GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Nocardioides daejeonensis MJ31

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_110206994.1 DNK54_RS11055 ABC transporter ATP-binding protein

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



>NCBI__GCF_003194585.1:WP_110206994.1
          Length = 368

 Score =  221 bits (564), Expect = 2e-62
 Identities = 142/365 (38%), Positives = 210/365 (57%), Gaps = 23/365 (6%)

Query: 3   SVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFI 62
           S+ V  +   +G+ T+L+ ++LDI  GEFL LLG+SG GKSTLLN IAG +    G + +
Sbjct: 15  SIEVDRIRKVYGSTTILNDIDLDIRAGEFLTLLGASGSGKSTLLNIIAGFIKADGGDVRV 74

Query: 63  KDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEILQ 122
             +++T      RG+GMVFQ YAL+P M+V  N+++GL+    P AEI   V  A E+++
Sbjct: 75  DGKSITSVPAHKRGLGMVFQHYALFPHMSVYDNVAYGLRRHGFPKAEIPGLVADALEMVE 134

Query: 123 IQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLHQS 182
           +  L KR+P+ELSGGQ+QRVA+ RA+V    V L DEPL  LD  LR +L++EI+RLH+ 
Sbjct: 135 MGHLGKRRPAELSGGQQQRVALARAVVFRPRVLLMDEPLGALDKMLREQLQLEIRRLHKE 194

Query: 183 LKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMNFF 242
           +  T ++VTHDQ EALT++DRIA+++ G I QL  P  +Y+AP   + A FIG    N  
Sbjct: 195 MGITFVFVTHDQEEALTMSDRIALLEKGDIVQLGTPEELYDAPSCRYAAEFIG--VSNIM 252

Query: 243 RGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPG--QKVVLGLRPEHVKVDEARDGEPTH 300
            G           RAG +  D      H ++  G     VL +RPE ++V   + G   H
Sbjct: 253 TGS----------RAGDVFTDTRNQTTH-KVSGGAADGTVLMVRPERLRVSAGQVGPAGH 301

Query: 301 Q----AVVDIEEPMGADNLLWL-TFAGQSMSVRIAGQRR---YPPGSTVRLSFDMGVASI 352
           +    A+V     +G+D  + + T +G+ M  R    R      PG  V L++++  A +
Sbjct: 302 ENALPAIVSDCVYLGSDRTVHVRTASGEEMVARTEVPRTDDGIQPGVPVTLTWNIEDARV 361

Query: 353 FDAES 357
              E+
Sbjct: 362 LAEEA 366


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: 353
Number of extensions: 17
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: 368
Length adjustment: 29
Effective length of query: 332
Effective length of database: 339
Effective search space:   112548
Effective search space used:   112548
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 24 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