GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fdh in Cereibacter sphaeroides ATCC 17029

Align D-threo-aldose 1-dehydrogenase (EC 1.1.1.122) (characterized)
to candidate WP_011841060.1 RSPH17029_RS07595 NAD(P)-dependent alcohol dehydrogenase

Query= BRENDA::Q97YM2
         (349 letters)



>NCBI__GCF_000015985.1:WP_011841060.1
          Length = 364

 Score =  169 bits (427), Expect = 1e-46
 Identities = 116/337 (34%), Positives = 176/337 (52%), Gaps = 14/337 (4%)

Query: 21  LSIEDVNIPE-PQGEEVLIRIGGAGVCRTDLR----VWKGVEAKQGFRLPIILGHENAGT 75
           L IEDV  P   + +EV++++G AG+CRTDL     VW+ +    G  LP I+GHENAG 
Sbjct: 17  LKIEDVPSPTIDRPDEVIVKVGAAGLCRTDLHIIEGVWRDIMDSHGSLLPYIMGHENAGW 76

Query: 76  IVEVGE-LAKVKKGDNVVVYATWGDLTCRYCREGKFNICKNQIIPGQTTNGGFSEYMLVK 134
           + +VG  +  VK GD V+ +       C  CR G    C+N + PG   +GGF+EY    
Sbjct: 77  VEDVGSGVTSVKPGDAVICHPLRTCGICLNCRHGHDMHCQNNLFPGLGLDGGFAEYFKT- 135

Query: 135 SSRWLVKLNS-LSPVEAAPLADAGTTSMGAIRQALPFISKFAEPVVIVNGIGGLAVYTIQ 193
           S R L+KLN+ ++P+  AP+ADAG T+  A ++A   ++     +++  G+GGL    +Q
Sbjct: 136 SERSLIKLNTGITPLSVAPMADAGITAYRAAKRAAKLLNPGDWALIL--GVGGLGHIALQ 193

Query: 194 ILKALMKNITIVGISRSKKHRDFALELGADYV-SEMKDAESLINKLTDGLGASIAIDLVG 252
           +L   M     + + R    +  A ELGAD V S   D    + ++T G GA + ID VG
Sbjct: 194 VLNE-MAGCRTIAVDREPGAQVLAKELGADKVLSGGPDLIEEVRQITGG-GARVVIDFVG 251

Query: 253 TEETTYNLGKLLAQEGAIILVGMEGKRVSLEAFDTAVWNKKLLGSNYGSLNDLEDVVRLS 312
                    KLL   G +I+VG  G  + +   +      ++ GS  G   +L +++ L+
Sbjct: 252 ELGIENLCWKLLKNGGDLIMVGY-GGTIEIPTLELVAREIRIGGSLVGDYTELVELMELN 310

Query: 313 ESGKIKPYIIKVPLDDINKAFTNLDEGRVDGRQVITP 349
             GK+K +  +  L+DIN A  +    R  GR VI P
Sbjct: 311 ADGKVKMHQTEFALEDINTAIDDFKNRRFTGRGVIVP 347


Lambda     K      H
   0.317    0.136    0.389 

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: 361
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: 349
Length of database: 364
Length adjustment: 29
Effective length of query: 320
Effective length of database: 335
Effective search space:   107200
Effective search space used:   107200
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. 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