GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Halomonas desiderata SP1

Align NatD, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate WP_086510701.1 BZY95_RS14925 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_002151265.1:WP_086510701.1
          Length = 335

 Score =  174 bits (442), Expect = 2e-48
 Identities = 100/326 (30%), Positives = 174/326 (53%), Gaps = 51/326 (15%)

Query: 8   LIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVN------------ 55
           +I+ G   GSI A+ A+G+TL + I+R ++FAH D +T GA++   +             
Sbjct: 11  VIIAGSVTGSIYAIGAIGVTLIFSIMRFAHFAHADMMTFGAFMVLLLTLAFPGVGGVVGL 70

Query: 56  -TFGVNIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIIL 114
            T  V + L+MI+     VG+    +K+ +  +R+       ++I S+G+ L L+  I L
Sbjct: 71  PTPIVMLPLAMILTAALAVGI----DKVFYKPLRAHGVKPIVIVIGSLGVTLMLQGLIRL 126

Query: 115 IWGGRNQN----------YNLPITPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTK 164
             G   QN          Y L +   L    + V + Q+++  L +  +  LH  L  T+
Sbjct: 127 FAGTSAQNMYLAGERKEIYRLDVPFELATRPIIVTEPQIILFILTIACVVGLHVFLNRTR 186

Query: 165 IGKAMRAVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLIL 224
           +GKAMRA++D+ DLA+ SGI+   ++  TW+IAG++ ++ G++  L    +P++ +FL+L
Sbjct: 187 LGKAMRAMSDNPDLARASGINTNYIVSVTWVIAGSLAAIAGTLLSLDVTFKPDLSFFLLL 246

Query: 225 PLFASVILGGIGNPYGAIAAAFIIGIVQEVST------------------------PFLG 260
           P+FA+ I+GG+G+PYGAIA  F++G  + ++                          F+G
Sbjct: 247 PIFAAAIVGGVGHPYGAIAGGFVVGFAETLAVFNWAVLLRPIAHLFPEWIEIPRNLAFVG 306

Query: 261 SQYKQGVALLIMILVLLIRPKGLFKG 286
           ++YK  V   I++ +L+ RP G+FKG
Sbjct: 307 TEYKIVVPFFILVAILVWRPTGIFKG 332


Lambda     K      H
   0.328    0.144    0.426 

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: 280
Number of extensions: 21
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: 288
Length of database: 335
Length adjustment: 27
Effective length of query: 261
Effective length of database: 308
Effective search space:    80388
Effective search space used:    80388
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