GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Skermanella stibiiresistens SB22

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate WP_037448510.1 N825_RS06700 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:Q6MNM2
         (347 letters)



>NCBI__GCF_000576635.1:WP_037448510.1
          Length = 378

 Score =  311 bits (797), Expect = 2e-89
 Identities = 170/360 (47%), Positives = 227/360 (63%), Gaps = 27/360 (7%)

Query: 1   MAKIQFSNIKKSFGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTI 60
           MA +   +++KSFG  +++ G+DLDI   EF V VGPSGCGKSTLLR +AGLE   SG +
Sbjct: 1   MADVTLRDVRKSFGGVEIIHGVDLDIRDNEFTVFVGPSGCGKSTLLRLIAGLEDITSGEM 60

Query: 61  SIDGKKINDIEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNEISEL 120
           +IDG ++ND+ P+ R I+MVFQSYALYPHMTV +NM FGLKL N     I ++V E +  
Sbjct: 61  TIDGVRVNDLPPKERGISMVFQSYALYPHMTVYDNMAFGLKLANSGKDAINRKVREAAGT 120

Query: 121 LQIKHLLDRKPKELSGGQRQRVALGRALSRQTPVILFDEPLSNLDAHLRSQMRLEIKRLH 180
           LQI+ LLDRKP++LSGGQRQRVA+GRA+ R+  V LFDEPLSNLDA LR QMR+E+ +L 
Sbjct: 121 LQIESLLDRKPRDLSGGQRQRVAIGRAIVREPKVFLFDEPLSNLDAALRVQMRIELAKLK 180

Query: 181 HNSKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGSPEMN 240
            +  +TM+YVTHDQ+EA TL D+I VL+ G +EQ G+P E+YH P+N F+A FIGSP MN
Sbjct: 181 DDLNATMVYVTHDQVEAMTLADKIVVLRAGHVEQAGSPLELYHHPRNLFVAGFIGSPRMN 240

Query: 241 FLEGAVLE--------KIPWPE-----------ARKADQILGIRPDAFA-LNQGPLGTQE 280
            +E  V+         +IP  +           A  A   LGIRP+     +QG      
Sbjct: 241 LIETKVVSTDRDGATIQIPGGDTMTVPAQAAGLAHGAPVTLGIRPEHLVEADQGD----- 295

Query: 281 VALGDFQIDISENLGGQQMLHGTLA-GNNVRILVDSMDNFSMKQTLPLKIDLTKAHLFDK 339
             + D  + + E LGG+   H  +A G  + +  D        + + + I     HLFD+
Sbjct: 296 -TILDCTVFVVERLGGETYCHVRIADGQTLVLRTDGETTVRPGEPIRVGIPAAACHLFDR 354


Lambda     K      H
   0.318    0.136    0.383 

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: 349
Number of extensions: 18
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: 347
Length of database: 378
Length adjustment: 29
Effective length of query: 318
Effective length of database: 349
Effective search space:   110982
Effective search space used:   110982
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 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