GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fucO in Klebsiella michiganensis M5al

Align L-lactaldehyde reductase (EC 1.1.1.77) (characterized)
to candidate BWI76_RS20780 BWI76_RS20780 alcohol dehydrogenase EutG

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



>FitnessBrowser__Koxy:BWI76_RS20780
          Length = 395

 Score =  253 bits (645), Expect = 9e-72
 Identities = 148/376 (39%), Positives = 212/376 (56%), Gaps = 6/376 (1%)

Query: 6   ALPKISLHGAGAIADMVNLVANKQWGKALIVTDGQLVKLGLLDSLFSALDEHQMSYHLFD 65
           ++P ++L G GA++        +      ++ D  L + GL   L  +L    ++  ++ 
Sbjct: 25  SVPPVTLCGLGALSACGQEAQARGVNHLFVMVDSFLHQAGLTAGLARSLAVKGVAMTVWP 84

Query: 66  EVFPNPTEELVQKGFAAYQSAECDYIIAFGGGSPIDTAKAVKILTANPGPSTAYSGVGKV 125
                P    V    A  + A+CD ++AFGGGS +D AKAV +L  NP  + +      V
Sbjct: 85  CPPGEPCVTDVCAAVAQLREAKCDGVVAFGGGSVLDAAKAVALLVTNPEQTLSEMTESSV 144

Query: 126 KNAGVPLVAINTTAGTAAEMTSNAVIIDSARKVKEVIIDPNIIPDIAVDDASVMLEIPAS 185
               +PL+A+ TTAGT +E T+  VIID+    K+V+   +++PD+A+ DA++   +P  
Sbjct: 145 LRPRLPLIAVPTTAGTGSETTNVTVIIDAVSGRKQVLAHASLMPDVAILDAALTEGVPPQ 204

Query: 186 VTAATGMDALTHAVEAYVSVGAHPLTDANALEAIRLINLWLPKAVDDGHNLEAREQMAFG 245
           VTA TG+DALTHAVEAY ++ A P TD+ AL AI +I   LPKAV  GH+L ARE M   
Sbjct: 205 VTAMTGIDALTHAVEAYSALNATPFTDSLALGAIAMIGQALPKAVGYGHDLAARESMLLA 264

Query: 246 QYLAGMAFNSAGLGLVHALAHQPGATHNLPHGVCNAILLPIVENFNRPNAVARFARIAQA 305
             +AGMAF+SAGLGL HA+AHQPGA  ++PHG  NA+LLP V  FNR     RF +I +A
Sbjct: 265 SCMAGMAFSSAGLGLCHAMAHQPGAALHIPHGQANAMLLPTVMAFNRMVCRERFRQIGRA 324

Query: 306 MGVETRGMSDEAASQEAINAIRTLSKRVGIPEGFSKLGVTKEDIEGWLDKALADPCAPCN 365
           +      ++ +    EAI A+  L   VG+ +  S  G   E    W   A  D C   N
Sbjct: 325 L------IAKKTDDHEAIAAVEALIAEVGLSKRLSDAGAKPEHFSAWAQAAQEDICLRAN 378

Query: 366 PRTASRDEVRGLYLEA 381
           PRTA+R+++  LY  A
Sbjct: 379 PRTATREQIIDLYAAA 394


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: 414
Number of extensions: 16
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: 395
Length adjustment: 30
Effective length of query: 352
Effective length of database: 365
Effective search space:   128480
Effective search space used:   128480
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 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