GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Desulfobacter vibrioformis DSM 8776

Align Homocitrate synthase AksA; EC 2.3.3.14; (R)-homo(2)citrate synthase; EC 2.3.3.-; (R)-homo(3)citrate synthase; EC 2.3.3.- (uncharacterized)
to candidate WP_035240746.1 Q366_RS15935 citramalate synthase

Query= curated2:Q8TW28
         (397 letters)



>NCBI__GCF_000745975.1:WP_035240746.1
          Length = 544

 Score =  179 bits (453), Expect = 2e-49
 Identities = 122/352 (34%), Positives = 183/352 (51%), Gaps = 22/352 (6%)

Query: 18  EVIVYDTTLRDGEQTPGVSFTPEQKLEIAHLLDELGVQQIEAGFPVVSEGER---DAVRR 74
           +V++YDTTLRDG Q   + F+P  KL+IA  LD+ G+  IE G+P  + G +   D VR 
Sbjct: 9   KVLLYDTTLRDGMQGENIFFSPGDKLKIAMRLDDAGIHYIEGGWPGSNPGAQAFFDLVRD 68

Query: 75  IAHEGLNADILCLARTLR--------GDVDAALDCDVDGVITFIATSELHLKHKLRMSRE 126
              +   A I     T R         ++ A +D     V  F  + +LH+   +  +RE
Sbjct: 69  TPFK--QAKICAFGSTRRQNSTCEKDSNIKALIDSGAPVVTIFGKSWDLHVSDIMNNTRE 126

Query: 127 EVLERIADTVEYAKDHGLWVAFSAE---DGTRTEFEFLERVYRTAEECGADRVHATDTVG 183
           E L  I ++V Y K  G  V + AE   DG +    F       A + G   +   DT G
Sbjct: 127 ENLAMITESVSYLKARGREVLYDAEHFYDGYKANPGFALETLGAALKGGTRCLVLCDTNG 186

Query: 184 VMIPAAM----RLFVAKIREVVDLPIGVHCHDDFGMAVANSLAAVEAGAQAISTTVNGIG 239
             +P  +    R  +A  ++  D+  GVH H+D  MAVAN++ AV AGA  +  TVNG G
Sbjct: 187 GCLPCDIDTITRETIAHFKDYEDVIFGVHTHNDCAMAVANAINAVHAGAIMVQGTVNGYG 246

Query: 240 ERAGNAALEEVI--MALKELYGIDPGFNTEVLAELSRKVSEYSGIDVPPNKAVVGENAFR 297
           ER GNA L  +I  +ALK         N   L  LSR VSE + +    ++  VG +AF 
Sbjct: 247 ERCGNADLTALIPILALKMNRACISEKNLAKLQNLSRFVSETANMPPVASRPFVGRSAFT 306

Query: 298 HESGIHVAAVLEEPRTYEPIDPKEVGMNRKIVLGKHTGRKAVVAKLEELGVE 349
           H+ G+HV+A+++ PR YE + P+ VG  R++++ + +G+  +  K +ELGV+
Sbjct: 307 HKGGVHVSAIMKNPRAYEHMSPEFVGNRRRVLVSEQSGKSNITYKAKELGVD 358


Lambda     K      H
   0.317    0.135    0.380 

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: 463
Number of extensions: 30
Number of successful extensions: 4
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: 397
Length of database: 544
Length adjustment: 33
Effective length of query: 364
Effective length of database: 511
Effective search space:   186004
Effective search space used:   186004
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 51 (24.3 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