GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Cereibacter sphaeroides ATCC 17029

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate WP_011841821.1 RSPH17029_RS13515 FAD-binding protein

Query= reanno::Phaeo:GFF2924
         (366 letters)



>NCBI__GCF_000015985.1:WP_011841821.1
          Length = 358

 Score =  392 bits (1008), Expect = e-114
 Identities = 215/367 (58%), Positives = 257/367 (70%), Gaps = 12/367 (3%)

Query: 1   MTPQSEAELAQIIVGATAPLAVSGGGTRGLS-TGGETLSVAGLNGVTLYEPGALTLVVQA 59
           M P +E ELA+I+ GA  PL + GGGTR +  T G  L  AGL GV LYEPGALTLV  A
Sbjct: 1   MRPSTEEELAEIVRGAAGPLRIRGGGTRAIGRTDGAPLETAGLAGVRLYEPGALTLVAGA 60

Query: 60  GTSVEEVQALLAGENQRLAFEPMDHRGLLGTKGTPTIGGVFAANVSGPRRIQCGAARDFL 119
           G+ + E++A+LA E QRL FE  D RGLLG +G  T+GGV AAN SGPRRIQ GA RD L
Sbjct: 61  GSPLGEIEAMLAAEGQRLPFEAPDLRGLLGREGVSTLGGVVAANGSGPRRIQAGACRDSL 120

Query: 120 LGVRFVDGRGDVLSNGGRVMKNVTGYDLVKLMAGSHGTLGVLSEVSLKVLPCSEACATVT 179
           +GVRFVDG G V+ NGGRVMKNVTGYDLVKLMAGSHGTLGVLSEV+ K+LP  E   T+ 
Sbjct: 121 IGVRFVDGAGQVVKNGGRVMKNVTGYDLVKLMAGSHGTLGVLSEVAFKLLPLPETELTLA 180

Query: 180 VHVADLTSAVAAMSTALGSPYDVTGAAYDPEAGAVYIRVEGFEASVTYRAEALKMALGKF 239
           +       AV AM+ ALGSP+DV+GAA+ P  G  ++R+EGFEASV YRAE L+  L  F
Sbjct: 181 LPDLAPERAVEAMAAALGSPFDVSGAAHWPGRG-TFLRIEGFEASVRYRAERLRRLLTGF 239

Query: 240 GEVSLALGAGDALWEGIRNVAAFHDRPGDVWRISVKPSDAVALAPALEAEGLLFDWGGGL 299
           GE +      ++ W  IR+VA FH R GDVWR+S+KPS+A A+A A      LFDWGGGL
Sbjct: 240 GEAAEV----ESPWAAIRDVAPFHGREGDVWRLSLKPSEAPAVA-ARAGGAALFDWGGGL 294

Query: 300 IWALVPAGRDLRFRLT-VPGHATLVRASAQTRAELGQFQPQPGPLAAISGGLRRQFDPRG 358
           +W L   G DLR R+    GHATLVR +A   A    F P+P PLAA++ GLR +FDPRG
Sbjct: 295 VWILTEPGTDLRARIAPFAGHATLVRGTAPVAA----FHPEPLPLAALAAGLRARFDPRG 350

Query: 359 ILNPGLM 365
           + NPGLM
Sbjct: 351 LFNPGLM 357


Lambda     K      H
   0.318    0.136    0.401 

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: 480
Number of extensions: 26
Number of successful extensions: 7
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: 366
Length of database: 358
Length adjustment: 29
Effective length of query: 337
Effective length of database: 329
Effective search space:   110873
Effective search space used:   110873
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 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