GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Marinobacter adhaerens HP15

Align Lactaldehyde reductase; Propanediol oxidoreductase; EC 1.1.1.77 (characterized)
to candidate GFF2063 HP15_2019 iron-containing alcohol dehydrogenase

Query= SwissProt::P0A9S1
         (382 letters)



>FitnessBrowser__Marino:GFF2063
          Length = 385

 Score =  217 bits (552), Expect = 5e-61
 Identities = 125/372 (33%), Positives = 208/372 (55%), Gaps = 8/372 (2%)

Query: 16  GAVGALTDEVKRRGYQKALIVTDKTLVQCGVVAKVTDKMDAAGLAWAIYDGVVPNPTITV 75
           G    L   VK    +K L+VTD  LV+ G++   T+ ++ AG+ + ++DGVV +P ++V
Sbjct: 17  GVTHRLGQIVKEHMGKKVLLVTDPGLVKAGLLDVATNSLNEAGVKYELFDGVVADPPVSV 76

Query: 76  VKEGLGVFQNSGADYLIAIGGGSPQDTCKAIGIISNNPEFADVRSLEGLSPTNKPSVPIL 135
           V+  L   + +G D +I  GGGS  D  K I ++    E  D   + G+       +P++
Sbjct: 77  VEAALADAREAGVDGVIGFGGGSSMDVAKLIALLIGGEEKLD--DVYGVGQAKGKRLPLI 134

Query: 136 AIPTTAGTAAEVTINYVITDEEKRRKFVCVDPHDIPQVAFIDADMMDGMPPALKAATGVD 195
            IPTTAGT +EVT   +IT  E  +K V V P  +P +A +DA++  G+P  + AATG+D
Sbjct: 135 QIPTTAGTGSEVTPISIITVGETEKKGV-VAPQLLPDIALLDAELTLGLPAHVTAATGID 193

Query: 196 ALTHAIEGYITRGAW--ALTDALHIKAIEIIAGALRGSVAGDKD--AGEEMALGQYVAGM 251
           A+ HAIE Y +  A    ++ AL  +A+ ++   +  +V    +  A  +M LG  +AG 
Sbjct: 194 AMVHAIESYTSASANNNPVSKALAREALRLLGANIETAVKDGSNVKARSDMLLGAMLAGQ 253

Query: 252 GFSNVGLGLVHGMAHPLGAFYNTPHGVANAILLPHVMRYNADFTGEKYRDIARVMGVKVE 311
            F+N  +  VH +A+P+G  ++ PHG++NA++LPHVMR+N +  GE Y  +A  +   + 
Sbjct: 254 AFANSPVAAVHALAYPIGGIFHVPHGLSNALVLPHVMRFNTEICGEAYSILATDVFPDLA 313

Query: 312 GMSLEEARNAAVEAVFALNRDVGIPPHLRDVGVRKEDIPALAQAALDDV-CTGGNPREAT 370
           G    +  N  ++ + AL+ D+G+   LR+VG+ + D+  LA  ++        NPRE +
Sbjct: 314 GTPAAKRANQFIDRLEALSADLGLEQTLREVGIGEADLATLASDSMKQTRLLVNNPREVS 373

Query: 371 LEDIVELYHTAW 382
             D + +Y  A+
Sbjct: 374 ETDALAIYKAAF 385


Lambda     K      H
   0.319    0.136    0.404 

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: 388
Number of extensions: 25
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: 382
Length of database: 385
Length adjustment: 30
Effective length of query: 352
Effective length of database: 355
Effective search space:   124960
Effective search space used:   124960
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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