GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Oleispira antarctica

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_046010654.1 OLEAN_RS19710 glutamine--fructose-6-phosphate transaminase (isomerizing)

Query= reanno::Korea:Ga0059261_1644
         (347 letters)



>NCBI__GCF_000967895.1:WP_046010654.1
          Length = 613

 Score =  132 bits (332), Expect = 2e-35
 Identities = 104/319 (32%), Positives = 157/319 (49%), Gaps = 39/319 (12%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVAS--LYDAPVAPGNGLCLAISQSGK 108
           ++ C  G+S H+    KY IE   G+P     + VAS   Y   V   N L + ISQSG+
Sbjct: 302 IIAC--GTSYHSGMVTKYWIEKYAGIP---CQVEVASEFRYRHTVIAKNTLLITISQSGE 356

Query: 109 SPDLLATVEHQRKAGAFV-VAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYICSLAA 167
           + D LA +   ++ G    + + N   S L   +D+ +   AGPE  VA+TK++   L A
Sbjct: 357 TADTLAALRKAKEQGLLASMTVCNVPGSSLVRESDLCLMTNAGPEIGVASTKAFTTQLTA 416

Query: 168 IAALVAAWAQ----DEALET----AVADLPAQLERAFALDWSAAVTALTGASGLFV---- 215
           +  L  A A+     EA ET    A+  LP  +E+A ALD       +   S LF     
Sbjct: 417 LLLLTVALAKRNGMSEAAETEIVTALHQLPGLVEKALALD-----PVIEKISQLFADKHH 471

Query: 216 ---LGRGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRAG 272
              LGRG  Y IAQE ALK KE   +HAE++ A E++HGP+A+V E   ++A A  +   
Sbjct: 472 SLFLGRGPMYPIAQEGALKLKEISYIHAEAYPAGELKHGPLALVDEDMPIIAVAPKNDLL 531

Query: 273 ESVRETVAEFRSRGAEV-LLADPAA--------RQAGLPAIAAHPAIEPILIVQSFYKMA 323
           E +   + E ++RG E+ + AD +             LP +     +EPI+ +     ++
Sbjct: 532 EKLVSNLEEVKARGGELFVFADESVNLYDLDDQHLVSLPTVPC--CLEPIVYIIPLQLLS 589

Query: 324 NALALARGCDPDSPPHLNK 342
             +A+ +G D D P +L K
Sbjct: 590 YHVAVLKGTDVDQPRNLAK 608


Lambda     K      H
   0.317    0.128    0.360 

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: 348
Number of extensions: 18
Number of successful extensions: 6
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: 347
Length of database: 613
Length adjustment: 33
Effective length of query: 314
Effective length of database: 580
Effective search space:   182120
Effective search space used:   182120
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 (21.7 bits)
S2: 51 (24.3 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