GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Marinobacter adhaerens HP15

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate GFF4361 HP15_p187g69 glucosamine--fructose-6-phosphate aminotransferase, isomerizing

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



>FitnessBrowser__Marino:GFF4361
          Length = 613

 Score =  133 bits (334), Expect = 1e-35
 Identities = 101/315 (32%), Positives = 158/315 (50%), Gaps = 27/315 (8%)

Query: 66  VVTCARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQSGKSP 125
           V+  A G+S +A   ARY +E  A +  S    S      + PN E  L + ISQSG++ 
Sbjct: 299 VLILACGTSSYAGMVARYWVEAIASIPCSVEIASEYRYRQSVPN-ERQLIVVISQSGETA 357

Query: 126 DLLAAVKAAKAAG-AHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSY---IAALV 181
           D +AA++ AK+ G  H +A+ NV +S +   A       AGPE+ VA+TK++   +A L 
Sbjct: 358 DTIAALEHAKSLGHRHTLAICNVPESAIVRQAALRFITRAGPEIGVASTKAFTTQLATLF 417

Query: 182 AVTQLIAAW------TEDAELTAALQDLPTALAAAWTLDWSLA--VERLKTASNLYVLGR 233
            +T L+A        +++      ++ LP A+    +L+ S+    +R     +   LGR
Sbjct: 418 LLTLLLAKARGTLDASDEQRYLGEIRHLPVAVEKVLSLEPSIRKLAQRFSQKRHALFLGR 477

Query: 234 GVGFGVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRASVDEM 293
           G  + +ALE ALK KE   +HAEA+ A E+ HGP+ALV D  P +V A ND+    +   
Sbjct: 478 GRHYPIALEGALKLKEISYIHAEAYPAGELKHGPLALVDDDMPVVVVAPNDQLLEKLKAN 537

Query: 294 AAGLRARGASVLIAGGGGDAPDALPTLAS----------HPVLEPILMIQSFYRMANALS 343
              +RARG  + +   G    D   T AS          +  L P+L + +   +A  ++
Sbjct: 538 MEEVRARGGELYVFADG----DTRVTSASGLHVLRMPEHYGELSPVLHVVALQLLAYHVA 593

Query: 344 VARGYDPDSPPHLNK 358
           + +G D D P +L K
Sbjct: 594 LVKGTDVDKPRNLAK 608


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: 387
Number of extensions: 14
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 363
Length of database: 613
Length adjustment: 33
Effective length of query: 330
Effective length of database: 580
Effective search space:   191400
Effective search space used:   191400
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