GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Methylocapsa aurea KYG

Align NAD-dependent glycerol dehydrogenase; Dha-forming NAD-dependent glycerol dehydrogenase; EC 1.1.1.6 (characterized)
to candidate WP_036257684.1 DL86_RS02605 SDR family oxidoreductase

Query= SwissProt::Q92EU6
         (254 letters)



>NCBI__GCF_000746085.1:WP_036257684.1
          Length = 2024

 Score =  129 bits (323), Expect = 6e-34
 Identities = 87/260 (33%), Positives = 144/260 (55%), Gaps = 27/260 (10%)

Query: 9   DFNITDKVAVVTGAASGIGKAMAELFSEKGAYVVL--LDIKEDVKDVAAQINPSRTLALQ 66
           D +++ K+ +VTG A  +GKA+A  F+E+GA+V++      E  K+ AA++   R + ++
Sbjct: 3   DGSLSGKLVLVTGGAKNVGKAIAMRFAERGAHVIVNFFHSLEASKETAAEL---RAMGVE 59

Query: 67  VDITK-----KENIEKVVAEIKKVYPKIDILANSAGVALLEKAEDLPEEYWDKTMELNLK 121
           VD+ +     K  ++++  EI   Y ++DIL N+A    L   +D+ EE++DK +  NLK
Sbjct: 60  VDVIRASVAQKNQVDRMFDEIAAKYGRLDILVNNAASGALLCVDDIAEEHFDKALSTNLK 119

Query: 122 GSF----LMAQIIGREMIATGGGKIVNMASQASVIALDKHVAYCASKAAIVSMTQVLAME 177
           G+F      A ++GR      GG IVN++S  + +    ++    SKAA+ S+T+ LA+E
Sbjct: 120 GAFWCSRRAASLMGR------GGAIVNVSSVGATLVPANYLVVGTSKAALESLTRYLAVE 173

Query: 178 WAPYNINVNAISPTVILTELGKKAWAGQVGEDMKK----LIPAGRFGYPEEVAACALFLV 233
           +AP  I VN  S T+I    G  A      E  K+      P  R    E++A   LFL 
Sbjct: 174 YAPRGIRVNTASATLI---DGSVAEMFPNSESTKRSSIAATPLKRLAAAEDLADLVLFLA 230

Query: 234 SDAASLITGENLIIDGGYTI 253
           SD++  ITG+ ++ DGG ++
Sbjct: 231 SDSSRWITGQVVVADGGLSL 250



 Score = 25.4 bits (54), Expect = 0.010
 Identities = 14/64 (21%), Positives = 33/64 (51%), Gaps = 3/64 (4%)

Query: 39   AYVVLLDIKE---DVKDVAAQINPSRTLALQVDITKKENIEKVVAEIKKVYPKIDILANS 95
            AY  L++ +E   +++++       R   L  D+    +I+  +A I     ++D++ N+
Sbjct: 1462 AYDRLINAREARRNIEEMRKHCGADRVHYLCADVLDAASIQNAIAAILAREAQVDLVVNA 1521

Query: 96   AGVA 99
            AG++
Sbjct: 1522 AGLS 1525


Lambda     K      H
   0.316    0.133    0.369 

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: 954
Number of extensions: 43
Number of successful extensions: 5
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: 254
Length of database: 2024
Length adjustment: 39
Effective length of query: 215
Effective length of database: 1985
Effective search space:   426775
Effective search space used:   426775
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: 54 (25.4 bits)

This GapMind analysis is from Apr 09 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