GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Dechlorosoma suillum PS

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate Dsui_3414 Dsui_3414 FAD/FMN-dependent dehydrogenase

Query= reanno::Cup4G11:RR42_RS17310
         (374 letters)



>FitnessBrowser__PS:Dsui_3414
          Length = 366

 Score =  379 bits (972), Expect = e-110
 Identities = 203/362 (56%), Positives = 249/362 (68%), Gaps = 19/362 (5%)

Query: 22  ATGTRTPLRLRGGGSKDFYGQHPQGTLLDTRAYSGIVDYDPPELVITARCGTPLAQIEAA 81
           A     PL LRGGGSKDFYG+  QG +LDTR++ G+V Y+P ELV+T + GT LA++EA 
Sbjct: 15  AASAGAPLLLRGGGSKDFYGRPVQGDILDTRSHRGVVAYEPTELVVTVKAGTSLAELEAV 74

Query: 82  LAERRQMLAFEPPHFSTGADGSDVATIGGAVAAGLSGPRRQAVGALRDFVLGTRVMDGRG 141
           LAE+ Q LA EPPHF     G D AT+GG VAAGLSGPRR   GA+RDFVLG R+MDG+G
Sbjct: 75  LAEKGQYLACEPPHF-----GPD-ATVGGMVAAGLSGPRRAQAGAVRDFVLGVRLMDGQG 128

Query: 142 DVLSFGGQVMKNVAGYDVSRLMSGSLGTLGLILEVSLKVLPVPFDDATLRFALDEAAALD 201
             L+FGGQVMKNVAGYDV RL++GSLG LGL+LEVSLKVLP P  +AT+R    +A AL 
Sbjct: 129 QALNFGGQVMKNVAGYDVPRLLAGSLGQLGLLLEVSLKVLPRPVAEATIRLETSQAKALA 188

Query: 202 RLNDWGGQPLPIAASAWHDG------VLHLRLSGAAAALRAARARLGGEAVDAAQADALW 255
            +N WGG+PLPI+A+ W D        + +RLSGA AA+ AA+A LGG  V+A  A A W
Sbjct: 189 LMNQWGGKPLPISATVWSDAGHPDGEAITVRLSGARAAVAAAQAALGGALVEAGPASAFW 248

Query: 256 RALREHSHAFFAPVQAGR--ALWRIAVPTTAAPLALPGGQLIEWGGGQRWWLGGSDSAAD 313
             +RE +H FF         ALWR+AVP+TA  L LPG  L+EWGG QRW +    S A+
Sbjct: 249 AGVREQTHPFFTGAGGANESALWRLAVPSTAPQLDLPGRTLVEWGGAQRWLV----SDAE 304

Query: 314 SAIVRAAAKAAGGHATLFRNGDKAVG-VFTPLSAPVAAIHQRLKATFDPAGIFNPQRMYA 372
              +R A + AGGHATLFR    A    F PL++P+  IH+RLKATFDP G+F   R+Y 
Sbjct: 305 PRRIREAVEKAGGHATLFRGPAAARDQAFHPLASPLLDIHRRLKATFDPRGVFAAGRLYE 364

Query: 373 GL 374
           GL
Sbjct: 365 GL 366


Lambda     K      H
   0.321    0.136    0.414 

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: 437
Number of extensions: 24
Number of successful extensions: 6
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: 374
Length of database: 366
Length adjustment: 30
Effective length of query: 344
Effective length of database: 336
Effective search space:   115584
Effective search space used:   115584
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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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