GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Oscillibacter ruminantium GH1

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_040661227.1 ON16_RS08265 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_000307265.1:WP_040661227.1
          Length = 394

 Score =  206 bits (524), Expect = 8e-58
 Identities = 118/321 (36%), Positives = 190/321 (59%), Gaps = 43/321 (13%)

Query: 1   MVRIIVKNVSKVF-----KKGK----------------VVALDNVNINIENGERFGILGP 39
           M  +I+KN+ KV+     KK +                V+A+ + N+ I + E   ++GP
Sbjct: 1   MAEVILKNIKKVYPNTEAKKHRKDGGEKLADLQITDEGVLAVQDFNLEIADKEFVVLVGP 60

Query: 40  SGAGKTTFMRIIAGLDVPSTGELYFDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTA 99
           SG GK+T +R++AGL+  S GELY   RL+       V P+DR I MVFQ +ALYP++T 
Sbjct: 61  SGCGKSTTLRMVAGLEEISGGELYMGGRLMND-----VAPKDRDIAMVFQNYALYPHMTV 115

Query: 100 FENIAFPLTNMKMSKEEIRKRVEEVAKILDIHHVLNHFPRELSGGQQQRVALARALVKDP 159
           +EN+AF L   K  K+E+ ++V E A+ILDI   L+  P+ LSGGQ+QRVA+ RA+V++P
Sbjct: 116 YENMAFSLKLKKTPKDEMDRKVREAAEILDITQYLDRKPKALSGGQRQRVAIGRAIVRNP 175

Query: 160 SLLLLDEPFSNLDARMRDSARALVKEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKL 219
            + L+DEP SNLDA++R+  RA + ++++R+  T L V+HD  +   + DR+ ++  G +
Sbjct: 176 QVFLMDEPLSNLDAKLRNQMRAELIKLRTRINTTFLYVTHDQTEAMTLGDRIVIMKGGVI 235

Query: 220 VQVGKPEDLYDNPVSIQVASLIG--EINELEGKVTNEGVV----IGSLRFPVSVSSDRAI 273
            Q+G P++++D+P+++ VA  IG  ++N  +GK+     V          P+   +  A+
Sbjct: 236 QQIGTPQEVFDHPINLFVAGFIGSPQMNFFDGKLIQTNGVWQAETAGAVIPLGQKTQAAL 295

Query: 274 -----------IGIRPEDVKL 283
                      IGIRPE ++L
Sbjct: 296 NAAGVAPMAVSIGIRPEHIQL 316


Lambda     K      H
   0.319    0.139    0.390 

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: 304
Number of extensions: 18
Number of successful extensions: 2
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: 353
Length of database: 394
Length adjustment: 30
Effective length of query: 323
Effective length of database: 364
Effective search space:   117572
Effective search space used:   117572
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 (21.7 bits)
S2: 50 (23.9 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