GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Dinoroseobacter shibae DFL-12

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate 3609758 Dshi_3141 ABC transporter related (RefSeq)

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



>FitnessBrowser__Dino:3609758
          Length = 352

 Score =  291 bits (745), Expect = 2e-83
 Identities = 169/361 (46%), Positives = 222/361 (61%), Gaps = 11/361 (3%)

Query: 1   MTSVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQI 60
           M  V ++DL+  +G    +D  +L +   EFLVLLG SGCGK+T +  IAGL D +DG+I
Sbjct: 1   MAEVILKDLTKRWGDFVGVDNQSLHVRDEEFLVLLGPSGCGKTTTMRMIAGLEDPTDGEI 60

Query: 61  FIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEI 120
           +I DR V  + PKDR + MVFQ+Y LYP MT+ +N+++ L+V  +  AEI  RV+RA+E 
Sbjct: 61  WIGDRMVNDDLPKDRDVAMVFQNYGLYPHMTIFENIAYPLRVRGVDKAEIPPRVQRAAEQ 120

Query: 121 LQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLH 180
           +++   L RKP  LSGGQRQRVA+ RA+VR   VFL DEPLSNLDAKLR  +R E+K L 
Sbjct: 121 VELTKFLHRKPKALSGGQRQRVALARAIVRKPKVFLMDEPLSNLDAKLRVTMRAELKHLS 180

Query: 181 QSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMN 240
           + L+ T +YVTHDQIEA+TLADR+AVMK GVIQQL  P  IYN P NLFVAGFIGSP+MN
Sbjct: 181 RELQITTVYVTHDQIEAMTLADRVAVMKHGVIQQLGTPDEIYNDPANLFVAGFIGSPAMN 240

Query: 241 FFRGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEPTH 300
              G VE  DG  FV  GG        P   R       +LG+R + ++V EA  G+   
Sbjct: 241 LINGSVE--DG-MFVTTGGTRLVKVPSPDRAR------AILGVRADDMQVHEAGQGD--I 289

Query: 301 QAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFDAESENR 360
              +   E  G   LL + +  Q +  R     R      V +S +     +FD ++E R
Sbjct: 290 DVTIYAFENTGESTLLTVQWGKQRVIARGDRHLRKEQDDVVGISLNTDHLYLFDPDTEER 349

Query: 361 L 361
           +
Sbjct: 350 I 350


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: 361
Number of extensions: 13
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: 361
Length of database: 352
Length adjustment: 29
Effective length of query: 332
Effective length of database: 323
Effective search space:   107236
Effective search space used:   107236
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.

Links

Downloads

Related tools

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