GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Thermodesulforhabdus norvegica DSM 9990

Align acetyl-CoA C-acetyltransferase (EC 2.3.1.9) (characterized)
to candidate WP_093394716.1 BM091_RS07565 acetyl-CoA C-acetyltransferase

Query= BRENDA::P45359
         (392 letters)



>NCBI__GCF_900114975.1:WP_093394716.1
          Length = 392

 Score =  538 bits (1386), Expect = e-157
 Identities = 259/392 (66%), Positives = 330/392 (84%), Gaps = 1/392 (0%)

Query: 1   MKEVVIASAVRTAIGSYGKSLKDVPAVDLGATAIKEAVKKAGIKPEDVNEVILGNVLQAG 60
           M   VIA+AVRT +GS+GK+L  V AVDLG  A+KEA+++  + PE V+EVILGNVLQAG
Sbjct: 1   MTRAVIATAVRTPVGSFGKTLASVSAVDLGVVALKEALRRINLTPEMVDEVILGNVLQAG 60

Query: 61  LGQNPARQASFKAGLPVEIPAMTINKVCGSGLRTVSLAAQIIKAGDADVIIAGGMENMSR 120
            GQNPARQ + K+G+P E+PA T+NKVC SGL++V LAAQ I  G+A++++AGG+ENMS+
Sbjct: 61  QGQNPARQVAVKSGIPYEVPAFTVNKVCASGLKSVILAAQAIMVGEAEIVVAGGIENMSQ 120

Query: 121 APYLANNARWGYRMGNAKFVDEMITDGLWDAFNDYHMGITAENIAERWNISREEQDEFAL 180
           APY    ARWG+RMG+   VD MI DGLWD FN YHMGITAEN+AER+ ISREEQD FAL
Sbjct: 121 APYAVPKARWGHRMGDGSLVDLMIFDGLWDIFNGYHMGITAENVAERFGISREEQDRFAL 180

Query: 181 ASQKKAEEAIKSGQFKDEIVPVVIKGRKGETVV-DTDEHPRFGSTIEGLAKLKPAFKKDG 239
            SQ+KAE AIK G+F++EIVPV +  RKG+ ++ DTDEHPRFG+T+E L+KL PAFKK+G
Sbjct: 181 RSQQKAEAAIKEGKFREEIVPVTVPQRKGDPIIFDTDEHPRFGTTLEALSKLPPAFKKEG 240

Query: 240 TVTAGNASGLNDCAAVLVIMSAEKAKELGVKPLAKIVSYGSAGVDPAIMGYGPFYATKAA 299
           TVTAGNASG+ND AAV+++MS +KA ELG++P+A+IVSY SAGVDPAIMG GP  A++ A
Sbjct: 241 TVTAGNASGINDGAAVVIVMSEKKASELGIEPMARIVSYASAGVDPAIMGTGPIPASRKA 300

Query: 300 IEKAGWTVDELDLIESNEAFAAQSLAVAKDLKFDMNKVNVNGGAIALGHPIGASGARILV 359
           +EKAGW+VD+LDLIE+NEAFAAQ++AV +++ +D+ KVNVNGGAIALGHPIGASGARIL 
Sbjct: 301 LEKAGWSVDDLDLIEANEAFAAQAIAVNREMGWDVEKVNVNGGAIALGHPIGASGARILT 360

Query: 360 TLVHAMQKRDAKKGLATLCIGGGQGTAILLEK 391
           TL++ M++R A++GLATLCIGGGQG A+ +E+
Sbjct: 361 TLLYEMKRRSARRGLATLCIGGGQGCALTVER 392


Lambda     K      H
   0.315    0.132    0.375 

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: 538
Number of extensions: 14
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: 392
Length of database: 392
Length adjustment: 31
Effective length of query: 361
Effective length of database: 361
Effective search space:   130321
Effective search space used:   130321
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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