GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Polaromonas naphthalenivorans CJ2

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate WP_011801983.1 PNAP_RS13005 ABC transporter permease

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_000015505.1:WP_011801983.1
          Length = 317

 Score =  227 bits (579), Expect = 3e-64
 Identities = 118/308 (38%), Positives = 187/308 (60%), Gaps = 6/308 (1%)

Query: 21  SLDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLS 80
           S+ + G  +  +L CV  A  +E F+T +N+  I++Q  + G++A+G T +ILT GIDLS
Sbjct: 8   SIAKLGPFIALLLACVFFATQNERFLTLQNFSLIMQQVMVVGVIAIGQTLIILTAGIDLS 67

Query: 81  VGSILAFAGLCSAMVATQ-GYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGML 139
            G ++A  G+    ++   G     A++ GM    + G++NG +V  + +PPF+ TLG L
Sbjct: 68  CGMVMALGGIVMTKLSADFGLPTPVAIACGMAVTMLFGLINGLLVTRIKLPPFIVTLGTL 127

Query: 140 SIARGMTFILNDGSPITDLPDAYLALG----IGKIGPIGVPIIIFAVVALIFWMVLRYTT 195
           +IA  +T + +    +TD+P     LG    IG    +G  +++   + +  W+ LR T 
Sbjct: 128 NIAFAITQLYSQSQTVTDIPAGMTFLGNTFTIGNTS-MGYGVVLMLALYVATWLWLRETA 186

Query: 196 YGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYE 255
            GR++YAVG + ++ R +GI   +V+  VYV++GL  G+A ++  ART +  P AG +  
Sbjct: 187 PGRHIYAVGNSPEATRLTGIATDRVLLGVYVLAGLFYGIASLLSVARTGAGDPNAGQTEN 246

Query: 256 LDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAV 315
           LDAI AVV+GGTSL GG G ++GTL GAL++GV  NGL L+GVSS YQ +  G++++ AV
Sbjct: 247 LDAITAVVLGGTSLFGGRGMLLGTLVGALIVGVFRNGLTLMGVSSVYQVLVTGILVILAV 306

Query: 316 LIDVWRKK 323
             D   +K
Sbjct: 307 TTDQMSRK 314


Lambda     K      H
   0.326    0.141    0.412 

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: 247
Number of extensions: 14
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: 325
Length of database: 317
Length adjustment: 28
Effective length of query: 297
Effective length of database: 289
Effective search space:    85833
Effective search space used:    85833
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 (21.6 bits)
S2: 48 (23.1 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