GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Phaeobacter inhibens BS107

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate GFF1915 PGA1_c19470 ABC transporter, ATP-binding protein

Query= uniprot:Q6MNM2
         (347 letters)



>FitnessBrowser__Phaeo:GFF1915
          Length = 363

 Score =  293 bits (751), Expect = 4e-84
 Identities = 164/345 (47%), Positives = 225/345 (65%), Gaps = 19/345 (5%)

Query: 13  FGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTISIDGKKINDIEP 72
           FG+ +VLK ++LDI  GEFLVL+G SGCGKSTLL T+AGL+ A  G I I+ + +   EP
Sbjct: 22  FGAVEVLKSLNLDIQKGEFLVLLGASGCGKSTLLNTIAGLQEATEGQIWINDENVTWREP 81

Query: 73  QNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNEISELLQIKHLLDRKPK 132
           ++R +AMVFQSYALYP MTV  N+ FGL++  +  AE  K V+E + +LQ++ LLDR+P 
Sbjct: 82  KDRGLAMVFQSYALYPKMTVRGNLAFGLRMNKVPKAEADKLVDEAARVLQLEELLDRRPG 141

Query: 133 ELSGGQRQRVALGRALSRQTPVILFDEPLSNLDAHLRSQMRLEIKRLHHNSKSTMIYVTH 192
           ELSGGQRQRVA+GRAL R+  V LFDEPLSNLDA LR+++R+E+KRLH    +TMIYVTH
Sbjct: 142 ELSGGQRQRVAIGRALVRKVDVFLFDEPLSNLDAKLRAELRVELKRLHQELGATMIYVTH 201

Query: 193 DQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGSPEMNFLEGAVLEKIPW 252
           DQ+EA TL DRIAV+KDGV++Q+ +P EIY RP N ++A F+G P MNF+ G V E    
Sbjct: 202 DQVEALTLADRIAVMKDGVVQQLDSPEEIYRRPANRYVAQFVGLPSMNFVNGVVTES--- 258

Query: 253 PEARKADQILGIRPDAFALNQGPLGTQEVAL----------GDFQIDIS--ENLGGQQML 300
              +  D  L +     A    P    E+ +          G F +D+   E LG ++++
Sbjct: 259 GAIQTEDFELALDQCNLASTPAPGTEVEIGIRPEHVHPANAGGFMLDVGMVELLGSERLI 318

Query: 301 HGTLAGNNVRILVDSMDNFSMKQTLPLKIDLTKA--HLFDKKTGL 343
            G + GN   ++ D  D  +++    ++I+L      +F  KTGL
Sbjct: 319 WGKV-GNTSIVMRDDPDT-TIRSGDQVRINLKPGAFSVFSAKTGL 361


Lambda     K      H
   0.318    0.136    0.383 

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: 289
Number of extensions: 14
Number of successful extensions: 1
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: 347
Length of database: 363
Length adjustment: 29
Effective length of query: 318
Effective length of database: 334
Effective search space:   106212
Effective search space used:   106212
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: 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