GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Prosthecochloris aestuarii DSM 271

Align kynurenine-oxoglutarate transaminase (EC 2.6.1.7); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized)
to candidate WP_041702288.1 PAES_RS06865 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q6YP21
         (454 letters)



>NCBI__GCF_000020625.1:WP_041702288.1
          Length = 402

 Score =  150 bits (379), Expect = 7e-41
 Identities = 106/352 (30%), Positives = 173/352 (49%), Gaps = 29/352 (8%)

Query: 29  FSTSAKMSLKFTNAKRIEGLDSNVWIEFTKLAADPSVVNLGQGFPDISPPTYVKEELSKI 88
           + T   ++++ +   RI GL   +  E         +V+L  G PD   P +V +  + I
Sbjct: 11  YLTRRVLNMQESQTMRITGLAKKMKAE------GKDIVSLSAGEPDFPTPLFVSQ--AGI 62

Query: 89  AAIDSLNQYTRGFGHPSLVKALSYLYEKLYQ-KQID-SNKEILVTVGAYGSLFNTIQALI 146
            AIDS   +TR   +  + +  S +  KL +  Q+D +  E++V+ G   +L N I AL 
Sbjct: 63  EAIDS--GFTRYTANSGIAELKSAVIAKLKRDNQLDYTPDEVIVSNGGKQTLINAILALC 120

Query: 147 DEGDEVILIVPFYDCYEPMVRMAGATPVFIPLRSKPVYGKRWSSSDWTLDPQELESKFNS 206
            EGDEVI+  P++  +  MVR+AGA+PV +P   +  Y          + P++LE+    
Sbjct: 121 QEGDEVIIPAPYWVSFPEMVRLAGASPVTVPTSIENGY---------KMTPEDLENAITD 171

Query: 207 KTKAIILNTPHNPLGKVYNREELQVIADLCIKYDTLCISDEVYEWLVYSGNKHLKIATFP 266
           KTK  ILN+P NP G VYN +E+  +  +        ISDE+Y+ +VY   K    A   
Sbjct: 172 KTKLFILNSPSNPSGAVYNEQEVTALMQVLEGRGIFVISDEMYDKIVYGDVKPYSPARIE 231

Query: 267 GMWERTITIGSAGKTFSVTGWKLGWSIGPNHLIKHLQTVQQNTIYTCATPLQEALAQAFW 326
            M +  +      KT+++TGW++G+  GP  +IK    +Q  T     +  Q+A A A  
Sbjct: 232 AMRDWVLVSNGVSKTYAMTGWRIGYLAGPKWIIKACDKIQSQTTSNPNSIAQKAAAAALN 291

Query: 327 IDIKRMDDPECYFNSLPKELEVKRDRMVRLLESV-GLKPIVPDGGYFIIADV 377
            D + ++D          E E +RD M + L  + G+   +P+G ++I   V
Sbjct: 292 GDQQVVEDRRL-------EFEKRRDYMYKALNEIPGITASLPEGAFYIFPSV 336


Lambda     K      H
   0.319    0.135    0.407 

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: 398
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: 454
Length of database: 402
Length adjustment: 32
Effective length of query: 422
Effective length of database: 370
Effective search space:   156140
Effective search space used:   156140
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 (21.8 bits)
S2: 51 (24.3 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