GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mcl in Escherichia coli BW25113

Align (S)-citramalyl-CoA lyase (EC 4.1.3.25); (R)-citramalyl-CoA lyase (EC 4.1.3.46) (characterized)
to candidate 14753 b0616 citrate lyase beta chain (acyl lyase subunit) (VIMSS)

Query= BRENDA::A0A172MLA1
         (322 letters)



>FitnessBrowser__Keio:14753
          Length = 302

 Score =  155 bits (393), Expect = 9e-43
 Identities = 103/301 (34%), Positives = 162/301 (53%), Gaps = 18/301 (5%)

Query: 8   RRALLYIPGSSQRFIDKSRTLTADCVAYDLEDSVTPHKKAEARSLVRRALDQPAPAGILE 67
           RR++L++PG++   +  S    AD + +DLEDSV   +K  AR +V  AL  P    I E
Sbjct: 14  RRSMLFVPGANAAMVSNSFIYPADALMFDLEDSVALREKDTARRMVYHALQHPLYRDI-E 72

Query: 68  RAVRINSVDSGLALADLTEVLQSPNLSTIVIPKVNSASDLTFVTDVITHTLSQLPLSQSA 127
             VR+N++DS   + DL  V++      + +PK ++A D+  +   I      L + ++ 
Sbjct: 73  TIVRVNALDSEWGVNDLEAVVRG-GADVVRLPKTDTAQDVLDIEKEI------LRIEKAC 125

Query: 128 SRPPIS--LLALVESAKSLTNLSQICAASPLLQGLIFAAEDFALDLSLTRTPALTEFLFA 185
            R P S  LLA +ES   +T   +I  AS  L G+   AED+  +L   R+P  TE LFA
Sbjct: 126 GREPGSTGLLAAIESPLGITRAVEIAHASERLIGIALGAEDYVRNLRTERSPEGTELLFA 185

Query: 186 RSAIATAARAANLPSTIDLVCTTYKSDKGDGSPPVVLQQECRDGKNLGFNGKQCIHPSQV 245
           R +I  AAR+A + +  D V +   ++ G         QE    K LGF+GK  I+P Q+
Sbjct: 186 RCSILQAARSAGIQA-FDTVYSDANNEAG-------FLQEAAHIKQLGFDGKSLINPRQI 237

Query: 246 STVQQIFGPELEEVQWAVRVTIADDKASKAGRGAWTLDGKMIDIPVAEKARAIVKKADAC 305
             +  ++ P  +EV  A RV  A + A++ G G  +L+GKM+D PV ++AR ++ +A+  
Sbjct: 238 DLLHNLYAPTQKEVDHARRVVEAAEAAAREGLGVVSLNGKMVDGPVIDRARLVLSRAELS 297

Query: 306 G 306
           G
Sbjct: 298 G 298


Lambda     K      H
   0.316    0.130    0.369 

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: 198
Number of extensions: 10
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: 322
Length of database: 302
Length adjustment: 27
Effective length of query: 295
Effective length of database: 275
Effective search space:    81125
Effective search space used:    81125
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: 48 (23.1 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