GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livG in Desulfatibacillum aliphaticivorans DSM 15576

Align High-affinity branched-chain amino acid transport ATP-binding protein LivG aka B3455, component of Leucine; leucine/isoleucine/valine porter (characterized)
to candidate WP_028316323.1 G491_RS0123750 ABC transporter ATP-binding protein

Query= TCDB::P0A9S7
         (255 letters)



>NCBI__GCF_000429905.1:WP_028316323.1
          Length = 287

 Score =  245 bits (626), Expect = 6e-70
 Identities = 130/282 (46%), Positives = 180/282 (63%), Gaps = 30/282 (10%)

Query: 3   QPLLSVNGLMMRFGGLLAVNNVNLELYPQEIVSLIGPNGAGKTTVFNCLTGFYKPTGGTI 62
           +P+L V  L M FGGL A++++++++ P EI +LIGPNGAGKTT FNC+TG Y PT G +
Sbjct: 2   KPILDVKNLTMDFGGLRALDSLDIDVRPGEIAALIGPNGAGKTTFFNCVTGMYNPTKGDV 61

Query: 63  LLRDQ-----HLEGLPGQQIARMGVVRTFQHVRLFREMTVIENLLVAQH----------- 106
           L+         L GL   ++   G+ RTFQ++RLF+ MTV+EN+++ +H           
Sbjct: 62  LVNSPSGYSTRLNGLKPNKVTERGLARTFQNIRLFQNMTVLENVMIGRHCHSGAGHEIIM 121

Query: 107 --------QQLKTGLFSG------LLKTPSFRRAQSEALDRAATWLERIGLLEHANRQAS 152
                   +   +  F G      LLK   F+  + E +  +   LE++GL + AN  A 
Sbjct: 122 NPDNSPVKRMAASAFFGGMEIAATLLKGKRFKEREQETVQYSYNVLEKVGLEKFANNFAK 181

Query: 153 NLAYGDQRRLEIARCMVTQPEILMLDEPAAGLNPKETKELDELIAELRNHHNTTILLIEH 212
           NL YG QRRLEIAR M T+P +L+LDEPAAG+NP+ETKELD+LI  +R+    +ILLIEH
Sbjct: 182 NLPYGLQRRLEIARAMATEPFLLLLDEPAAGMNPQETKELDDLIQRIRDKEGISILLIEH 241

Query: 213 DMKLVMGISDRIYVVNQGTPLANGTPEQIRNNPDVIRAYLGE 254
           DM+LVM IS RI+V++ G  +A GTP +IR N  VI+AYLGE
Sbjct: 242 DMRLVMSISQRIFVMDYGKKIAQGTPGEIRTNDAVIKAYLGE 283


Lambda     K      H
   0.320    0.137    0.395 

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: 204
Number of extensions: 9
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: 255
Length of database: 287
Length adjustment: 25
Effective length of query: 230
Effective length of database: 262
Effective search space:    60260
Effective search space used:    60260
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: 47 (22.7 bits)

This GapMind analysis is from Sep 24 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