GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pco in Brucella inopinata BO1

Align acyl-CoA oxidase (EC 1.3.3.6) (characterized)
to candidate WP_134789776.1 BIBO1_RS08430 acyl-CoA dehydrogenase

Query= BRENDA::Q96329
         (436 letters)



>NCBI__GCF_000182725.1:WP_134789776.1
          Length = 395

 Score =  224 bits (570), Expect = 5e-63
 Identities = 132/386 (34%), Positives = 207/386 (53%), Gaps = 6/386 (1%)

Query: 47  DYYHFNDLLTPEEQAIRKKVRECMEKEVAP-IMTEYWEKAEFP--FHITPKLGAMGVAGG 103
           D +   + LT +E+ IR   +      + P +   Y E+   P  F +  + G +GV   
Sbjct: 11  DPFLLEEQLTEDERMIRDSAKAFASDVLLPRVEKAYLEETTDPELFRLMGQAGLLGVT-- 68

Query: 104 SIKGYGCPGLSITANAIATAEIARVDASCSTFILVHSSLGMLTIALCGSEAQKEKYLPSL 163
             + YG    S  A  +   E+ RVD+   + + V SSL M  I   GS+ Q++KYLP L
Sbjct: 69  LPEDYGAANASYVAYGLVAREVERVDSGYRSMMSVQSSLVMYPIYAYGSDEQRKKYLPGL 128

Query: 164 AQLNTVACWALTEPDNGSDASGLGTTATKVEGGWKINGQKRWIGNSTFADLLIIFARNTT 223
                + C+ LTEPD GSD +G+ T A K++GG++++G K WI NS  AD+ +++A++  
Sbjct: 129 VSGELIGCFGLTEPDAGSDPAGMKTRAEKIDGGYRLSGSKMWISNSPIADVFVVWAKSAA 188

Query: 224 -TNQINGFIVKKDAPGLKATKIPNKIGLRMVQNGDILLQNVFVPDEDRLPGVNSFQDTSK 282
             N I GFI++K   GL A KI  K+ LR    G+I++  V VP++  LP V+  +    
Sbjct: 189 HDNAIRGFILEKGMKGLSAPKIGGKLSLRASITGEIVMDGVEVPEDAILPNVSGLKGPFG 248

Query: 283 VLAVSRVMVAWQPIGISMGIYDMCHRYLKERKQFGAPLAAFQLNQQKLVQMLGNVQAMFL 342
            L  +R  ++W  +G +   +    +Y  +RKQF  PLA  QL Q+KL  M   +     
Sbjct: 249 CLNRARYGISWGVLGAAEDCWFRARQYGLDRKQFNKPLAGTQLYQKKLADMQTEIALGLQ 308

Query: 343 MGWRLCKLYETGQMTPGQASLGKAWISSKARETASLGRELLGGNGILADFLVAKAFCDLE 402
              R+ +L++ G+M P   S+ K     KA + A   R++ GGNGI  ++ V +   +LE
Sbjct: 309 ASLRVGRLFDEGKMAPEMISIVKRNNCGKALDIARQARDMHGGNGIQIEYHVMRHAQNLE 368

Query: 403 PIYTYEGTYDINTLVTGREVTGIASF 428
            + TYEGT+D++ L+ GR  TGI +F
Sbjct: 369 TVNTYEGTHDVHALILGRAQTGIQAF 394


Lambda     K      H
   0.319    0.133    0.399 

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: 371
Number of extensions: 15
Number of successful extensions: 2
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: 436
Length of database: 395
Length adjustment: 31
Effective length of query: 405
Effective length of database: 364
Effective search space:   147420
Effective search space used:   147420
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 (21.7 bits)
S2: 50 (23.9 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