGRDVTTVEPADRDLAMVFQSYALYPHMTVRENMEFGMKVNGFEPDLRKERI 114
            S G++   G+DVT + P  R++A VFQ   LY  MTV EN+ F +K      D   +R+
Sbjct: 61  PSHGKVLYDGKDVTKLPPEQRNIAQVFQFPVLYDTMTVYENLAFPLKNRKIPKDQVNKRV 120

Query: 115 AEAARVLQLEDYLDRKPGQLSGGQRQRVAIGRAIVKNP-SVFLFDEPLSNLDAKLRVQMR 173
            E A  L L   L+++   LS   +Q++++GR +V++  +  LFDEPL+ +D  L+ Q+R
Sbjct: 121 HEIADSLDLTADLNKRAAGLSADAKQKISLGRGLVRSDVAAILFDEPLTVIDPHLKWQLR 180

Query: 174 VELEGLHKQLGATMIYVTHDQVEAMTMADKIVVLNRGRIEQVGSPMDLYHKPNSRFVAEF 233
            +L+ +HK+   T+IYVTHDQVEAMT ADKIVV+  G + Q+G+P +L+  P   FV  F
Sbjct: 181 RKLKEIHKRFEHTLIYVTHDQVEAMTFADKIVVMYEGELVQIGTPEELFEHPEHTFVGYF 240

Query: 234 IGSPAMNVFSSDV--------GLQ-----------DISLDASAAFVGCRPEHIEI-VPDG 273
           IGSP MN+    V        GL+             +   S   +G RP +I+I   D 
Sbjct: 241 IGSPGMNLVECSVADGIAKAAGLEIPVPGIGTRRAAEASGTSKVELGIRPMYIDIRGKDA 300

Query: 274 DGHIAATVHVKERLGGESLLYLGLKGGGQIVARVGGDDE 312
           +G  A   +V+++ G   ++ L L G     ARV  D E
Sbjct: 301 EGLEARITNVEDQ-GSAKIVTLAL-GDATFKARVSEDQE 337


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: 309
Number of extensions: 22
Number of successful extensions: 2
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: 362
Length adjustment: 29
Effective length of query: 309
Effective length of database: 333
Effective search space:   102897
Effective search space used:   102897
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 Apr 09 2024. 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