GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bcd in Escherichia coli BW25113

Align butyryl-CoA dehydrogenase; EC 1.3.99.2 (characterized)
to candidate 15814 b1695 putative oxidoreductase (VIMSS)

Query= CharProtDB::CH_091787
         (383 letters)



>FitnessBrowser__Keio:15814
          Length = 383

 Score =  172 bits (436), Expect = 1e-47
 Identities = 125/390 (32%), Positives = 192/390 (49%), Gaps = 19/390 (4%)

Query: 1   MDFNLTDIQQDFLK-----LAHDFGEKKLAPTVTERDHKGIYDKELIDELLSLGITGAYF 55
           MDF+LT+ Q+  L      +  +F E+         D  G Y +E +  L   GI+    
Sbjct: 1   MDFSLTEEQELLLASIRELITTNFPEEYFRTC----DQNGTYPREFMRALADNGISMLGV 56

Query: 56  EEKYGGSGDDGGDVLSYILAVEELAKYDAGVAITLSATVSLCANPIWQFGTEAQKEKFLV 115
            E++GG      D ++ +LA+ E++K  A   +    T   C + + +FG+  Q  K   
Sbjct: 57  PEEFGGIP---ADYVTQMLALMEVSKCGAPAFLI---TNGQCIHSMRRFGSAEQLRKTAE 110

Query: 116 PLVE-GTKLGAFGLTEPNAGTDASGQQTIATKNDDGTYTLNGSKIFITNGGAADIYIVFA 174
             +E G    A  LTEP AG+D +   T  T+ +   Y +NG K FIT        +V A
Sbjct: 111 STLETGDPAYALALTEPGAGSDNNSATTTYTRKNGKVY-INGQKTFITGAKEYPYMLVLA 169

Query: 175 MTDKSKG-NHGITAFILEDGTPGFTYGKKEDKMGIHTSQTMELVFQDVKVPAENMLGEEG 233
              + K      T + ++   PG        K+G H   T E+   +V+V   +M+GEEG
Sbjct: 170 RDPQPKDPKKAFTLWWVDSSKPGIKINPLH-KIGWHMLSTCEVYLDNVEVEESDMVGEEG 228

Query: 234 KGFKIAMMTLDGGRIGVAAQALGIAEAALADAVEYSKQRVQFGKPLCKFQSISFKLADMK 293
            GF   M   +  R+  AA++ G AE A  DA  Y+ QR+ FGKP+   Q I  KLA M 
Sbjct: 229 MGFLNVMYNFEMERLINAARSTGFAECAFEDAARYANQRIAFGKPIGHNQMIQEKLALMA 288

Query: 294 MQIEAARNLVYKAACKKQEGKPFTVDAAIAKRVASDVAMRVTTEAVQIFGGYGYSEEYPV 353
           ++I+  RN+V K A +  + +     AA+AK   +  AM V  +A+QI GG GY++E  V
Sbjct: 289 IKIDNMRNMVLKVAWQADQHQSLRTSAALAKLYCARTAMEVIDDAIQIMGGLGYTDEARV 348

Query: 354 ARHMRDAKITQIYEGTNEVQLMVTGGALLR 383
           +R  RD +  +I  GT+E+ + V G  +L+
Sbjct: 349 SRFWRDVRCERIGGGTDEIMIYVAGRQILK 378


Lambda     K      H
   0.316    0.135    0.380 

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: 302
Number of extensions: 14
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: 383
Length of database: 383
Length adjustment: 30
Effective length of query: 353
Effective length of database: 353
Effective search space:   124609
Effective search space used:   124609
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 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