GapMind for catabolism of small carbon sources

 

Alignments for a candidate for amaD in Azospirillum brasilense Sp245

Align glycine oxidase (EC 1.4.3.19) (characterized)
to candidate AZOBR_RS30970 AZOBR_RS30970 glycine oxidase

Query= BRENDA::O31616
         (369 letters)



>FitnessBrowser__azobra:AZOBR_RS30970
          Length = 374

 Score =  173 bits (439), Expect = 6e-48
 Identities = 123/368 (33%), Positives = 184/368 (50%), Gaps = 18/368 (4%)

Query: 9   VIGGGIIGSAIAYYLAKENKNTALFESGTMGGRTTSAAAGMLGAHAECEE-RDAFFDFAM 67
           VIG G+IG +IA+ LA       +F+ G  G   + AA GML A  E E   ++      
Sbjct: 3   VIGAGVIGLSIAWRLAAAGCRVEVFDRGAAGRGASHAAGGMLAACVETEPGEESLLPLTR 62

Query: 68  HSQRLYKGLGEELYALSGVDIRQHNGGMFKLAFSEEDVLQLRQMDDLDS-----VSWYSK 122
            SQ L+     EL A SG+ +     G   +A + +D  ++R + D  +     V W S 
Sbjct: 63  ASQDLWPAFAAELEAASGMAVDLRGEGTMVIALNADDAAKVRFLHDFQTRLGLPVEWLSG 122

Query: 123 EEVLEKEPYASGDIFGASFIQDDVHVEPYFVCKAYVKAAKMLGAEIFEHTPVLHVE-RDG 181
            EV  +EPY    + GA F   D  V+   V  A   AA   GA + E+  V  +E R G
Sbjct: 123 AEVRRREPYLQPGVAGALFCAGDHQVDNRKVATALHAAALRAGAVVHEYAEVSRIEVRGG 182

Query: 182 EALFIKTPSGDVWANHVVVASGVWSGMFFKQLGLNNAFLP----VKGECLSVWNDD-IPL 236
            A+ I+     V A+ VV+A+G WSG      GL+ A  P    VKG+ L +  D  +PL
Sbjct: 183 RAVGIQVEDRLVEADQVVLAAGAWSGWID---GLSPAVRPPVRPVKGQMLCLRMDARLPL 239

Query: 237 TK-TLYHDHCYIVPRKSGRLVVGATMKPGDWSETPDLGGLESVMKKAKTMLPAIQNMKVD 295
            +  ++    Y++PR  GRL+VGAT +   + +    GG  ++++ A   LP I  + ++
Sbjct: 240 LRHVVWTPGTYLIPRLDGRLLVGATTEERGFDDRLTAGGQFALLEGAWRALPGIAELPIE 299

Query: 296 RFWAGLRPGTKDGKPYIGRHPEDSRILFAAGHFRNGILLAPATGALISDLIMNKEVNQDW 355
             WAG RPGT+D  P +G   E   +++A GH RNGILL P T   ++ L++  E +   
Sbjct: 300 EAWAGFRPGTRDDAPILGL-SEVEGLVYATGHHRNGILLTPVTADSVARLVLTGEAD-PV 357

Query: 356 LHAFRIDR 363
           +  F +DR
Sbjct: 358 IRPFALDR 365


Lambda     K      H
   0.320    0.137    0.419 

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: 376
Number of extensions: 26
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: 369
Length of database: 374
Length adjustment: 30
Effective length of query: 339
Effective length of database: 344
Effective search space:   116616
Effective search space used:   116616
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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