GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nagB in Stenotrophomonas chelatiphaga DSM 21508

Align Glucosamine-6-phosphate deaminase [isomerizing], alternative (EC 3.5.99.6) (characterized)
to candidate WP_057508080.1 ABB28_RS07710 glutamine--fructose-6-phosphate transaminase (isomerizing)

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



>NCBI__GCF_001431535.1:WP_057508080.1
          Length = 612

 Score =  128 bits (322), Expect = 4e-34
 Identities = 99/307 (32%), Positives = 152/307 (49%), Gaps = 19/307 (6%)

Query: 70  ARGSSDHAATFARYLIETKAGVLTSSAGPSVSSVYDASPNLEGALYLAISQSGKSPDLLA 129
           A G+S +A   ARY IE+ AG L  +   +    Y A+      L + +SQSG++ D + 
Sbjct: 302 ACGTSYYAGMTARYWIESIAG-LPCNVEIASEYRYRAAYADPKHLVVTLSQSGETLDTME 360

Query: 130 AVKAAKAAG-AHAVALVNVVDSPLAALADEVIPLHAGPELSVAATKSYIAALVAVTQLIA 188
           A+K AK+ G  H +++ NV +S +   ++ V    AG E+ VA+TK++   L A+ QL  
Sbjct: 361 ALKYAKSLGHLHTLSICNVPESAIPRASELVCYTRAGAEIGVASTKAFTTQLAALFQLTV 420

Query: 189 AW---------TEDAELTAALQDLPTALAAAWTLDWSLAV--ERLKTASNLYVLGRGVGF 237
                      T +A+    L+ LP ++  A  ++  +A   ER    S+   LGRG+ +
Sbjct: 421 VLGKLHGRVDATREADYLEQLRFLPGSVQHALNMEPQIAAWAERFARKSSALFLGRGLHY 480

Query: 238 GVALEAALKFKETCGLHAEAFSAAEVLHGPMALVKDGFPALVFAQNDESRASVDEMAAGL 297
            +ALE ALK KE   +HAEA+ A E+ HGP+ALV +  P +V A ND     V      +
Sbjct: 481 PIALEGALKLKEITYIHAEAYPAGELKHGPLALVDEDMPVVVIAPNDSLLEKVKSNMQEV 540

Query: 298 RARGASVLIAGG------GGDAPDALPTLASHPVLEPILMIQSFYRMANALSVARGYDPD 351
           RARG  + +           +    + T     VL PI+       +A   ++ARG D D
Sbjct: 541 RARGGELFVFADQDSNFVESEGVHVIRTPRHAGVLSPIVHTIPVQLLAYHTALARGTDVD 600

Query: 352 SPPHLNK 358
            P +L K
Sbjct: 601 KPRNLAK 607


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: 395
Number of extensions: 17
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: 612
Length adjustment: 33
Effective length of query: 330
Effective length of database: 579
Effective search space:   191070
Effective search space used:   191070
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