GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Desulfitobacterium hafniense DCB-2

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate WP_015943904.1 DHAF_RS10835 alcohol dehydrogenase

Query= metacyc::STM4044-MONOMER
         (382 letters)



>NCBI__GCF_000021925.1:WP_015943904.1
          Length = 405

 Score =  227 bits (578), Expect = 5e-64
 Identities = 142/371 (38%), Positives = 208/371 (56%), Gaps = 10/371 (2%)

Query: 12  LHGAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQMSYHLFDEVFPNP 71
           L GA ++  +  +++ K   K LIVTD  +  LGL++S    LD+  + Y ++D+  PNP
Sbjct: 28  LEGANSLNKLPEVISRKGISKILIVTDQGISSLGLVNSFLQDLDKAGVRYTVYDKTVPNP 87

Query: 72  TEELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAY-SGVGKVKNAGV 130
           T + +++    YQ  +C+ I+AFGGGSP+D AK V    ANP  S +   GV KV+    
Sbjct: 88  TLDNIEEALKLYQEQQCEGIVAFGGGSPMDCAKGVGARVANPHKSISQMKGVLKVRRKLP 147

Query: 131 PLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPASVTAAT 190
           PL AI TTAGT +E T  AVI D   + K  + D  +IP  AV D  + + +P  +T+ T
Sbjct: 148 PLFAIPTTAGTGSEATLAAVISDPRNREKYPVNDTALIPHYAVLDPLLTVGLPKHITSTT 207

Query: 191 GMDALTHAVEAYVSVGAHPLTDANALEAIRLI--NLWLPKAVDDGHNLEAREQMAFGQYL 248
           G+DALTHAVEAY+       T   + +A+RLI  NL++  A   G N++ARE M    Y 
Sbjct: 208 GLDALTHAVEAYIGRSNTQETTELSRKAVRLIFDNLYI--AYSQGENVKARENMLKASYY 265

Query: 249 AGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQAMGV 308
           AG+AF  A +G +HALAH  G  + +PHG+ NA++LP V  +       R A +A  + +
Sbjct: 266 AGVAFTRAYVGYIHALAHALGGFYGVPHGLANAVILPCVLEYYGEAVHERLAELADVLEM 325

Query: 309 ETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKAL--ADPCAPCNP 366
            + G S E  +   I AI+ LSK++ IP      G+  EDI   ++ A   A P  P  P
Sbjct: 326 GSPGDSHEQKATLFIEAIKELSKKMNIPRKID--GILAEDIPLLVEHAWKEATPLYPV-P 382

Query: 367 RTASRDEVRGL 377
           R  SR+++  +
Sbjct: 383 RLLSRNDLNNI 393


Lambda     K      H
   0.317    0.133    0.384 

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: 378
Number of extensions: 14
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: 382
Length of database: 405
Length adjustment: 31
Effective length of query: 351
Effective length of database: 374
Effective search space:   131274
Effective search space used:   131274
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 (21.7 bits)
S2: 50 (23.9 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