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_011459150.1 DHAF_RS02645 alcohol dehydrogenase

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



>NCBI__GCF_000021925.1:WP_011459150.1
          Length = 387

 Score =  313 bits (801), Expect = 7e-90
 Identities = 167/377 (44%), Positives = 243/377 (64%), Gaps = 2/377 (0%)

Query: 7   LPKISLHGAGAIADMVNLVANKQWGK-ALIVTDGQLVKLGLLDSLFSALDEHQMSYHLFD 65
           +P ++L GAGA A      A    GK AL+VTD  L + GL   +   ++   +   ++ 
Sbjct: 12  MPTVNLMGAGA-AQEAGKQAKILGGKTALLVTDAFLNQSGLAKQIAEIIEAEGVKVVIYP 70

Query: 66  EVFPNPTEELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKV 125
              PNPT++ V  G A ++   C+ I++ GGGS  D AK V ++  N G    + GV K 
Sbjct: 71  GAEPNPTDKNVHDGVAVFEKENCNMIVSLGGGSAHDCAKGVGLVAGNGGNIRDFEGVDKS 130

Query: 126 KNAGVPLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPAS 185
               VP++A+NTTAGTA+EMT   +I D+ R +K  I+D +  P+++++D  +M+  PA 
Sbjct: 131 AKPMVPMIAVNTTAGTASEMTRFCIITDTDRHIKMAIVDWHATPNVSINDPLLMIGKPAP 190

Query: 186 VTAATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQMAFG 245
           +TAATGMDALTHAVEAYVS  A P+TD+ AL AI+LI+ +L +AV +G + EAR+QMA+ 
Sbjct: 191 LTAATGMDALTHAVEAYVSTAATPITDSAALMAIKLISKYLRRAVANGQDFEARDQMAYA 250

Query: 246 QYLAGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQA 305
           Q+LAGMAFN+A LG VHA+AHQ G  +NLPHGVCNAILLP V  FN    + RF  IA+A
Sbjct: 251 QFLAGMAFNNASLGYVHAMAHQLGGFYNLPHGVCNAILLPRVSRFNLIGNLERFVDIAEA 310

Query: 306 MGVETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPCAPCN 365
           +G E + +S   A+++A+ A+ TLS+ + IP G ++LGV +ED++     A+ D C+  N
Sbjct: 311 LGEEIKNLSARDAAEKALTAMTTLSQDISIPSGLTELGVKEEDLQTMAVNAMKDACSLTN 370

Query: 366 PRTASRDEVRGLYLEAL 382
           PR A  +++  +Y  +L
Sbjct: 371 PRLAKLEDIIQIYKNSL 387


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: 403
Number of extensions: 21
Number of successful extensions: 1
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: 387
Length adjustment: 30
Effective length of query: 352
Effective length of database: 357
Effective search space:   125664
Effective search space used:   125664
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