GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Tistlia consotensis USBA 355

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_085123761.1 B9O00_RS16330 ABC transporter ATP-binding protein

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



>NCBI__GCF_900177295.1:WP_085123761.1
          Length = 361

 Score =  275 bits (702), Expect = 2e-78
 Identities = 158/364 (43%), Positives = 216/364 (59%), Gaps = 8/364 (2%)

Query: 1   MTSVSVRDLSLNFGAVTV-LDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQ 59
           M SV  + L   FG  +V L   +L++  GEFL  LG SGCGK+T L   AGL   + G+
Sbjct: 1   MVSVRYQHLHKAFGDGSVALQDFSLEVADGEFLTFLGPSGCGKTTTLRMTAGLETPTSGE 60

Query: 60  IFIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASE 119
           IF  +R V    P  R I MVFQSYALYP MTV++NL + L+   +   E  +R    + 
Sbjct: 61  IFFGERPVVDLPPGRRNIAMVFQSYALYPHMTVQQNLEYPLRKQGVARDERARRATALAA 120

Query: 120 ILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRL 179
            LQ+  LL R+P  LSGGQ+QRVA+GRAL+R+ +VFL DEPLSNLDA+LR+++R E+ +L
Sbjct: 121 TLQLDALLHRRPKHLSGGQQQRVALGRALIREPEVFLLDEPLSNLDAELRTQMRAELIQL 180

Query: 180 HQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSM 239
           H+ +  TMIYVTHDQ+EA+T++ RIAVM  G +QQ+  P+ IY  P N FVA F+GSP+M
Sbjct: 181 HRRIGRTMIYVTHDQVEAMTMSTRIAVMSKGELQQVGTPLEIYREPRNRFVAAFVGSPAM 240

Query: 240 NFFRGEVEPKDGRSFVRAGG--IAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGE 297
           NF  G +E +DGR+  RA G  +A           L     V+ G+RPEH+ ++      
Sbjct: 241 NFVEGGIELRDGRAVFRAAGLEVALPDARSARLAGLARASGVLAGIRPEHLSLEPG---- 296

Query: 298 PTHQAVVDIEEPMGADNLLWLTFAGQSMSVRIAGQRRYPPGSTVRLSFDMGVASIFDAES 357
            + +  V + E MG ++++        + VR AG      G  V L  D     +FDA S
Sbjct: 297 -SGEGRVLVVEAMGHEDIVTAETPAGRIVVRSAGTATAAAGDLVPLRVDPEKLHLFDAAS 355

Query: 358 ENRL 361
             RL
Sbjct: 356 GERL 359


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: 359
Number of extensions: 15
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: 361
Length adjustment: 29
Effective length of query: 332
Effective length of database: 332
Effective search space:   110224
Effective search space used:   110224
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 Apr 09 2024. 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