GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Caulobacter crescentus NA1000

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate CCNA_00569 CCNA_00569 glucosamine-6-phosphate deaminase

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



>FitnessBrowser__Caulo:CCNA_00569
          Length = 358

 Score =  560 bits (1443), Expect = e-164
 Identities = 297/363 (81%), Positives = 314/363 (86%), Gaps = 5/363 (1%)

Query: 1   MEATVLTRHETPAPTGASPPSLAPASTHMFREAGEAARVAAVQLTANAPKIQALAQRLRA 60
           MEATVLTR     P GA+P  L+P  T MF EAGE A V    L ANA ++ ALA+RLRA
Sbjct: 1   MEATVLTR-----PEGAAPARLSPEDTRMFLEAGEGAAVVRTLLAANAERVAALAERLRA 55

Query: 61  NPPRVVVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQ 120
           +PPRVVVTCARGSSDHAATFARYLIETKAGVLTSSAG SVSSVYDASPNLEGAL LA+SQ
Sbjct: 56  HPPRVVVTCARGSSDHAATFARYLIETKAGVLTSSAGLSVSSVYDASPNLEGALCLAVSQ 115

Query: 121 SGKSPDLLAAVKAAKAAGAHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAAL 180
           SGKSPDLLA+VKAAKAAGAHAVA VNV DSPLAALAD VIPLHAGPELSVAATKSYIAAL
Sbjct: 116 SGKSPDLLASVKAAKAAGAHAVAFVNVEDSPLAALADVVIPLHAGPELSVAATKSYIAAL 175

Query: 181 VAVTQLIAAWTEDAELTAALQDLPTALAAAWTLDWSLAVERLKTASNLYVLGRGVGFGVA 240
            A+TQLIAAWT+D  LTAAL+ LP  L AAW LDWS AVE L+ A NLYVLGRGVGFGVA
Sbjct: 176 AAITQLIAAWTQDEALTAALEGLPLQLEAAWNLDWSSAVEGLRHAINLYVLGRGVGFGVA 235

Query: 241 LEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRASVDEMAAGLRAR 300
           LEAALKFKETCGLHAEAFSAAEVLHGPMALVK+GFPALVFAQNDESR SV EMA GLR R
Sbjct: 236 LEAALKFKETCGLHAEAFSAAEVLHGPMALVKEGFPALVFAQNDESRESVVEMAQGLRQR 295

Query: 301 GASVLIAGGGGDAPDALPTLASHPVLEPILMIQSFYRMANALSVARGYDPDSPPHLNKVT 360
           GASVL+A  G DAP  LPT  SHPVLEPILM+QSFYRMANALSVARGY+PDSPPHLNKVT
Sbjct: 296 GASVLMAAPGDDAPGGLPTPLSHPVLEPILMVQSFYRMANALSVARGYNPDSPPHLNKVT 355

Query: 361 ETI 363
           ET+
Sbjct: 356 ETL 358


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: 502
Number of extensions: 10
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: 358
Length adjustment: 29
Effective length of query: 334
Effective length of database: 329
Effective search space:   109886
Effective search space used:   109886
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: 49 (23.5 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