GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Dechlorosoma suillum PS

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate Dsui_0258 Dsui_0258 sulfate ABC transporter, ATP-binding protein

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



>FitnessBrowser__PS:Dsui_0258
          Length = 360

 Score =  199 bits (507), Expect = 7e-56
 Identities = 123/342 (35%), Positives = 186/342 (54%), Gaps = 22/342 (6%)

Query: 3   SVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFI 62
           S+ +R+++  FG    LD ++L I  GE + LLG SGCGK+TLL  IAG+    +GQ+  
Sbjct: 2   SIEIRNIAKRFGNFVALDDVSLSIPTGELVALLGPSGCGKTTLLRIIAGMETADEGQVMF 61

Query: 63  KDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVA--KIPP--AEIEKRVKRAS 118
           +    T    ++R +G VFQ YAL+  M V +N++FGL+V   K  P  +EI KRV    
Sbjct: 62  EGSEATHLHARERQVGFVFQHYALFRHMNVFENVAFGLRVKPRKERPCESEIRKRVMDLL 121

Query: 119 EILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKR 178
            ++Q+  L  R P++LSGGQRQR+A+ RAL  +  V L DEP   LD K+R ELR  ++R
Sbjct: 122 SLVQLDWLADRYPTQLSGGQRQRIALARALAVEPKVLLLDEPFGALDTKVRKELRRWLRR 181

Query: 179 LHQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPS 238
           LH  +  + ++VTHDQ EAL +ADR+ VM  G I+Q+  P  +Y+ P + FV  F+G  +
Sbjct: 182 LHDEMHISSVFVTHDQEEALEVADRVVVMNKGRIEQVGSPDEVYSNPASPFVYQFLG--N 239

Query: 239 MNFFRGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEP 298
           +N F   V                   A  A   +  GQ+ V  +RP  + +D     E 
Sbjct: 240 VNVFHSRVH---------------GAWAEVARDDVPAGQEAVAFIRPHDIDIDTVATPE- 283

Query: 299 THQAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGST 340
           + +A V   + +G    + +   G+ + V +  +R+   G T
Sbjct: 284 SLEAKVSYVQTIGPLVRVEVIHQGELVEVELTRERQQVLGLT 325


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: 312
Number of extensions: 12
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: 361
Length of database: 360
Length adjustment: 29
Effective length of query: 332
Effective length of database: 331
Effective search space:   109892
Effective search space used:   109892
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