GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Pontibacillus litoralis JSM 072002

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_036834129.1 N784_RS08505 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_000775615.1:WP_036834129.1
          Length = 321

 Score =  287 bits (735), Expect = 2e-82
 Identities = 150/318 (47%), Positives = 209/318 (65%), Gaps = 6/318 (1%)

Query: 2   KPKVFITRQIPENGIKMIEKFYEIELWKDPKAP-PRGVLLEKVREVDALVTLVTDKVDKE 60
           KP +FITR +PE  I      ++I++W   + P  R +L+++  + DAL+T+++D++D++
Sbjct: 3   KPYIFITRTLPEEIIAPFRANWDIQMWDSEEKPVDRTILIQETAKADALITMLSDRIDEQ 62

Query: 61  LLENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIV 120
           LLE   +LK+IA  AVG+DNID++ A K+GI VTNTP VLT+ TADL F LL+A ARR +
Sbjct: 63  LLEQGAQLKVIANLAVGFDNIDVKAAQKKGIIVTNTPDVLTETTADLTFGLLMATARRFI 122

Query: 121 EADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYS 180
           EA   +R+G W+     W PL+  G  +  KT+GIVG GRIG+A+A RA+GF M ++Y++
Sbjct: 123 EASDHIRNGNWEN----WAPLLLAGLDIHHKTIGIVGMGRIGRAVAHRAQGFHMNVLYHN 178

Query: 181 RTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTS 240
           R+R  EAE  +GA YV FE LL++SDF+    P T+ET  M   K  + MK +A+ IN S
Sbjct: 179 RSRDTEAESALGATYVSFEELLQQSDFVVCLAPFTEETAGMFNAKAFQTMKSSAMFINAS 238

Query: 241 RGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEE-LFKLKNVVLAPHIGSATHEAREG 299
           RGA V    L +AL  G IAGAGLDVF +EP  N+  L  LK VV  PHIGSA+ E R+ 
Sbjct: 239 RGANVVEEDLYEALVAGDIAGAGLDVFTKEPIANDHPLLTLKQVVALPHIGSASVETRQA 298

Query: 300 MAELVAKNLIAFAKGEIP 317
           M  L  +N+     G+ P
Sbjct: 299 MMHLCLENINLVLSGQQP 316


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: 249
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: 321
Length adjustment: 28
Effective length of query: 303
Effective length of database: 293
Effective search space:    88779
Effective search space used:    88779
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 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