GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Steroidobacter denitrificans DSM 18526

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_083536601.1 ACG33_RS08120 hypothetical protein

Query= SwissProt::F4QV02
         (369 letters)



>NCBI__GCF_001579945.1:WP_083536601.1
          Length = 363

 Score =  230 bits (587), Expect = 4e-65
 Identities = 130/323 (40%), Positives = 178/323 (55%), Gaps = 17/323 (5%)

Query: 61  LDFGGTLTQKRVIGRLHGKANAPLIVVAGGISADRYVHRTETKGLGWWSGAVGVRAPIDL 120
           L FGG L    V  R+ G   APL+   GGISA R V   +    GWW G +GV   +DL
Sbjct: 29  LTFGGRLDTVSVAWRVSGNPQAPLVAALGGISAGRAVADVDKTQKGWWGGIIGVGKALDL 88

Query: 121 TRFRVLAFDFAPEFGEDVKDAKTPL---TITTQDQARLLALLLDHLG------------- 164
            +++VL  DF    G         +   +I+T DQA +L  +L H+              
Sbjct: 89  NQYQVLGIDFLGGSGTTTGPRPGQVDFPSISTTDQAEILRQVLAHVRQSAIPGKGASTGR 148

Query: 165 VEKVAAFIGCSYGGMIALAFGELFPDWAEQLVVVSAAHRPHPLATAWRGIQRRILQLGLE 224
           +  +AA IG SYGGM+ALAF + +P   E++VV+SAA +PHPL+TAWR ++R +++    
Sbjct: 149 IHPLAAIIGASYGGMVALAFAQRWPQLVERIVVISAADQPHPLSTAWRSVERAVVRYATA 208

Query: 225 TGRIDQAVGLARELAMTTYRTQEEFGDRFDSEAPSHAGQ-AYPVCDYLQARGRAYRDRTT 283
            G   + + LAR LAMTTYR+  EF DRFD  A    G+  +PV  YL ARG AY     
Sbjct: 209 RGDGPEGLRLARALAMTTYRSAREFADRFDQPAVRIDGRYQFPVESYLLARGDAYAANYI 268

Query: 284 PSRWLSLSDSIDRHRVEPEAITAPVTLIGFTTDRLCPIEDMRELADRLPNLWRFEQHASV 343
           P  ++ LS+SID HR++   +    TL+G   D+L PI DMR L  RL    R  + +S+
Sbjct: 269 PEAFVCLSESIDLHRIDASQVRVSTTLVGIVEDQLVPIADMRRLQQRLGGPVRLVELSSL 328

Query: 344 YGHDAFLKEDKLVADILTSVLKD 366
           YGHDAFLKE   +  +  + L D
Sbjct: 329 YGHDAFLKETDALRQVFAAALND 351


Lambda     K      H
   0.321    0.137    0.412 

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: 354
Number of extensions: 12
Number of successful extensions: 3
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: 369
Length of database: 363
Length adjustment: 30
Effective length of query: 339
Effective length of database: 333
Effective search space:   112887
Effective search space used:   112887
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: 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