GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Pseudomonas stutzeri RCH2

Align Probable c4-dicarboxylate-binding protein (characterized, see rationale)
to candidate GFF773 Psest_0787 tripartite ATP-independent periplasmic transporter solute receptor, DctP family

Query= uniprot:Q9HVH5
         (332 letters)



>FitnessBrowser__psRCH2:GFF773
          Length = 332

 Score =  431 bits (1107), Expect = e-125
 Identities = 208/332 (62%), Positives = 265/332 (79%)

Query: 1   MFKPFVGVALAALFAVSAVAHAEDAGPVVIKFSHVVSDDTPKGKGALLFKKLAEERLPGK 60
           M+K  V   +AAL+  SA A A +A P+VIKF+HVV+DDTPKGKGALL K+L E+R+ GK
Sbjct: 1   MYKSCVAALVAALYWFSAPAMAAEAEPIVIKFAHVVADDTPKGKGALLLKQLVEQRMAGK 60

Query: 61  VKVEVYPNSTLFGDADEIEALRANKVQMLATSLSKFEPYTKQLQVFDLPFLFDDLEALKR 120
           VKVEVYPNSTL GDA+E++AL  NKVQ+LA S+SKF PYTK+LQVFDLPFLFDD EAL+R
Sbjct: 61  VKVEVYPNSTLVGDAEEMQALFDNKVQLLAPSMSKFAPYTKKLQVFDLPFLFDDAEALQR 120

Query: 121 FQKRDKSRELLRSMAKHGIYGLAYWNNGMKQLSATRELHRPDDAKGLVFRIQPSSVLEAQ 180
           FQKR+ +R+LLRSMA HG+YGLAYWNNG+KQLSAT  L +P DA GL FRIQPS VLEAQ
Sbjct: 121 FQKREAARQLLRSMADHGVYGLAYWNNGLKQLSATTPLRKPSDANGLAFRIQPSPVLEAQ 180

Query: 181 FAMLGATAKQLSYAETLKAMQAGSVQGTENTWSNLAGQKIDSVQPYITETNHGALSYMLI 240
           FA +GA +  L +A+  ++++ G VQG EN WSN+  Q + SVQPYITE+NHG L YMLI
Sbjct: 181 FAAVGAKSVVLPFAKVYESLKGGVVQGAENPWSNILSQNMHSVQPYITESNHGVLDYMLI 240

Query: 241 TSSAFWTGIPYQTRTELESIVDEVTLVVNKEAEALNQKEREHLLAAGKSRLVSLSAEEHE 300
           T++ FW  +P+  R+ELE I+ EVT  VN+EA A+N+++RE +LA+G S+L++L+ EE +
Sbjct: 241 TNNDFWLSMPFAVRSELEGIILEVTQAVNREAAAVNRRDRERILASGSSQLITLTPEERQ 300

Query: 301 AWRNAMKPLWKNYEAQIGSDVLRAAQVVNRKR 332
           AWR  M P+WK YEA IG+D++RAA  VNR+R
Sbjct: 301 AWREQMLPVWKTYEADIGADLIRAAMTVNRRR 332


Lambda     K      H
   0.316    0.130    0.367 

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: 321
Number of extensions: 7
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: 332
Length of database: 332
Length adjustment: 28
Effective length of query: 304
Effective length of database: 304
Effective search space:    92416
Effective search space used:    92416
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 17 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