GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcF in Dyella japonica UNC79MFTsu3.2

Align D-lactate oxidase, iron-sulfur subunit (EC 1.1.3.15) (characterized)
to candidate N515DRAFT_2104 N515DRAFT_2104 glycolate oxidase iron-sulfur subunit

Query= reanno::Phaeo:GFF2923
         (444 letters)



>FitnessBrowser__Dyella79:N515DRAFT_2104
          Length = 400

 Score =  140 bits (352), Expect = 9e-38
 Identities = 123/400 (30%), Positives = 171/400 (42%), Gaps = 35/400 (8%)

Query: 25  CVHCGFCTATCPTYQVLGDELDSPRGRIYLIKDMLENERVPDAKTVKHIDRCLSCLACMT 84
           CV CG C   CPTY +  +E +SPRGRI +   +   +  P A+  +H+D CL C+ C  
Sbjct: 20  CVQCGLCLPVCPTYALDRNEAESPRGRIAIAAALARGQASPTAELREHLDHCLGCMGCEK 79

Query: 85  TCPSGVHYMHLVDHARAYIDKHYNRPWSDRAL-----RWLLARILPYPGRFRLALIGAKL 139
            CP+ V Y  L+   RA +     RP  +  L     RW   R     G   L   G K 
Sbjct: 80  VCPANVRYGELLVETRALLGPALQRPEHEIGLVRDPRRWRRLR----RGLGWLGFAGWKS 135

Query: 140 AQPFKRLVPDARLRAMLDMAPRHIPPVSRNDDPQSFAAKAPRRKRVALMTGCAQKALNTD 199
           A   K L   + LR+ L + PR   P+      Q  + KA     VAL  GC     + D
Sbjct: 136 ALA-KSLPARSALRSALALWPR--TPLPEPYLAQPASDKAADGDTVALFPGCIASVEDAD 192

Query: 200 INDATIRLLTRLGCEVVVAAGAGCCGALTHHMGREEESHATAAKNIRAWTDEIDGQGLDA 259
              A   LL   G   VV   A CCGA+  H G    +   AA+   AW D       D 
Sbjct: 193 AQRAARTLLRAAGYR-VVELPAFCCGAMDLHGGDTARAEQAAAQVSAAWQD----AQADH 247

Query: 260 IVINTSGCGTTVKDYGHMFRNDALAEDAARVSAIAMDISELLMQLDLPEGEDKETTVAYH 319
           +V  T GC  T++   H+     +A+  A ++A A  +S       LP      T VA H
Sbjct: 248 LVTVTPGCVGTLR---HVLPGVRVADPMALLAARAQRLS----FRPLP------TRVAVH 294

Query: 320 AACSLQHGQQIKTHPKTLLKRA-GFTVVEPADSHLCCGSAGTYNLLQPEISAELKARKVT 378
             C+  +  +       LL+R  G  V        CCG+AGT+ L  PE +A L+   + 
Sbjct: 295 LPCTQSNVARSDDALLRLLRRVPGLDVAPLPKPPHCCGAAGTHVLEFPERAARLREDTLR 354

Query: 379 SLEARQPDLIAAGNIGCMMQIGSA----TDIPILHTVELL 414
            + A  P  + + NIGC + + +      D P  H + LL
Sbjct: 355 QVAALAPRRLLSSNIGCRLHLAAGMQNERDWPHQHPLVLL 394


Lambda     K      H
   0.321    0.135    0.419 

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: 2
Number of HSP's successfully gapped: 2
Length of query: 444
Length of database: 400
Length adjustment: 32
Effective length of query: 412
Effective length of database: 368
Effective search space:   151616
Effective search space used:   151616
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 (21.9 bits)
S2: 50 (23.9 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