GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Pseudovibrio axinellae Ad2

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_068004539.1 PsAD2_RS07415 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_001623255.1:WP_068004539.1
          Length = 290

 Score =  209 bits (532), Expect = 6e-59
 Identities = 108/279 (38%), Positives = 170/279 (60%), Gaps = 3/279 (1%)

Query: 9   IVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNT-FGVNIWLSMIV 67
           ++ GI +GSI AL AVG+TL +GILR ++ AHGD  TLGA+    V T FGV+ W+++ V
Sbjct: 11  LMPGIVLGSIYALGAVGITLVFGILRFAHLAHGDLATLGAFAALGVVTIFGVSPWVALPV 70

Query: 68  AVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRNQNYNLPI 127
           A+V    + +  +KL +  +         +++ S+G+AL LR  + ++WG   + Y   I
Sbjct: 71  AMVACAFMAIGIDKLFYDYLSE--RPKIIVVMSSLGIALMLRAVVQVVWGVDTETYTRGI 128

Query: 128 TPALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMRAVADDLDLAKVSGIDVE 187
               D +G+++   ++  +    L +G L   LQ TK GKAMRA++D+ DLA +SG+D  
Sbjct: 129 VRPDDYWGIRIRDREIYTIIAMFLIVGVLWAFLQKTKWGKAMRAMSDNPDLALLSGVDNR 188

Query: 188 QVIFWTWLIAGTVTSLGGSMYGLITAVRPNMGWFLILPLFASVILGGIGNPYGAIAAAFI 247
           ++   TW I G + +  G   G+ T ++P MGW ++LP+FA+ ILGG+G   GA+    I
Sbjct: 189 KITMLTWGIVGVLCAASGFFLGINTELKPLMGWTMLLPMFAAAILGGVGRVEGAVIGGLI 248

Query: 248 IGIVQEVSTPFLGSQYKQGVALLIMILVLLIRPKGLFKG 286
           +GI +E S  F+  +YK  +A  I++L+LL+RP GL KG
Sbjct: 249 VGIAEETSVLFIPGEYKAAMAFAILLLILLVRPTGLLKG 287


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: 271
Number of extensions: 22
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: 288
Length of database: 290
Length adjustment: 26
Effective length of query: 262
Effective length of database: 264
Effective search space:    69168
Effective search space used:    69168
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