GapMind for catabolism of small carbon sources

 

Alignments for a candidate for LRA5 in Cereibacter sphaeroides ATCC 17029

Align 2-dehydro-3-deoxy-L-rhamnonate dehydrogenase (NAD(+)); 2-keto-3-deoxy-L-rhamnonate dehydrogenase; KDRDH; L-KDR dehydrogenase; EC 1.1.1.401 (characterized)
to candidate WP_011842438.1 RSPH17029_RS17935 L-idonate 5-dehydrogenase

Query= SwissProt::P0DOW0
         (331 letters)



>NCBI__GCF_000015985.1:WP_011842438.1
          Length = 345

 Score =  123 bits (309), Expect = 6e-33
 Identities = 102/305 (33%), Positives = 147/305 (48%), Gaps = 18/305 (5%)

Query: 1   MKTLTWTAKETMSILSAPAPVPEPGWIALRVAGVGICGSELSGYLGH----NELRKPPLV 56
           M+     A   +SI     P  + G + L +A  GICGS+L  Y  H    N + + P++
Sbjct: 1   MRACVIRAARDLSIEPWAEPALQAGEVRLDLAWGGICGSDLH-YFQHGRVANSILREPMI 59

Query: 57  MGHEFSGVVEEVGHGVTNVKIGDLVTANPLVTCGRCIHCLRGERQRCESRRIIG--IDFP 114
           +GHEFSG + EVG GV  +K G  V  NP   CG C  C  G    C S R +G    FP
Sbjct: 60  LGHEFSGRIREVGPGVQWLKPGMAVAVNPSRPCGSCDQCSAGLTHLCRSMRFMGSAAHFP 119

Query: 115 ---GAYAERVLVPSNQCYAVKDAID---GALVEPLACAVRAVGLARIKVGDTAVVIGAGI 168
              G +AER +V ++QC A+ + +D    AL EP A A+ AV LA+I  G + +V GAG 
Sbjct: 120 HTHGGFAERPVVLASQCVALPETVDLALAALSEPYAVALHAVELAQIAAGASVLVTGAGT 179

Query: 169 IGLMTVRLLGLSGAKRIAVVDPNDERL-KISQLWGA-TEMAPNLGAL-LTDNHPQSFDCV 225
           IG +       +GA R+ V D  +  L ++ ++ GA T +  +  A    +      D V
Sbjct: 180 IGSLVAVAARQAGAGRLIVTDIAEPALARVRKVTGAETHLVGDPEATRAAEAAIGEVDVV 239

Query: 226 IDAVGLSTTRRDSLNALIRGGRAVWIGL--HEALTHLDGNQIVRDELEVRGSFCYTDDEF 283
           ++A G+S     ++  +   GR V +G    EA   L G  I    L     F    DE 
Sbjct: 240 LEASGVSAALDMAIRCIRPRGRIVQVGFLPPEARLSLAGLLIREATLVGAYRFLGEFDEA 299

Query: 284 IRAVS 288
           +R +S
Sbjct: 300 VRQIS 304


Lambda     K      H
   0.322    0.139    0.424 

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: 270
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: 331
Length of database: 345
Length adjustment: 28
Effective length of query: 303
Effective length of database: 317
Effective search space:    96051
Effective search space used:    96051
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: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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