GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Rhodobacter ovatus JA234

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate WP_097030568.1 CRO07_RS10110 FAD-binding protein

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



>NCBI__GCF_900207575.1:WP_097030568.1
          Length = 360

 Score =  366 bits (939), Expect = e-106
 Identities = 201/367 (54%), Positives = 245/367 (66%), Gaps = 10/367 (2%)

Query: 1   MTPQSEAELAQIIVGATAPLAVSGGGTRGLST-GGETLSVAGLNGVTLYEPGALTLVVQA 59
           M P +E E+A+I+  A  PL + GGGTRG+    G  L   GL G+ LYEPGALTLV  A
Sbjct: 1   MRPGTEQEVAEIVRAAEGPLRIVGGGTRGIGRCAGAVLETCGLAGIRLYEPGALTLVAGA 60

Query: 60  GTSVEEVQALLAGENQRLAFEPMDHRGLLGTKGTPTIGGVFAANVSGPRRIQCGAARDFL 119
           GT + +V+A LA + QRL FE  D RGLLG  G  T+GGV A+N SGPRR+Q GA RD L
Sbjct: 61  GTRLADVEAALAAQGQRLPFEVPDLRGLLGRGGCSTLGGVVASNASGPRRVQAGACRDSL 120

Query: 120 LGVRFVDGRGDVLSNGGRVMKNVTGYDLVKLMAGSHGTLGVLSEVSLKVLPCSEACATVT 179
           +GVRFVDG G V+ NGGRVMKNVTGYDLVKL+AGSHGTLGVL+EV+ K+LP  E   T+ 
Sbjct: 121 IGVRFVDGTGAVVKNGGRVMKNVTGYDLVKLLAGSHGTLGVLTEVAFKLLPVPEDEVTLM 180

Query: 180 VHVADLTSAVAAMSTALGSPYDVTGAAYDPEAGAVYIRVEGFEASVTYRAEALKMALGKF 239
           +       AVAAM+ ALGSP++V+GAA+ P  G  ++R+EGF ASV YRA  L   L  F
Sbjct: 181 LSGVSAERAVAAMAAALGSPFEVSGAAHWPGRG-TFLRIEGFAASVAYRAGRLAALLAPF 239

Query: 240 GEVSLALGAGDALWEGIRNVAAFHDRPGDVWRISVKPSDAVALAPALEAEGLLFDWGGGL 299
           G V    G     W  IR+V  F  R GDVWR+ VKPS+A  +A     E +L DWGGGL
Sbjct: 240 GAVEQVAGP----WRSIRDVEPFQGREGDVWRVLVKPSEAPGVAVRSGGE-VLIDWGGGL 294

Query: 300 IWALVPAGRDLRFRL-TVPGHATLVRASAQTRAELGQFQPQPGPLAAISGGLRRQFDPRG 358
           +W LV  G DLR R+  + GHATLVR       +L  F P+P  +AA+S GLR +FDPRG
Sbjct: 295 VWVLVEPGCDLRARIGPLAGHATLVRGG--EAGDLPVFPPEPAAVAALSRGLRARFDPRG 352

Query: 359 ILNPGLM 365
           + NPGLM
Sbjct: 353 LFNPGLM 359


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: 487
Number of extensions: 28
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: 366
Length of database: 360
Length adjustment: 29
Effective length of query: 337
Effective length of database: 331
Effective search space:   111547
Effective search space used:   111547
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 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