GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Microvirga lotononidis WSM3557

Align L-iditol 2-dehydrogenase; EC 1.1.1.14 (characterized)
to candidate WP_009763936.1 MICLODRAFT_RS21540 NAD(P)-dependent alcohol dehydrogenase

Query= CharProtDB::CH_000596
         (353 letters)



>NCBI__GCF_000262405.1:WP_009763936.1
          Length = 357

 Score =  160 bits (404), Expect = 6e-44
 Identities = 111/367 (30%), Positives = 179/367 (48%), Gaps = 37/367 (10%)

Query: 9   MKAAVMHNTREIKIETLPVPDINHDEVLIKVMAVGICGSDLHYYTNGRIGNYVVEKPFIL 68
           M+AA+      I ++  P+P+I   + L+++    ICG+D+H       G Y V     +
Sbjct: 4   MRAAIFVEPGRIVLDEKPIPNIGPLDALVRISTTTICGTDIHILK----GEYPVAPGLTI 59

Query: 69  GHECAGEIAAVGSSVDQFKVGDRVAVEPGVTCGRCEACKEGRYNLCPDVQFLATP----- 123
           GHE  G I  +GS+V  ++ G RV        G  EAC  G    C       T      
Sbjct: 60  GHEPVGIIEKLGSAVQGYREGQRVIAGAITPSGYSEACLCG----CHSQDGAGTKHGWKA 115

Query: 124 --------PVDGAFVQYIKMRQDFVFL--IPDSLSYEEAALI-EPFSVGIHAAARTKLQP 172
                    +DG   +Y+++      L  +PD L+ E+  +  +  S G   A   +++ 
Sbjct: 116 MGGWKFGNTIDGCQAEYLRVPDAMANLAPVPDGLTDEQVLMCPDILSTGFSGAESGRIRI 175

Query: 173 GSTIAIMGMGPVGLMAVAAAKAFGAGTIIVTDLEPLRLEAAKKMGATHIINIREQDALEE 232
           G T+A+   GP+GL A A AK  GA TII  +  P R++ +++MGA H+I+  + D +EE
Sbjct: 176 GDTVAVFAQGPIGLCATAGAKLMGATTIIAVESLPERIDMSRRMGADHVIDFTKADPVEE 235

Query: 233 IKTITNDRGVDVAWETAGNPAALQSALASVRRGGKLAIVGLPSQNEIPLNVPFIADNEID 292
           I+ +T+ RGVDV+ E  G     ++AL  +R GG L+ +G+ S +   L +P   D  + 
Sbjct: 236 IRRLTDGRGVDVSIEALGRQQTFEAALRVLRPGGTLSSLGVYSGD---LRIPL--DGFLA 290

Query: 293 IYGIFRYANTYPKG--------IEFLASGIVDTKHLVTDQYSLEQTQDAMERALQFKNEC 344
             G +    T   G        I  +ASG VDT+ LVT ++ L+Q ++A +     ++  
Sbjct: 291 GLGDYTIRTTLCPGGKERMRRLISAIASGRVDTRPLVTHRFKLDQIEEAYDLFSHQRDGV 350

Query: 345 LKVMVYP 351
           LKV + P
Sbjct: 351 LKVAIAP 357


Lambda     K      H
   0.320    0.137    0.401 

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: 319
Number of extensions: 18
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: 353
Length of database: 357
Length adjustment: 29
Effective length of query: 324
Effective length of database: 328
Effective search space:   106272
Effective search space used:   106272
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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