GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Pseudomonas benzenivorans DSM 8628

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_090448703.1 BLS63_RS26060 low specificity L-threonine aldolase

Query= BRENDA::O50584
         (346 letters)



>NCBI__GCF_900100495.1:WP_090448703.1
          Length = 347

 Score =  629 bits (1622), Expect = 0.0
 Identities = 296/345 (85%), Positives = 326/345 (94%)

Query: 1   MTDQSQQFASDNYSGICPEAWAAMEKANHGHERAYGDDQWTARAADHFRKLFETDCEVFF 60
           M+D SQQFASDNYSGICPEAWAAM +ANHGH+RAYGDDQWTARAAD FR+LFETDCEVFF
Sbjct: 1   MSDSSQQFASDNYSGICPEAWAAMAEANHGHDRAYGDDQWTARAADQFRQLFETDCEVFF 60

Query: 61  AFNGTAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLTARSEGGKLTPA 120
           AFNGTAANSLAL++LCQSYHSVICSETAHVETDECGAPEFFSNGSKLL A +E GKLTPA
Sbjct: 61  AFNGTAANSLALAALCQSYHSVICSETAHVETDECGAPEFFSNGSKLLLAHTENGKLTPA 120

Query: 121 SIREVALKRQDIHYPKPRVVTITQATEVGSVYRPDELKAISATCKELGLNLHMDGARFSN 180
           +IRE+ALKRQDIHYPKP+VV++TQATEVG+VYRP E++AISATC+ELGLNLHMDGARFSN
Sbjct: 121 AIREIALKRQDIHYPKPKVVSLTQATEVGTVYRPAEVRAISATCRELGLNLHMDGARFSN 180

Query: 181 ACAFLGCTPAELTWKAGIDVLCFGGTKNGMAVGEAILFFNRKLAEDFDYRCKQAGQLASK 240
           ACAFLGCTPAELTW+AG+DVLCFGGTKNGMAVGEAILFFN+ LAEDFDYRCKQAGQLASK
Sbjct: 181 ACAFLGCTPAELTWEAGVDVLCFGGTKNGMAVGEAILFFNKALAEDFDYRCKQAGQLASK 240

Query: 241 MRFLSAPWVGLLEDGAWLRHAAHANHCAQLLSSLVADIPGVELMFPVEANGVFLQMSEPA 300
           MR+LSAPWVGLL++ AWL +A HAN CA+LL+ LV+D+PGV LMFPVEANGVFLQMSEPA
Sbjct: 241 MRYLSAPWVGLLQNDAWLYYAGHANRCARLLAELVSDVPGVSLMFPVEANGVFLQMSEPA 300

Query: 301 LEALRNKGWRFYTFIGSGGARFMCSWDTEEARVRELAADIRAVMS 345
           LEALR +GWRFYTFIG+GGARFMCSWDT E RVRELAADIR  M+
Sbjct: 301 LEALRARGWRFYTFIGAGGARFMCSWDTAEERVRELAADIRTAMA 345


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: 502
Number of extensions: 10
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: 346
Length of database: 347
Length adjustment: 29
Effective length of query: 317
Effective length of database: 318
Effective search space:   100806
Effective search space used:   100806
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.

Links

Downloads

Related tools

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