GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Pseudomonas benzenivorans DSM 8628

Align Acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_090447771.1 BLS63_RS21120 acetyl-CoA C-acyltransferase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2411
         (393 letters)



>NCBI__GCF_900100495.1:WP_090447771.1
          Length = 394

 Score =  594 bits (1531), Expect = e-174
 Identities = 301/394 (76%), Positives = 340/394 (86%), Gaps = 1/394 (0%)

Query: 1   MNTPEIYVVSAARTAIGTFGGSLKDVPLADLATTAVKAALERAAVDPALVGHLVMGNVIP 60
           M  PE+Y+VSA RTAIG+FGG+LKD P  +LATTAV AAL+R+      VGH+VMGNVIP
Sbjct: 1   MPNPEVYIVSAVRTAIGSFGGTLKDTPPCELATTAVSAALQRSGCAAERVGHVVMGNVIP 60

Query: 61  TETRDAYISRVAAMNAGIPKETPAYNVNRLCGSGLQAIINAAQTLMLGDADIVVGAGAES 120
           TETRDAYISRVAAMNAGIPKE PA+NVNRLCGSGLQAI++AAQ+L+LGD +I +GAGAES
Sbjct: 61  TETRDAYISRVAAMNAGIPKEVPAFNVNRLCGSGLQAIVSAAQSLLLGDCEIAIGAGAES 120

Query: 121 MSRGPYLMPAARWGSRMGNAQVIDYMLGILHDPFHGIHMGITAENVAARNGITREMQDAL 180
           MSRGPYL+P ARWG RMG+ Q +DYMLGILHDPF  +HMGITAEN+A  +GI+R  QDAL
Sbjct: 121 MSRGPYLLPGARWGGRMGDMQAVDYMLGILHDPFQRMHMGITAENIAELHGISRADQDAL 180

Query: 181 AFEDQQRAAHAIANGYFSEQIATVEIQDRKGVKLFSVDEHPRA-TSLEQLAAMKPAFKKD 239
           A   QQRAA AIA G F+ QI  VEI+ RKG +LF VDEH R  TSLEQLA M+ AFK+ 
Sbjct: 181 ALVSQQRAARAIAEGRFAGQIVPVEIKSRKGTQLFEVDEHVRGDTSLEQLAGMRTAFKQG 240

Query: 240 GSVTAGNASGLNDGAAALVMASGNAVQANNLKPLARLVSYAHAGVEPEFMGLGPIPATRL 299
           G+VTAGNASGLNDGAAA+V+A+G AVQA+NL+PLARLVSYAHAGVEPE MGLGPIPATRL
Sbjct: 241 GTVTAGNASGLNDGAAAVVLATGAAVQADNLRPLARLVSYAHAGVEPELMGLGPIPATRL 300

Query: 300 ALKRAGLTVADLDVIEANIAFAAQACAVSQELDLDPAKVNPNGSGIALGHPVGATGAIIA 359
           AL+RAGL V+DLDVIE+N AFAAQACAV++ LD DPAKVNPNGSGI+LGHPVGATGAII 
Sbjct: 301 ALQRAGLKVSDLDVIESNEAFAAQACAVARALDFDPAKVNPNGSGISLGHPVGATGAIIV 360

Query: 360 TKAIHELHRTGGRYALVTMCIGGGQGIAAIFERV 393
           TKAIHEL RT GRYAL TMCIGGGQGIAAIFERV
Sbjct: 361 TKAIHELQRTQGRYALATMCIGGGQGIAAIFERV 394


Lambda     K      H
   0.318    0.133    0.378 

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: 548
Number of extensions: 16
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: 393
Length of database: 394
Length adjustment: 31
Effective length of query: 362
Effective length of database: 363
Effective search space:   131406
Effective search space used:   131406
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