GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Thiomicrospira cyclica ALM1

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_013834891.1 THICY_RS01725 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000214825.1:WP_013834891.1
          Length = 377

 Score =  509 bits (1310), Expect = e-149
 Identities = 247/366 (67%), Positives = 294/366 (80%), Gaps = 3/366 (0%)

Query: 20  VEPKTARFSEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAET 79
           V+P+T + S PL L  G  LPSY+LVYETYG+LN + SNAVLICHALSGDHH  G++ E 
Sbjct: 7   VKPQTLQVSMPLQLVSGAELPSYDLVYETYGELNADASNAVLICHALSGDHHVTGYY-EG 65

Query: 80  DRKPGWWDSAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVK 139
           D KPGWW   IGPGKP+DT+ FFVVC NNLGGC+GS+GP S++PA+GK YGPDFPIVT +
Sbjct: 66  DTKPGWWSDYIGPGKPVDTNEFFVVCSNNLGGCRGSSGPASLNPATGKVYGPDFPIVTCR 125

Query: 140 DWVHAQYRLMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIA 199
           DWV++Q  L Q+LG+  WAAVIGGS+GGMQV+QW+I +PD + HA+VIAAAP+LSAQNIA
Sbjct: 126 DWVNSQNTLRQHLGIEQWAAVIGGSMGGMQVMQWAIDHPDKLRHALVIAAAPKLSAQNIA 185

Query: 200 FNEVARQAIITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELRAGQ 259
           FNEVAR+AI+TDPEF GGR+ +    P+ GL LARMLGH+TYLSDD M AKFGRELR+  
Sbjct: 186 FNEVARRAIMTDPEFNGGRFIEAGTTPKGGLALARMLGHLTYLSDDMMGAKFGRELRSES 245

Query: 260 VQYGFDVEFQVESYLRYQGTSFVDR--FDANTYLLMTKALDYFDPAQASNDDLVAALAEV 317
           ++Y FDVEFQVESYLRYQG  F  +  FDANTYLLMTKALDYFDPA   +++L AA A+ 
Sbjct: 246 LKYSFDVEFQVESYLRYQGEKFATKQNFDANTYLLMTKALDYFDPAAEFDNNLSAAFAQT 305

Query: 318 KAHFLVVSFTSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLA 377
           +A FLVVSFTSDWRFSP RSREIVRALL + + VSYAEIES HGHDAFL+   +Y  +  
Sbjct: 306 QASFLVVSFTSDWRFSPTRSREIVRALLDNDRAVSYAEIESEHGHDAFLLPNTHYEGIFR 365

Query: 378 GYMANI 383
            YM  I
Sbjct: 366 AYMNRI 371


Lambda     K      H
   0.320    0.135    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: 539
Number of extensions: 20
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: 403
Length of database: 377
Length adjustment: 30
Effective length of query: 373
Effective length of database: 347
Effective search space:   129431
Effective search space used:   129431
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: 50 (23.9 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