GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Mycolicibacterium vanbaalenii PYR-1

Align Uncharacterized lactate 2-monooxygenase PB1A11.03; EC 1.13.12.4 (characterized)
to candidate WP_011778563.1 MVAN_RS06560 alpha-hydroxy-acid oxidizing enzyme

Query= SwissProt::Q9HDX2
         (407 letters)



>NCBI__GCF_000015305.1:WP_011778563.1
          Length = 391

 Score =  187 bits (475), Expect = 5e-52
 Identities = 121/360 (33%), Positives = 190/360 (52%), Gaps = 24/360 (6%)

Query: 40  EQLAVERMTKDAAGYVYGCAGKRETYDKNMESFKKWSIIPNRLIKSGFPDLSTTVFGQKY 99
           +Q A +R+ K A   +   + K  T   N+ESF +    P+ +  +   D++T+V GQ  
Sbjct: 14  QQRAKKRLPKSAYSSLISASEKGVTVTDNVESFAELGFAPHVIGATEKRDMATSVLGQDI 73

Query: 100 PFPIALAPVGVQKIFNPEGESGSCAAATREHIPYIISTASATSFEDIEKASGPGERWYQL 159
             P+ ++P GVQ I +P+GE     AA        +S+ ++   ED+   +   + ++Q+
Sbjct: 74  SLPVIISPTGVQAI-DPDGEVAVARAAAARGTAMGLSSFASKPMEDVTAVND--KIFFQI 130

Query: 160 YWPSNDHQDITISLLNRAKKTGCRVLIVTLDTFILGWR-------PSDMDNGYDPFLNPD 212
           YW  +  +D  ++ + RA+  G + LI+T D      R       P  MD      ++P+
Sbjct: 131 YWLGS--RDDILARMERARAAGAKGLILTTDWSFAHGRDWGSPKIPERMDLKTMIRMSPE 188

Query: 213 SIGVEHGFSD-------PVFRKQFKEKHGVEVEENMLEAAKEFAGIVFPGISHDWEDLKF 265
            I     F         P  R   + + G E      EA  ++ G   P     WED+ +
Sbjct: 189 VITKPRWFFSFAKHLRPPDLRVPNQGRRG-EAGPTFFEAYGQWMGTPPP----TWEDVAW 243

Query: 266 LRKHWDGPIVLKGIMNVPDAKKAVEYGMQGIVVSNHGGRQQDGGVASLTMLPKIVDAVGD 325
           LR+ W GP +LKG + V DAK+AV+ G+  I VSNHGG   DG  A++  LP I DAVGD
Sbjct: 244 LREQWGGPFLLKGTVRVDDAKRAVDAGVSAITVSNHGGNNLDGTPAAIRCLPAIADAVGD 303

Query: 326 KLDVLFDSGVRSGADIAKALALGAKMVLIGRPYVYGLALEGSSGVSHVIRCLLGDLELTL 385
           +++VL D G+R G+D+ KA+ALGA+ V+IGR Y++GLA  G +GV +V+  L G ++  L
Sbjct: 304 QVEVLLDGGIRRGSDVVKAVALGARAVMIGRAYLWGLAANGQAGVENVLDILRGGIDSAL 363


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: 376
Number of extensions: 17
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: 407
Length of database: 391
Length adjustment: 31
Effective length of query: 376
Effective length of database: 360
Effective search space:   135360
Effective search space used:   135360
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