GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Beijerinckia mobilis UQM 1969

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_280949214.1 DL88_RS17420 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_000745425.1:WP_280949214.1
          Length = 411

 Score =  373 bits (958), Expect = e-108
 Identities = 185/365 (50%), Positives = 249/365 (68%), Gaps = 5/365 (1%)

Query: 29  EPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWDS 88
           +PLA+D G SL    + Y+TYG LN++ SNA+L+CHAL+GD H A  H  T  KPGWW  
Sbjct: 27  QPLAMDAGVSLAPLTIAYQTYGTLNEDKSNAILVCHALTGDQHVASDHPITG-KPGWWWI 85

Query: 89  AIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYRL 148
            +GPG+PIDT+R+FV+  N +GGC G+TGP S++PA+G+ +G D PIVT++D V AQ  L
Sbjct: 86  MVGPGRPIDTNRYFVISSNVVGGCMGTTGPASLNPATGRAWGLDLPIVTIRDMVKAQAML 145

Query: 149 MQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQAI 208
           + +LG+     V GGS+GGMQVLQW+ ++P  V  A+ IA A + S+QNIAF+EV RQ+I
Sbjct: 146 IDHLGIKTLFCVAGGSMGGMQVLQWAASFPGRVFAAMPIATAAKHSSQNIAFHEVGRQSI 205

Query: 209 ITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELRAGQV-QYGFDVE 267
           + DP +  GRY D    P +GL +ARM  HITYLSD+A+++KFGR+L+      + FD +
Sbjct: 206 MADPNWLAGRYLDQGTFPNKGLAVARMAAHITYLSDEALQSKFGRKLQGRSAPTFSFDAD 265

Query: 268 FQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVKAHFLVVSFT 327
           FQVE+YLR+QG SFVDRFDAN+YL +T+A DYFD A      L  A    K  F VVSF 
Sbjct: 266 FQVENYLRHQGASFVDRFDANSYLYVTRACDYFDLAADYGGSLAMAFKGTKTRFCVVSFQ 325

Query: 328 SDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGYMANIDFAS 387
           SDW ++   SR IV AL A G  VS+ +IE++ GHDAFL+  P +     G+   +D A+
Sbjct: 326 SDWLYTTADSRAIVHALNAGGASVSFVDIETDRGHDAFLLNEPEFIATTRGF---LDAAA 382

Query: 388 TPRGV 392
             RG+
Sbjct: 383 RARGL 387


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: 500
Number of extensions: 16
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: 411
Length adjustment: 31
Effective length of query: 372
Effective length of database: 380
Effective search space:   141360
Effective search space used:   141360
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 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