GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Rhodanobacter denitrificans 2APBS1

Align D-xylulose reductase; Xylitol dehydrogenase; XDH; EC 1.1.1.9 (characterized)
to candidate WP_015449047.1 R2APBS1_RS18135 S-(hydroxymethyl)glutathione dehydrogenase/class III alcohol dehydrogenase

Query= SwissProt::Q07993
         (356 letters)



>NCBI__GCF_000230695.2:WP_015449047.1
          Length = 370

 Score = 88.6 bits (218), Expect = 2e-22
 Identities = 94/312 (30%), Positives = 136/312 (43%), Gaps = 46/312 (14%)

Query: 9   AIVLERPGKITLTNVSIPKISDPNEVIIQIKATGICGSDIHYYTHGRIANYVVESPMVLG 68
           A V  +P  I   +V+ PK     EV+++I ATG+C +D    +    A+   + P++LG
Sbjct: 8   AWVAGQPLSIEQVDVAGPKAG---EVLVRIVATGVCHTDAFTLSG---ADPEGQFPVILG 61

Query: 69  HESSGIVALIGENVKTLKVGDRVALEPGIPDRFSPEMKE------GRYNLDPNLKFAATP 122
           HE  GIV  +GE V +LKVGD V     IP  ++PE  E      G+ NL   ++     
Sbjct: 62  HEGGGIVEEVGEGVTSLKVGDHV-----IP-LYTPECGECKFCRSGKTNLCQKIRATQGQ 115

Query: 123 PF--DGT---------LTKYYKTMKDFVYKLPDDVSFEEGALIEPL----------SVAI 161
               DGT         L  Y  T     Y +  ++S  +     PL          +  I
Sbjct: 116 GLMPDGTSRFSLNGKPLLHYMGTSTFSEYTVLPEISLAKINPAAPLDKVCLLGCGITTGI 175

Query: 162 HA-NKLAKIKFGARCVVFGAGPIGLLAGKVASVFGAADVVFVDLLENKLETARQFGATHI 220
            A    AK++ GA   VFG G IGL   + A +  A  ++ +D    K   A+  GAT  
Sbjct: 176 GAVLNTAKVEPGATVAVFGLGGIGLSVVQGAVMAKAGRIIAIDRHPEKFAMAKALGATDC 235

Query: 221 VNSGDLPHGVTVDSVIKKAIGKKGADVVFECSGAEPCVRAGIEVCKAG---GTIVQV-GM 276
           VN  D P       +++   G  G D  FEC G    +R+ +E C  G     I+ V G 
Sbjct: 236 VNVNDYPDTPIQQVIVELTDG--GVDYSFECIGNVQVMRSALECCHKGWGESIIIGVAGA 293

Query: 277 GQEEIQFPISII 288
           GQE    P  ++
Sbjct: 294 GQEICTRPFQLV 305


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: 352
Number of extensions: 25
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: 1
Length of query: 356
Length of database: 370
Length adjustment: 29
Effective length of query: 327
Effective length of database: 341
Effective search space:   111507
Effective search space used:   111507
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