GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PfGW456L13_1897 in Dinoroseobacter shibae DFL-12

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate 3607842 Dshi_1250 ABC transporter related (RefSeq)

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>FitnessBrowser__Dino:3607842
          Length = 351

 Score =  295 bits (754), Expect = 2e-84
 Identities = 160/366 (43%), Positives = 232/366 (63%), Gaps = 18/366 (4%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           M+ + LR   K YG      +  ++L I DGEF + VGPSGCGKSTL+  IAGLE  S G
Sbjct: 1   MSGITLRGAVKRYGE--TQVVHGVDLSIADGEFCVFVGPSGCGKSTLLRMIAGLEETSEG 58

Query: 61  AILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVS 120
           +I +   D++ + P +R +AMVFQ+YALYP M+V +N+ FGLK+  +P AEI  +VA  S
Sbjct: 59  SIHIGARDVTRLDPSERGVAMVFQTYALYPHMTVAENMGFGLKMNGVPKAEIKAKVAAAS 118

Query: 121 KLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           ++L+++  L+RKP  LSGGQ+QRVA+GRA+ R P+++LFDEPLSNLDA+LRVEMR E+  
Sbjct: 119 EILKLDDYLARKPKALSGGQRQRVAIGRAIVRGPEVFLFDEPLSNLDAELRVEMRVEIAR 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPP 240
           +H+ +  T +YVTHDQ+EAMTL DK+ V++ G ++Q G P ++Y +P N+FVA FIGSP 
Sbjct: 179 LHKEIGATMIYVTHDQVEAMTLADKIVVLRAGRVEQVGAPLELYRDPDNVFVAGFIGSPA 238

Query: 241 MNFIPLRLQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQIILANGEANG 300
           MNF+  R++     L  L          PL +  A      V +G+RP+ I L  G    
Sbjct: 239 MNFLDGRIENDAVHLAGL---------PPLPVPGAAGRSGPVTVGVRPQHIALEPGGDGY 289

Query: 301 LPTIRAEVQVTEPTGPDTLVFVNLND-TKVCCRLAPDVAPAVGETLTLQFDPAKVLLFDA 359
           L      V++TE  G  + +++   D +++      +   A G  + L   P +V+LF+A
Sbjct: 290 L------VELTESLGGVSYLYLRGADGSRLTVEAGEEDPIAEGTPVGLSLAPDRVMLFEA 343

Query: 360 KTGERL 365
           +TG+RL
Sbjct: 344 ETGQRL 349


Lambda     K      H
   0.319    0.138    0.393 

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: 382
Number of extensions: 14
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: 386
Length of database: 351
Length adjustment: 30
Effective length of query: 356
Effective length of database: 321
Effective search space:   114276
Effective search space used:   114276
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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