GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Streptacidiphilus oryzae TH49

Align Uncharacterized lactate 2-monooxygenase PB1A11.03; EC 1.13.12.4 (characterized)
to candidate WP_037571249.1 BS73_RS10185 lactate 2-monooxygenase

Query= SwissProt::Q9HDX2
         (407 letters)



>NCBI__GCF_000744815.1:WP_037571249.1
          Length = 386

 Score =  344 bits (883), Expect = 2e-99
 Identities = 178/375 (47%), Positives = 246/375 (65%), Gaps = 9/375 (2%)

Query: 15  SYESEIYAKGLKFQRPQITVDGRHWEQLAVERMTKDAAGYVYGCAGKRETYDKNMESFKK 74
           +++ EIY  GL  + P++  D     ++A  R+     GYV G AG  +T   N E+  +
Sbjct: 6   AFQYEIYLNGLLGKVPRLPTDLSRLAEIAEARLPAGPYGYVAGNAGGGKTEAANREALDR 65

Query: 75  WSIIPNRLIKSGFPDLSTTVFGQKYPFPIALAPVGVQKIFNPEGESGSCAAATREHIPYI 134
           W I+P  L   G  DLS  V G++ P P+ALAPVGV  I +P+ E+ +  AA    +P+ 
Sbjct: 66  WRIVPRMLRDVGTRDLSVEVLGRRLPAPVALAPVGVLSIMHPDAETAAARAAAEVGVPFT 125

Query: 135 ISTASATSFEDIEKASGPGERWYQLYWPSNDHQDITISLLNRAKKTGCRVLIVTLDTFIL 194
           +S+AS+TS ED+ +ASG GERW+QLYWP +  +++T S L RAK++G   L+VTLDT++L
Sbjct: 126 LSSASSTSMEDVAEASGEGERWFQLYWPKD--REVTKSFLRRAKESGYSALLVTLDTWLL 183

Query: 195 GWRPSDMDNGYDPFLNPDSIGVEHGFSDPVFRKQFKEKHGVEVEENMLEAAKEFAGIVFP 254
            WRP D+D  Y PFL+   IG E+ F+DP F     +       E++  A   F G+ F 
Sbjct: 184 SWRPRDLDQAYLPFLH--GIGTENYFTDPAFLAGLAKPP----VEDLQAAVMHFVGM-FN 236

Query: 255 GISHDWEDLKFLRKHWDGPIVLKGIMNVPDAKKAVEYGMQGIVVSNHGGRQQDGGVASLT 314
             +  W+DL F+R++WDGPIVLKG+++  DA++A + GM GIVVSNHGGRQ  G + +  
Sbjct: 237 DPTKTWDDLDFIRENWDGPIVLKGVLHPDDARRAADAGMDGIVVSNHGGRQVAGAIGAAD 296

Query: 315 MLPKIVDAVGDKLDVLFDSGVRSGADIAKALALGAKMVLIGRPYVYGLALEGSSGVSHVI 374
            LP I +AVGD+LDVLFDSG+R G D AKALALGAK VL+GRP+VY L L+G +GV HV+
Sbjct: 297 ALPAIAEAVGDRLDVLFDSGIRGGEDTAKALALGAKTVLLGRPWVYALGLDGQAGVEHVL 356

Query: 375 RCLLGDLELTLHLSG 389
           R  L +L+LTL LSG
Sbjct: 357 RAHLAELDLTLALSG 371


Lambda     K      H
   0.319    0.138    0.421 

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: 445
Number of extensions: 21
Number of successful extensions: 3
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: 407
Length of database: 386
Length adjustment: 31
Effective length of query: 376
Effective length of database: 355
Effective search space:   133480
Effective search space used:   133480
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 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