GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Aquimarina longa SW024

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_062053929.1 N456_RS03480 glutamine--fructose-6-phosphate transaminase (isomerizing)

Query= reanno::Caulo:CCNA_00453
         (363 letters)



>NCBI__GCF_001401755.1:WP_062053929.1
          Length = 615

 Score =  111 bits (278), Expect = 5e-29
 Identities = 91/317 (28%), Positives = 143/317 (45%), Gaps = 23/317 (7%)

Query: 61  NPPRVVVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQ 120
           N  R+++  A G+S HA   A Y+ E    +       S     +   + +  + +AISQ
Sbjct: 298 NAKRIIII-ACGTSWHAGLVAEYIFEELVRIPVEVEYASEFRYRNPVIHQDDVV-IAISQ 355

Query: 121 SGKSPDLLAAVKAAKAAGAHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAAL 180
           SG++ D +AA+K AK  GA    + NVV S ++         HAGPE+ VA+TK++   +
Sbjct: 356 SGETADTMAAIKLAKENGAFVFGVCNVVGSSISRETHAGAYTHAGPEIGVASTKAFTTQI 415

Query: 181 VAVTQLIAAWTE------DAELTAALQDLP-----TALAAAWTLDWSLAVERLKTASNLY 229
             ++ +     E      +++    LQ+L        LA           E  K A N  
Sbjct: 416 TVLSLIALKLAERKGTISNSDFHYYLQELERIPEKVKLALESNDHIKFIAETYKDAKNCL 475

Query: 230 VLGRGVGFGVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRAS 289
            LGRG  F VALE ALK KE   +HAE + AAE+ HGP+AL+ +  P +V A        
Sbjct: 476 YLGRGFNFPVALEGALKLKEISYIHAEGYPAAEMKHGPIALIDEQMPVIVIATKKGHYDK 535

Query: 290 VDEMAAGLRARGASVLIAGGGGDAPDALPTLASHPV--------LEPILMIQSFYRMANA 341
           V      +++R   ++     GD  + +  LA H +        L P+L       ++  
Sbjct: 536 VVSNIQEIKSRKGKIIAIVTEGD--ETVKNLADHVIEVPETEEFLTPLLTTIPLQLLSYH 593

Query: 342 LSVARGYDPDSPPHLNK 358
           ++V    + D P +L K
Sbjct: 594 IAVMLDKNVDQPRNLAK 610


Lambda     K      H
   0.315    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: 353
Number of extensions: 16
Number of successful extensions: 2
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: 363
Length of database: 615
Length adjustment: 33
Effective length of query: 330
Effective length of database: 582
Effective search space:   192060
Effective search space used:   192060
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 (21.6 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