GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Nitratifractor salsuginis DSM 16511

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_245526293.1 NITSA_RS07550 pyridoxal phosphate-dependent aminotransferase

Query= BRENDA::Q8YMS6
         (388 letters)



>NCBI__GCF_000186245.1:WP_245526293.1
          Length = 378

 Score =  383 bits (983), Expect = e-111
 Identities = 184/374 (49%), Positives = 268/374 (71%), Gaps = 2/374 (0%)

Query: 14  ITLAIAAKAKAMKAEGIDVCSFSAGEPDFDTPAHIKAAAAKALDEGKTKYGAAAGEPKLR 73
           +T+A++  A+ +KA+G D+ SFSAGEPDFDTP  IK AA  A+ +G TKY + AG P+L 
Sbjct: 1   MTIAVSTLARELKAQGKDILSFSAGEPDFDTPERIKEAAIDAIRQGHTKYTSVAGIPELL 60

Query: 74  EAIARKLQKDNHLDYKPENVIVTNGGKHSLYNLIVALIDPGDEVIIPAPYWLSYPEMVTL 133
           +AI+ K +++N L+Y  E+++V+NG K SL+NL  ALID GDEVIIPAPYW++YPE+V+ 
Sbjct: 61  DAISEKFRRENRLEYAREHLLVSNGAKQSLFNLTQALIDEGDEVIIPAPYWVTYPELVSY 120

Query: 134 VGGKSVIVPTDASTGYKITPEQLRKAITPKTKLFVLNSPSNPTGMVYTPEEIKALAQVVV 193
            GGK VI+ TD  +G+KITP+QL  AITP+TK+ +L SPSNPTG VY  +E++AL +V+ 
Sbjct: 121 AGGKPVIIDTDDRSGFKITPDQLEAAITPRTKMLILTSPSNPTGSVYDGKELEALGKVLE 180

Query: 194 DADIYVVSDEIYEKILYDGAQHISIGSLGKEIFNRTLISNGFAKAYSMTGWRLGYLAGP- 252
              + VVSDE+YEK+++DG + ++  S+ ++++ RT+  NG +K+ +MTGWR+GYLA P 
Sbjct: 181 GTPVTVVSDEMYEKLVFDGTEFVATASISEDLYRRTVTVNGLSKSVAMTGWRMGYLATPD 240

Query: 253 VDIIKAASSIQGHSTSNVCTFAQYGAI-AALEDSQDCVEEMRQAFAKRRQVMLDRLNAIP 311
            +++K   S+Q  STSN+ T  QY +I   L +  D +E MRQAF  R    ++  NAI 
Sbjct: 241 TELVKKMISLQSQSTSNINTITQYASIPPLLGEVDDEIETMRQAFEARMHEAVELFNAID 300

Query: 312 GLSTAKPDGAFYLFPDISKTGLKSLEFCDALIEEHKVAVIPGIAFGADDNIRLSYATDLA 371
           G+S  +P GAFYLF +I   G+ S+ F   L++++ VAV+PGI FG++   R SYA D+ 
Sbjct: 301 GISVLRPKGAFYLFVNIKDLGIDSMTFSQELLKKYGVAVVPGIGFGSEGYFRFSYAADIV 360

Query: 372 TIEKGLDRLEKFVR 385
           TI +G+ R+EKFV+
Sbjct: 361 TIREGVRRIEKFVK 374


Lambda     K      H
   0.317    0.134    0.381 

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: 374
Number of extensions: 13
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: 388
Length of database: 378
Length adjustment: 30
Effective length of query: 358
Effective length of database: 348
Effective search space:   124584
Effective search space used:   124584
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: 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