GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Azohydromonas australica DSM 1124

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_028997414.1 H537_RS0107560 2-hydroxyacid dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_000430725.1:WP_028997414.1
          Length = 317

 Score =  204 bits (519), Expect = 2e-57
 Identities = 132/311 (42%), Positives = 176/311 (56%), Gaps = 12/311 (3%)

Query: 2   KPKVF-ITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKE 60
           KP+V  I R  P    ++   F    L + P A  R  L E      A VT     +D  
Sbjct: 5   KPRVLQIGRLTPWLEQQLAADFDLTLLAQQPDA--RAYLAEHGAGFVAAVTSAAVGIDAA 62

Query: 61  LLENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIV 120
           L+E+ PKL++I+ + VG D ID++ A +RGI V  TP VL D  AD AF LLL VARR  
Sbjct: 63  LIESLPKLQVISSFGVGLDKIDLQAAARRGIPVGYTPEVLNDCVADTAFTLLLDVARRAT 122

Query: 121 EADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYS 180
           EAD FVR G W K +        L   + GK LGIVG GRIG+ +A+RA GF M+I Y++
Sbjct: 123 EADRFVRQGGWLKDKFP------LATRVSGKRLGIVGLGRIGRTIARRASGFDMEIRYHN 176

Query: 181 RTRKPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTS 240
           R  +P      G E    E L + SDF+ +      E+ +++  + L  + P   L+N +
Sbjct: 177 R--RPAEGVSFGYEPSLVE-LARWSDFLVIAAAGGAESRNLVSAEVLDALGPQGFLVNIA 233

Query: 241 RGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREGM 300
           RG VVD   L++ L+E  IAGAGLDV+ +EP   E L +L N VL PH+ SATHE R+ M
Sbjct: 234 RGTVVDEAVLVQYLQEKRIAGAGLDVYVDEPRVPEALLQLDNAVLLPHVASATHETRQAM 293

Query: 301 AELVAKNLIAF 311
           +ELV +NL AF
Sbjct: 294 SELVLENLRAF 304


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: 244
Number of extensions: 10
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: 331
Length of database: 317
Length adjustment: 28
Effective length of query: 303
Effective length of database: 289
Effective search space:    87567
Effective search space used:    87567
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 Apr 09 2024. 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