GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Paraburkholderia bryophila 376MFSha3.1

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate H281DRAFT_04682 H281DRAFT_04682 glycolate oxidase FAD binding subunit

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



>FitnessBrowser__Burk376:H281DRAFT_04682
          Length = 362

 Score =  421 bits (1081), Expect = e-122
 Identities = 211/368 (57%), Positives = 266/368 (72%), Gaps = 13/368 (3%)

Query: 7   DQQATLTAFRDAIRHATGTRTPLRLRGGGSKDFYGQHPQGTLLDTRAYSGIVDYDPPELV 66
           ++   +  + + +R A+     LR+RGGG+KD+YGQ  +G +LDTRAY GI+ YDP ELV
Sbjct: 2   EEDDIVAMWSERVRSASAAGRALRVRGGGTKDWYGQTLEGEILDTRAYRGIIAYDPAELV 61

Query: 67  ITARCGTPLAQIEAALAERRQMLAFEPPHFSTGADGSDVATIGGAVAAGLSGPRRQAVGA 126
           ITAR GTPL +IEAALAE  QMLAFEPPHF   A      T GG +AAG++GPRR + GA
Sbjct: 62  ITARAGTPLLEIEAALAEHHQMLAFEPPHFGPQA------TFGGCIAAGIAGPRRPSAGA 115

Query: 127 LRDFVLGTRVMDGRGDVLSFGGQVMKNVAGYDVSRLMSGSLGTLGLILEVSLKVLPVPFD 186
            RDFVLG  VM+G+G  L FGGQV+KNVAGYDVSRLM+GSLGTLGLILE+S+KVLP P  
Sbjct: 116 ARDFVLGAVVMNGQGQALHFGGQVVKNVAGYDVSRLMAGSLGTLGLILELSVKVLPQPQA 175

Query: 187 DATLRFALDEAAALDRLNDWGGQPLPIAASAWHDGVLHLRLSGAAAALRAARARLGGEAV 246
           +ATL+F ++   A+ +LN+WGG+PLPI ASAW  G L +RL+GA +A+++ARA LGGE V
Sbjct: 176 EATLKFDVNGTDAVRKLNEWGGRPLPITASAWRHGTLAVRLAGAESAVKSARASLGGEVV 235

Query: 247 DAAQADALWRALREHSHAFFAPVQAGRALWRIAVPTTAAPLALPGGQLIEWGGGQRWWLG 306
           DA +A+  W  LRE +  FFA +    ALWR+A+P+   PL LPG QL+EWGG QRWW+ 
Sbjct: 236 DAVEAERFWAGLREQTDTFFAAIPPKAALWRLALPSITEPLQLPGAQLMEWGGAQRWWI- 294

Query: 307 GSDSAADSAIVRAAAKAAGGHATLFRNG---DKAVGVFTPLSAPVAAIHQRLKATFDPAG 363
              +  D+  VR +AK AGGHAT+FR G   D+  GVFTPL AP+  IH+ LK  FDPA 
Sbjct: 295 ---TDTDAQTVRISAKQAGGHATIFRTGHGYDRGAGVFTPLPAPLMKIHRGLKTAFDPAR 351

Query: 364 IFNPQRMY 371
           IFN  R+Y
Sbjct: 352 IFNRGRLY 359


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: 465
Number of extensions: 17
Number of successful extensions: 4
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: 362
Length adjustment: 30
Effective length of query: 344
Effective length of database: 332
Effective search space:   114208
Effective search space used:   114208
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.

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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