GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_068174208.1 HTA01S_RS18420 D-glycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_001592305.1:WP_068174208.1
          Length = 331

 Score =  243 bits (619), Expect = 6e-69
 Identities = 135/312 (43%), Positives = 191/312 (61%), Gaps = 6/312 (1%)

Query: 2   KPKVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKEL 61
           +P + I R +    +  + + +E+E  +         L+E+++    ++T  ++++D  L
Sbjct: 4   RPAILIARAVFPEVVARLREHFEVETNEQDAPFTPAQLIERLQGKVGVMTTGSERIDAAL 63

Query: 62  LENAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVE 121
           L   P+L++ A  AVGY+N D+   T  G+  TNTP VLT+ TAD  FALL+A ARRI E
Sbjct: 64  LAACPQLRVAANIAVGYNNFDVPAMTAAGVLATNTPDVLTETTADFGFALLMATARRICE 123

Query: 122 ADAFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKR-AKGFGMKIIYYS 180
           ++ F+R+G+W +    W   MF G  + G TLGI+G GRIGQA+A+R A GFGM +IY++
Sbjct: 124 SEHFLRAGQWNR----WALDMFAGAEVHGSTLGILGMGRIGQAIARRGAHGFGMNVIYHN 179

Query: 181 RTRKPEAEEEI-GAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINT 239
           R+R     E    A YV    LL+++D + L VP + E++H IG  EL  MKP A L+N 
Sbjct: 180 RSRLDTGSEAACRARYVSKAELLQQADHLVLVVPYSAESHHTIGAAELAQMKPTATLVNI 239

Query: 240 SRGAVVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREG 299
           +RG +VD  AL  AL+E  IA AGLDVFE EP  + +L  + NVVL PHI SAT   R  
Sbjct: 240 ARGGIVDDAALAVALREKRIAAAGLDVFEGEPKVHPDLLTVPNVVLTPHIASATLPTRLA 299

Query: 300 MAELVAKNLIAF 311
           MA L A NLIA+
Sbjct: 300 MANLAADNLIAY 311


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: 232
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: 331
Length of database: 331
Length adjustment: 28
Effective length of query: 303
Effective length of database: 303
Effective search space:    91809
Effective search space used:    91809
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: 49 (23.5 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