GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Burkholderia phytofirmans PsJN

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate BPHYT_RS27190 BPHYT_RS27190 sugar ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>FitnessBrowser__BFirm:BPHYT_RS27190
          Length = 343

 Score =  245 bits (625), Expect = 1e-69
 Identities = 135/321 (42%), Positives = 195/321 (60%), Gaps = 13/321 (4%)

Query: 35  QKLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVG 94
           QK  A  SL+++I+ FS  S  F  V NL+++         L +A T VIIT GIDLSVG
Sbjct: 25  QKFAALGSLVVLIVAFSLTSAAFFSVGNLMTVALQVTSIAYLGVAATCVIITGGIDLSVG 84

Query: 95  TMMTFCAVMAGVVLTNWGMPLPLGIAAAIFFGALSGWISGMVIAKLKVPPFIATLGMMML 154
           +++    V A  +L   G+P+P+ +   +  GA  GW++G+ + ++ +PPFIATLGMM++
Sbjct: 85  SVLALAGV-AAALLVKAGVPIPVAMLGGMLVGAACGWVNGICVTRMGLPPFIATLGMMLV 143

Query: 155 LKGLSLVISGTRPIY-FNDTEG---------FSAIAQDSLIGDLIPSLPIPNAVLILFLV 204
            +GL+L I+G RP+    D  G          S I  D     + P +P P  ++++   
Sbjct: 144 ARGLALQITGARPVSGLGDAFGELGNGALFRISHIGADGFPDTVFPGIPYPVVIMVVLFA 203

Query: 205 AIGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRL 264
           A+  SI+L++T  GR+ +A+GSN EA RLSGV V   K+  Y  SG + G  G ++ SRL
Sbjct: 204 AV--SILLSRTSLGRHIYAVGSNAEAARLSGVNVQGVKLFTYVLSGLLAGATGCVLMSRL 261

Query: 265 NSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQ 324
            +AQP  G  YELDAIA+ VIGGTSL GG GTI GT IGAF++ VL NGL +  V+   Q
Sbjct: 262 VTAQPNEGVMYELDAIASAVIGGTSLMGGVGTISGTAIGAFVIGVLRNGLNMNGVSSFIQ 321

Query: 325 TVVTGVIIILAVYLDILRRRR 345
            ++ GV+I+  V++D LR R+
Sbjct: 322 QIIIGVVILGTVWIDQLRNRK 342


Lambda     K      H
   0.326    0.139    0.398 

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: 277
Number of extensions: 7
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 347
Length of database: 343
Length adjustment: 29
Effective length of query: 318
Effective length of database: 314
Effective search space:    99852
Effective search space used:    99852
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: 49 (23.5 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