GapMind for catabolism of small carbon sources

 

Alignments for a candidate for liuA in Cupriavidus basilensis 4G11

Align acyl-CoA dehydrogenase subunit (EC 1.3.8.4; EC 1.3.8.5) (characterized)
to candidate RR42_RS00895 RR42_RS00895 acyl-CoA dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS00895
          Length = 376

 Score =  291 bits (746), Expect = 2e-83
 Identities = 163/378 (43%), Positives = 236/378 (62%), Gaps = 5/378 (1%)

Query: 5   LTPELEELRRTVEEFAHDVVAPKIGDFYERHEFPYEIVREMGRMGLFGLPFPEEYGGMGG 64
           LTPE E +R  V +FA   +AP    +     FP  + RE+  +G +G+  PE+YGG G 
Sbjct: 3   LTPEQEMIRDAVRQFAQQEIAPHAAAWDRDKTFPQAVHRELAALGAYGVAVPEQYGGAGL 62

Query: 65  DYLALGIALEELARVDSSVAITLEAGVSLGAMPIHLFGTDAQKAEWLPRLCSGEILGAFG 124
           DYL+L + LEE+A  D   +  +          +  F ++AQK +WL  L  GE+LGAF 
Sbjct: 63  DYLSLALILEEIAAGDGGTSTVISVNNCPVCSMLMAFASEAQKQQWLVPLARGEMLGAFC 122

Query: 125 LTEPDGGSDAGATRTTARLDESTNEWVINGTKCFITNSGTDITGLVTVTAVTGRKPDGKP 184
           LTEP  GSDA A RT+A  D   +++V+NG K FIT+       +  V AVT  K  GK 
Sbjct: 123 LTEPHVGSDAAALRTSAVRDG--DDYVLNGVKQFITSGKN--ADVAIVLAVTD-KAAGKR 177

Query: 185 LISSIIVPSGTPGFTVAAPYSKVGWNASDTRELSFADVRVPAANLLGEQGRGYAQFLRIL 244
            IS+ +VP+ TPG+ VA    K+G ++SDT ++ F D RVPAAN+LGE+G GY   L  L
Sbjct: 178 GISAFLVPTATPGYIVARLEEKLGQHSSDTAQILFEDCRVPAANMLGEEGAGYKMALSGL 237

Query: 245 DEGRIAISALATGLAQGCVDESVKYAGERHAFGRNIGAYQAIQFKIADMEMKAHMARVGW 304
           + GRI I++ + G+A+   D ++ YA ER +FG+ + A+QA+QF++ADM  K  +AR   
Sbjct: 238 EGGRIGIASQSIGMARAAFDAALAYAKERESFGQPLFAHQAVQFRLADMATKIEVARQMV 297

Query: 305 RDAASRLVAGEPFKKEAAIAKLYSSTVAVDNAREATQIHGGYGFMNEYPVARMWRDSKIL 364
             AAS   AG P  KEAA+ KLY+S +A +    A Q+ GGYG+++++PV R++RD ++ 
Sbjct: 298 WHAASLKDAGRPCLKEAAMGKLYASEMAEEVCSAAIQVFGGYGYVSDFPVERIYRDVRVC 357

Query: 365 EIGEGTSEVQRMLIAREL 382
           +I EGTS++Q++LIAR L
Sbjct: 358 QIYEGTSDIQKILIARAL 375


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: 17
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 17 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