GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livH in Azohydromonas australica DSM 1124

Align ABC transporter permease (characterized, see rationale)
to candidate WP_028999461.1 H537_RS0121280 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A165KC95
         (309 letters)



>NCBI__GCF_000430725.1:WP_028999461.1
          Length = 307

 Score =  470 bits (1209), Expect = e-137
 Identities = 232/309 (75%), Positives = 273/309 (88%), Gaps = 2/309 (0%)

Query: 1   MDILLQQIINGLVLGSMYALIALGYTMVYGIIQLINFAHGEVLMIGALTSWSCIGMMQGA 60
           MDI LQQIINGLVLGSMYAL+ALGYTMVYGII LINFAHGEVLM+GA+ SW+ + ++  +
Sbjct: 1   MDIFLQQIINGLVLGSMYALVALGYTMVYGIINLINFAHGEVLMVGAMVSWTVVTVLGDS 60

Query: 61  MPGAPGWVILLLATIIACVVAATLNFVIEKVAYRPLRSSPRLAPLITAIGMSILLQTLAM 120
             G PGW+++L++ I A V+ + LNF IEK+AYRPLR++PRLAPLITA+GMS+LLQTLAM
Sbjct: 61  --GLPGWLLMLISLICAVVICSALNFTIEKLAYRPLRNAPRLAPLITAMGMSLLLQTLAM 118

Query: 121 IIWKPNYKPYPTMLPSSPFEIGGAFITPTQILILGVTAVALASLVYLVNHTNLGRAMRAT 180
           IIWKPN KP+P +LP+ P EI GA I+ TQILILG+TA+ LA+L+YLVN T LGRAMRAT
Sbjct: 119 IIWKPNPKPFPQLLPTDPIEIAGAVISVTQILILGITALVLAALLYLVNKTKLGRAMRAT 178

Query: 181 AENPRVASLMGVKPDMVISATFIIGAVLAAIAGIMYASNYGTAQHTMGFLPGLKAFTAAV 240
           AENPRVASLMGV+PD VISATFIIGA LAA+AGIM+A+NYGT QHTMGFLPGLKAFTAAV
Sbjct: 179 AENPRVASLMGVRPDWVISATFIIGASLAALAGIMWAANYGTVQHTMGFLPGLKAFTAAV 238

Query: 241 FGGIGNLAGAVVGGILLGLIEAIGSGYIGTLTGGLLGSHYTDIFAFIVLIIILTLRPSGL 300
            GGIGNLAGAVVG +LLGL+EAIG+GY+G LTGG+LGSHY DIFAF+ L+++LTLRP GL
Sbjct: 239 LGGIGNLAGAVVGALLLGLLEAIGAGYLGDLTGGVLGSHYADIFAFMALVLVLTLRPQGL 298

Query: 301 LGERVADRA 309
           LGER ADRA
Sbjct: 299 LGERTADRA 307


Lambda     K      H
   0.327    0.142    0.419 

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: 336
Number of extensions: 7
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: 309
Length of database: 307
Length adjustment: 27
Effective length of query: 282
Effective length of database: 280
Effective search space:    78960
Effective search space used:    78960
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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