GapMind for catabolism of small carbon sources

 

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

Align Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate 3608008 Dshi_1416 ABC transporter related (RefSeq)

Query= SwissProt::Q9YGA6
         (372 letters)



>FitnessBrowser__Dino:3608008
          Length = 347

 Score =  342 bits (876), Expect = 1e-98
 Identities = 191/368 (51%), Positives = 238/368 (64%), Gaps = 24/368 (6%)

Query: 1   MAGVRLVDVWKVFGEVTAVREMSLEVKDGEFMILLGPSGCGKTTTLRMIAGLEEPSRGQI 60
           MA +RL  V K +G    V +  L + D EF++LLGPSGCGKTTT+RMIAGLEEPS G+I
Sbjct: 1   MAEIRLNHVQKRWGSFVGVEDFHLTIPDREFLVLLGPSGCGKTTTMRMIAGLEEPSSGEI 60

Query: 61  YIGDKLVADPEKGIFVPPKDRDIAMVFQSYALYPHMTVYDNIAFPLKLRKVPRQEIDQRV 120
           +IGD++V        + PKDRD+AMVFQSY LYP+M VY+NI FPLK+RKVP  E + RV
Sbjct: 61  WIGDRMVNA------LDPKDRDVAMVFQSYGLYPNMNVYENIRFPLKVRKVPEVEHEARV 114

Query: 121 REVAELLGLTELLNRKPRELSGGQRQRVALGRAIVRKPQVFLMDEPLSNLDAKLRVRMRA 180
              + ++ L + L+RKP  LSGGQRQRVAL RAIVR+P VFLMDEPLSNLDAKLRV  RA
Sbjct: 115 MRASAMVELDDFLHRKPAALSGGQRQRVALARAIVREPNVFLMDEPLSNLDAKLRVSTRA 174

Query: 181 ELKKLQRQLGVTTIYVTHDQVEAMTMGDRIAVMNRGVLQQVGSPDEVYDKPANTFVAGFI 240
           ++K L  +L VTTIYVTHDQ+EAMT+ DR+ VM+ GV+QQVG+P E+YD+PANTFVA FI
Sbjct: 175 QIKNLSHELQVTTIYVTHDQIEAMTLADRVVVMSAGVVQQVGTPMEIYDRPANTFVASFI 234

Query: 241 GSPPMNFLDAIVTEDGFVDFGEFRLKLLPDQFEVLGELGYVGREVIFGIRPEDLYDAMFA 300
           GSP MN ++  VT+  F            D+  + G  G  GR V  G R ED      A
Sbjct: 235 GSPAMNLMEGAVTDGTFHG----------DRVAIAGLSGAAGR-VTLGFRAED------A 277

Query: 301 QVRVPGENLVRAVVEIVENLGSERIVHLRVGGVTFVGSFRSESRVREGVEVDVVFDMKKI 360
           QV V  +  + A V  +E LG   +V ++ GG         E R   G  V +       
Sbjct: 278 QV-VDSDGQIAAPVYSMELLGDATMVTVKAGGTLVAVKAPKEFRAEIGAPVQIRIPTGIC 336

Query: 361 HIFDKTTG 368
           H+FD  TG
Sbjct: 337 HLFDAQTG 344


Lambda     K      H
   0.323    0.142    0.406 

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: 397
Number of extensions: 12
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: 372
Length of database: 347
Length adjustment: 29
Effective length of query: 343
Effective length of database: 318
Effective search space:   109074
Effective search space used:   109074
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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