GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Sinorhizobium meliloti 1021

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate SMc04393 SMc04393 ABC transporter ATP-binding protein

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



>FitnessBrowser__Smeli:SMc04393
          Length = 370

 Score =  327 bits (838), Expect = 3e-94
 Identities = 174/369 (47%), Positives = 241/369 (65%), Gaps = 8/369 (2%)

Query: 1   MTSVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQI 60
           M+ + + +L  ++GA+ +L  +NL+I+ G FLVL+G SGCGKSTLLN IAGL  ++ G I
Sbjct: 1   MSFLKITNLRKSYGALEILKDINLEIEEGGFLVLVGPSGCGKSTLLNTIAGLEPITSGDI 60

Query: 61  FIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEI 120
            I  R+V+   P  R I MVFQSYALYP MTV  N++FG+++  +P  E EK +K+ +++
Sbjct: 61  AINGRSVSGLHPSKRDIAMVFQSYALYPNMTVAGNIAFGMEIRGVPKEEREKAIKQVADM 120

Query: 121 LQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLH 180
           LQI  LL RKPS+LSGGQRQRVA+GRALVR+  VFLFDEPLSNLDAKLR ++R EIKRLH
Sbjct: 121 LQIGHLLDRKPSQLSGGQRQRVAMGRALVRNPQVFLFDEPLSNLDAKLRVDMRTEIKRLH 180

Query: 181 QSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMN 240
             +K T++YVTHDQIEA+TLA +IAV+K GV+QQ   P  IYN P N+FVA F+GSP+MN
Sbjct: 181 HRMKTTIVYVTHDQIEAMTLATKIAVLKDGVLQQFGTPAEIYNNPANMFVADFMGSPAMN 240

Query: 241 FFRGEVEPKDGRSFVRAGGIAFDV--TAYPAHTRLQ--PGQKVVLGLRPEHVKVDEARDG 296
             + ++E    +  V       +    A P +  L    G++VV G+RPE +   +  D 
Sbjct: 241 LLKAQIETAGSQVSVTLARPNAEPLRLAVPHNGALSAYAGKEVVFGIRPEALTDPDGADR 300

Query: 297 EPTH----QAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASI 352
                   + ++++ EP G+D        G+ +  R+    R  PG T RL+F++  A  
Sbjct: 301 NAQFVAEGECLIEVVEPAGSDTFAVTRLGGKEIVARLRADARIAPGQTSRLAFNLDKAVF 360

Query: 353 FDAESENRL 361
           FD +SE R+
Sbjct: 361 FDPQSEKRI 369


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: 397
Number of extensions: 10
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: 370
Length adjustment: 30
Effective length of query: 331
Effective length of database: 340
Effective search space:   112540
Effective search space used:   112540
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