GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Pseudomonas benzenivorans DSM 8628

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_090446180.1 BLS63_RS15310 glutamine--fructose-6-phosphate transaminase (isomerizing)

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



>NCBI__GCF_900100495.1:WP_090446180.1
          Length = 620

 Score =  132 bits (331), Expect = 3e-35
 Identities = 108/323 (33%), Positives = 164/323 (50%), Gaps = 41/323 (12%)

Query: 51  VVTCARGSSDHAATYAKYLIETLTGVPTASAALSVAS--LYDAPVAPGNGLCLAISQSGK 108
           +V C  G+S HA   A+Y +E L G+P     + VAS   Y   V   + L ++ISQSG+
Sbjct: 303 IVAC--GTSYHAGMVARYWLEELAGIP---CQVEVASEFRYRKVVVQPDSLFISISQSGE 357

Query: 109 SPDLLATVEHQRKA----GAFV--VAMVNAEDSPLAALADIVIPLKAGPERSVAATKSYI 162
           + D LA + + +      G ++  +A+ N   S L   +D+ +  +AGPE  VA+TK++ 
Sbjct: 358 TADTLAALRNAKALPAGQGGYLASLAICNVGISSLVRESDLCLLTQAGPEIGVASTKAFT 417

Query: 163 CSLAAIAALVAAWAQ-----DEALETAVAD----LPAQLERAFALDWSAAVTALTGAS-- 211
             L A+  L  +  Q     D ALE  + D    LP +L  A A+D      A   A   
Sbjct: 418 TQLVALMLLTLSIGQVRGSLDPALEAELVDELRRLPTRLGEALAMDAVVEKIAELFAEKH 477

Query: 212 -GLFVLGRGYGYGIAQEAALKFKETCALHAESFSAAEVRHGPMAIVGEAFHVLAFASSDR 270
             LF LGRG  Y +A E ALK KE   +HAE++ A E++HGP+A+V     V+  A ++ 
Sbjct: 478 HALF-LGRGAQYPVAMEGALKLKEISYIHAEAYPAGELKHGPLALVDSDMPVVTVAPNNE 536

Query: 271 AGESVRETVAEFRSRGAEVLLADPAARQAGL-----------PAIAAHPAIEPILIVQSF 319
             E ++  + E R+RG E+++   A +QAGL           P I  H A+ PIL     
Sbjct: 537 LLEKLKSNLQEVRARGGELIVF--ADQQAGLSNGEGTHVVNMPHI--HDALAPILYTLPL 592

Query: 320 YKMANALALARGCDPDSPPHLNK 342
             ++  +A+ +G D D P +L K
Sbjct: 593 QLLSYYVAVLKGTDVDQPRNLAK 615


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: 405
Number of extensions: 21
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: 620
Length adjustment: 33
Effective length of query: 314
Effective length of database: 587
Effective search space:   184318
Effective search space used:   184318
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