GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Sphingomonas koreensis DSMZ 15582

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate Ga0059261_3665 Ga0059261_3665 glucosamine--fructose-6-phosphate aminotransferase (isomerizing)

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



>FitnessBrowser__Korea:Ga0059261_3665
          Length = 607

 Score =  162 bits (411), Expect = 2e-44
 Identities = 112/313 (35%), Positives = 162/313 (51%), Gaps = 26/313 (8%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVAS--LYDAPVAPGNGLCLAISQSGK 108
           +V C  G+S +A   AKY  E    V   +  + VAS   Y APV    GL + ISQSG+
Sbjct: 295 IVAC--GTSYYAGMVAKYWFEQFARV---AVDIDVASEFRYRAPVMEDGGLMIVISQSGE 349

Query: 109 SPDLLATVEHQRKAGAFVVAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYICSLAAI 168
           + D LA + H +  G  + A+VN   S +A  AD+++P  AGPE  VA+TK++ C LA +
Sbjct: 350 TADTLAALRHAKAEGQTIAAVVNVPTSTMAREADLLLPTHAGPEIGVASTKAFTCQLAVL 409

Query: 169 AALVAAW---------AQDEALETAVADLPAQLERAFALDWS--AAVTALTGASGLFVLG 217
           AAL A           A+++ +   +A+ PA L  A A D +      A+ GA  +  LG
Sbjct: 410 AALAANLAKAKGRMDAAEEKEIVRHLAEAPAALNAALAYDEAIEGMAGAVAGARDVLYLG 469

Query: 218 RGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDRAGESVRE 277
           RG  Y +A E ALK KE   +HAE ++A E++HGP+A++ E   V+  A S    E    
Sbjct: 470 RGTDYPLALEGALKLKEISYIHAEGYAAGEMKHGPIALIDENVPVIVIAPSGPLFEKTVS 529

Query: 278 TVAEFRSRGAEVLLAD--PAARQAGLPAIA------AHPAIEPILIVQSFYKMANALALA 329
            + E ++RG +V+L         AG   IA       HP I PI+       +A  +A+A
Sbjct: 530 NMQEVQARGGKVVLISDYDGIAAAGDGCIATITMPKVHPLIAPIVYAVPVQLLAYHVAVA 589

Query: 330 RGCDPDSPPHLNK 342
           +G D D P +L K
Sbjct: 590 KGTDVDQPRNLAK 602


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: 432
Number of extensions: 26
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: 347
Length of database: 607
Length adjustment: 33
Effective length of query: 314
Effective length of database: 574
Effective search space:   180236
Effective search space used:   180236
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 17 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