GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Pedobacter sp. GW460-11-11-14-LB5

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate CA265_RS17230 CA265_RS17230 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>FitnessBrowser__Pedo557:CA265_RS17230
          Length = 319

 Score =  243 bits (619), Expect = 6e-69
 Identities = 143/318 (44%), Positives = 196/318 (61%), Gaps = 7/318 (2%)

Query: 4   KVFITRQIPENGIKMIEKF-YEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELL 62
           KVFI+  I   GIK +E+    I  WK+ +      L+   ++ DAL+++  +K++   L
Sbjct: 2   KVFISGNIASVGIKELEENNITITQWKENRQITAEELIAACQDQDALISVGPNKINAAFL 61

Query: 63  ENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEA 122
           +    LK+IA ++VGYD +D+  A K  I + NTPGVL+ ATAD AF L+LAV+R+   A
Sbjct: 62  KACSHLKVIALHSVGYDQVDVAAAKKLNIPIGNTPGVLSKATADTAFLLMLAVSRKAFFA 121

Query: 123 DAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKG-FGMKIIYYSR 181
              +  GEWK  E    P   LG  + GKTLGI G G+IG  +AK+  G + M +IY++R
Sbjct: 122 HKKIIKGEWKNYE----PTPELGIEVNGKTLGIFGLGKIGLEMAKKCIGAYQMPVIYHNR 177

Query: 182 TRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSR 241
           +R  EAE+EIGA+YV FETLL +SD +S+H  LT ET         K MK N+I INT+R
Sbjct: 178 SRNEEAEKEIGAKYVSFETLLAQSDVLSVHTALTPETKDKFTLDVFKQMKANSIFINTAR 237

Query: 242 GAVVDTNALIKALKEGWIAGAGLDVFEEEPY-YNEELFKLKNVVLAPHIGSATHEAREGM 300
           GA+ +   LIKAL++  I GAGLDV   EP   N  L  ++NV + PHIGSAT E R  M
Sbjct: 238 GAIHNEKDLIKALEKKIIWGAGLDVTNPEPMDKNNPLLSMENVAVLPHIGSATEETRAAM 297

Query: 301 AELVAKNLIAFAKGEIPP 318
           A+++ KN+IA   GE  P
Sbjct: 298 AQIIVKNIIAGLNGEKLP 315


Lambda     K      H
   0.317    0.137    0.392 

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: 262
Number of extensions: 9
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: 331
Length of database: 319
Length adjustment: 28
Effective length of query: 303
Effective length of database: 291
Effective search space:    88173
Effective search space used:    88173
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: 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