GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Beijerinckia indica ATCC 9039

Align acetyl-CoA C-acetyltransferase [EC: 2.3.1.9] (characterized)
to candidate WP_012384743.1 BIND_RS08905 acetyl-CoA C-acyltransferase

Query= reanno::pseudo5_N2C3_1:AO356_21640
         (393 letters)



>NCBI__GCF_000019845.1:WP_012384743.1
          Length = 378

 Score =  277 bits (708), Expect = 4e-79
 Identities = 171/397 (43%), Positives = 231/397 (58%), Gaps = 27/397 (6%)

Query: 1   MQEVVIVAATRTAIG-SFQGSLAAIPAPELGAAVIRRLLEQTGLSGEQVDEVILGQVLTA 59
           M +VVI    R+    + +G LA +   +L A V++ L+++TG+  E +++++LG     
Sbjct: 1   MTKVVIAGYIRSPFTLAKKGELATVRPDDLAAQVVKGLIKKTGIPAEDIEDLLLGCAFPE 60

Query: 60  GS-GQNPARQASILAGLPHAVPALTLNKVCGSGLKALHLGAQAIRCGDAEVIIAGGMENM 118
           G  G N AR  S LAGLP +V A T+N+ CGS +  +H+ A AI+       IA G+E+M
Sbjct: 61  GEQGFNVARLVSFLAGLPLSVGASTVNRFCGSSMTTVHMAAGAIQMNAGNAFIAAGVESM 120

Query: 119 SLAPYV----LPAARTGLRMGHAKMIDSMITDGLWDAFNDYHMGITAENLVDKYGISREE 174
           S  P +    LP       M  A M                 MG TAEN+  K+ ISR+E
Sbjct: 121 SRVPMMGFNPLPNPELAATMPGAYM----------------GMGDTAENVAAKWTISRKE 164

Query: 175 QDAFAAASQQKAVAAIEGGRFADEITPILIPQRKGDPVAFATDEQPRAGTTAESLGKLKP 234
           Q+ FA  S Q+A AA + GR   EI PI    RKG      TD   R  TT E L +LKP
Sbjct: 165 QEEFALRSHQRATAAQKEGRLTGEIIPIT--GRKG---TITTDGCIRPDTTLEGLAELKP 219

Query: 235 AFKKDGSVTAGNASSLNDGAAAVILMSAEKAKALGLPVLAKISAYANAGVDPAIMGIGPV 294
           AF  +G VTAG +S L DGAAAV++ S + AK   L VLA + A A +G  P IMGIGPV
Sbjct: 220 AFSANGVVTAGTSSPLTDGAAAVLVCSEDYAKHHHLDVLASVKAIAVSGCSPEIMGIGPV 279

Query: 295 SATRRCLDKAGWSLEQLDLIEANEAFAAQSLAVARELKWDMDKVNVNGGAIALGHPIGAS 354
           +A+R+ L +AG    Q+D++E NEAFA+QS+A  REL    D+VN++GGAIALGHP+GA+
Sbjct: 280 AASRKALARAGLEAGQIDIVELNEAFASQSIACMRELNLSPDRVNIDGGAIALGHPLGAT 339

Query: 355 GCRVLVSLLHEMIKRDAKKGLATLCIGGGQGVALALE 391
           G R++      + +   K  LAT CIGGGQG+A  LE
Sbjct: 340 GARIVGKAASLLKREKGKYALATQCIGGGQGIATVLE 376


Lambda     K      H
   0.317    0.133    0.376 

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: 364
Number of extensions: 11
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: 393
Length of database: 378
Length adjustment: 30
Effective length of query: 363
Effective length of database: 348
Effective search space:   126324
Effective search space used:   126324
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.

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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