GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Neiella marina J221

Align D-xylulose reductase; Xylitol dehydrogenase; XDH; EC 1.1.1.9 (characterized)
to candidate WP_087506147.1 CBE68_RS11035 S-(hydroxymethyl)glutathione dehydrogenase/class III alcohol dehydrogenase

Query= SwissProt::Q07993
         (356 letters)



>NCBI__GCF_002165625.1:WP_087506147.1
          Length = 382

 Score = 91.7 bits (226), Expect = 3e-23
 Identities = 101/375 (26%), Positives = 165/375 (44%), Gaps = 58/375 (15%)

Query: 15  PGKITLTNVSIPKISDPNEVIIQIKATGICGSDIHYYTHGRIANYVVESPMVLGHESSGI 74
           P  +   +V +PK     EV+++I ATG+C +D  +   G     +   P +LGHE  GI
Sbjct: 25  PLSMAEVDVELPK---HGEVLVRIVATGVCHTDA-FTLSGDDPEGIF--PAILGHEGGGI 78

Query: 75  VALIGENVKTLKVGDRVALEPGIPDRFSPEMKE------GRYNLDPNLKFAATPPFDGTL 128
           V ++GE V +++VGD V     IP  ++ E  E      G+ NL   ++           
Sbjct: 79  VEMVGEGVTSVEVGDHV-----IP-LYTAECGECKFCTSGKTNLCQAVRETQGQGLMPDG 132

Query: 129 TKYYKTMKDFVYKLPDDVSFEEGALIEPLSVAIHANKL---------------------- 166
           T  +      +Y      +F E  ++  +S+A  + K                       
Sbjct: 133 TSRFSIDGMPIYHYMGCSTFSEYTVLPEISLAKVSPKAPLEEVCLLGCGVTTGMGAVLNT 192

Query: 167 AKIKFGARCVVFGAGPIGLLAGKVASVFGAADVVFVDLLENKLETARQFGATHIVNSGDL 226
           AK++ GA   +FG G IGL A   A +  A+ ++ +D+ ++K E A Q GAT ++N    
Sbjct: 193 AKVEAGATVAIFGLGGIGLSAIIGARMADASRIIGIDINDSKFELATQLGATDLINP--- 249

Query: 227 PHGVTVDSVIKKAI---GKKGADVVFECSGAEPCVRAGIEVCKAG---GTIVQV-GMGQE 279
               T+D  I++AI      G D  FEC G    +R  +E C  G     I+ V G GQE
Sbjct: 250 ---QTLDQPIQQAIIDMTDGGVDYSFECIGNVNVMRQALECCHKGWGESVIIGVAGAGQE 306

Query: 280 EIQFPISIIPTKELTFQGCFRYCQG--DYSDSIELVSSRKLSLKPFITHRYSFKDAVEAF 337
               P  ++ T  +     F   +G  +  + +E   + +  L+ FITH     +  +AF
Sbjct: 307 ISTRPFQLV-TGRVWRGSAFGGVKGRSELPEIVERYMAGEFGLQEFITHTMGLAEINKAF 365

Query: 338 EETSHHPLNNIKTII 352
           +    H   +I+T+I
Sbjct: 366 D--LMHEGKSIRTVI 378


Lambda     K      H
   0.319    0.138    0.402 

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: 333
Number of extensions: 21
Number of successful extensions: 4
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: 356
Length of database: 382
Length adjustment: 30
Effective length of query: 326
Effective length of database: 352
Effective search space:   114752
Effective search space used:   114752
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 (21.7 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