GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpT in Stenotrophomonas chelatiphaga DSM 21508

Align GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized)
to candidate WP_057508148.1 ABB28_RS08100 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= TCDB::G3LHY9
         (356 letters)



>NCBI__GCF_001431535.1:WP_057508148.1
          Length = 362

 Score =  195 bits (496), Expect = 1e-54
 Identities = 115/322 (35%), Positives = 184/322 (57%), Gaps = 18/322 (5%)

Query: 1   MARITLDHIRHAYGANPKSDKDYSLKEVDHEWNDGGAYALLGPSGCGKTTLLNIISGLLQ 60
           MA++ L  +R  Y      +   ++K+   E  DG    L+GPSGCGK+TLL +I+GL +
Sbjct: 1   MAKVQLQGVRKVY-----DNGQVAVKDATFEVADGELMVLVGPSGCGKSTLLRMIAGLEE 55

Query: 61  PSHGRILFDGKDVTNLSTQSRNIAQVFQFPVIYDTMTVYDNLAFPLRNRGVAEADVDRRV 120
            S G +    + V +++ + R+IA VFQ   +Y  MTV +NLAF L+ RG  +A +D+R+
Sbjct: 56  ISGGTLTIGERVVNDVAPKDRDIAMVFQSYALYPHMTVAENLAFGLKLRGHDKATIDKRI 115

Query: 121 RDILEMIDLASWARRKAQGLTADQKQKISLGRGLVRNDVNAILFDEPLTVIDPHMKWVLR 180
            +  + + L     +  + ++  Q+Q+++LGR LVR      L DEPL+ +D  ++  +R
Sbjct: 116 SEAAQTLGLTDMMDKLPKAMSGGQRQRVALGRALVREPA-VFLLDEPLSNLDAKLRHSVR 174

Query: 181 SQLKRLHKQFGFTMVYVTHDQTEALTFAEKVVVMYDGQIVQIGTPAELFERPSHTFVGYF 240
           +++ +LH++ G TM+YVTHDQ EA+T  +++VV+ DG I QI TP EL++RP++ FV  F
Sbjct: 175 TEIAQLHRKLGTTMIYVTHDQVEAMTLGQRIVVLKDGVIQQIDTPMELYDRPANLFVAGF 234

Query: 241 IGSPGMNF----MPARIEGSTVKVGDETLTLEYA---PKTSGTAKTELGIRPEFIRLGRE 293
           +GSP MN     + A   G  V  GD    L +A   P+        +G+RPE ++    
Sbjct: 235 LGSPAMNVLRGTLQASASGVVVSDGDWKAPLGHATIDPRWL-DKPIAVGVRPEHLQPADA 293

Query: 294 GMPIT----ISKVEDIGRQKIV 311
           G   T    I  +E +G +  V
Sbjct: 294 GAEWTFEARIEGIEPVGNEIFV 315


Lambda     K      H
   0.321    0.137    0.405 

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: 324
Number of extensions: 17
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 356
Length of database: 362
Length adjustment: 29
Effective length of query: 327
Effective length of database: 333
Effective search space:   108891
Effective search space used:   108891
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