GapMind for catabolism of small carbon sources

 

Alignments for a candidate for alr in Collinsella tanakaei YIT 12063

Align lysine racemase (EC 5.1.1.5) (characterized)
to candidate WP_009141067.1 HMPREF9452_RS05125 alanine racemase

Query= BRENDA::Q04HB7
         (371 letters)



>NCBI__GCF_000225705.1:WP_009141067.1
          Length = 383

 Score =  162 bits (411), Expect = 1e-44
 Identities = 119/383 (31%), Positives = 193/383 (50%), Gaps = 36/383 (9%)

Query: 11  IEFSKSSLAYNVQYTKQVSG-AKTLWLAVKSNAYGHGLLQVSKIARECGVDGLAVSVLDE 69
           +E  + +L  N +  K + G  K L   VK++AYGHG +Q +KI    G D  AV+ + E
Sbjct: 14  VEIDQGALRRNTRAFKNLLGYGKRLCCVVKADAYGHGAVQCAKIMHATGADMFAVATVSE 73

Query: 70  GIAIRQAGIDDFILILGPIDVKYAPIASKYHFLTTVSSLDWLKSADK------ILGKEKL 123
           G+ +R+ GI   IL+L    +       +Y  + +V S ++  +  +       +GK   
Sbjct: 74  GVQLREGGIKSPILVLNEPPIDACDTLLEYQIMPSVYSSEFALAYGERAVEMGCVGK--- 130

Query: 124 SVNLAVDTGMNRIGVRSKKDLKDEIEFLQEHSDH--FSYDGIFTHFASSDNPDDHYFQRQ 181
             ++A++TGMNRIGVR      D +EF +E   H     DG+FTHFA++D+PD   ++ Q
Sbjct: 131 -YHMAIETGMNRIGVR----FTDVLEFRREIDFHRGIECDGVFTHFATADDPDGWDYRLQ 185

Query: 182 KNRWYELI----DGLIMPRYVHVMNSGAAMY-HSKELPGCNSIARVGTVVYGVEPSEGVL 236
             R+ E +    D       VH  N+ A+M  HS +      + R G  +YG++P E   
Sbjct: 186 CTRFSEAVAAMKDAGFECGIVHCSNTPASMLDHSMQF----DMIRAGIGLYGLQPCE-KS 240

Query: 237 GPIDKLKPVFELKSALTFVKKIPAGEGISYGSKF-VTSRDTWIGTLPIGYGDGWLAEYQD 295
            PI  L+PV  +++ +T       GEG+ YG  F V      + T+P+GY DG      +
Sbjct: 241 APIMPLEPVMSVRARVTRTIHPAMGEGVGYGFTFRVPRARVQVCTIPVGYADGLPRTLSN 300

Query: 296 -FQLLIDGQKCRQVGQIAMDQMMVALPH-------EYPIGTEVTLIGKSGKYENTLYDLH 347
              +L  GQ+ RQVG I MDQ MVA+         E  +G  +T++GK G    ++ ++ 
Sbjct: 301 KMDVLYRGQRIRQVGNICMDQCMVAIQQTPARQMPEAEVGDLITIVGKDGDAVISMDEMA 360

Query: 348 KHSGVPPWKITVAFSDRLKRMVV 370
           +  G   +++   F  RL+++ +
Sbjct: 361 RLRGTINYEVACGFGMRLEKVYI 383


Lambda     K      H
   0.319    0.137    0.410 

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: 348
Number of extensions: 20
Number of successful extensions: 7
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: 371
Length of database: 383
Length adjustment: 30
Effective length of query: 341
Effective length of database: 353
Effective search space:   120373
Effective search space used:   120373
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 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