GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metA in Caulobacter crescentus NA1000

Align Homoserine O-succinyltransferase; HST; Homoserine transsuccinylase; HTS; EC 2.3.1.46 (characterized)
to candidate CCNA_00559 CCNA_00559 homoserine O-acetyltransferase

Query= SwissProt::D0L1T6
         (403 letters)



>FitnessBrowser__Caulo:CCNA_00559
          Length = 382

 Score =  398 bits (1022), Expect = e-115
 Identities = 191/358 (53%), Positives = 255/358 (71%), Gaps = 2/358 (0%)

Query: 28  SEPLALDCGRSLPSYELVYETYGQLNDEGSNAVLICHALSGDHHAAGFHAETDRKPGWWD 87
           +EPL LD G  +   E+ Y+TYGQLN + SNAVLICHAL+GD H A  H  T  KPGWW 
Sbjct: 20  NEPLRLDSGGVIEGLEIAYQTYGQLNADKSNAVLICHALTGDQHVASPHPTTG-KPGWWQ 78

Query: 88  SAIGPGKPIDTDRFFVVCLNNLGGCKGSTGPLSVDPASGKPYGPDFPIVTVKDWVHAQYR 147
             +GPGKP+D  R F++C N +GGC GSTGP S++PA+GK YG  FP++T+ D V AQ  
Sbjct: 79  RLVGPGKPLDPARHFIICSNVIGGCMGSTGPASINPATGKTYGLSFPVITIADMVRAQAM 138

Query: 148 LMQYLGLSGWAAVIGGSLGGMQVLQWSITYPDAVAHAVVIAAAPRLSAQNIAFNEVARQA 207
           L+  LG+    AV+GGS+GGMQV QW++ YP+ +  AVV+A+A R SAQNIAF+EV RQA
Sbjct: 139 LVSALGVETLFAVVGGSMGGMQVQQWAVDYPERMFSAVVLASASRHSAQNIAFHEVGRQA 198

Query: 208 IITDPEFYGGRYADHNALPRRGLMLARMLGHITYLSDDAMRAKFGRELRAGQVQYGFDVE 267
           I+ DP++ GG YA+H   P +GL +ARM  HITYLS+ A++ KFGREL+   + +GFD +
Sbjct: 199 IMADPDWRGGAYAEHGVRPEKGLAVARMAAHITYLSEPALQRKFGRELQRDGLSWGFDAD 258

Query: 268 FQVESYLRYQGTSFVDRFDANTYLLMTKALDYFDPAQASNDDLVAALAEVK-AHFLVVSF 326
           FQVESYLR+QG+SFVDRFDAN+YL +T+A+DYFD A +    L  A    +   F V+SF
Sbjct: 259 FQVESYLRHQGSSFVDRFDANSYLYITRAMDYFDIAASHGGVLAKAFTRARNVRFCVLSF 318

Query: 327 TSDWRFSPERSREIVRALLASGKQVSYAEIESNHGHDAFLMTIPYYHRVLAGYMANID 384
           +SDW +    +R +VRAL A+G + ++AEIES+ GHDAFL+  P     L G++A+ +
Sbjct: 319 SSDWLYPTAENRHLVRALTAAGARAAFAEIESDKGHDAFLLDEPVMDAALEGFLASAE 376


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: 497
Number of extensions: 15
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: 382
Length adjustment: 31
Effective length of query: 372
Effective length of database: 351
Effective search space:   130572
Effective search space used:   130572
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 09 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