GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Hyphomicrobium sulfonivorans WDL6

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate WP_068464883.1 APY04_RS16095 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>NCBI__GCF_001541235.1:WP_068464883.1
          Length = 399

 Score =  397 bits (1019), Expect = e-115
 Identities = 190/365 (52%), Positives = 259/365 (70%), Gaps = 5/365 (1%)

Query: 29  EPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWDS 88
           +PL L C + L    + YETYG+LN + SNA+L+CHAL+GD + A  H  T +KPGWW +
Sbjct: 37  QPLRLACDQLLAPISIAYETYGELNADKSNAILVCHALTGDQYVASEHPVT-KKPGWWST 95

Query: 89  AIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYRL 148
            +GPGKP+DT+R+FV+C N LGGC GSTGP S+DPA+GKPYG +FP++T+ D V+AQ RL
Sbjct: 96  LVGPGKPVDTNRYFVICSNILGGCMGSTGPASIDPATGKPYGLNFPVITIGDMVNAQVRL 155

Query: 149 MQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQAI 208
           + + G+    +V+GGS+GGMQVL+W+ ++ + V  AV IA APR S+QNIAF+EV RQA+
Sbjct: 156 IDHFGIDQLFSVVGGSMGGMQVLEWAASHSERVFSAVPIATAPRHSSQNIAFHEVGRQAV 215

Query: 209 ITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELR-AGQVQYGFDVE 267
           + DP++ GG Y  H  +PR GL +ARM  HITYLS+DA+  KFGR L+   Q+ + F+ +
Sbjct: 216 MADPDWCGGDYHSHGKVPRNGLSVARMAAHITYLSEDALHHKFGRNLQNRSQLTFSFNAD 275

Query: 268 FQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVKAHFLVVSFT 327
           FQVESYLR+QG++FVDRFDAN+YL +T+A+DYFD   +  D L  A    K  F VVSFT
Sbjct: 276 FQVESYLRHQGSTFVDRFDANSYLYITRAMDYFDLGASRGDVLANAFRGTKTRFCVVSFT 335

Query: 328 SDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGYMANIDFAS 387
           SDW +    SR IV AL A    VS+ EI+S+ GHDAFL+  P +   + G++++   A 
Sbjct: 336 SDWLYPTRESRAIVHALNAVAANVSFVEIDSDKGHDAFLLKEPEFFATIHGFLSS---AG 392

Query: 388 TPRGV 392
             RG+
Sbjct: 393 VKRGL 397


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: 488
Number of extensions: 17
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: 399
Length adjustment: 31
Effective length of query: 372
Effective length of database: 368
Effective search space:   136896
Effective search space used:   136896
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