GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Herbaspirillum aquaticum IEH 4430

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate WP_088755699.1 CEJ45_RS13985 glycolate oxidase subunit GlcE

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



>NCBI__GCF_002213425.1:WP_088755699.1
          Length = 357

 Score =  400 bits (1028), Expect = e-116
 Identities = 212/368 (57%), Positives = 260/368 (70%), Gaps = 16/368 (4%)

Query: 7   DQQATLTAFRDAIRHATGTRTPLRLRGGGSKDFYGQHPQGTLLDTRAYSGIVDYDPPELV 66
           D +A L +FR+ I         L++RGGG+KD+YGQ P G LLDTR YSGI+DY+P ELV
Sbjct: 6   DMEAVLASFRERILSGRA----LQIRGGGTKDWYGQVPSGDLLDTRPYSGIIDYEPTELV 61

Query: 67  ITARCGTPLAQIEAALAERRQMLAFEPPHFSTGADGSDVATIGGAVAAGLSGPRRQAVGA 126
           ITARCGTPLA+I+AALA   QMLA+EPP F         AT+GG VAAGLSGP R A GA
Sbjct: 62  ITARCGTPLAEIDAALAGHNQMLAWEPPRFG------GAATVGGMVAAGLSGPSRAAAGA 115

Query: 127 LRDFVLGTRVMDGRGDVLSFGGQVMKNVAGYDVSRLMSGSLGTLGLILEVSLKVLPVPFD 186
           +RDFVLG  +MD +G+ L FGGQVMKNVAGYD+SRL++GSLGTLGLIL+VSLKVLP P  
Sbjct: 116 VRDFVLGAVLMDAQGEQLHFGGQVMKNVAGYDISRLLAGSLGTLGLILQVSLKVLPRPIA 175

Query: 187 DATLRFALDEAAALDRLNDWGGQPLPIAASAWHDGVLHLRLSGAAAALRAARARLGGEAV 246
            +T  F +++  AL  LN   GQPLP+ ASAW + VL +RLSGA AA+ +A  ++GG   
Sbjct: 176 SSTRVFEINQEGALRLLNQSAGQPLPLVASAWVNNVLTIRLSGAQAAVDSAIKKMGG--T 233

Query: 247 DAAQADALWRALREHSHAFFAPVQAGRALWRIAVPTTAAPLALPGGQLIEWGGGQRWWLG 306
           + +  +  W  LRE +H FFA  QA   LWR++VP+ A P+ LPG QLIEWGG QRW   
Sbjct: 234 ELSNPEDYWTDLREQTHPFFADPQA--PLWRLSVPSVAPPIDLPGRQLIEWGGAQRWL-- 289

Query: 307 GSDSAADSAIVRAAAKAAGGHATLFRNGDKAVGVFTPLSAPVAAIHQRLKATFDPAGIFN 366
             +   D+  +RAAA A GGHA+L R GDKA+GVF PL   V +IH+RLK  FDP GIFN
Sbjct: 290 RPEGNVDAVAIRAAALAVGGHASLHRGGDKAIGVFHPLQPAVESIHRRLKQQFDPQGIFN 349

Query: 367 PQRMYAGL 374
           P R+YA L
Sbjct: 350 PGRLYASL 357


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: 443
Number of extensions: 20
Number of successful extensions: 5
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: 357
Length adjustment: 30
Effective length of query: 344
Effective length of database: 327
Effective search space:   112488
Effective search space used:   112488
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 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