GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimC in Cupriavidus basilensis 4G11

Align pimeloyl-CoA dehydrogenase small subunit (EC 1.3.1.62) (characterized)
to candidate RR42_RS36390 RR42_RS36390 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-20677
         (380 letters)



>FitnessBrowser__Cup4G11:RR42_RS36390
          Length = 381

 Score =  320 bits (820), Expect = 4e-92
 Identities = 175/373 (46%), Positives = 228/373 (61%), Gaps = 3/373 (0%)

Query: 1   MDFDLSEEQRLLKESVEGLLKGSYDFDSRKKYAKEKGGWSRAVWGKFAEQ-GLLGLPFSE 59
           MDF  SEEQ +L++++   L   Y F++R+   +   GW  + W   A++ GLLG  F E
Sbjct: 1   MDFQFSEEQSMLRDTLARYLADHYSFEARQAAIRSPAGWRASCWQALAQELGLLGAAFPE 60

Query: 60  EDGGFGAGAVETMIVMEALGHSLVLEPYLPTVVIGGGFLRRAGSAAQKAAHLPGIIDGSK 119
             GG G  AVE  IVME  G  LV+EPYL TVV+GGG L   GS    A+ LP II G  
Sbjct: 61  RFGGLGGNAVEHTIVMEQFGRHLVVEPYLSTVVLGGGALLH-GSETLAASWLPAIIGGEA 119

Query: 120 TFAFAQLEKNSRWDLGDVSTTAKKSGDGWVIDGEKFVVLNGEAADTLIVTARTKGGQRDR 179
           T A+A  E  SR+ L DV  +A ++  GW +DG K VV+    A  L+V+ART G +RDR
Sbjct: 120 TVAWAHAEPRSRYCLHDVQASAARAQGGWRLDGHKAVVVAAPWATHLVVSARTGGSRRDR 179

Query: 180 TGVGVFLVPADAKGITRKGYPTQDGLHAADITFTGVQVGADAAIGDPENALELIEAVVDD 239
            G+ +F +  DA G+T + YPT DG  AADI    V V     +G    AL LIE + D+
Sbjct: 180 DGISLFWIARDAPGVTLQEYPTVDGSRAADIRLDNVFVPDGGLLGAEGEALTLIERLSDE 239

Query: 240 ARTALCAEAVGLMDESLTTTVEYIKTRKQFGVPIGSFQVLQHRAADMFVATEQARSMAMF 299
           A  ALCAEA G M   L  TV+Y + RKQFGVPI +FQVLQHR ADM+V  EQ  ++   
Sbjct: 240 AAVALCAEAGGAMSRMLGDTVDYARQRKQFGVPIATFQVLQHRMADMYVQLEQTVALTQV 299

Query: 300 ATMAAEFDDAKERAGAIAAAKVQIGKSGKFVGQQSIQLHGGIGMTMEAKIGHYFKRLTMI 359
           A M        +RA A +AAK Q G++G+FVGQ ++Q+HGG+G+T E  +GHYFKR+T I
Sbjct: 300 AAMQVGAQPT-QRALAASAAKAQAGQAGRFVGQAAVQIHGGMGVTEELAVGHYFKRVTAI 358

Query: 360 EQTFGDTDHHLAR 372
           +  FG  +HHL R
Sbjct: 359 DLQFGSAEHHLRR 371


Lambda     K      H
   0.318    0.135    0.388 

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: 416
Number of extensions: 24
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: 380
Length of database: 381
Length adjustment: 30
Effective length of query: 350
Effective length of database: 351
Effective search space:   122850
Effective search space used:   122850
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