GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bkdC in Hyphomicrobium sulfonivorans WDL6

Align Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial; Branched-chain alpha-keto acid dehydrogenase complex component E2; Dihydrolipoamide branched-chain transacylase E2; EC 2.3.1.168 (characterized)
to candidate WP_068463170.1 APY04_RS12525 2-oxo acid dehydrogenase subunit E2

Query= SwissProt::Q23571
         (448 letters)



>NCBI__GCF_001541235.1:WP_068463170.1
          Length = 343

 Score =  120 bits (300), Expect = 9e-32
 Identities = 97/326 (29%), Positives = 151/326 (46%), Gaps = 32/326 (9%)

Query: 148 TPAVRRIAIENKIKLAEVRGTGKDGRVLKEDVLKFLG--------------QVPADHTSG 193
           +P  RR+A +  + L  + G+G  GR++K D+ K L               Q P    S 
Sbjct: 20  SPLARRLAKDAALSLDAIAGSGPHGRIIKRDIEKALAGGAQSSASQSQAAQQAPDTTASR 79

Query: 194 STNIRTTHQA--PQPSSKSYEPLKEDVAVPIRG---------YTRAMVKTMTEALK-IPH 241
           +     T  A  PQP S S    +  +A+  +G           R + + +T A + IPH
Sbjct: 80  AMTPSATAAALKPQPPSPSGMSDESVLALYDKGSYEVQPHDKMRRVIAERLTLAKRTIPH 139

Query: 242 FGYNDEINVDSLVKYRAELKEFAKE---RHIKLSYMPFFIKAASLALLEYPSLNSTTDEK 298
           F  + +  +D L++ R  +   +     R  KLS   F IKA +LAL   P  N T  E 
Sbjct: 140 FYLSIDCRIDELMRARERMNASSPPEGPRAYKLSVNDFLIKALALALQHVPDANVTWTE- 198

Query: 299 MENVIHKASHNICLAMDTPGGLVVPNIKNCEQRSIFEIAQELNRLLEAGKKQQIKREDLI 358
            E ++     +I +A+   GGL  P I++ E +S+ EI+ E+  L E  +K+++   +  
Sbjct: 199 -EGMLRHKYSDIGVAVAVEGGLFTPVIRHAEMKSLSEISNEMRDLAERARKRRLAPHEYQ 257

Query: 359 DGTFSLSNIGNIGGTYASPVVFPPQVAIGAIGKIEKLPRFDKHDNVIPVNIMKVSWCADH 418
            GT S+SN+G  G      V+ PP   I A+G  ++ P     D+V    +M V+   DH
Sbjct: 258 GGTTSISNLGMYGIKNFDAVINPPHATILAVGAADRRP-VVVGDSVEVATVMDVTLSCDH 316

Query: 419 RVVDGATMARFSNRWKFYLEHPSAML 444
           R VDGA  A     +K ++E P  ML
Sbjct: 317 RAVDGAIGAELLRAFKAFVEDPVRML 342


Lambda     K      H
   0.316    0.132    0.377 

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: 291
Number of extensions: 17
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: 448
Length of database: 343
Length adjustment: 31
Effective length of query: 417
Effective length of database: 312
Effective search space:   130104
Effective search space used:   130104
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 Apr 09 2024. 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