GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gyaR in Methanosarcina acetivorans C2A

Align Glyoxylate reductase; EC 1.1.1.26 (characterized)
to candidate WP_011020641.1 MA_RS03105 phosphoglycerate dehydrogenase

Query= SwissProt::Q9C4M5
         (331 letters)



>NCBI__GCF_000007345.1:WP_011020641.1
          Length = 523

 Score =  211 bits (538), Expect = 2e-59
 Identities = 107/319 (33%), Positives = 190/319 (59%), Gaps = 10/319 (3%)

Query: 4   KVFITRQIPENGIKMIEKFYEIELWKDPKAPPRGVLLEKVREVDALVTLVTDKVDKELLE 63
           KV ++  +   G++++++ + +++           L+EK+ E DALV     +V + ++E
Sbjct: 2   KVLVSDSLSNEGLEILKEHFTVDV---NTGLSEDELVEKIGEYDALVIRSGTQVTQRVIE 58

Query: 64  NAPKLKIIAQYAVGYDNIDIEEATKRGIYVTNTPGVLTDATADLAFALLLAVARRIVEAD 123
            A  LKI+ +  VG DN+D++ ATK+GI V N P     + A+    +++A++R I +A+
Sbjct: 59  AADNLKIVGRAGVGVDNVDVDAATKKGIIVANAPEGNMISAAEHTIGMMMAMSRNIPQAN 118

Query: 124 AFVRSGEWKKSEVGWHPLMFLGYGLKGKTLGIVGFGRIGQALAKRAKGFGMKIIYYSRTR 183
           A ++  EWK+++       F+G  +KGKTLGI+G GRIG  +AKRA G  M ++ Y    
Sbjct: 119 ASLKGREWKRNK-------FMGVEVKGKTLGIIGLGRIGSEVAKRASGLEMNLMGYDPFI 171

Query: 184 KPEAEEEIGAEYVDFETLLKESDFISLHVPLTKETYHMIGEKELKLMKPNAILINTSRGA 243
             +   E+G +      + KE+D+I++H PL KET +++ +++  LMK    ++N +RG 
Sbjct: 172 SEKRAMELGVKLATVNEISKEADYITVHTPLIKETRNILDDEQFDLMKSGVRILNCARGG 231

Query: 244 VVDTNALIKALKEGWIAGAGLDVFEEEPYYNEELFKLKNVVLAPHIGSATHEAREGMAEL 303
           +++  AL++AL+ G + GA LDVF EEP +   L    NV++ PH+G++T EA+  +A  
Sbjct: 232 IINEAALVRALESGKVGGAALDVFVEEPPFGSPLLNFDNVIVTPHLGASTQEAQVNVAID 291

Query: 304 VAKNLIAFAKGEIPPNLVN 322
           +AK +++   G +  N +N
Sbjct: 292 IAKEVVSVLTGGLAKNAIN 310


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: 443
Number of extensions: 18
Number of successful extensions: 2
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: 523
Length adjustment: 31
Effective length of query: 300
Effective length of database: 492
Effective search space:   147600
Effective search space used:   147600
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: 50 (23.9 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