GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Burkholderia phytofirmans PsJN

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 BPHYT_RS15605 BPHYT_RS15605 ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>FitnessBrowser__BFirm:BPHYT_RS15605
          Length = 316

 Score =  134 bits (338), Expect = 2e-36
 Identities = 93/315 (29%), Positives = 167/315 (53%), Gaps = 40/315 (12%)

Query: 1   MDIQTIQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNTFGV- 59
           MDI  IQ ++NG+ +GS+ A+ A+G T+ YGIL + NFAHGD L +GA +   ++  GV 
Sbjct: 1   MDI-FIQQVLNGLVLGSVYAIIALGYTMVYGILGIINFAHGDVLMVGAMVA--LSAIGVL 57

Query: 60  -----------NIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFL 108
                       + +++I+A +    V    E++ +  +R  +A     +I +IG+++ L
Sbjct: 58  QNHFPGLGNVPTLIIALIIAAIVCAAVGYTIERVAYRPLR--KAPRLAPLITAIGVSILL 115

Query: 109 RNGIILIWGGRNQNY-NLPITPALDIF-------GVKVPQNQLLVLALAVLSIGALHYLL 160
           +   ++IW      +  L  T  L++        G  +   +++++ +A L +G L  L+
Sbjct: 116 QTLAMMIWSRNPLPFPQLLPTDPLNVIKATDTTPGAVISMTEIVIIVVAFLVMGGLLLLV 175

Query: 161 QNTKIGKAMRAVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSM----YGLITAVRP 216
             TK+G+AMRA+A++   A + G++   VI  T++I   + +L G M    YG       
Sbjct: 176 HKTKLGRAMRAIAENPGNASLMGVNPNFVISATFMIGSALAALAGVMIASEYG---NAHF 232

Query: 217 NMGWFLILPLFASVILGGIGNPYGAIAAAFIIGIVQEVSTPFL--------GSQYKQGVA 268
            MG+   L  F + +LGGIGN  GA+    I+G+++++   ++        GS Y+   A
Sbjct: 233 YMGFIPGLKAFTAAVLGGIGNLGGAMVGGVILGLIEQLGAGYIGNLTGGVFGSNYQDVFA 292

Query: 269 LLIMILVLLIRPKGL 283
            +++I+VL+ RP GL
Sbjct: 293 FIVLIIVLVFRPSGL 307


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: 273
Number of extensions: 19
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: 316
Length adjustment: 27
Effective length of query: 261
Effective length of database: 289
Effective search space:    75429
Effective search space used:    75429
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 17 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