GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Desulfoscipio geothermicus DSM 3669

Align C4-dicarboxylate-binding periplasmic protein DctP (characterized)
to candidate WP_092483242.1 BM299_RS09090 TRAP transporter substrate-binding protein

Query= SwissProt::P37735
         (333 letters)



>NCBI__GCF_900115975.1:WP_092483242.1
          Length = 345

 Score =  301 bits (771), Expect = 2e-86
 Identities = 161/306 (52%), Positives = 208/306 (67%), Gaps = 4/306 (1%)

Query: 27  EPIVIKFSHVVAPDTPKGKGAAKFEELAEKYTNGAVDVEVYPNSQLYKDKEELEALQLGA 86
           E IVIKFSHVVA +TPKG+ A  FEELAEKYT G VDV+V+PNSQLY D E L A+Q   
Sbjct: 38  EKIVIKFSHVVAENTPKGQAAIMFEELAEKYTEGRVDVQVFPNSQLYNDDEVLAAVQQNN 97

Query: 87  VQMLAPSLAKFGPLGVQDFEVFDLPYIFKDYEALHKVTQGEA-GKMLLSKLEAKGITGLA 145
           VQM AP+ +K   L  Q + +FD P+ F D +A+    + E  G  L S L+ + + GLA
Sbjct: 98  VQMAAPATSKVSKLFPQ-WTIFDFPFAFPDTDAVQTAMESEEIGGKLFSMLKEQQLLGLA 156

Query: 146 FWDNGFKIMSANT-PLTMPDDFLGLKMRIQSSKVLEAEMNALGAVPQVMAFSEVYQALQT 204
            WDNGFK M+ +  PL MP+DF G K R+ SS+VLEA+  ALGA P  M FSEVY AL+ 
Sbjct: 157 MWDNGFKQMTLDEHPLYMPEDFKGQKFRVMSSRVLEAQFKALGANPVPMPFSEVYSALEQ 216

Query: 205 GVVDGTENPPSNMFTQKMNEVQKHATVSNHGYLGYAVIVNKQFWDGLPADVRTGLEKAMA 264
           GV+DG EN  SN++++K +EVQK+ T+SNHGYLGYAVI N  FW+GLP DVR GLEKA+ 
Sbjct: 217 GVIDGQENTLSNIYSKKFHEVQKYMTISNHGYLGYAVITNSAFWEGLPTDVREGLEKALD 276

Query: 265 ESTDYANGIAKEENEKALQAMKDAGT-TEFHELTAEERAAWEEVLTPVHDEMAERIGAET 323
           E+T +    A+  N++ L+ +K  GT  E HELT EE+ AW +    V+++  E +G + 
Sbjct: 277 ETTRWVRENAQRLNQENLEKIKADGTLVEIHELTQEEKEAWMKATDVVYEQFKEEVGEDL 336

Query: 324 IAAVKA 329
           I AV A
Sbjct: 337 INAVMA 342


Lambda     K      H
   0.314    0.130    0.364 

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: 279
Number of extensions: 11
Number of successful extensions: 5
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: 333
Length of database: 345
Length adjustment: 28
Effective length of query: 305
Effective length of database: 317
Effective search space:    96685
Effective search space used:    96685
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 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