GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Sulfuritalea hydrogenivorans sk43H DSM 22779

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate WP_041099979.1 SUTH_RS13630 NADP(H)-dependent aldo-keto reductase

Query= BRENDA::F2YCN5
         (340 letters)



>NCBI__GCF_000828635.1:WP_041099979.1
          Length = 345

 Score =  107 bits (266), Expect = 6e-28
 Identities = 108/344 (31%), Positives = 162/344 (47%), Gaps = 61/344 (17%)

Query: 20  DKSATRVALGTWAIGGWMWGGTDDDASIKTIHRAIDLG----INIIDTAPAYG------- 68
           D   +RV LGT   G      ++ DA     HR +D      +N IDTA  Y        
Sbjct: 10  DLKVSRVCLGTMTFGTQ---NSEADA-----HRQLDFALARDVNFIDTAEMYSVPPNAES 61

Query: 69  RGHAEEVVGKAIKGQ-RDNLIIATKV-----GLDWTLTPDQSMRRNSSASRIKKEIEDSL 122
            G  E  +G  +K Q RD +++ATK+     G+ W    + +  R +    I+  IE SL
Sbjct: 62  YGKTETYIGTWLKRQARDRIVLATKISGPGRGMKWIRNGELAFNRKN----IRAAIEGSL 117

Query: 123 RRLGTDYIDLYQVHWPD---PL--------------VPIEETATILEALRKEGKIRSIGV 165
           RRL TDY+DLYQ+HWPD   PL              VP+ ET   L  L KEG++R IG+
Sbjct: 118 RRLQTDYVDLYQLHWPDRNTPLFGQYQFDPEKERDFVPLAETLEALAELVKEGRVRCIGL 177

Query: 166 SNYSVQQMDEFKKYAE------LAVSQSPYNLFEREIDKDILPYAKKNDLVVLGYGALCR 219
           SN +   + +F + AE      +   Q+ Y+L  R  +  +     + ++ +L Y  L  
Sbjct: 178 SNETPWGVMQFVRLAEERNLPRVVSVQNAYSLLNRTWETGLAEIGFRENVGLLAYSPLAF 237

Query: 220 GLLSGRMTADRAFTGDDLRKT-DPKF-QKPRFEHYLAAVEELKKLAKEHYNKSVLALAIR 277
           GLLSG+  AD   +G   R T  P F Q+    + L AV     LA+ H   S+  LA+ 
Sbjct: 238 GLLSGKYLADAQTSG---RVTLFPGFGQRYSKINVLPAVAAYADLARRH-GISLTRLALA 293

Query: 278 WMLEQG-PTLALWGACKPEQI-DGIDEVFGWQISDEDLKQIDAI 319
           ++  +      + GA   EQ+ + ID   G  + +E + +I+A+
Sbjct: 294 FVASRPFVDSTIIGATTMEQLHEDIDGCTG-TLPEEVVNEIEAL 336


Lambda     K      H
   0.317    0.136    0.407 

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: 262
Number of extensions: 15
Number of successful extensions: 3
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: 340
Length of database: 345
Length adjustment: 29
Effective length of query: 311
Effective length of database: 316
Effective search space:    98276
Effective search space used:    98276
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: 49 (23.5 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