GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Sulfuritalea hydrogenivorans DSM 22779

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_041096967.1 SUTH_RS02960 glutamine--fructose-6-phosphate transaminase (isomerizing)

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



>NCBI__GCF_000828635.1:WP_041096967.1
          Length = 609

 Score =  132 bits (332), Expect = 2e-35
 Identities = 102/314 (32%), Positives = 161/314 (51%), Gaps = 26/314 (8%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVASLYDAPVAPGNG--LCLAISQSGK 108
           V+  A G+S HA   A+Y IE L G+     ++ +AS Y   V+  N   L +AISQSG+
Sbjct: 295 VLILACGTSFHAGLVARYWIEQLAGI---GCSVEIASEYRYRVSVPNPEQLVVAISQSGE 351

Query: 109 SPDLLATVEHQRKAG-AFVVAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYICSLAA 167
           + D LA+++H +  G    +A+ N  +S +     +    +AGPE  VA+TK++   LAA
Sbjct: 352 TADTLASIKHAKALGMGRTLAICNVPESAIVRECALRFLTRAGPEIGVASTKAFTTQLAA 411

Query: 168 IAALVAAWAQDEALET---------AVADLPAQLERAFALDWSAAVTALTGAS---GLFV 215
           +  L    A+               A+  LP  +++  AL+    V A   A     LF 
Sbjct: 412 LFLLAVTLAKQNGRLAPEHEAGHLKALRHLPVAVQKVLALEPDIKVWATRFADKHHALF- 470

Query: 216 LGRGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRAGESV 275
           LGRG+ Y IA E ALK KE   +HAE + A E++HGP+A+V +   V++ A +D   E +
Sbjct: 471 LGRGHHYPIALEGALKLKEISYIHAEGYPAGELKHGPLALVDKDMPVISIAPNDALLEKL 530

Query: 276 RETVAEFRSRGAEVLL---ADPAA-RQAGLPAIAA---HPAIEPILIVQSFYKMANALAL 328
           +  + E  +RG E+ +   AD A   +AG+  +     +  + P+L V +   ++   AL
Sbjct: 531 KSNLKEVAARGGELYVFADADSAVDEEAGVHVLRLPEHYGLLSPVLHVIALQLLSYHAAL 590

Query: 329 ARGCDPDSPPHLNK 342
            +G D D P +L K
Sbjct: 591 VKGTDVDKPRNLAK 604


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: 424
Number of extensions: 19
Number of successful extensions: 5
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: 609
Length adjustment: 33
Effective length of query: 314
Effective length of database: 576
Effective search space:   180864
Effective search space used:   180864
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 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