GapMind for catabolism of small carbon sources

 

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

Align AraV, component of Arabinose, fructose, xylose porter (characterized)
to candidate H281DRAFT_02040 H281DRAFT_02040 putative spermidine/putrescine transport system ATP-binding protein

Query= TCDB::Q97UF2
         (371 letters)



>FitnessBrowser__Burk376:H281DRAFT_02040
          Length = 356

 Score =  199 bits (505), Expect = 1e-55
 Identities = 119/298 (39%), Positives = 176/298 (59%), Gaps = 22/298 (7%)

Query: 1   MTTIRVENLSKIFKKGKTEVKAVDNVSITIDSGMAFGVLGPSGHGKTTFLRLIAGLEEPT 60
           M  + +ENL K F    T + A+ +  + I+ G     LGPSG GKTT LR+IAG E PT
Sbjct: 1   MAFLEIENLHKSFG---TNI-ALHHFDMKIERGEFITFLGPSGCGKTTVLRMIAGFETPT 56

Query: 61  SGYIYFDNEAVSSPRRVMMSPEKRGIAMVFQNWALYPNMTVFDNIAFPLKLAKVPKDKIE 120
            G I  DN+ V+  R       +R + MVFQ++AL+PNMTV +NI F LK+   P+ +I 
Sbjct: 57  RGVIRLDNKDVTHLRT-----RQRKVGMVFQSYALFPNMTVAENIGFGLKITHRPQAEIS 111

Query: 121 NKVKEVSEELGLSGVLNRYPKELSGGQMQRTAIARALVKDPKVLLLDEPFSNLDAQIRES 180
            +V+E+   + L  +  RYP +LSGGQ QR A+ARAL   P+VLLLDEP S LDA+IR S
Sbjct: 112 QRVEEMLHLIKLPQLGGRYPWQLSGGQQQRVALARALAGKPQVLLLDEPLSALDAKIRIS 171

Query: 181 ARALVRKIQRERKLTTLIVSHDPADIFAIANKAGVIVNGKFAQIGTPTEIYEYPATDLIA 240
            R  +R +QRE  +T++ V+HD  +  +I+++  V+  G+  QIG+P+EIY YP T  +A
Sbjct: 172 LRQDIRALQRELGITSIFVTHDQEEALSISDRIVVMNEGRVEQIGSPSEIYNYPRTRFVA 231

Query: 241 RLTGEINLIQAKIIENNAIIANLKVPLNNMELKGQSNI---------VIGLRPDDLTL 289
              G +N++   +I+     A  K+ ++  EL     +         ++ LRP+ + L
Sbjct: 232 SFVGTLNILAGHVIDP----ATGKMVVDGQELTTTQELPAGDAGKKRLLALRPEAIVL 285


Lambda     K      H
   0.317    0.136    0.374 

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: 302
Number of extensions: 5
Number of successful extensions: 2
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: 371
Length of database: 356
Length adjustment: 29
Effective length of query: 342
Effective length of database: 327
Effective search space:   111834
Effective search space used:   111834
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 (21.6 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