GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylE_Tm in Paraburkholderia bryophila 376MFSha3.1

Align Sugar ABC transporter, periplasmic sugar-binding protein (characterized, see rationale)
to candidate H281DRAFT_03378 H281DRAFT_03378 monosaccharide ABC transporter substrate-binding protein, CUT2 family

Query= uniprot:Q9WXW9
         (335 letters)



>FitnessBrowser__Burk376:H281DRAFT_03378
          Length = 315

 Score =  133 bits (334), Expect = 7e-36
 Identities = 96/294 (32%), Positives = 148/294 (50%), Gaps = 22/294 (7%)

Query: 34  IGVIGKSVHP-YWSQVEQGVKAA-GKALGVDTKFFVPQKEDINA-QLQMLESFIAEGVNG 90
           I VI K+ +  YW  V++G  AA   A G    F  P  E   A ++ M+E+ +   V G
Sbjct: 28  IAVIVKTANSNYWQNVQKGATAAMADAKGYTMTFQGPAAESAIADEVNMVENAVNRHVAG 87

Query: 91  IAIAPSDPTAVIPTIKKALEMGIPVVTLDTDSPDSGRYVY---IGTDNYQAGYTAGLIMK 147
           I +APSDP A++P +KKA E  IPVV +D+   D+G+  Y   + TDN +AG      M 
Sbjct: 88  IVLAPSDPDALVPAMKKAWEAHIPVVLIDSTVSDAGKQYYQSFLSTDNVKAGELCAKAMI 147

Query: 148 ELLGGKGKVVIGTGSLTAMNSLQRIQGFKDAIK-DSEIEIVDILNDEEDGARAVSLAEAA 206
           + +G  GKV + +    A + + R+ GF+  I   S++++V     +   A A++     
Sbjct: 148 DRVGQTGKVAVMSYVPGAGSEVGRVGGFRKYIAAHSKLQLVGPFYSQSQMANALNQTTDV 207

Query: 207 LNAHPDLDAFFGVYAYNGPAQALVVKNAGKVGKVKIVCFDTTPDILQYVKEGVIQATMGQ 266
           L+A+PDL   FG            ++ +GK GKV  + FD   D+  +V++G IQA   Q
Sbjct: 208 LSANPDLKGIFGANEPTAVGMGRALQQSGKGGKVIAIGFDGNQDLQGFVRDGTIQAIAVQ 267

Query: 267 RPYMMGYLSVTVLYLMNKIGVQNTLMMLPKVKVDGKVDYVIDTGVDVVTPENLD 320
             Y MGY            G+Q  + ++ +  V  +V    DTGV +V  +NLD
Sbjct: 268 SSYQMGYK-----------GIQTLVNVIERKPVSKQV----DTGVMMVEKQNLD 306


Lambda     K      H
   0.318    0.137    0.388 

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: 238
Number of extensions: 16
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: 335
Length of database: 315
Length adjustment: 28
Effective length of query: 307
Effective length of database: 287
Effective search space:    88109
Effective search space used:    88109
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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