GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Sinorhizobium meliloti 1021

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate SMa1351 SMa1351 enolase

Query= BRENDA::A9CEQ8
         (378 letters)



>FitnessBrowser__Smeli:SMa1351
          Length = 402

 Score =  180 bits (456), Expect = 7e-50
 Identities = 120/390 (30%), Positives = 184/390 (47%), Gaps = 44/390 (11%)

Query: 3   ITAVRTHLLEHRLDTPFESASMRFDRRAHVLVEIECDDGTVGWGE---CLGPARPNAAVV 59
           I A R H  +    T F++A +R          IE DDG VGWGE     G A     +V
Sbjct: 28  IEANRQHQSDFGRLTTFDAAILR----------IETDDGIVGWGEGKNAAGSAGSYGTLV 77

Query: 60  QAYS----GWLIGQDPRQTEKIWAVLYNALRDQ------------GQRGLSLTALSGIDI 103
              +      L+G+D      +W +LYN +R +             +RGLS+ A+S +DI
Sbjct: 78  HMLNYEVGPRLVGRDAADISAVWEMLYNGVRHERAAMSGHAMPELSRRGLSIAAISAVDI 137

Query: 104 ALWDIKGKHYGASISMLLGGRWRESVRAYATGSFKRDNVDRVSDNASEMAERRAEGFHAC 163
           ALWDI GK  G  +  LLGGR  + + AYA+G +  ++ +++           + GF A 
Sbjct: 138 ALWDILGKSLGVPVWKLLGGRKADRLPAYASGGW--ESAEKIGGQLQSYLA--SGGFKAV 193

Query: 164 KIKIGF---GVEEDLRVIAAVREAIGPDMRLMIDANHGYTVTEAITLGDRAAGFGIDWFE 220
           K+++G            + A R+A+GP + +M+DA+  YTV +A           + WFE
Sbjct: 194 KMRVGAMDGAPYVSAARVRAARKALGPSVDIMVDAHGTYTVADAKRFIQLVRDCDLAWFE 253

Query: 221 EPVVPEQLDAYARVRAGQPIPVAGGETWHGRYGMWQALSAGAVDILQPDLCGCGGFSEIQ 280
           EPV+ +     A VRA   +P+A GE+   R+         + DI QPD   CGG +E  
Sbjct: 254 EPVIADDKAGMAEVRAAGNVPIATGESEATRFAFRDLAVLRSADIFQPDPAFCGGITEAM 313

Query: 281 KIATLATLHGVRIVPHVWGTGVQIAAALQFMAAMTPDPVRVNPIEPIMEFDRTHNPFRQA 340
           +I  +A+   +R+ PH+W       + L   AA        +P   ++E+    NP    
Sbjct: 314 RIGAIASAFNLRLAPHLWAGAPCFFSGLHICAA--------SPASFVVEYSVGANPMIHD 365

Query: 341 VLREPLEAVNGVVTIPDGPGLGIEINRDAL 370
           ++ E +   +G++ IPD PGLG  IN   L
Sbjct: 366 LVEETVAVKDGMLEIPDKPGLGFTINERVL 395


Lambda     K      H
   0.321    0.138    0.431 

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: 429
Number of extensions: 16
Number of successful extensions: 5
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: 378
Length of database: 402
Length adjustment: 30
Effective length of query: 348
Effective length of database: 372
Effective search space:   129456
Effective search space used:   129456
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 (21.9 bits)
S2: 50 (23.9 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