GapMind for catabolism of small carbon sources

 

Alignments for a candidate for adh in Methanobacterium veterum MK4

Align Alcohol dehydrogenase; EC 1.1.1.1; EC 1.1.1.4; EC 1.2.1.3 (characterized)
to candidate WP_048081448.1 EJ01_RS05805 NAD(P)-dependent alcohol dehydrogenase

Query= SwissProt::Q0KDL6
         (366 letters)



>NCBI__GCF_000745485.1:WP_048081448.1
          Length = 356

 Score =  217 bits (552), Expect = 4e-61
 Identities = 126/343 (36%), Positives = 188/343 (54%), Gaps = 21/343 (6%)

Query: 5   MKAAVFVEPGRIELADKPIPDIGPNDALVRITTTTICGTDVH-ILKGEYPVAKGLTVGHE 63
           MK    ++ G     +K  P  GP DA+VR T    C +DVH + +G       + +GHE
Sbjct: 1   MKGFAMLKIGETGWIEKDRPKCGPRDAIVRPTCLAPCTSDVHTVWEGAIGDRHNMILGHE 60

Query: 64  PVGIIEKLGSAVTGYREGQRVIAGAICPNFNSYAAQDGVASQDGSYLMASGQCGCHGYKA 123
            VGI++++G+ V  ++ G RVI  AI P+++S A Q G  SQ G      G CG      
Sbjct: 61  AVGIVDEVGTEVKDFKPGDRVIVPAITPDWDSEAVQRGFPSQTG------GACG------ 108

Query: 124 TAGWRFGNMIDGTQAEYVLVPDAQANLTPIPDGLTDEQVLMCPDIMSTGFKGAENANIRI 183
             GW++ N  DG   E+  V  A  NL  +P+G++ E  +M  D+MSTGF GAENA I +
Sbjct: 109 --GWKYSNFKDGVFGEFFHVNLADNNLAHLPEGMSQEAAVMITDMMSTGFMGAENAGIEL 166

Query: 184 GDTVAVFAQGPIGLCATAGARLCGATTIIAIDGNDHRLEIARKMGADVVLNFRNCDVVDE 243
           G TVAV   G +GLC  AGA+L GA  I A+      +E+A+K GA  ++++R+ D  ++
Sbjct: 167 GSTVAVLGIGAVGLCGIAGAKLRGAGRIFAVGTRPVSVEVAKKYGATDIISYRDGDTAEQ 226

Query: 244 VMKLTGGRGVDASIEALGTQATFEQSLRVLKPGGTLSSLGVYSSDL----TIPLS--AFA 297
           ++  T G GVDA I + G       + ++ K G  +S+   +        T+PL    + 
Sbjct: 227 ILDATDGEGVDAVIISGGGPDILIDACKMAKAGSKISNNNYFGKGEGEKDTLPLCRVGWG 286

Query: 298 AGLGDHKINTALCPGGKERMRRLINVIESGRVDLGALVTHQYR 340
            G+ D  I T LCPGG+ RM RL +++  GR+D   LVTH+++
Sbjct: 287 FGMADKDIITGLCPGGRVRMERLADIVTYGRMDPELLVTHKFK 329


Lambda     K      H
   0.320    0.138    0.408 

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: 409
Number of extensions: 24
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: 366
Length of database: 356
Length adjustment: 29
Effective length of query: 337
Effective length of database: 327
Effective search space:   110199
Effective search space used:   110199
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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