GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Methyloferula stellata AR4 AR4T

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_020173422.1 A3OQ_RS0100680 low specificity L-threonine aldolase

Query= BRENDA::A0T1V9
         (348 letters)



>NCBI__GCF_000385335.1:WP_020173422.1
          Length = 355

 Score =  303 bits (775), Expect = 6e-87
 Identities = 156/349 (44%), Positives = 217/349 (62%), Gaps = 4/349 (1%)

Query: 1   MIFSSDNWAGAHPAIAESLVTHAKGYASAYGTSELDRKVEERFSEVFERDVAVFFVGTGT 60
           M F+SDN  GAHP I E++V    G  ++YG     +K   R SE+FE + +VFFV TGT
Sbjct: 1   MDFTSDNTFGAHPKILEAIVATNSGPVASYGEDPFTQKAAARLSEIFEHETSVFFVATGT 60

Query: 61  AANSLALSIANRAGGIAFCHREAHVNVDECGAPQFFSHGARLSAVGGARGKMDPAKLEAE 120
           AAN+LAL       G  FCH +AH++ DECGAP+ F+ GA++  + G  GK+  A  +  
Sbjct: 61  AANALALGAVCPPWGAVFCHEDAHISEDECGAPEMFTAGAKIVGIPGFAGKISTANFKKA 120

Query: 121 IRRFPKENVHGGQPMAVTLTQATESGTVYSLGEIEAIASIARSQTLPLHMDGARFANALV 180
           +  FP+  V   QP  ++L+Q TE+GT Y+  +I ++A++A    L +HMDGARFANALV
Sbjct: 121 LASFPRGQVKQVQPAVLSLSQLTEAGTAYACEDIASLAALAHEAGLKVHMDGARFANALV 180

Query: 181 SLGTTPAEMTWKRGIDLLSFGGTKNGCWCAEALVLFDPSRAQEMHFLRKRSAQLFSKSRF 240
           +   +PA M+W+ GID+LS G TKNG    EA++ FDP+ A+   + RKRS    SK RF
Sbjct: 181 AQNCSPAAMSWQAGIDVLSLGATKNGALACEAVIFFDPAMAEAFAYQRKRSGHTVSKGRF 240

Query: 241 VAAQFDAYLAGDLWLDLARHANAMARRLADGITASAESRLAWAPDANEVFVVLKREAASR 300
           + AQ  AYL   LWL LA+ AN  A RLA G+      RL W PDANE+FV++     +R
Sbjct: 241 LGAQMLAYLDAGLWLGLAKIANDHAARLAAGLAKIPGVRLPWLPDANEIFVIIPGAIDNR 300

Query: 301 LRQQGALFYDW---EVPHDLEGSLAEDEGLFRLVTSFATRAEDVDRFVA 346
           L+  GA +Y+W   + P ++    +E E   RLVTS+AT + D+DR +A
Sbjct: 301 LKAAGAAYYEWGLRDYPPEVIPP-SEGEVFVRLVTSYATASADIDRLIA 348


Lambda     K      H
   0.320    0.132    0.394 

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: 326
Number of extensions: 10
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: 348
Length of database: 355
Length adjustment: 29
Effective length of query: 319
Effective length of database: 326
Effective search space:   103994
Effective search space used:   103994
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 Jul 25 2024. The underlying query database was built on Jul 25 2024.

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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