GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Sinorhizobium fredii NGR234

Align low-specificity L-threonine aldolase (EC 4.1.2.48) (characterized)
to candidate WP_164923841.1 NGR_RS03350 low-specificity L-threonine aldolase

Query= BRENDA::P75823
         (333 letters)



>NCBI__GCF_000018545.1:WP_164923841.1
          Length = 344

 Score =  324 bits (831), Expect = 2e-93
 Identities = 168/327 (51%), Positives = 225/327 (68%), Gaps = 3/327 (0%)

Query: 2   IDLRSDTVTRPSRAMLEAMMAAPVGDDVYGDDPTVNALQDYAAELSGKEAAIFLPTGTQA 61
           +D RSDTVTRP+  M  AM AA VGDDV GDDPTV AL+   A L GKEA +F+PTGT +
Sbjct: 8   LDFRSDTVTRPTLGMRAAMAAAEVGDDVLGDDPTVKALEARLASLLGKEAGLFVPTGTMS 67

Query: 62  NLVALLSHCERGEEYIVGQAAHNYLFEAGGAAVLGSIQPQPIDAAADGTLPLDKVAMKIK 121
           NL A++SHC+RGEE++    AH YL+EAGGAAVLGS+QPQP+    DGT+PL+ +   +K
Sbjct: 68  NLAAIMSHCQRGEEFLCATGAHAYLWEAGGAAVLGSVQPQPLPVRTDGTIPLEDLHAAVK 127

Query: 122 PDDIHFARTKLLSLENTHNGKVLPREYLKEAWEFTRERNLALHVDGARIFNAVVAYGCEL 181
            DD HFA T+L+++ENT  G+VL R++L E  +F RER LA H+DGAR+FNA  A G ++
Sbjct: 128 DDDPHFAITRLVTIENTFAGRVLRRDHLAEVADFARERKLATHLDGARLFNAAAALGVDV 187

Query: 182 KEITQYCDSFTICLSKGLGTPVGSLLVGNRDYIKRAIRWRKMTGGGMRQSGILAAAGIYA 241
             +    D+ ++CLSKGLG P+GS+LVG+   + RA RWRKM GGGMRQ+GI+AAAG+YA
Sbjct: 188 GCLADGYDTVSLCLSKGLGAPLGSVLVGDAPLLARARRWRKMLGGGMRQAGIIAAAGLYA 247

Query: 242 LKNNVARLQEDHDNAAWMAEQLRE-AGADVMRQDTNMLFVRVGEENAAALGEYMKARNVL 300
           L ++V RL EDH NA  +A+      G  V    +N++FV +  + A  L E ++   + 
Sbjct: 248 LDHHVDRLVEDHANAQVLAQAFAGIEGMKVTPPQSNVVFVELAPDLATRLSEALRELGIA 307

Query: 301 INASP--IVRLVTHLDVSREQLAEVAA 325
            +  P   +R VTHLDV+R  + E  A
Sbjct: 308 ASFWPGGRMRWVTHLDVNRAAVDEAIA 334


Lambda     K      H
   0.319    0.134    0.391 

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: 348
Number of extensions: 13
Number of successful extensions: 2
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: 333
Length of database: 344
Length adjustment: 28
Effective length of query: 305
Effective length of database: 316
Effective search space:    96380
Effective search space used:    96380
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: 49 (23.5 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