GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Methylocapsa aurea KYG T

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_036258293.1 DL86_RS03570 low specificity L-threonine aldolase

Query= BRENDA::A0T1V9
         (348 letters)



>NCBI__GCF_000746085.1:WP_036258293.1
          Length = 354

 Score =  313 bits (802), Expect = 4e-90
 Identities = 165/349 (47%), Positives = 221/349 (63%), Gaps = 4/349 (1%)

Query: 1   MIFSSDNWAGAHPAIAESLVTHAKGYASAYGTSELDRKVEERFSEVFERDVAVFFVGTGT 60
           M F+SDN  GA   I ++++   KG + AYG      +  E   EVFE+++A F V TGT
Sbjct: 1   MDFTSDNTTGASQPILDAILAANKGPSPAYGADPFSARAAELLGEVFEKEIACFLVATGT 60

Query: 61  AANSLALSIANRAGGIAFCHREAHVNVDECGAPQFFSHGARLSAVGGARGKMDPAKLEAE 120
           A+N+LAL       G  FCH++AHV  DECGAP+ F+ GA+L  + G  GK+ P    A 
Sbjct: 61  ASNALALGALCPPWGAVFCHQDAHVLDDECGAPEMFTAGAKLVGIPGHAGKIAPRDFAAA 120

Query: 121 IRRFPKENVHGGQPMAVTLTQATESGTVYSLGEIEAIASIARSQTLPLHMDGARFANALV 180
           +  FP+  V   QP A++L+QATE G +Y+  E+  +A+IA    L +HMDGARFANALV
Sbjct: 121 LANFPRGVVKTVQPAALSLSQATECGALYTCAELSELAAIAHDAKLQVHMDGARFANALV 180

Query: 181 SLGTTPAEMTWKRGIDLLSFGGTKNGCWCAEALVLFDPSRAQEMHFLRKRSAQLFSKSRF 240
           +LGTTPAEM+WK GID+LSFG TKNG    EAL+ FDP RA  + + RKR     SK RF
Sbjct: 181 ALGTTPAEMSWKAGIDVLSFGATKNGALACEALIFFDPRRALNLPYQRKRGGHTLSKGRF 240

Query: 241 VAAQFDAYLAGDLWLDLARHANAMARRLADGITASAESRLAWAPDANEVFVVLKREAASR 300
           + AQ  AYL     L+LA+ ANA A RLA+G+  +   RL W  +ANEVF +L R+  + 
Sbjct: 241 LGAQMVAYLEKGHGLELAKTANARAVRLAEGLAKAPGVRLPWTREANEVFAILPRKTDAA 300

Query: 301 LRQQGALFYDWEVPHDLEGSL---AEDEGLFRLVTSFATRAEDVDRFVA 346
           L+  GAL+Y+W      +  +   +EDE   RLVTSFAT+A D++RF+A
Sbjct: 301 LKAAGALYYEWSF-RSFDPKIVLPSEDEVFVRLVTSFATQASDIERFLA 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: 328
Number of extensions: 13
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: 354
Length adjustment: 29
Effective length of query: 319
Effective length of database: 325
Effective search space:   103675
Effective search space used:   103675
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 Apr 10 2024. The underlying query database was built on Apr 09 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