GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctC in Dechlorosoma suillum PS

Align lactate dehydrogenase (NAD+, ferredoxin) (subunit 2/3) (EC 1.3.1.110) (characterized)
to candidate Dsui_3149 Dsui_3149 electron transfer flavoprotein, alpha subunit

Query= BRENDA::H6LBB1
         (418 letters)



>FitnessBrowser__PS:Dsui_3149
          Length = 360

 Score =  222 bits (565), Expect = 2e-62
 Identities = 127/335 (37%), Positives = 194/335 (57%), Gaps = 10/335 (2%)

Query: 63  KVAIDKSL--YRGITVYVDHIEGQIHPVTFELIGKARELAAVIGHPVYALLMGT---NIT 117
           K+ +D+ L  Y+G+ V+V+   G +HPV++EL+G+ R LA  +G  +  ++MG    ++ 
Sbjct: 14  KIKLDEELLAYKGVWVFVESERGHVHPVSWELMGQGRRLADQLGVELCGVVMGAPGPDLE 73

Query: 118 EKADELLKYGVDKVFVYDKPELKHFVIEPYANVLEDFIEKVKPSSILVGATNVGRSLAPR 177
            +      YG D+ +    P L  +   P+   L D +   KP  +L+GAT +GR LA  
Sbjct: 74  AQCRAAFAYGADRCYRIASPVLAEYRNVPFTRALTDLVNAHKPEILLLGATTLGRDLAGS 133

Query: 178 VAARYRTGLTADCTILEMK-ENTDLVQIRPAFGGNIMAQIVTENTRPQFCTVRYKVFTAP 236
           VA   +TGLTADCT L +  E+  L+  RP FGG+++  IVT N RPQ  TVR++V   P
Sbjct: 134 VATTLKTGLTADCTELAIDPEDRCLLSTRPTFGGSLLCTIVTLNYRPQMATVRHRVMPMP 193

Query: 237 ERVNEPWG---DVEMMDIEKAKLVSAIEVMEVIKKEKGIDLSEAETIVAVGRGVKCEKDL 293
           +   E  G   D E   IE   +   +E +   +++K   L  AE +V+ G+G+   ++ 
Sbjct: 194 DPQPERTGLIVDFEAGLIETDIVTKVLEFIPDDQRDKP-QLPYAEIVVSGGKGLGKAENF 252

Query: 294 DMIHEFAEKIGATVACTRPGIEAGWFDARLQIGLSGRTVKPKLIIALGISGAVQFAAGMQ 353
             + + A+ +G  V  +R  I AGW  A  Q+G +G+TV+P L IA GISGA+Q   GM+
Sbjct: 253 KHVWDLAKVLGGEVGASRAAIHAGWISADRQVGQTGKTVRPALYIAAGISGAIQHRVGME 312

Query: 354 NSEYIIAINSDPKAPIFNIAHCGMVGDLYEILPEL 388
            ++ IIAIN+DP APIF+ AH  +VGD  ++LP L
Sbjct: 313 GADCIIAINNDPNAPIFDFAHYAIVGDCNQVLPAL 347


Lambda     K      H
   0.319    0.137    0.395 

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: 417
Number of extensions: 19
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: 418
Length of database: 360
Length adjustment: 30
Effective length of query: 388
Effective length of database: 330
Effective search space:   128040
Effective search space used:   128040
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 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