GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Neiella marina J221

Align L-iditol 2-dehydrogenase (EC 1.1.1.14) (characterized)
to candidate WP_087506848.1 CBE68_RS14645 fructuronate reductase

Query= BRENDA::Q9KWR5
         (485 letters)



>NCBI__GCF_002165625.1:WP_087506848.1
          Length = 492

 Score =  237 bits (605), Expect = 6e-67
 Identities = 133/381 (34%), Positives = 207/381 (54%), Gaps = 7/381 (1%)

Query: 3   TRETLKSLPANVQAPPYDIDGIKPGIVHFGVGNFFRAHEAFYVEQILEHAPD-WAIVGVG 61
           T   L+SL  N +   +D   ++  IVH G G F R H+A Y +   + +   W I  + 
Sbjct: 5   TEVNLESLGFN-EKTSFDRSKLETNIVHIGFGAFHRGHQAVYNDLTNDQSDKLWGICEIN 63

Query: 62  LTGSDRSKKKAEEFKAQDCLYSLTETAPSGKSTVRVMGALRDYLLAPADP-EAVLKHLVD 120
           + G     +   + +AQ  L+S+ E +     + R++ ++ + +  P D  +A +  L +
Sbjct: 64  MFGGP---ELIADLQAQQHLFSVVERSADSMVS-RLIRSVTESIHTPVDGIQAAIDKLAE 119

Query: 121 PAIRIVSMTITEGGYNINETTGAFDLENAAVKADLKNPEKPSTVFGYVVEALRRRWDAGG 180
           P ++IVS+TITE GY  +  +G  D+ N  ++ DL NP+ P +  G + EALR R D G 
Sbjct: 120 PQVKIVSLTITEKGYCSDPQSGQLDINNGLIQHDLNNPQTPQSALGLITEALRVRRDKGL 179

Query: 181 KAFTVMSCDNLRHNGNVARKAFLGYAKARDPELAKWIEENATFPNGMVDRITPTVSAEIA 240
             F+V+SCDN+  NG + ++A L +AK  D  LA WIE+N TFP+ MVDRI P ++ +  
Sbjct: 180 APFSVLSCDNIPENGLLTKEAVLSFAKQLDSALAAWIEQNVTFPSTMVDRIVPAMTDDAF 239

Query: 241 KKLNAASGLDDDLPLVAEDFHQWVLEDQFADGRPPLEKAGVQMVGDVTDWEYVKIRMLNA 300
             ++   G  D   +V ED+ QWV+ED F  GRP  +KAG   V DV  +E +K+RMLN 
Sbjct: 240 AVIDECIGYRDPCGIVCEDYRQWVIEDNFVAGRPDWDKAGAMFVADVLPYEEMKLRMLNG 299

Query: 301 GHVMLCFPGILVGYENVDDAIEDSELLGNLKNYLNKDVIPTLKAPSGMTLEGYRDSVISR 360
            H  L + G L GY+ +   +EDS+        + ++   +L     + LE Y   +I R
Sbjct: 300 SHSFLAYNGFLAGYDFIYQCMEDSDFRATTLRLMLEEQAKSLNPSLKVDLEQYASLLIGR 359

Query: 361 FSNKAMSDQTLRIASDGCSKV 381
           FSN  +  +T +IA DG  K+
Sbjct: 360 FSNPNIKHKTAQIAMDGTQKL 380


Lambda     K      H
   0.317    0.135    0.398 

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: 532
Number of extensions: 15
Number of successful extensions: 2
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: 485
Length of database: 492
Length adjustment: 34
Effective length of query: 451
Effective length of database: 458
Effective search space:   206558
Effective search space used:   206558
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: 52 (24.6 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