GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_17605 in Desulfatiglans anilini DSM 4660

Align ATP-binding cassette domain-containing protein; SubName: Full=Amino acid transporter; SubName: Full=Histidine ABC transporter ATP-binding protein; SubName: Full=Histidine transport system ATP-binding protein (characterized, see rationale)
to candidate WP_244155490.1 H567_RS0115555 ABC transporter ATP-binding protein

Query= uniprot:A0A1N7U8S3
         (276 letters)



>NCBI__GCF_000422285.1:WP_244155490.1
          Length = 243

 Score =  129 bits (323), Expect = 8e-35
 Identities = 91/252 (36%), Positives = 129/252 (51%), Gaps = 25/252 (9%)

Query: 4   SAQALAAYPVDEPVAQPVTAAIKLQVEGIHKRYGEH----EVLKGVSLNARQGDVISLIG 59
           S  A AA  + EP+         +++  + K YG      + LKG+ L    G+ ++++G
Sbjct: 2   SRNAAAAETMLEPI---------IRLTNVTKTYGSGSAAMQALKGIDLAIHPGEFVAVMG 52

Query: 60  ASGSGKSTMLRCINFLEQPDAGVITLDGISIEMRQGRAGTRAPHQDQLQNLRTRLAMVFQ 119
            SGSGKST +  +  L+ P +GV   DG+ +         R     +    R  L  VFQ
Sbjct: 53  PSGSGKSTCMNILGCLDTPSSGVFLFDGVDV--------ARLTRDQRALLRRHDLGFVFQ 104

Query: 120 HFNLWSHMTVLENITMAPRRVLDVSAAEAEKRARMYLDKVGLPSRVADQYPAFLSGGQQQ 179
            FNL S  + LEN+ + P     V AA   + A   L  VGL S      PA LSGGQQQ
Sbjct: 105 GFNLLSRTSALENVEL-PLIYRRVPAARRRELALRALAAVGL-SGWESHTPAELSGGQQQ 162

Query: 180 RVAIARALAMEPEIILFDEPTSALDPELVGEVLKVIQTL-AEEGRTMLMVTHEMGFARQV 238
           RVAI RA+  EP+++L DEPT  LD  L  EV++++Q+     G T++MVTHE   A   
Sbjct: 163 RVAITRAIVTEPKVLLADEPTGNLDSALSREVMELLQSFNRSRGLTIVMVTHEADMAAYA 222

Query: 239 SSQVLFLHQGRV 250
             ++LF   GR+
Sbjct: 223 ERRILF-RDGRI 233


Lambda     K      H
   0.319    0.133    0.372 

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: 157
Number of extensions: 10
Number of successful extensions: 4
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: 276
Length of database: 243
Length adjustment: 24
Effective length of query: 252
Effective length of database: 219
Effective search space:    55188
Effective search space used:    55188
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 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