GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Dinoroseobacter shibae DFL-12

Align D-xylose ABC transporter, periplasmic D-xylose-binding protein (characterized)
to candidate 3608607 Dshi_2000 D-xylose ABC transporter, periplasmic substrate-binding protein (RefSeq)

Query= CharProtDB::CH_003787
         (330 letters)



>FitnessBrowser__Dino:3608607
          Length = 340

 Score =  236 bits (603), Expect = 5e-67
 Identities = 125/315 (39%), Positives = 191/315 (60%), Gaps = 7/315 (2%)

Query: 10  LCTSLLLTNVAAHA-KEVKIGMAIDDLRLERWQKDRDIFVKKAESLGAKVFVQSANGNEE 68
           L  +++   V   A  +V +G++  + + ERW+ D        E+ GA      A  +  
Sbjct: 6   LAAAIVAAGVTTSAYADVTVGVSWSNFQEERWKTDEAAIKAALEAAGATYVSADAQSSSA 65

Query: 69  TQMSQIENMINRGVDVLVIIPYNGQVLSNVVKEAKQEGIKVLAYDRMINDADIDFYISFD 128
            Q+S +E++I +GVD L+I+  + Q +   V+ A  EGI V+ YDR+I D    FY++FD
Sbjct: 66  KQLSDVESLIAQGVDALIILAQDSQAIGPAVQAAADEGIPVVGYDRLIEDPRA-FYLTFD 124

Query: 129 NEKVGELQAKALVDIVPQGNYFLMGGSPVDNNAKLFRAGQMKVLKPYVDSGKIKVVGDQW 188
           N +VG +QA+A+++  P+GNY ++ GSP D NA   R GQ ++L+  +D+GKI +VG+ +
Sbjct: 125 NVEVGRMQARAVLEQAPEGNYVMIKGSPTDPNADFLRGGQQEILQDAIDAGKITIVGEAY 184

Query: 189 VDGWLPENALKIMENALTANNNKIDAVVASNDATAGGAIQALSAQGLSGKVAISGQDADL 248
            DGWLP NA + ME  LTA +N++DAVVASND TAGG + AL+AQG+ G + +SGQD D 
Sbjct: 185 TDGWLPANAQRNMEQILTAQDNQVDAVVASNDGTAGGVVAALTAQGMEG-IPVSGQDGDH 243

Query: 249 AGIKRIAAGTQTMTVYKPITLLANTAAEIAVELGNGQE----PKADTTLNNGLKDVPSRL 304
           A + R+A GTQT++V+K    L   A EIAV + NG        A +  + G  ++ +R 
Sbjct: 244 AALNRVAKGTQTVSVWKDARDLGRAAGEIAVAMANGTAMADIEGATSWTSPGGTELTARF 303

Query: 305 LTPIDVNKNNIKDTV 319
           L P+ V  +N+   V
Sbjct: 304 LAPVPVTADNLTAVV 318


Lambda     K      H
   0.314    0.132    0.366 

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: 265
Number of extensions: 15
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: 330
Length of database: 340
Length adjustment: 28
Effective length of query: 302
Effective length of database: 312
Effective search space:    94224
Effective search space used:    94224
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: 42 (22.0 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