GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Phaeobacter inhibens BS107

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate GFF1915 PGA1_c19470 ABC transporter, ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__Phaeo:GFF1915
          Length = 363

 Score =  371 bits (952), Expect = e-107
 Identities = 208/365 (56%), Positives = 252/365 (69%), Gaps = 14/365 (3%)

Query: 1   MTS-VSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQ 59
           MTS VS RDLS+ FGAV VL  LNLDI  GEFLVLLG+SGCGKSTLLN IAGL + ++GQ
Sbjct: 9   MTSHVSARDLSVRFGAVEVLKSLNLDIQKGEFLVLLGASGCGKSTLLNTIAGLQEATEGQ 68

Query: 60  IFIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASE 119
           I+I D NVTW EPKDRG+ MVFQSYALYP+MTV  NL+FGL++ K+P AE +K V  A+ 
Sbjct: 69  IWINDENVTWREPKDRGLAMVFQSYALYPKMTVRGNLAFGLRMNKVPKAEADKLVDEAAR 128

Query: 120 ILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRL 179
           +LQ++ LL R+P ELSGGQRQRVAIGRALVR VDVFLFDEPLSNLDAKLR+ELRVE+KRL
Sbjct: 129 VLQLEELLDRRPGELSGGQRQRVAIGRALVRKVDVFLFDEPLSNLDAKLRAELRVELKRL 188

Query: 180 HQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSM 239
           HQ L  TMIYVTHDQ+EALTLADRIAVMK GV+QQL  P  IY  P N +VA F+G PSM
Sbjct: 189 HQELGATMIYVTHDQVEALTLADRIAVMKDGVVQQLDSPEEIYRRPANRYVAQFVGLPSM 248

Query: 240 NFFRGEVEPKDGRSFVRAGGIAFD---VTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDG 296
           NF  G V  + G        +A D   + + PA     PG +V +G+RPEHV    A   
Sbjct: 249 NFVNG-VVTESGAIQTEDFELALDQCNLASTPA-----PGTEVEIGIRPEHVHPANAGG- 301

Query: 297 EPTHQAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFDAE 356
                  V + E +G++ L+W      S+ +R         G  VR++   G  S+F A+
Sbjct: 302 ---FMLDVGMVELLGSERLIWGKVGNTSIVMRDDPDTTIRSGDQVRINLKPGAFSVFSAK 358

Query: 357 SENRL 361
           +  R+
Sbjct: 359 TGLRI 363


Lambda     K      H
   0.320    0.137    0.392 

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: 396
Number of extensions: 16
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: 361
Length of database: 363
Length adjustment: 29
Effective length of query: 332
Effective length of database: 334
Effective search space:   110888
Effective search space used:   110888
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