GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Methylobacterium sp. 4-46

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_043702076.1 M446_RS05285 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000019365.1:WP_043702076.1
          Length = 390

 Score =  374 bits (960), Expect = e-108
 Identities = 182/353 (51%), Positives = 241/353 (68%), Gaps = 2/353 (0%)

Query: 30  PLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWDSA 89
           PLA+D G +L  +++ Y+T G+LN   SNAVL+CHAL+GD H A  H  T  KPGWW++ 
Sbjct: 31  PLAMDAGVALAPWQIAYQTVGRLNAARSNAVLVCHALTGDQHVASRHPLTG-KPGWWETV 89

Query: 90  IGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYRLM 149
           +GPGKP+DTDR+FV+C N +G C G+TGP S++PA+G PYG DFP+VT++D V  Q  L+
Sbjct: 90  VGPGKPVDTDRYFVICANVVGSCMGTTGPASINPATGHPYGLDFPLVTIRDMVRGQAMLL 149

Query: 150 QYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQAII 209
             LG+      IGGS+GGMQVLQW+ +YP+ V  A+ IA   R SAQNIAF+EV RQA++
Sbjct: 150 DRLGIPDLFLCIGGSMGGMQVLQWAASYPERVFAAMPIATGARHSAQNIAFHEVGRQAVM 209

Query: 210 TDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELRAGQV-QYGFDVEF 268
            DP ++GGRY D    P +GL +ARM  HITYLS+ A+  KFGR  +      + FD +F
Sbjct: 210 ADPAWHGGRYLDVGTRPAKGLAVARMGAHITYLSEPALHRKFGRRFQDRDAPTFSFDADF 269

Query: 269 QVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVKAHFLVVSFTS 328
           Q+ESYLR+QG SFV+RFDAN YL +T+A+DYFD A      L  A    +  F V+SFTS
Sbjct: 270 QIESYLRHQGISFVERFDANAYLYLTRAMDYFDLAADHGGVLANAFRGSRTRFCVMSFTS 329

Query: 329 DWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGYMA 381
           DW F    SR IV AL A+  +V++ E+ES+ GHDAFL+  P       G++A
Sbjct: 330 DWLFPTPDSRAIVHALNAAAARVAFVEVESDKGHDAFLLDEPAMFAAACGFIA 382


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: 476
Number of extensions: 14
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: 390
Length adjustment: 31
Effective length of query: 372
Effective length of database: 359
Effective search space:   133548
Effective search space used:   133548
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