GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Bacteroides thetaiotaomicron VPI-5482

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate 350082 BT0554 glucosamine--fructose-6-phosphate aminotransferase (NCBI ptt file)

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



>FitnessBrowser__Btheta:350082
          Length = 614

 Score =  118 bits (296), Expect = 4e-31
 Identities = 94/312 (30%), Positives = 145/312 (46%), Gaps = 22/312 (7%)

Query: 65  VVVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQSGKS 124
           ++V C  G+S HA    ++LIE+   +       S     D   + E  + +AISQSG++
Sbjct: 302 IIVAC--GTSWHAGLIGKHLIESFCRIPVEVEYASEFRYRDPVID-EHDVVIAISQSGET 358

Query: 125 PDLLAAVKAAKAAGAHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAALVAVT 184
            D LAAV+ AK+ GA    + N + S +         +H GPE+ VA+TK++   +  +T
Sbjct: 359 ADTLAAVELAKSRGAFIYGICNAIGSSIPRATHTGSYIHVGPEIGVASTKAFTGQVTVLT 418

Query: 185 QLIAAW---------TEDAELTAALQDLPTALAAAWTLDWSLAVERLKT---ASNLYVLG 232
            L             T+   +   L  +P  +     L+  LA E  KT   A N   LG
Sbjct: 419 MLALTLAREKGTIDETQYLNIVRELNSIPGKMKEVLKLNDKLA-ELSKTFTYAHNFIYLG 477

Query: 233 RGVGFGVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRASVDE 292
           RG  + VALE ALK KE   +HAE + AAE+ HGP+AL+    P +V A  +     V  
Sbjct: 478 RGYSYPVALEGALKLKEISYIHAEGYPAAEMKHGPIALIDAEMPVVVIATQNGLYEKVLS 537

Query: 293 MAAGLRARGASVLIAGGGGD------APDALPTLASHPVLEPILMIQSFYRMANALSVAR 346
               ++AR   V+     GD      A  ++    +   L+P++       +A  ++V +
Sbjct: 538 NIQEIKARKGKVIAFVTKGDTVISKIADCSIELPETIECLDPLITTVPLQLLAYHIAVCK 597

Query: 347 GYDPDSPPHLNK 358
           G D D P +L K
Sbjct: 598 GMDVDQPRNLAK 609


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: 329
Number of extensions: 12
Number of successful extensions: 4
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: 614
Length adjustment: 33
Effective length of query: 330
Effective length of database: 581
Effective search space:   191730
Effective search space used:   191730
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 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