GapMind for catabolism of small carbon sources

 

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

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_011778448.1 MVAN_RS05945 threonine aldolase

Query= BRENDA::O50584
         (346 letters)



>NCBI__GCF_000015305.1:WP_011778448.1
          Length = 343

 Score =  219 bits (557), Expect = 1e-61
 Identities = 132/339 (38%), Positives = 187/339 (55%), Gaps = 5/339 (1%)

Query: 5   SQQFASDNYSGICPEAWAAMEKANHGHERAYGDDQWTARAADHFRKLFETD-CEVFFAFN 63
           S  FASDN +   P    A+   N G   +YGDD  TA AA+  R  FE+   +V FAF 
Sbjct: 6   SAAFASDNAAPAHPRVLEALHHVNQGPAPSYGDDPVTAEAAEALRTAFESPGADVLFAFT 65

Query: 64  GTAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLTARSEGGKLTPASIR 123
           GTAAN +AL+S  + +H + CS+ AHV  DE G P   S G++L    S+ G ++P  + 
Sbjct: 66  GTAANIIALASAVRPWHEIFCSDVAHVLVDEAGGPVRLS-GAQLTRLASDDGLISPDELE 124

Query: 124 EVALKRQDIHYPKPRVVTITQATEVGSVYRPDELKAISATCKELGLNLHMDGARFSNACA 183
                R  +H+ +PR+V+ITQ+TE G V+    +         LGL +H+DGAR +NA A
Sbjct: 125 RRVRGRSAVHHSQPRIVSITQSTENGRVWSATAVAQFVDRAHALGLLVHVDGARIANAVA 184

Query: 184 FLGCTPAELTWKAGIDVLCFGGTKNGMAVGEAILFFNRKLAEDFDYRCKQAGQLASKMRF 243
            L  +P E    A  D++  GGTKNG+  G+AIL       +   +  KQ G LASK RF
Sbjct: 185 ALSISPLEAIGDA--DIVSVGGTKNGLMFGDAILVRRPAHFDGIHFVQKQIGHLASKHRF 242

Query: 244 LSAPWVGLLEDGAWLRHAAHANHCAQLLSSLVADIPGVELMFPVEANGVFLQMSEPALEA 303
           ++A + GL E G WLR+AAHAN  A+ LS+ +  + G++L  P E+N VF+++   A   
Sbjct: 243 VAAQFAGLFEGGLWLRNAAHANAMARRLSTGLEAL-GLQLASPTESNEVFVKLDGEAHRR 301

Query: 304 LRNKGWRFYTFIGSGGARFMCSWDTEEARVRELAADIRA 342
           L  +        G    RF+CSW T E  V +  A +R+
Sbjct: 302 LAERYLVHQPDPGQPVVRFVCSWSTTETEVDDALAALRS 340


Lambda     K      H
   0.321    0.133    0.413 

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: 318
Number of extensions: 18
Number of successful extensions: 6
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: 346
Length of database: 343
Length adjustment: 29
Effective length of query: 317
Effective length of database: 314
Effective search space:    99538
Effective search space used:    99538
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 (21.9 bits)
S2: 49 (23.5 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