GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SM_b21106 in Phaeobacter inhibens BS107

Align ABC transporter for L-Fucose, ATPase component (characterized)
to candidate GFF729 PGA1_c07440 ABC transporter, ATP binding protein

Query= reanno::Smeli:SM_b21106
         (365 letters)



>FitnessBrowser__Phaeo:GFF729
          Length = 353

 Score =  328 bits (841), Expect = 1e-94
 Identities = 185/369 (50%), Positives = 233/369 (63%), Gaps = 23/369 (6%)

Query: 1   MAPVTLKKLVKRYGALEVVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGGAI 60
           M  VTL K VK+YG ++V+H +DL + D EF   VGPSGCGKST LRMIAGLEE S G I
Sbjct: 1   MTGVTLAKAVKKYGDVQVIHDVDLSIDDGEFCVFVGPSGCGKSTLLRMIAGLEETSSGNI 60

Query: 61  EIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAAAI 120
            IG R V  L    R ++MVFQSYALYPHMTV +NMGF LK+ G P E+I+ +VAEA+ I
Sbjct: 61  HIGDRDVTRLDAADRGVAMVFQSYALYPHMTVEDNMGFGLKMNGHPKEKIREKVAEASRI 120

Query: 121 LDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKKLH 180
           L L   L+R+P  LSGGQRQRVA+GRAIVR P+VFLFDEPLSNLDA+LR  +R EI +LH
Sbjct: 121 LKLDDYLKRKPKALSGGQRQRVAIGRAIVRGPEVFLFDEPLSNLDAELRVDMRVEIARLH 180

Query: 181 ARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPPMN 240
             + ATMIYVTHDQVEAMTL+D+IV++R G +EQVG+P +++  P  +FVAGFIGSP MN
Sbjct: 181 KEIGATMIYVTHDQVEAMTLADKIVVLRAGRVEQVGSPMELYANPDNRFVAGFIGSPSMN 240

Query: 241 MEEAVLTDGKLAFASGATLPLPPRFR-----SLVREGQKVTFGLRPDDVYPSGHGLHAGD 295
             E  +         G  +P     R     +L  +G KV  GLRP  +      + A D
Sbjct: 241 FLEGTVQ------GDGVVVPALENRRVATSVALPADGSKVLLGLRPQHL-----SVTAAD 289

Query: 296 ADAVHEIELPVTITEPLGNETLVFTQF-NGRDWVSRMLNPRPLRPGEAVPMSFDLARAHL 354
           +  V      + + E LG  +  +     G   +        L  G AV + FD A A++
Sbjct: 290 SSLV------LDLRERLGGVSYDYLSTPTGEKLIVETRGDEALPEGTAVALGFDDADAYI 343

Query: 355 FDGETGRAL 363
           FDG T + L
Sbjct: 344 FDGATEQRL 352


Lambda     K      H
   0.320    0.137    0.397 

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: 339
Number of extensions: 15
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: 365
Length of database: 353
Length adjustment: 29
Effective length of query: 336
Effective length of database: 324
Effective search space:   108864
Effective search space used:   108864
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 (21.8 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