GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Stenotrophomonas chelatiphaga DSM 21508

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_057508708.1 ABB28_RS11195 homoserine acetyltransferase

Query= SwissProt::Q8P6V8
         (369 letters)



>NCBI__GCF_001431535.1:WP_057508708.1
          Length = 343

 Score =  489 bits (1259), Expect = e-143
 Identities = 253/332 (76%), Positives = 277/332 (83%), Gaps = 2/332 (0%)

Query: 40  DTYTPAAD--SDAPPAVRGELVINLPMRHAGQRELRLRYELVGAEQAPVVFVAGGISAHR 97
           D++ P +    D   A RGE    L MRHAG R +RLRYE VG   APVV +AGGISA+R
Sbjct: 12  DSFVPVSVPVEDRVHAARGEFAAVLDMRHAGPRPIRLRYEWVGPADAPVVVLAGGISANR 71

Query: 98  HLAASAVFPEKGWVEGLVGAGRALDPASRRLLAFDFLGADGSLDAPIDTADQADAIAALL 157
           H+AA+A F EKGW EGLVG GR LDP   R+LAFDF+GADG+LD PIDTADQADA+A LL
Sbjct: 72  HVAANAQFVEKGWAEGLVGPGRTLDPQLLRVLAFDFIGADGALDVPIDTADQADALAILL 131

Query: 158 DALGIARLHGFVGYSYGALVGLQFASRHAARLHTLVAVSGAHRAHPYAAAWRALQRRAVA 217
           D LGIA+L  FVGYSYGALV  QF  RH  R+  LV VSGAHRAHPYAAAWRALQRRAVA
Sbjct: 132 DHLGIAQLQAFVGYSYGALVAQQFGVRHRPRVQRLVVVSGAHRAHPYAAAWRALQRRAVA 191

Query: 218 LGQLQCAEHHGLALARQFAMLSYRTPEEFSERFDAPPELINGRVRVAAEDYLDAAGAQYV 277
           LGQLQC++ +GLALARQFAMLSYRTPEEFSERFDA PE+INGRVRVAAEDYLDAA AQYV
Sbjct: 192 LGQLQCSDENGLALARQFAMLSYRTPEEFSERFDAAPEVINGRVRVAAEDYLDAAAAQYV 251

Query: 278 ARTPVNAYLRLSESIDLHRIDPAAVAVPTVVVAVEGDRLVPLADLVSLVEGLGPRGSLRV 337
           ARTPV A+LRLSESIDLHRI+PA + +PTVVVAVEGDRLVPLADLVSLVEGLGPRGSLRV
Sbjct: 252 ARTPVTAWLRLSESIDLHRIEPAQLLLPTVVVAVEGDRLVPLADLVSLVEGLGPRGSLRV 311

Query: 338 LRSPFGHDAFLKEIDRIDAILTTALRTTGETA 369
           LRSP+GHDAFLKE DRIDAIL  A+R  GETA
Sbjct: 312 LRSPYGHDAFLKETDRIDAILANAIRIPGETA 343


Lambda     K      H
   0.321    0.135    0.393 

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: 434
Number of extensions: 8
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: 369
Length of database: 343
Length adjustment: 29
Effective length of query: 340
Effective length of database: 314
Effective search space:   106760
Effective search space used:   106760
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