GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdhA in Halomonas xinjiangensis TRM 0175

Align xylitol 2-dehydrogenase (EC 1.1.1.9) (characterized)
to candidate WP_043531534.1 JH15_RS14530 Zn-dependent oxidoreductase

Query= reanno::BFirm:BPHYT_RS16050
         (365 letters)



>NCBI__GCF_000759345.1:WP_043531534.1
          Length = 340

 Score =  177 bits (450), Expect = 3e-49
 Identities = 114/338 (33%), Positives = 177/338 (52%), Gaps = 19/338 (5%)

Query: 13  MTAIVCHAPKDYRVEQVSKPRAGAHELVIRIAACGICASDCKCHSGAKMFWGGPSPWVKA 72
           M A    AP DY + ++  P+A   E+++R+A  GIC SD     G   F       V+ 
Sbjct: 1   MQAFQVSAPLDYTITEIETPQAAPGEVLVRVAYAGICGSDMHIIHGENAF-------VRF 53

Query: 73  PVIPGHEFFGFVEEIGEGAADHFGVKMGDRVIAEQIVPCGKCRYCKSGQYWMCEVHNIFG 132
           P I GHEF G VE +GEG     G+ +GDRV  + ++ CG+C  C+ G+  +C    + G
Sbjct: 54  PRITGHEFAGTVEALGEGVE---GLSIGDRVCIDPVINCGECYPCRIGRPNVCTALEVIG 110

Query: 133 FQREVADGGMAEYMRIPPTAIVHKIPDGISLEDAAIIEPLACAIHTVNRGEVQLDDVVVI 192
             R   +GG  E + +P  A  H++PD + L+ AA++EP   A + ++R +    D ++I
Sbjct: 111 VHR---NGGFEEQVNVP-AANAHRLPDNVGLDAAALVEPYTIAANVLDRMQPVAGDRLLI 166

Query: 193 AGAGPLGLMMTQIAHLKTPKKLVVIDLVEERLALAREYGADVTINPKQDDALAIIHSLTD 252
            GAG +GL + Q+A     + + V D+++ERLA ARE GA  T N +QDD  A +  LT 
Sbjct: 167 FGAGVIGLTILQMARALGLEDITVTDVIDERLATARELGASRTFNGRQDDIEAAMQELTG 226

Query: 253 GYGCDVYIETTGAPIGVNQGMDLIRKLGR--FVEFSVFGADTTLDWSVIGDRKELDVRGA 310
           G G  +  +    P  + Q + +    GR   + F+   +D  +   VI  +KEL + G+
Sbjct: 227 GEGIPLIADAACVPALLPQILRIASPAGRVGLLGFNPNPSD-LVQLEVI--KKELTLVGS 283

Query: 311 HLGPYCYPIAIDLLARGLVTSKGIVTHGFSLEEWDEAI 348
            L    +P  IDL+A G + +  +V+H   L E   AI
Sbjct: 284 RLNNRKFPEVIDLMASGRLDALALVSHRLPLAEMPGAI 321


Lambda     K      H
   0.322    0.140    0.435 

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: 283
Number of extensions: 23
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: 365
Length of database: 340
Length adjustment: 29
Effective length of query: 336
Effective length of database: 311
Effective search space:   104496
Effective search space used:   104496
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 (21.9 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