GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Methylobacterium sp. 4-46

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate WP_012333698.1 M446_RS18850 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-11693
         (386 letters)



>NCBI__GCF_000019365.1:WP_012333698.1
          Length = 376

 Score =  270 bits (690), Expect = 5e-77
 Identities = 156/371 (42%), Positives = 226/371 (60%), Gaps = 5/371 (1%)

Query: 12  LRRTVEEFAHDVVAPKIGDFYERHEFPYEIVREMGRMGLFGLPFPEEYGGMGGDYLALGI 71
           +R T   FA   + P   ++     FP E V  +G +G  G+  PE YGG   D+++  +
Sbjct: 9   IRDTARSFAQARLRPFAAEWDRDSRFPREAVAALGELGFLGMLVPEAYGGSAVDHVSYAL 68

Query: 72  ALEELARVDSSVAITLEAGVSLGAMPIHLFGTDAQKAEWLPRLCSGEILGAFGLTEPDGG 131
           A+EE+A  D +V+  +    S+  +PI  FGT+AQK  +L  L  G  LGAF LTEP  G
Sbjct: 69  AIEEIAAGDGAVSTIMSVHNSVACVPILRFGTEAQKERFLVPLARGAQLGAFCLTEPGAG 128

Query: 132 SDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVTVTAVTGRKPDGKPLISSIIV 191
           SDAGA   TAR     N +V++GTK FIT+  +    L  V AVT  +  GK  IS+ IV
Sbjct: 129 SDAGAV--TARARRVGNRYVLSGTKQFITSGRS--ADLAIVFAVTDPEA-GKRGISAFIV 183

Query: 192 PSGTPGFTVAAPYSKVGWNASDTRELSFADVRVPAANLLGEQGRGYAQFLRILDEGRIAI 251
           P+ TPG+ VA    K+G  ASDT ++ F D+ +    LLG++G G    L  L+ GRI I
Sbjct: 184 PTATPGYRVARIEHKLGQRASDTAQIVFEDMELTPDLLLGQEGEGLRIALSNLEGGRIGI 243

Query: 252 SALATGLAQGCVDESVKYAGERHAFGRNIGAYQAIQFKIADMEMKAHMARVGWRDAASRL 311
           +A A G+A+   + ++ YAGER  FG+ + A+QA+ F++ADM  +   AR+   +AA   
Sbjct: 244 AAQAVGMARAAFEAALAYAGERETFGQKLTAHQAVAFRLADMATRIEAARLLVHNAARLR 303

Query: 312 VAGEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRDSKILEIGEGTS 371
            AG+P  KEAA+AKL++S +A     +A QIHGGYG++ +YPV R++RD ++ +I EGTS
Sbjct: 304 DAGQPCLKEAAMAKLFASEMAEAVCSDAIQIHGGYGYLADYPVERIYRDVRVCQIYEGTS 363

Query: 372 EVQRMLIAREL 382
           +VQR++I+R L
Sbjct: 364 DVQRIVISRAL 374


Lambda     K      H
   0.318    0.136    0.402 

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: 399
Number of extensions: 11
Number of successful extensions: 3
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: 386
Length of database: 376
Length adjustment: 30
Effective length of query: 356
Effective length of database: 346
Effective search space:   123176
Effective search space used:   123176
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