GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Stenotrophomonas chelatiphaga DSM 21508

Align Solute-binding protein Bpro_3107 (characterized)
to candidate WP_057509040.1 ABB28_RS12855 C4-dicarboxylate ABC transporter

Query= SwissProt::Q128M1
         (330 letters)



>NCBI__GCF_001431535.1:WP_057509040.1
          Length = 333

 Score =  244 bits (623), Expect = 2e-69
 Identities = 125/324 (38%), Positives = 200/324 (61%), Gaps = 9/324 (2%)

Query: 13  SAALAALLAGLGMGAAQATE-------FRSADTHNADDYPTVAAVKYMGELLEKKSGGKH 65
           + +L AL A   +G ++A +         + D H AD YPTV AVK++G+ LE+++GG+ 
Sbjct: 9   ATSLGALAAPALIGCSKAGDSVAGGHLLTATDVHVAD-YPTVTAVKWIGQTLERETGGRL 67

Query: 66  KIKVFNKQALGSEKETIDQVKIGALDFTRVNVGPMNAICPLTQVPTMPFLFSSIAHMRKS 125
           +++ ++   LG E E ID  + GA+D TRV  G +N   PLTQ   +P++F S+AHMR +
Sbjct: 68  RLRQYHSGQLGRESEAIDMARFGAIDITRVYSGALNNAFPLTQALCLPYVFDSVAHMRAA 127

Query: 126 LDGPVGDEILKSCESAGFIGLAFYDSGARSIY-AKKPIRTVADAKGLKIRVQQSDLWVAL 184
           LDG V D +L+  ES   +GLA YDSGAR  Y  K PI    D +GLK+RV  SD+++ L
Sbjct: 128 LDGGVADAVLRGFESRDLVGLAIYDSGARCFYNTKHPIVAPQDLRGLKLRVASSDIFIQL 187

Query: 185 VSAMGANATPMPYGEVYTGLKTGLIDAAENNIPSFDTAKHVEAVKVYSKTEHSMAPEILV 244
           +   GAN TPM  G+ ++G++T +ID AENN+ SF +++H EA   +S+++HS AP++L+
Sbjct: 188 MRLFGANPTPMSLGDTFSGMETHMIDGAENNMRSFHSSRHFEAAHYWSQSDHSYAPDVLL 247

Query: 245 MSKIIYDKLPKAEQDMIRAAAKESVAFERQKWDEQEAKSLANVKAAGAEIVEVDKKSFQA 304
           MS+  YD+L   ++ ++   A+ SV   R++WD  E  +   V   G +  EVD  +F+ 
Sbjct: 248 MSRASYDQLRPDDRQLLLETARASVKVMREQWDASEDAARKAVVDFGVKTNEVDLVAFRK 307

Query: 305 VMGPVYDKFMTTPDMKRLVKAVQD 328
              P+  +++  P++  +V  ++D
Sbjct: 308 AADPLLQEYLKQPELAAMVSRIRD 331


Lambda     K      H
   0.316    0.130    0.362 

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: 226
Number of extensions: 10
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: 330
Length of database: 333
Length adjustment: 28
Effective length of query: 302
Effective length of database: 305
Effective search space:    92110
Effective search space used:    92110
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 (21.6 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