GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Brucella inopinata BO1

Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_008510811.1 BIBO1_RS18185 acetyl-CoA C-acetyltransferase

Query= BRENDA::Q0KAI3
         (392 letters)



>NCBI__GCF_000182725.1:WP_008510811.1
          Length = 402

 Score =  263 bits (671), Expect = 9e-75
 Identities = 158/406 (38%), Positives = 228/406 (56%), Gaps = 18/406 (4%)

Query: 1   MQQAVIVDAIRSPMGRSKPGSAFTELHATELLAQVIKGLVERNKLDPGLVDDVITGCVTQ 60
           M +A I D +R+P GR K   +  E+ A  L A+V++ L +RN +D   VDD+I GCV  
Sbjct: 1   MAEAYIYDHVRTPRGRGKKDGSLHEVPAVRLGAKVLESLRDRNGIDTAKVDDIIFGCVDP 60

Query: 61  AGEQSAGPGRVAWLAAGFPDHVPATTIDRKCGSSQQAVHFAAQGIMAGAYDIVIACGIES 120
            GE  A   R A   AG+    P   I R C S   A++ AA  +  G+ D+VIA G+ES
Sbjct: 61  VGEAGAVIPRSAAFEAGYDFKAPGIQISRFCASGLDAINLAAAKVAFGSDDLVIAGGVES 120

Query: 121 MSRVPMGSARIGQNPYGPSMEARYAPG-LVSQGVAAELVAAKYELSRHDMDSYSARSHEL 179
           MSRV MG +  G     PS+     PG  + QGV+A+L+A KY  SR D+D+Y+  S + 
Sbjct: 121 MSRVGMGMSG-GAWYMDPSVGF---PGYFMPQGVSADLIATKYGFSRDDVDAYAVESQKR 176

Query: 180 AATARESGAFRREILGISTPNGL--VEQDETIRPGTSVEKLGTLQASFRNDELSARFPQI 237
           AA + E G F+  ++ I   NGL  +++DE +RPGT ++ LG L  SF        F  +
Sbjct: 177 AANSWEKGCFKNSVITIKDQNGLTILDRDEHMRPGTDMQALGQLNPSFVMPGEMGGFNAV 236

Query: 238 GWNVT-----------AGNASQISDGASAMLLMSESMAQRLGLKPRARFVAFDVCGDDPV 286
           G               AGN+S I DGA+ +L+ S    +   +KPRAR  AF   G +P 
Sbjct: 237 GIQAHPEIETVNHVHHAGNSSGIVDGAAGVLVGSRKAGKAFDIKPRARIRAFANIGSEPA 296

Query: 287 MMLTAPIPASQRAIKKSGLKLDQIDHYEINEAFACVPLAWQRALGADPARLNPRGGAIAL 346
           +MLT P+  +++ +K++ +K+  ID +E+NEAFA V L + +A      ++N  GGAIA+
Sbjct: 297 LMLTGPVDVTEKLLKQAKMKISDIDLFELNEAFAAVVLRYMQAFDIPHDKINVNGGAIAM 356

Query: 347 GHPLGASGVRLMTTMLHALEDSGQRYGLQSMCEAGGMANATIIERL 392
           GHPLGA+G  ++ T+L  LE       L ++C   GM  ATIIER+
Sbjct: 357 GHPLGATGAMILGTVLDELERRNLNTALVTLCIGAGMGTATIIERV 402


Lambda     K      H
   0.318    0.132    0.384 

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: 435
Number of extensions: 16
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: 392
Length of database: 402
Length adjustment: 31
Effective length of query: 361
Effective length of database: 371
Effective search space:   133931
Effective search space used:   133931
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 (21.7 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